Celera Corporation

United States of America

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C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids 38
C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material 30
C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical 22
C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides 14
C12Q 1/6827 - Hybridisation assays for detection of mutation or polymorphism 14
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1.

Genetic polymorphisms associated with stroke, methods of detection and uses thereof

      
Application Number 17849982
Grant Number 12077825
Status In Force
Filing Date 2022-06-27
First Publication Date 2023-04-13
Grant Date 2024-09-03
Owner Celera Coporation (USA)
Inventor
  • Luke, May
  • Devlin, James J.

Abstract

The present invention provides compositions and methods based on genetic polymorphisms that are associated with vascular diseases such as stroke. In particular, the present invention relates to genetic polymorphisms that have utility for such uses as predicting disease risk or predicting an individual's response to a treatment such as statins, including groups of polymorphisms that may be used as a signature marker set for such uses, as well as nucleic acid molecules containing the polymorphisms, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • A61K 31/22 - Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
  • A61K 31/35 - Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
  • A61K 31/40 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
  • A61K 31/404 - Indoles, e.g. pindolol
  • A61K 31/435 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom

2.

GENETIC POLYMORPHISMS ASSOCIATED WITH CARDIOVASCULAR DISEASES, METHODS OF DETECTION AND USES THEREOF

      
Application Number 17852737
Status Pending
Filing Date 2022-06-29
First Publication Date 2023-03-30
Owner
  • Celera Corporation (USA)
  • University of Texas Board of Regents (USA)
Inventor
  • Shiffman, Dov
  • Devlin, James J.
  • Louie, Judy Z.
  • Boerwinkle, Eric

Abstract

The present invention provides compositions and methods based on genetic polymorphisms that are associated with cardiovascular diseases, particularly coronary heart disease (especially myocardial infarction) or hypertension. For example, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material

3.

GENETIC POLYMORPHISMS ASSOCIATED WITH VENOUS THROMBOSIS AND STATIN RESPONSE, METHODS OF DETECTION AND USES THEREOF

      
Application Number 17668697
Status Pending
Filing Date 2022-02-10
First Publication Date 2022-10-27
Owner
  • Celera Corporation (USA)
  • Leiden University Medical Center (LUMC) Acting on behalf of Academic Hospital Lieden (AZL) (Netherlands)
Inventor
  • Bare, Lance
  • Devlin, James J.
  • Rosendaal, Frits R.
  • Reitsma, Pieter H.
  • Bezemer, Irene D.

Abstract

The present invention provides compositions and methods based on genetic polymorphisms that are associated with response to statin treatment (particularly for reducing the risk of venous thrombosis). For example, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • A61K 31/00 - Medicinal preparations containing organic active ingredients
  • A61K 31/137 - Arylalkylamines, e.g. amphetamine, epinephrine, salbutamol, ephedrine
  • A61K 31/37 - Coumarins, e.g. psoralen
  • A61K 31/4439 - Non-condensed pyridinesHydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
  • A61K 31/4545 - Non-condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
  • A61K 31/5377 - 1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
  • A61K 45/06 - Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • A61K 45/00 - Medicinal preparations containing active ingredients not provided for in groups
  • A61K 31/22 - Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
  • A61K 31/366 - Lactones having six-membered rings, e.g. delta-lactones
  • A61K 31/40 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil

4.

Genetic polymorphisms associated with coronary events and drug response, methods of detection and uses thereof

      
Application Number 17215307
Grant Number 11814684
Status In Force
Filing Date 2021-03-29
First Publication Date 2022-05-19
Grant Date 2023-11-14
Owner Celera Corporation (USA)
Inventor
  • Iakoubova, Olga
  • Devlin, James J.
  • Tong, Carmen
  • Rowland, Charles

Abstract

The present invention provides compositions and methods based on genetic polymorphisms that are associated with coronary heart disease (particularly myocardial infarction), aneurysm/dissection, and/or response to drug treatment, particularly statin treatment. For example, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • G01N 33/68 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving proteins, peptides or amino acids

5.

Genetic polymorphisms associated with psoriasis, methods of detection and uses thereof

      
Application Number 17177433
Grant Number 11788143
Status In Force
Filing Date 2021-02-17
First Publication Date 2021-10-14
Grant Date 2023-10-17
Owner Celera Corporation (USA)
Inventor
  • Li, Yonghong
  • Schrodi, Steven
  • Begovich, Ann
  • Chang, Monica

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with psoriasis and related pathologies. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, including groups of nucleic acid molecules that may be used as a signature marker set, such as a haplotype, a diplotype, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • G01N 33/68 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving proteins, peptides or amino acids

6.

CANCER TARGETS AND USES THEREOF

      
Application Number 17152136
Status Pending
Filing Date 2021-01-19
First Publication Date 2021-09-23
Owner CELERA CORPORATION (USA)
Inventor
  • Fang, Dong
  • Moore, Paul
  • Ruben, Steve
  • Aggarwal, Sudeepta

Abstract

Methods and compositions are provided for assessing, treating, and preventing diseases, especially cancer, using cancer-associated targets (“CAT”). Methods and compositions are also provided for determining or predicting the effectiveness of a treatment for these diseases or for selecting a treatment, using CAT. Methods and compositions are further provided for modulating cell function using CAT. Also provided are compositions that modulate CAT (e.g., antagonists or agonists), such as antibodies, proteins, small molecule compounds, and nucleic acid agents (e.g., RNAi and antisense agents), as well as pharmaceutical compositions thereof. Further provided are methods of screening for agents that modulate CAT, and agents identified by these screening methods.

IPC Classes  ?

  • C07K 16/24 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
  • C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
  • A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum
  • C07K 16/18 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans
  • G01N 33/574 - ImmunoassayBiospecific binding assayMaterials therefor for cancer
  • C07K 14/47 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from animalsPeptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from humans from vertebrates from mammals
  • C12N 15/113 - Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides
  • G01N 33/50 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing
  • C07K 14/57 - IFN-gamma
  • C07K 16/30 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells

7.

Genetic polymorphisms associated with cardiovascular diseases, methods of detection and uses thereof

      
Application Number 16739408
Grant Number 11408034
Status In Force
Filing Date 2020-01-10
First Publication Date 2021-06-03
Grant Date 2022-08-09
Owner Celera Corporation (USA)
Inventor
  • Shiffman, Dov
  • Devlin, James J.
  • Louie, Judy Z.
  • Boerwinkle, Eric

Abstract

The present invention provides compositions and methods based on genetic polymorphisms that are associated with cardiovascular diseases, particularly coronary heart disease (especially myocardial infarction) or hypertension. For example, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material

8.

Genetic polymorphisms associated with stroke, methods of detection and uses thereof

      
Application Number 16814085
Grant Number 11401555
Status In Force
Filing Date 2020-03-10
First Publication Date 2020-12-03
Grant Date 2022-08-02
Owner Celera Corporation (USA)
Inventor
  • Luke, May
  • Devlin, James J.

Abstract

The present invention provides compositions and methods based on genetic polymorphisms that are associated with vascular diseases such as stroke. In particular, the present invention relates to genetic polymorphisms that have utility for such uses as predicting disease risk or predicting an individual's response to a treatment such as statins, including groups of polymorphisms that may be used as a signature marker set for such uses, as well as nucleic acid molecules containing the polymorphisms, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • A61K 31/22 - Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
  • A61K 31/35 - Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
  • A61K 31/40 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
  • A61K 31/404 - Indoles, e.g. pindolol
  • A61K 31/435 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom

9.

Methods and compositions for diagnosing and treating diseases

      
Application Number 16747791
Grant Number 11802164
Status In Force
Filing Date 2020-01-21
First Publication Date 2020-09-17
Grant Date 2023-10-31
Owner Celera Corporation (USA)
Inventor
  • Ruben, Steve
  • He, Tao
  • Lee, Candy
  • Van Orden, Karen
  • Moore, Paul

Abstract

Methods and compositions are provided for assessing, treating, and preventing diseases, especially cancer, using cancer-associated targets (CAT). Methods and compositions are also provided for determining or predicting the effectiveness of a treatment for these diseases or for selecting a treatment, using CAT. Methods and compositions are further provided for modulating cell function using CAT. Also provided are compositions that modulate CAT (e.g., antagonists or agonists), such as antibodies, proteins, small molecule compounds, and nucleic acid agents (e.g., RNAi and antisense agents), as well as pharmaceutical compositions thereof. Further provided are methods of screening for agents that modulate CAT, and agents identified by these screening methods.

IPC Classes  ?

  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C07K 16/30 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
  • C07K 14/705 - ReceptorsCell surface antigensCell surface determinants
  • C07K 16/40 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against enzymes
  • C12N 9/64 - Proteinases derived from animal tissue, e.g. rennin
  • C12N 15/113 - Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides
  • C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
  • G01N 33/574 - ImmunoassayBiospecific binding assayMaterials therefor for cancer
  • C07K 14/47 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from animalsPeptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from humans from vertebrates from mammals
  • C07K 16/18 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans
  • C07K 16/28 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
  • C12N 9/18 - Carboxylic ester hydrolases
  • A61K 39/00 - Medicinal preparations containing antigens or antibodies
  • A61K 38/00 - Medicinal preparations containing peptides

10.

Genetic polymorphisms associated with statin response and cardiovascular diseases, methods of detection and uses thereof

      
Application Number 16728333
Grant Number 11827937
Status In Force
Filing Date 2019-12-27
First Publication Date 2020-08-27
Grant Date 2023-11-28
Owner Celera Corporation (USA)
Inventor Shiffman, Dov

Abstract

The present invention provides compositions and methods based on genetic polymorphisms that are associated with response to statin treatment, particularly for reducing the risk of cardiovascular disease, especially coronary heart disease (such as myocardial infarction) and stroke. For example, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents and kits for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents and kits for their detection.

IPC Classes  ?

  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • G16B 20/50 - Mutagenesis
  • G16B 20/30 - Detection of binding sites or motifs
  • G16B 20/20 - Allele or variant detection, e.g. single nucleotide polymorphism [SNP] detection
  • G16B 25/20 - Polymerase chain reaction [PCR]Primer or probe designProbe optimisation
  • A61K 31/22 - Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
  • A61K 31/366 - Lactones having six-membered rings, e.g. delta-lactones
  • A61K 31/397 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
  • A61K 31/40 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
  • A61K 31/405 - Indole-alkanecarboxylic acidsDerivatives thereof, e.g. tryptophan, indomethacin
  • A61K 31/455 - Nicotinic acid, i.e. niacinDerivatives thereof, e.g. esters, amides
  • A61K 31/505 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim
  • G16B 20/00 - ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
  • G16B 25/00 - ICT specially adapted for hybridisationICT specially adapted for gene or protein expression

11.

Polymorphism in the Apo(a) gene predict responsiveness to acetylsalicylic acid treatment

      
Application Number 16716193
Grant Number 11697850
Status In Force
Filing Date 2019-12-16
First Publication Date 2020-08-06
Grant Date 2023-07-11
Owner
  • The Brigham and Women's Hospital, Inc. (USA)
  • Celera Corporation (USA)
Inventor
  • Ridker, Paul M.
  • Chasman, Daniel
  • Shiffman, Dov

Abstract

This invention relates to nucleotide polymorphisms in the human Apo(a) gene and to the use of Apo(a) nucleotide polymorphisms in identifying whether a human subject will respond or not to treatment with acetylsalicylic acid.

IPC Classes  ?

  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • G01N 33/92 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving lipids, e.g. cholesterol
  • A61K 31/616 - Salicylic acidDerivatives thereof having the hydroxy group in position 2 esterified, e.g. salicylsulfuric acid by carboxylic acids, e.g. acetylsalicylic acid
  • C12Q 1/6876 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes

12.

Genetic polymorphisms associated with coronary events and drug response, methods of detection and uses thereof

      
Application Number 16553592
Grant Number 10988809
Status In Force
Filing Date 2019-08-28
First Publication Date 2020-04-23
Grant Date 2021-04-27
Owner Celera Corporation (USA)
Inventor
  • Iakoubova, Olga
  • Devlin, James J.
  • Tong, Carmen
  • Rowland, Charles

Abstract

The present invention provides compositions and methods based on genetic polymorphisms that are associated with coronary heart disease (particularly myocardial infarction), aneurysm/dissection, and/or response to drug treatment, particularly statin treatment. For example, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • G01N 33/68 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving proteins, peptides or amino acids

13.

Lung cancer markers and uses thereof

      
Application Number 16456363
Grant Number 11105806
Status In Force
Filing Date 2019-06-28
First Publication Date 2020-02-27
Grant Date 2021-08-31
Owner Celera Corporation (USA)
Inventor
  • Birse, Charles
  • Ruben, Steve
  • Lewis, Marcia
  • Mesri, Mehdi

Abstract

Methods and compositions are provided for assessing (e.g., diagnosing), treating, and preventing diseases, especially cancer, and particular lung cancer, using lung cancer markers (LCM). Individual LCM and panels comprising multiple LCM are provided for these and other uses. Methods and compositions are also provided for determining or predicting the effectiveness of a treatment or for selecting a treatment using LCM. Methods and compositions are further provided for modulating cell function using LCM. Also provided are compositions that modulate LCM (e.g., antagonists or agonists), such as antibodies, proteins, small molecule compounds, and nucleic acid agents (e.g., RNAi and antisense agents), as well as pharmaceutical compositions thereof. Further provided are methods of screening for agents that modulate LCM, and agents identified by these screening methods.

IPC Classes  ?

  • C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
  • G01N 33/574 - ImmunoassayBiospecific binding assayMaterials therefor for cancer

14.

Genetic polymorphisms associated with psoriasis, methods of detection and uses thereof

      
Application Number 16149492
Grant Number 10954565
Status In Force
Filing Date 2018-10-02
First Publication Date 2019-07-25
Grant Date 2021-03-23
Owner Celera Corporation (USA)
Inventor
  • Li, Yonghong
  • Schrodi, Steven
  • Begovich, Ann
  • Chang, Monica

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with psoriasis and related pathologies. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, including groups of nucleic acid molecules that may be used as a signature marker set, such as a haplotype, a diplotype, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • G01N 33/68 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving proteins, peptides or amino acids

15.

Molecular prognostic signature for predicting breast cancer metastasis, and uses thereof

      
Application Number 16003682
Grant Number 11028445
Status In Force
Filing Date 2018-06-08
First Publication Date 2019-05-09
Grant Date 2021-06-08
Owner Celera Corporation (USA)
Inventor
  • Lau, Kit
  • Wang, Alice

Abstract

The present invention is based on the discovery of a unique 14-gene molecular prognostic signature that is useful for predicting breast cancer metastasis. In particular, the present invention relates to methods and reagents for detecting and profiling the expression levels of these genes, and methods of using the expression level information in predicting risk of breast cancer metastasis.

IPC Classes  ?

  • C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer

16.

Genetic polymorphisms associated with statin response and cardiovascular diseases, methods of detection and uses thereof

      
Application Number 15952792
Grant Number 10563263
Status In Force
Filing Date 2018-04-13
First Publication Date 2019-01-31
Grant Date 2020-02-18
Owner Celera Corporation (USA)
Inventor Shiffman, Dov

Abstract

The present invention provides compositions and methods based on genetic polymorphisms that are associated with response to statin treatment, particularly for reducing the risk of cardiovascular disease, especially coronary heart disease (such as myocardial infarction) and stroke. For example, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents and kits for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents and kits for their detection.

IPC Classes  ?

  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • A61K 31/00 - Medicinal preparations containing organic active ingredients
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • A61K 31/22 - Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
  • A61K 31/366 - Lactones having six-membered rings, e.g. delta-lactones
  • A61K 31/397 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
  • A61K 31/40 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
  • A61K 31/405 - Indole-alkanecarboxylic acidsDerivatives thereof, e.g. tryptophan, indomethacin
  • A61K 31/455 - Nicotinic acid, i.e. niacinDerivatives thereof, e.g. esters, amides
  • A61K 31/505 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim
  • G16B 20/00 - ICT specially adapted for functional genomics or proteomics, e.g. genotype-phenotype associations
  • G16B 25/00 - ICT specially adapted for hybridisationICT specially adapted for gene or protein expression

17.

Genetic polymorphisms associated with psoriasis, methods of detection and uses thereof

      
Application Number 15991247
Grant Number 10920276
Status In Force
Filing Date 2018-05-29
First Publication Date 2019-01-24
Grant Date 2021-02-16
Owner Celera Corporation (USA)
Inventor
  • Begovich, Ann
  • Beasley, Ellen
  • Schrodi, Steven

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with psoriasis and related pathologies. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, including groups of nucleic acid molecules that may be used as a signature marker set, such as a haplotype, a diplotype, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • A61K 31/5377 - 1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
  • C07K 16/24 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
  • G01N 33/68 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving proteins, peptides or amino acids

18.

Genetic polymorphisms associated with autoinflammatory diseases, methods of detection and uses thereof

      
Application Number 15788125
Grant Number 11008618
Status In Force
Filing Date 2017-10-19
First Publication Date 2018-06-21
Grant Date 2021-05-18
Owner Celera Corporation (USA)
Inventor
  • Schrodi, Steven
  • Li, Yonghong

Abstract

The present invention provides compositions and methods based on genetic polymorphisms that are associated with autoinflammatory diseases such as psoriasis. For example, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • C07K 16/24 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons

19.

Polymorphism in the Apo(a) gene predict responsiveness to acetylsalicylic acid treatment

      
Application Number 15477206
Grant Number 10550433
Status In Force
Filing Date 2017-04-03
First Publication Date 2017-11-23
Grant Date 2020-02-04
Owner
  • The Brigham and Women's Hospital, Inc. (USA)
  • Celera Corporation (USA)
Inventor
  • Ridker, Paul M.
  • Chasman, Daniel
  • Shiffman, Dov

Abstract

This invention relates to nucleotide polymorphisms in the human Apo(a) gene and to the use of Apo(a) nucleotide polymorphisms in identifying whether a human subject will respond or not to treatment with acetylsalicylic acid.

IPC Classes  ?

  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • G01N 33/92 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving lipids, e.g. cholesterol
  • A61K 31/616 - Salicylic acidDerivatives thereof having the hydroxy group in position 2 esterified, e.g. salicylsulfuric acid by carboxylic acids, e.g. acetylsalicylic acid
  • C12Q 1/6876 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes

20.

Genetic polymorphisms associated with cardiovascular diseases, methods of detection and uses thereof

      
Application Number 15409162
Grant Number 10584384
Status In Force
Filing Date 2017-01-18
First Publication Date 2017-10-12
Grant Date 2020-03-10
Owner Celera Corporation (USA)
Inventor
  • Shiffman, Dov
  • Devlin, James J.
  • Louie, Judy Z.
  • Boerwinkle, Eric

Abstract

The present invention provides compositions and methods based on genetic polymorphisms that are associated with cardiovascular diseases, particularly coronary heart disease (especially myocardial infarction) or hypertension. For example, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material

21.

Lung cancer markers and uses thereof

      
Application Number 15346547
Grant Number 10338075
Status In Force
Filing Date 2016-11-08
First Publication Date 2017-06-01
Grant Date 2019-07-02
Owner Celera Corporation (USA)
Inventor
  • Birse, Charles
  • Ruben, Steve
  • Lewis, Marcia
  • Mesri, Mehdi

Abstract

Methods and compositions are provided for assessing (e.g., diagnosing), treating, and preventing diseases, especially cancer, and particular lung cancer, using lung cancer markers (LCM). Individual LCM and panels comprising multiple LCM are provided for these and other uses. Methods and compositions are also provided for determining or predicting the effectiveness of a treatment or for selecting a treatment using LCM. Methods and compositions are further provided for modulating cell function using LCM. Also provided are compositions that modulate LCM (e.g., antagonists or agonists), such as antibodies, proteins, small molecule compounds, and nucleic acid agents (e.g., RNAi and antisense agents), as well as pharmaceutical compositions thereof. Further provided are methods of screening for agents that modulate LCM, and agents identified by these screening methods.

IPC Classes  ?

  • G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor
  • G01N 33/574 - ImmunoassayBiospecific binding assayMaterials therefor for cancer
  • C12Q 1/6886 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer

22.

Genetic polymorphisms, associated with rheumatoid arthritis, methods of detection and uses thereof

      
Application Number 15284752
Grant Number 10301679
Status In Force
Filing Date 2016-10-04
First Publication Date 2017-05-25
Grant Date 2019-05-28
Owner Celera Corporation (USA)
Inventor
  • Schrodi, Steven J.
  • Begovich, Ann

Abstract

The present invention provides compositions and methods based on genetic polymorphisms that are associated with autoimmune disease, particularly rheumatoid arthritis. For example, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids

23.

Genetic polymorphisms associated with coronary events and drug response, methods of detection and uses thereof

      
Application Number 15150636
Grant Number 10435749
Status In Force
Filing Date 2016-05-10
First Publication Date 2017-01-26
Grant Date 2019-10-08
Owner Celera Corporation (USA)
Inventor
  • Iakoubova, Olga
  • Devlin, James J.
  • Tong, Carmen
  • Rowland, Charles

Abstract

The present invention provides compositions and methods based on genetic polymorphisms that are associated with coronary heart disease (particularly myocardial infarction), aneurysm/dissection, and/or response to drug treatment, particularly statin treatment. For example, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • G01N 33/68 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving proteins, peptides or amino acids

24.

Genetic polymorphisms associated with psoriasis, methods of detection and uses thereof

      
Application Number 15151643
Grant Number 10006088
Status In Force
Filing Date 2016-05-11
First Publication Date 2017-01-26
Grant Date 2018-06-26
Owner Celera Corporation (USA)
Inventor
  • Begovich, Ann
  • Beasley, Ellen
  • Cargill, Michele
  • Schrodi, Steven

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with psoriasis and related pathologies. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, including groups of nucleic acid molecules that may be used as a signature marker set, such as a haplotype, a diplotype, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • A61K 31/5377 - 1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
  • C07K 16/24 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans against cytokines, lymphokines or interferons
  • G01N 33/68 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving proteins, peptides or amino acids

25.

Genetic polymorphisms associated with psoriasis, methods of detection and uses thereof

      
Application Number 14963923
Grant Number 10131949
Status In Force
Filing Date 2015-12-09
First Publication Date 2016-08-25
Grant Date 2018-11-20
Owner Celera Corporation (USA)
Inventor
  • Li, Yonghong
  • Schrodi, Steven
  • Begovich, Ann
  • Chang, Monica

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with psoriasis and related pathologies. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, including groups of nucleic acid molecules that may be used as a signature marker set, such as a haplotype, a diplotype, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides
  • C07H 21/02 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with ribosyl as saccharide radical
  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • G01N 33/68 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving proteins, peptides or amino acids

26.

Genetic polymorphisms associated with psoriasis, methods of detection and uses thereof

      
Application Number 14605115
Grant Number 09371565
Status In Force
Filing Date 2015-01-26
First Publication Date 2015-09-17
Grant Date 2016-06-21
Owner Celera Corporation (USA)
Inventor
  • Begovich, Ann
  • Beasley, Ellen
  • Cargill, Michelle
  • Schrodi, Steven

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with psoriasis and related pathologies. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, including groups of nucleic acid molecules that may be used as a signature marker set, such as a haplotype, a diplotype, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides

27.

Composite metastasis score with weighted coefficients for predicting breast cancer metastasis, and uses thereof

      
Application Number 13406221
Grant Number 08557525
Status In Force
Filing Date 2012-02-27
First Publication Date 2013-10-15
Grant Date 2013-10-15
Owner Celera Corporation (USA)
Inventor
  • Wang, Alice
  • Lagier, Robert J.
  • Rowland, Charles M.

Abstract

The present invention relates to a composite metastasis score (“cMS”) based on expression of a 14-gene molecular signature (referred to as a metastasis score, or “MS”) in combination with progesterone receptor (PR) expression that is useful for predicting breast cancer metastasis. In preferred embodiments, the cMS is determined by applying weighted coefficients to MS and PR. The present invention provides methods and reagents for detecting and profiling the expression levels of these genes, and methods of using the expression level information for predicting risk of breast cancer metastasis, among other embodiments.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids

28.

Genetic polymorphisms associated with psoriasis, methdos of detection and uses thereof

      
Application Number 13712430
Grant Number 08975022
Status In Force
Filing Date 2012-12-12
First Publication Date 2013-08-22
Grant Date 2015-03-10
Owner Celera Corporation (USA)
Inventor
  • Begovich, Ann
  • Beasley, Ellen
  • Cargill, Michele
  • Schrodi, Steven

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with psoriasis and related pathologies. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, including groups of nucleic acid molecules that may be used as a signature marker set, such as a haplotype, a diplotype, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides
  • C07H 21/02 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with ribosyl as saccharide radical
  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical

29.

Cancer targets and uses thereof

      
Application Number 13436411
Grant Number 08524238
Status In Force
Filing Date 2012-03-30
First Publication Date 2013-03-28
Grant Date 2013-09-03
Owner Celera Corporation (USA)
Inventor
  • Fang, Dong
  • Moore, Paul
  • Ruben, Steve
  • Aggarwal, Sudeepta

Abstract

Methods and compositions are provided for assessing, treating, and preventing diseases, especially cancer, using cancer-associated targets (“CAT”). Methods and compositions are also provided for determining or predicting the effectiveness of a treatment for these diseases or for selecting a treatment, using CAT. Methods and compositions are further provided for modulating cell function using CAT. Also provided are compositions that modulate CAT (e.g., antagonists or agonists), such as antibodies, proteins, small molecule compounds, and nucleic acid agents (e.g., RNAi and antisense agents), as well as pharmaceutical compositions thereof. Further provided are methods of screening for agents that modulate CAT, and agents identified by these screening methods.

IPC Classes  ?

  • A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum
  • A61K 39/00 - Medicinal preparations containing antigens or antibodies

30.

GENETIC POLYMORPHISMS ASSOCIATED WITH VENOUS THROMBOSIS AND STATIN RESPONSE, METHODS OF DETECTION AND USES THEREOF

      
Document Number 03159981
Status In Force
Filing Date 2011-11-02
Open to Public Date 2012-05-10
Grant Date 2023-12-19
Owner
  • LEIDEN UNIVERSITY MEDICAL CENTRE (LUMC) ACTING ON BEHALF OF ACADEMIC HOS (USA)
  • CELERA CORPORATION (USA)
Inventor
  • Bare, Lance
  • Devlin, James J.
  • Bezemer, Irene D.
  • Reitsma, Pieter H.
  • Rosendaal, Frits R.

Abstract

The disclosure provides compositions and methods based on genetic polymorphisms that are associated with response to statin treatment (particularly for reducing the risk of venous thrombosis). Specifically, the disclosure provides nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • A61K 31/22 - Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
  • A61K 31/366 - Lactones having six-membered rings, e.g. delta-lactones
  • A61K 31/40 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
  • A61K 31/405 - Indole-alkanecarboxylic acidsDerivatives thereof, e.g. tryptophan, indomethacin
  • A61K 31/505 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim
  • A61P 7/02 - Antithrombotic agentsAnticoagulantsPlatelet aggregation inhibitors
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6827 - Hybridisation assays for detection of mutation or polymorphism
  • C12Q 1/6858 - Allele-specific amplification
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material

31.

GENETIC POLYMORPHISMS ASSOCIATED WITH VENOUS THROMBOSIS AND STATIN RESPONSE, METHODS OF DETECTION AND USES THEREOF

      
Document Number 02814414
Status In Force
Filing Date 2011-11-02
Open to Public Date 2012-05-10
Grant Date 2022-07-26
Owner
  • CELERA CORPORATION (USA)
  • LEIDEN UNIVERSITY MEDICAL CENTRE (LUMC) ACTING ON BEHALF OF ACADEMIC HOS (USA)
Inventor
  • Bare, Lance
  • Devlin, James J.
  • Rosendaal, Frits R.
  • Reitsma, Pieter H.
  • Bezemer, Irene D.

Abstract

The disclosure provides compositions and methods based on genetic polymorphisms that are associated with response to statin treatment (particularly for reducing the risk of venous thrombosis). Specifically, the disclosure provides nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6827 - Hybridisation assays for detection of mutation or polymorphism
  • C12Q 1/6858 - Allele-specific amplification
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material

32.

Cancer targets and uses thereof

      
Application Number 12275779
Grant Number 08168586
Status In Force
Filing Date 2008-11-21
First Publication Date 2012-05-01
Grant Date 2012-05-01
Owner Celera Corporation (USA)
Inventor
  • Fang, Dong
  • Moore, Paul
  • Ruben, Steve
  • Aggarwal, Sudeepta

Abstract

Methods and compositions are provided for assessing, treating, and preventing diseases, especially cancer, using cancer-associated targets (“CAT”). Methods and compositions are also provided for determining or predicting the effectiveness of a treatment for these diseases or for selecting a treatment, using CAT. Methods and compositions are further provided for modulating cell function using CAT. Also provided are compositions that modulate CAT (e.g., antagonists or agonists), such as antibodies, proteins, small molecule compounds, and nucleic acid agents (e.g., RNAi and antisense agents), as well as pharmaceutical compositions thereof. Further provided are methods of screening for agents that modulate CAT, and agents identified by these screening methods.

IPC Classes  ?

  • A61K 38/00 - Medicinal preparations containing peptides
  • G01N 33/574 - ImmunoassayBiospecific binding assayMaterials therefor for cancer
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • A61K 51/10 - Antibodies or immunoglobulinsFragments thereof
  • A61K 39/00 - Medicinal preparations containing antigens or antibodies

33.

Lung cancer markers, and uses thereof

      
Application Number 13005031
Grant Number 08808997
Status In Force
Filing Date 2011-01-12
First Publication Date 2012-03-29
Grant Date 2014-08-19
Owner Celera Corporation (USA)
Inventor
  • Birse, Charles
  • Lewis, Marcia
  • Ruben, Steve
  • Mesri, Mehdi

Abstract

Methods and compositions are provided for assessing (e.g., diagnosing), treating, and preventing diseases, especially cancer, and particular lung cancer, using lung cancer markers (LCM). Individual LCM and panels comprising multiple LCM are provided for these and other uses. Methods and compositions are also provided for determining or predicting the effectiveness of a treatment or for selecting a treatment using LCM. Methods and compositions are further provided for modulating cell function using LCM. Also provided are compositions that modulate LCM (e.g., antagonists or agonists), such as antibodies, proteins, small molecule compounds, and nucleic acid agents (e.g., RNAi and antisense agents), as well as pharmaceutical compositions thereof. Further provided are methods of screening for agents that modulate LCM, and agents identified by these screening methods.

IPC Classes  ?

  • G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor

34.

Genetic polymorphisms associated with venous thrombosis, methods of detection and uses thereof

      
Application Number 13023295
Grant Number 08227189
Status In Force
Filing Date 2011-02-08
First Publication Date 2012-02-16
Grant Date 2012-07-24
Owner Celera Corporation (USA)
Inventor
  • Bare, Lance
  • Devlin, James J.
  • Rosendaal, Frits R.
  • Reitsma, Pieter H.
  • Bezemer, Irene D.

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with coronary heart disease and in particular VT and response to drug treatment. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids

35.

GENETIC POLYMORPHISMS ASSOCIATED WITH STATIN RESPONSE AND CARDIOVASCULAR DISEASES, METHODS OF DETECTION AND USES THEREOF

      
Document Number 02796880
Status In Force
Filing Date 2011-04-15
Open to Public Date 2011-10-27
Grant Date 2020-12-01
Owner CELERA CORPORATION (USA)
Inventor
  • Shiffman, Dov
  • Devlin, James J.
  • Luke, May
  • Ross, David

Abstract


Compositions and methods based on genetic polymorphisms that are associated
with response to statin treatment,
particularly for reducing the risk of cardiovascular disease, especially
coronary heart disease (such as myocardial infarction) and
stroke are provided. For example, nucleic acid molecules containing the
polymorphisms, variant proteins encoded by these nucleic
acid molecules, reagents and kits for detecting the polymorphic nucleic acid
molecules and variant proteins, and methods of using
the nucleic acid molecules and proteins as well as methods of using reagents
and kits for their detection are disclosed.

IPC Classes  ?

  • C12N 9/04 - Oxidoreductases (1.), e.g. luciferase acting on CHOH groups as donors, e.g. glucose oxidase, lactate dehydrogenase (1.1)
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6813 - Hybridisation assays
  • C12Q 1/6858 - Allele-specific amplification
  • C12Q 1/6876 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
  • C40B 30/00 - Methods of screening libraries
  • G01N 33/48 - Biological material, e.g. blood, urineHaemocytometers

36.

GENETIC POLYMORPHISMS ASSOCIATED WITH STATIN RESPONSE AND CARDIOVASCULAR DISEASES, METHODS OF DETECTION AND USES THEREOF

      
Document Number 03060628
Status In Force
Filing Date 2011-04-15
Open to Public Date 2011-10-27
Grant Date 2024-04-30
Owner CELERA CORPORATION (USA)
Inventor
  • Shiffman, Dov
  • Devlin, James J.
  • Luke, May
  • Ross, David

Abstract

Compositions and methods based on genetic polymorphisms that are associated with response to statin treatment, particularly for reducing the risk of cardiovascular disease, especially coronary heart disease (such as myocardial infarction) and stroke are provided. For example, nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents and kits for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents and kits for their detection are disclosed.

IPC Classes  ?

  • A61K 31/22 - Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
  • A61K 31/366 - Lactones having six-membered rings, e.g. delta-lactones
  • A61K 31/397 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
  • A61K 31/40 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
  • A61K 31/405 - Indole-alkanecarboxylic acidsDerivatives thereof, e.g. tryptophan, indomethacin
  • A61K 31/4422 - 1,4-Dihydropyridines, e.g. nifedipine, nicardipine
  • A61K 31/455 - Nicotinic acid, i.e. niacinDerivatives thereof, e.g. esters, amides
  • A61P 9/00 - Drugs for disorders of the cardiovascular system
  • A61P 9/10 - Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6827 - Hybridisation assays for detection of mutation or polymorphism
  • C12Q 1/6858 - Allele-specific amplification
  • C12Q 1/6876 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes

37.

Methods and compositions for diagnosing and treating diseases

      
Application Number 12901254
Grant Number 08486392
Status In Force
Filing Date 2010-10-08
First Publication Date 2011-10-13
Grant Date 2013-07-16
Owner Celera Corporation (USA)
Inventor
  • Ruben, Steve
  • Moore, Paul
  • He, Tao
  • Lee, Candy N.
  • Van Orden, Karen

Abstract

Methods and compositions are provided for assessing, treating, and preventing diseases, especially cancer, using cancer-associated targets (CAT). Methods and compositions are also provided for determining or predicting the effectiveness of a treatment for these diseases or for selecting a treatment, using CAT. Methods and compositions are further provided for modulating cell function using CAT. Also provided are compositions that modulate CAT (e.g., antagonists or agonists), such as antibodies, proteins, small molecule compounds, and nucleic acid agents (e.g., RNAi and antisense agents), as well as pharmaceutical compositions thereof. Further provided are methods of screening for agents that modulate CAT, and agents identified by these screening methods.

IPC Classes  ?

  • A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum

38.

Molecular prognostic signature for predicting breast cancer metastasis, and uses thereof

      
Application Number 12638040
Grant Number 08614058
Status In Force
Filing Date 2009-12-15
First Publication Date 2010-12-23
Grant Date 2013-12-24
Owner Celera Corporation (USA)
Inventor
  • Lau, Kit
  • Wang, Alice

Abstract

The present invention is based on the discovery of a unique 14-gene molecular prognostic signature that is useful for predicting breast cancer metastasis. In particular, the present invention relates to methods and reagents for detecting and profiling the expression levels of these genes, and methods of using the expression level information in predicting risk of breast cancer metastasis.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids

39.

Methods and compositions for diagnosing and treating diseases

      
Application Number 11802321
Grant Number 07842291
Status In Force
Filing Date 2007-05-22
First Publication Date 2010-11-30
Grant Date 2010-11-30
Owner Celera Corporation (USA)
Inventor
  • Ruben, Steve
  • Moore, Paul A.
  • He, Tao
  • Lee, Candy N.
  • Van Orden, Karen
  • Birse, Charles E.
  • Mesri, Mehdi
  • Joseloff, Elizabeth G.

Abstract

Methods and compositions are provided for assessing, treating, and preventing diseases, especially cancer, using cancer-associated targets (CAT). Methods and compositions are also provided for determining or predicting the effectiveness of a treatment for these diseases or for selecting a treatment, using CAT. Methods and compositions are further provided for modulating cell function using CAT. Also provided are compositions that modulate CAT (e.g., antagonists or agonists), such as antibodies, proteins, small molecule compounds, and nucleic acid agents (e.g., RNAi and antisense agents), as well as pharmaceutical compositions thereof. Further provided are methods of screening for agents that modulate CAT, and agents identified by these screening methods.

IPC Classes  ?

40.

Genetic polymorphisms associated with cardiovascular diseases, methods of detection and uses thereof

      
Application Number 12500378
Grant Number 08216786
Status In Force
Filing Date 2009-07-09
First Publication Date 2010-02-11
Grant Date 2012-07-10
Owner Celera Corporation (USA)
Inventor
  • Shiffman, Dov
  • Devlin, James J.
  • Louie, Judy Z.
  • Boerwinkle, Eric

Abstract

The present invention provides compositions and methods based on genetic polymorphisms that are associated with cardiovascular diseases, particularly coronary heart disease (especially myocardial infarction) or hypertension. For example, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical

41.

GENETIC POLYMORPHISMS ASSOCIATED WITH VENOUS THROMBOSIS, METHODS OF DETECTION AND USES THEREOF

      
Document Number 02717045
Status In Force
Filing Date 2009-03-13
Open to Public Date 2009-12-17
Grant Date 2018-04-10
Owner
  • CELERA CORPORATION (USA)
  • LEIDEN UNIVERSITY MEDICAL CENTRE (LUMC) ACTING ON BEHALF OF ACADEMIC HOS (USA)
Inventor
  • Bare, Lance
  • Devlin, James
  • Rosendaal, Frits R.
  • Reitsma, Pieter H.
  • Bezemer, Irene D.

Abstract


The present invention is based on the discovery of genetic polymorphisms that
are associated
with venous thrombosis (VT) and, in particular, methods of determining whether
a human has
an increased risk for VT based on the nucleotide content at F11 polymorphism
rs2036914
corresponding to position 101 of SEQ ID NO:710. The invention further pertains
to nucleic acid
molecules useful for such methods.

IPC Classes  ?

  • A61P 7/02 - Antithrombotic agentsAnticoagulantsPlatelet aggregation inhibitors
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6827 - Hybridisation assays for detection of mutation or polymorphism
  • C12Q 1/6858 - Allele-specific amplification
  • C12Q 1/686 - Polymerase chain reaction [PCR]
  • C12Q 1/6876 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
  • C40B 30/04 - Methods of screening libraries by measuring the ability to specifically bind a target molecule, e.g. antibody-antigen binding, receptor-ligand binding
  • C40B 40/06 - Libraries containing nucleotides or polynucleotides, or derivatives thereof

42.

Genetic polymorphisms associated with venous thrombosis, methods of detection and uses thereof

      
Application Number 12403552
Grant Number 08071291
Status In Force
Filing Date 2009-03-13
First Publication Date 2009-10-29
Grant Date 2011-12-06
Owner Celera Corporation (USA)
Inventor
  • Bare, Lance
  • Devlin, James J.
  • Rosendaal, Frits R.
  • Reitsma, Pieter H.
  • Bezemer, Irene D.

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with venous thrombosis. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides
  • C07H 21/02 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with ribosyl as saccharide radical
  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical

43.

GENETIC POLYMORPHISMS ASSOCIATED WITH STROKE, METHODS OF DETECTION AND USES THEREOF

      
Document Number 02716368
Status In Force
Filing Date 2009-02-20
Open to Public Date 2009-08-27
Grant Date 2022-03-01
Owner CELERA CORPORATION (USA)
Inventor
  • Luke, May
  • Devlin, James

Abstract


The present invention is based on the discovery of genetic polymorphisms that
are associated with stroke and
relat-ed pathologies, such as other vascular diseases. In particular, the
present invention relates to nucleic acid molecules containing the
polymorphisms, including groups of nucleic acid molecules that may be used as
a signature marker set, such as a haplotype, a
diplotype, variant proteins encoded by such nucleic acid molecules, reagents
for detecting the polymorphic nucleic acid molecules
and proteins, and methods of using the nucleic acid and proteins as well as
methods of using reagents for their detection.

IPC Classes  ?

  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6827 - Hybridisation assays for detection of mutation or polymorphism
  • C12Q 1/6858 - Allele-specific amplification
  • C12Q 1/6876 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
  • C40B 30/04 - Methods of screening libraries by measuring the ability to specifically bind a target molecule, e.g. antibody-antigen binding, receptor-ligand binding
  • C40B 40/06 - Libraries containing nucleotides or polynucleotides, or derivatives thereof

44.

GENETIC POLYMORPHISMS ASSOCIATED WITH STROKE, METHODS OF DETECTION AND USES THEREOF

      
Document Number 02882487
Status In Force
Filing Date 2009-02-20
Open to Public Date 2009-08-27
Grant Date 2021-11-30
Owner CELERA CORPORATION (USA)
Inventor
  • Luke, May
  • Devlin, James

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with stroke and related pathologies, such as other vascular diseases. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, including groups of nucleic acid molecules that may be used as a signature marker set, such as a haplotype, a diplotype, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C07H 21/00 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6827 - Hybridisation assays for detection of mutation or polymorphism
  • C12Q 1/6858 - Allele-specific amplification
  • C12Q 1/6876 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
  • C40B 30/04 - Methods of screening libraries by measuring the ability to specifically bind a target molecule, e.g. antibody-antigen binding, receptor-ligand binding

45.

Lung cancer markers, and uses thereof

      
Application Number 12273994
Grant Number 07892760
Status In Force
Filing Date 2008-11-19
First Publication Date 2009-07-09
Grant Date 2011-02-22
Owner Celera Corporation (USA)
Inventor
  • Birse, Charles
  • Lewis, Marcia
  • Ruben, Steve
  • Mesri, Mehdi

Abstract

Methods and compositions are provided for assessing (e.g., diagnosing), treating, and preventing diseases, especially cancer, and particular lung cancer, using lung cancer markers (LCM). Individual LCM and panels comprising multiple LCM are provided for these and other uses. Methods and compositions are also provided for determining or predicting the effectiveness of a treatment or for selecting a treatment using LCM. Methods and compositions are further provided for modulating cell function using LCM. Also provided are compositions that modulate LCM (e.g., antagonists or agonists), such as antibodies, proteins, small molecule compounds, and nucleic acid agents (e.g., RNAi and antisense agents), as well as pharmaceutical compositions thereof. Further provided are methods of screening for agents that modulate LCM, and agents identified by these screening methods.

IPC Classes  ?

  • G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor

46.

LUNG CANCER MARKERS AND USES THEREOF

      
Document Number 02705486
Status In Force
Filing Date 2008-11-19
Open to Public Date 2009-05-28
Grant Date 2019-04-02
Owner CELERA CORPORATION (USA)
Inventor
  • Birse, Charles
  • Ruben, Steve
  • Lewis, Marcia
  • Mesri, Mehdi

Abstract


Methods and compositions are provided for assessing (e.g., diagnosing),
treating, and preventing diseases,
especially cancer, and particular lung cancer, using lung cancer markers
(LCM). Individual LCM and panels comprising multiple
LCM are provided for these and other uses. Methods and compositions are also
provided for determining or predicting the
effectiveness of a treatment or for selecting a treatment using LCM. Methods
and compositions are further provided for modulating cell
function using LCM. Also provided are compositions that modulate LCM (e.g.,
antagonists or agonists), such as antibodies,
proteins, small molecule compounds, and nucleic acid agents (e.g., RNAi and
antisense agents), as well as pharmaceutical
compositions thereof. Further provided are methods of screening for agents
that modulate LCM, and agents identified by these screening
methods.

IPC Classes  ?

  • A61K 45/00 - Medicinal preparations containing active ingredients not provided for in groups
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6809 - Methods for determination or identification of nucleic acids involving differential detection
  • C40B 30/04 - Methods of screening libraries by measuring the ability to specifically bind a target molecule, e.g. antibody-antigen binding, receptor-ligand binding
  • C40B 40/10 - Libraries containing peptides or polypeptides, or derivatives thereof
  • G01N 33/574 - ImmunoassayBiospecific binding assayMaterials therefor for cancer
  • G01N 33/68 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing involving proteins, peptides or amino acids

47.

Genetic polymorphisms associated with liver fibrosis, methods of detection and uses thereof

      
Application Number 12264501
Grant Number 08039212
Status In Force
Filing Date 2008-11-04
First Publication Date 2009-05-21
Grant Date 2011-10-18
Owner Celera Corporation (USA)
Inventor
  • Li, Yonghong
  • Huang, Hongjin

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with liver fibrosis and related pathologies. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, including groups of nucleic acid molecules that may be used as a signature marker set, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides

48.

GENETIC POLYMORPHISMS ASSOCIATED WITH LIVER FIBROSIS, METHODS OF DETECTION AND USES THEREOF

      
Document Number 02703877
Status In Force
Filing Date 2008-11-05
Open to Public Date 2009-05-14
Grant Date 2018-12-18
Owner CELERA CORPORATION (USA)
Inventor
  • Li, Yonghong
  • Huang, Hongjin

Abstract


The present invention is based on the discovery of genetic polymorphisms that
are associated with liver fibrosis
and related pathologies. In particular, the present invention relates to
nucleic acid molecules containing the polymorphisms,
in-cluding groups of nucleic acid molecules that may be used as a signature
marker set, variant proteins encoded by such nucleic acid
molecules, reagents for detecting the polymorphic nucleic acid molecules and
proteins, and methods of using the nucleic acid and
proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • A61K 45/00 - Medicinal preparations containing active ingredients not provided for in groups
  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6827 - Hybridisation assays for detection of mutation or polymorphism
  • C12Q 1/6858 - Allele-specific amplification
  • C12Q 1/686 - Polymerase chain reaction [PCR]
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • C40B 30/00 - Methods of screening libraries
  • C40B 40/06 - Libraries containing nucleotides or polynucleotides, or derivatives thereof

49.

Genetic polymorphisms associated with liver fibrosis, methods of detection and uses thereof

      
Application Number 11796733
Grant Number 07727725
Status In Force
Filing Date 2007-04-26
First Publication Date 2008-12-04
Grant Date 2010-06-01
Owner Celera Corporation (USA)
Inventor
  • Huang, Hongjin
  • Venkatesh, Ramasubbu
  • Cargill, Michele

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with liver fibrosis and related pathologies. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, including groups of nucleic acid molecules that may be used as a signature marker set, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides

50.

POLYMORPHISM IN THE APO(A) GENE PREDICT RESPONSIVENESS TO ACETYLSALICYLIC ACID TREATMENT

      
Document Number 02686874
Status In Force
Filing Date 2008-05-09
Open to Public Date 2008-11-20
Grant Date 2021-10-19
Owner
  • THE BRIGHAM AND WOMEN'S HOSPITAL, INC (USA)
  • CELERA CORPORATION (USA)
Inventor
  • Ridker, Paul
  • Chasman, Daniel
  • Shiffman, Dov

Abstract

This invention relates to nucleotide polymorphisms in the human Apo(a) gene and to the use of Apo(a) nucleotide polymorphisms in identifying whether a human subject will respond or not to treatment with acetylsalicylic acid.

IPC Classes  ?

  • A61K 31/397 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
  • A61K 31/4462 - Non-condensed piperidines, e.g. piperocaine only substituted in position 3
  • A61K 31/542 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and at least one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
  • A61K 31/616 - Salicylic acidDerivatives thereof having the hydroxy group in position 2 esterified, e.g. salicylsulfuric acid by carboxylic acids, e.g. acetylsalicylic acid
  • A61K 31/702 - Oligosaccharides, i.e. having three to five saccharide radicals attached to each other by glycosidic linkages
  • A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum
  • A61P 9/10 - Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6827 - Hybridisation assays for detection of mutation or polymorphism
  • C12Q 1/6858 - Allele-specific amplification
  • C12Q 1/6876 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes

51.

CELERA

      
Application Number 007304223
Status Registered
Filing Date 2008-10-10
Registration Date 2010-10-18
Owner Celera Corporation (USA)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Medical diagnostic reagents assays and assay systems, clinical medical reagents, assays and assay systems.

52.

GENETIC POLYMORPHISMS ASSOCIATED WITH CORONARY EVENTS AND DRUG RESPONSE, METHODS OF DETECTION AND USES THEREOF

      
Document Number 02680024
Status In Force
Filing Date 2008-03-24
Open to Public Date 2008-10-02
Grant Date 2017-07-04
Owner CELERA CORPORATION (USA)
Inventor
  • Iakoubova, Olga
  • Devlin, James
  • Tong, Carmen
  • Rowland, Charles

Abstract

The present invention provides compositions and methods based on genetic polymorphisms that are associated with coronary heart disease (particularly myocardial infarction), aneurysm/dissection, and/or response to drug treatment, particularly statin treatment. For example, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by these nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and variant proteins, and methods of using the nucleic acid molecules and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6858 - Allele-specific amplification
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • C40B 30/04 - Methods of screening libraries by measuring the ability to specifically bind a target molecule, e.g. antibody-antigen binding, receptor-ligand binding
  • C40B 40/06 - Libraries containing nucleotides or polynucleotides, or derivatives thereof

53.

CELERA

      
Application Number 007269236
Status Registered
Filing Date 2008-09-29
Registration Date 2010-12-08
Owner Celera Corporation (USA)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Medical diagnostic reagents assays and assay systems, clinical medical reagents, assays and assay systems.

54.

Molecular prognostic signature for predicting breast cancer distant metastasis, and uses thereof

      
Application Number 12012530
Grant Number 07695915
Status In Force
Filing Date 2008-01-31
First Publication Date 2008-08-28
Grant Date 2010-04-13
Owner Celera Corporation (USA)
Inventor
  • Lau, Kit
  • Wang, Alice

Abstract

The present invention is based on the discovery of a unique 14-gene molecular prognostic signature that is useful for predicting breast cancer metastasis. In particular, the present invention relates to methods and reagents for detecting and profiling the expression levels of these genes, and methods of using the expression level information in predicting risk of breast cancer metastasis.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids

55.

A MOLECULAR PROGNOSTIC SIGNATURE FOR PREDICTING BREAST CANCER DISTANT METASTASIS, AND USES THEREOF

      
Document Number 02674907
Status In Force
Filing Date 2008-01-31
Open to Public Date 2008-08-07
Grant Date 2017-04-04
Owner CELERA CORPORATION (USA)
Inventor
  • Lau, Kit
  • Wang, Alice

Abstract

The present invention is based on the discovery of a unique 14-gene molecular prognostic signature that is useful for predicting breast cancer metastasis. In particular, the present invention relates to methods and reagents for detecting and profiling the expression levels of these genes, and methods of using the expression level information in predicting risk of breast cancer metastasis.

IPC Classes  ?

  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C40B 30/00 - Methods of screening libraries
  • C40B 30/04 - Methods of screening libraries by measuring the ability to specifically bind a target molecule, e.g. antibody-antigen binding, receptor-ligand binding
  • C40B 40/06 - Libraries containing nucleotides or polynucleotides, or derivatives thereof

56.

Genetic polymorphisms associated with psoriasis, methods of detection and uses thereof

      
Application Number 11899017
Grant Number 07993833
Status In Force
Filing Date 2007-08-31
First Publication Date 2008-05-08
Grant Date 2011-08-09
Owner Celera Corporation (USA)
Inventor
  • Begovich, Ann
  • Beasley, Ellen
  • Cargill, Michele
  • Schrodi, Steven

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with psoriasis and related pathologies. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, including groups of nucleic acid molecules that may be used as a signature marker set, such as a haplotype, a diplotype, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides
  • C07H 21/02 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with ribosyl as saccharide radical
  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical

57.

GENETIC POLYMORPHISMS ASSOCIATED WITH VENOUS THROMBOSIS, METHODS OF DETECTION AND USES THEREOF

      
Document Number 02666346
Status In Force
Filing Date 2007-10-19
Open to Public Date 2008-05-02
Grant Date 2016-02-23
Owner
  • LEIDEN UNIVERSITY MEDICAL CENTRE (LUMC) ACTING ON BEHALF OF ACADEMIC HOS (USA)
  • CELERA CORPORATION (USA)
Inventor
  • Devlin, James J.
  • Rosendaal, Frits R.
  • Reitsma, Pieter H.
  • Bezemer, Irene D.
  • Bare, Lance

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with coronary heart disease and in particular VT and response to drug treatment. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • A61K 39/395 - AntibodiesImmunoglobulinsImmune serum, e.g. antilymphocytic serum
  • C07H 21/00 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor

58.

GENETIC POLYMORPHISMS ASSOCIATED WITH VENOUS THROMBOSIS, METHODS OF DETECTION AND USES THEREOF

      
Document Number 02915679
Status In Force
Filing Date 2007-10-19
Open to Public Date 2008-05-02
Grant Date 2017-12-12
Owner
  • LEIDEN UNIVERSITY MEDICAL CENTRE (LUMC) ACTING ON BEHALF OF ACADEMIC HOS (USA)
  • CELERA CORPORATION (USA)
Inventor
  • Bare, Lance
  • Devlin, James J.
  • Rosendaal, Frits R.
  • Reitsma, Pieter H.
  • Bezemer, Irene D.

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with coronary heart disease and in particular VT and response to drug treatment. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C12Q 1/6827 - Hybridisation assays for detection of mutation or polymorphism
  • C12Q 1/6858 - Allele-specific amplification
  • C12Q 1/686 - Polymerase chain reaction [PCR]
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material

59.

POLYMORPHISM IN THE KIF6 GENE AS A DIAGNOSTIC FOR MYOCARDIAL INFARCTION RISK AND RESPONSIVENESS TO STATIN TREATMENT

      
Document Number 02613521
Status In Force
Filing Date 2006-09-25
Open to Public Date 2007-03-29
Grant Date 2017-06-20
Owner CELERA CORPORATION (USA)
Inventor
  • Iakoubova, Olga
  • Devlin, James J.

Abstract

The present invention pertains to the association of a specific single polynucleotide polymorphism (SNP) in the human genome with increased risk for myocardial infarction (MI). In particular, the present invention pertains to a whether a human has an increased risk for a myocardial infarction (MI), or whether a human's risk for MI is reduced by treatment with an HMG-CoA reductase inhibitor, e.g. a statin. The method comprises determining whether a human has an increased risk for MI based on the presence or absence of G in gene KIF6 at position 101 of SEQ ID NO: 263, or C at position 101 of its complement. Presence of G at position 101 of SEQ ID NO:263 or C at position 101 of the complement indicates that the human has increased risk for MI and that the risk is reduced by such treatment. Also provided are polynucleotides useful for performing such methods.

IPC Classes  ?

  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C07K 14/47 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from animalsPeptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from humans from vertebrates from mammals
  • C07K 16/18 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans
  • C40B 30/04 - Methods of screening libraries by measuring the ability to specifically bind a target molecule, e.g. antibody-antigen binding, receptor-ligand binding
  • C40B 40/06 - Libraries containing nucleotides or polynucleotides, or derivatives thereof
  • G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor

60.

Genetic polymorphisms associated with cardiovascular disorders and drug response, methods of detection and uses thereof

      
Application Number 11526137
Grant Number 07799530
Status In Force
Filing Date 2006-09-22
First Publication Date 2007-03-29
Grant Date 2010-09-21
Owner Celera Corporation (USA)
Inventor
  • Iakoubova, Olga
  • Devlin, James

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with cardiovascular disorders, particularly acute coronary events such as myocardial infarction and stroke, and genetic polymorphisms that are associated with responsiveness of an individual having a cardiovascular disorder to treatment of the disorder with statin. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C12P 19/34 - Polynucleotides, e.g. nucleic acids, oligoribonucleotides

61.

Genetic polymorphisms associated with coronary heart disease, methods of detection and uses thereof

      
Application Number 11375359
Grant Number 07977052
Status In Force
Filing Date 2006-03-13
First Publication Date 2006-10-05
Grant Date 2011-07-12
Owner Celera Corporation (USA)
Inventor
  • Luke, May M.
  • Devlin, James J.
  • Shiffman, Dov

Abstract

The present invention is based on the discovery of genetic polymorphisms that are associated with coronary heart disease and in particular stenosis and MI and response to drug treatment. In particular, the present invention relates to nucleic acid molecules containing the polymorphisms, variant proteins encoded by such nucleic acid molecules, reagents for detecting the polymorphic nucleic acid molecules and proteins, and methods of using the nucleic acid and proteins as well as methods of using reagents for their detection.

IPC Classes  ?

  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids

62.

GENETIC POLYMORPHISMS ASSOCIATED WITH CORONARY HEART DISEASE, METHODS OF DETECTION AND USES THEREOF

      
Document Number 02600794
Status In Force
Filing Date 2006-03-13
Open to Public Date 2006-09-21
Grant Date 2014-08-12
Owner CELERA CORPORATION (USA)
Inventor
  • Luke, May
  • Cargill, Michele
  • Devlin, James
  • Shiffman, Dov

Abstract


The present invention is based on the discovery of genetic polymorphisms that
are associated with coronary heart disease and in particular stenosis and MI
and response to drug treatment. In particular, the present invention relates
to nucleic acid molecules containing the polymorphisms, variant proteins
encoded by such nucleic acid molecules, reagents for detecting the polymorphic
nucleic acid molecules and proteins, and methods of using the nucleic acid and
proteins as well as methods of using reagents for their detection.

63.

SINGLE NUCLEOTIDE POLYMORPHISMS ASSOCIATED WITH CARDIOVASCULAR DISORDERS AND STATIN RESPONSE, METHODS OF DETECTION AND USES THEREOF

      
Document Number 02832293
Status In Force
Filing Date 2004-11-24
Open to Public Date 2005-06-23
Grant Date 2015-08-04
Owner
  • CELERA CORPORATION (USA)
  • BRISTOL-MYERS SQUIBB COMPANY (USA)
Inventor
  • Cargill, Michele
  • Iakoubova, Olga
  • Devlin, James J.
  • Tsuchihashi, Zenta
  • Shaw, Peter
  • Ploughman, Lynn Marie
  • Zerba, Kim E.
  • Koustubh, Ranade
  • Kirchgessner, Todd

Abstract


A method is provided for indicating whether a human has an increased risk for
a
myocardial infarction (MI), or whether a human's risk for MI is reduced by
treatment with an
HMG-CoA reductase inhibitor, e.g. a statin such as pravastatin, atorvastatin,
simvastatin,
cerevastatin, or lovastatin. The method comprises testing nucleic acid from
the human for
presence or absence of a single nucleotide polymorphism at position 101 of SEQ
ID NO:205 or
its complement. Presence of T at position 101 of SEQ ID NO:205 or A at
position 101 of the
complement indicates that the human has increased risk for MI and that the
risk is reduced by
such treatment. Also provided are polynucleotides useful for such testing.

IPC Classes  ?

  • C07K 14/47 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from animalsPeptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from humans from vertebrates from mammals
  • C07K 16/18 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans
  • C12N 15/12 - Genes encoding animal proteins
  • C12Q 1/6827 - Hybridisation assays for detection of mutation or polymorphism
  • C12Q 1/6858 - Allele-specific amplification
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • C40B 30/04 - Methods of screening libraries by measuring the ability to specifically bind a target molecule, e.g. antibody-antigen binding, receptor-ligand binding
  • C40B 40/06 - Libraries containing nucleotides or polynucleotides, or derivatives thereof
  • G01N 33/48 - Biological material, e.g. blood, urineHaemocytometers
  • G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor
  • G01N 33/577 - ImmunoassayBiospecific binding assayMaterials therefor involving monoclonal antibodies
  • G01N 35/00 - Automatic analysis not limited to methods or materials provided for in any single one of groups Handling materials therefor

64.

SINGLE NUCLEOTIDE POLYMORPHISMS ASSOCIATED WITH CARDIOVASCULAR DISORDERS AND STATIN RESPONSE, METHODS OF DETECTION AND USES THEREOF

      
Document Number 02860272
Status In Force
Filing Date 2004-11-24
Open to Public Date 2005-06-23
Grant Date 2017-12-19
Owner
  • CELERA CORPORATION (USA)
  • BRISTOL-MYERS SQUIBB COMPANY (USA)
Inventor
  • Cargill, Michele
  • Iakoubova, Olga
  • Devlin, James J.
  • Tsuchihashi, Zenta
  • Shaw, Peter
  • Ploughman, Lynn Marie
  • Zerba, Kim E.
  • Koustubh, Ranade
  • Kirchgessner, Todd

Abstract


A method is provided for indicating whether a human has an increased risk for
a
myocardial infarction (MI), or whether a human's risk for MI is reduced by
treatment with an
HMG-CoA reductase inhibitor, e.g. a statin such as pravastatin, atorvastatin,
simvastatin,
cerevastatin, or lovastatin. The method comprises testing nucleic acid from
the human for
presence or absence of a single nucleotide polymorphism at position 101 of SEQ
ID NO:197 or
its complement. Presence of G at position 101 of SEQ ID NO:197 or C at
position 101 of the
complement indicates that the human has increased risk for MI and that the
risk is reduced by
such treatment. Also provided are polynucleotides useful for such testing.

IPC Classes  ?

  • A61K 31/22 - Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
  • A61K 31/366 - Lactones having six-membered rings, e.g. delta-lactones
  • A61K 31/40 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
  • A61K 31/4418 - Non-condensed pyridinesHydrogenated derivatives thereof having a carbocyclic ring directly attached to the heterocyclic ring, e.g. cyproheptadine
  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C07K 14/47 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from animalsPeptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from humans from vertebrates from mammals
  • C07K 16/18 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans
  • C12N 15/12 - Genes encoding animal proteins
  • C12Q 1/6827 - Hybridisation assays for detection of mutation or polymorphism
  • C12Q 1/6858 - Allele-specific amplification
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • C40B 30/04 - Methods of screening libraries by measuring the ability to specifically bind a target molecule, e.g. antibody-antigen binding, receptor-ligand binding
  • C40B 40/06 - Libraries containing nucleotides or polynucleotides, or derivatives thereof
  • G01N 33/48 - Biological material, e.g. blood, urineHaemocytometers
  • G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor

65.

SINGLE NUCLEOTIDE POLYMORPHISMS ASSOCIATED WITH CARDIOVASCULAR DISORDERS AND STATIN RESPONSE, METHODS OF DETECTION AND USES THEREOF

      
Document Number 03050151
Status In Force
Filing Date 2004-11-24
Open to Public Date 2005-06-23
Grant Date 2023-03-07
Owner
  • CELERA CORPORATION (USA)
  • BRISTOL-MYERS SQUIBB COMPANY (USA)
Inventor
  • Cargill, Michele
  • Iakoubova, Olga
  • Devlin, James J.
  • Tsuchihashi, Zenta
  • Shaw, Peter
  • Ploughman, Lynn Marie
  • Zerba, Kim E.
  • Koustubh, Ranade
  • Kirchgessner, Todd

Abstract


A method is provided for indicating whether a human has an increased risk for
a
coronary heart disease (CHD), or whether a human's risk for CHD is reduced by
treatment with
an HMG-CoA reductase inhibitor, e.g. a statin such as pravastatin,
atorvastatin, simvastatin,
cerevastatin, or lovastatin. The method comprises testing nucleic acid from
the human for
presence or absence of a single nucleotide polymorphism at position 101 of SEQ
ID NO:195 or
its complement. Presence of G at position 101 of SEQ ID NO:195 or C at
position 101 of the
complement indicates that the human has increased risk for CHD and that the
risk is reduced by
such treatment. Also provided are polynucleotides useful for such testing.

IPC Classes  ?

  • A61K 31/22 - Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
  • A61P 9/00 - Drugs for disorders of the cardiovascular system
  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6827 - Hybridisation assays for detection of mutation or polymorphism
  • C12Q 1/6876 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor
  • G01N 35/00 - Automatic analysis not limited to methods or materials provided for in any single one of groups Handling materials therefor

66.

SINGLE NUCLEOTIDE POLYMORPHISMS ASSOCIATED WITH CARDIOVASCULAR DISORDERS AND STATIN RESPONSE, METHODS OF DETECTION AND USES THEREOF

      
Document Number 02547072
Status In Force
Filing Date 2004-11-24
Open to Public Date 2005-06-23
Grant Date 2015-06-23
Owner
  • BRISTOL-MYERS SQUIBB COMPANY (Switzerland)
  • CELERA CORPORATION (USA)
Inventor
  • Cargill, Michele
  • Iakoubova, Olga
  • Devlin, James J.
  • Tsuchihashi, Zenta
  • Shaw, Peter
  • Ploughman, Lynn Marie
  • Zerba, Kim E.
  • Koustubh, Ranade
  • Kirchgessner, Todd

Abstract



A method is provided for indicating whether a human has an increased risk for
a
myocardial infarction (MI), or whether a human's risk for MI is reduced by
treatment with an
HMG-CoA reductase inhibitor, e.g. a statin such as pravastatin, atorvastatin,
simvastatin,
cerevastatin, or lovastatin. The method comprises testing nucleic acid from
the human for
presence or absence of a single nucleotide polymorphism at position 101 of SEQ
ID NO:190 or
its complement. Presence of G at position 101 of SEQ ID NO:190 or C at
position 101 of the
complement indicates that the human has increased risk for MI and that the
risk is reduced by
such treatment. Also provided are polynucleotides useful for such testing.

IPC Classes  ?

  • C04B 40/06 - Inhibiting the setting, e.g. mortars of the deferred action type containing water in breakable containers
  • C07H 21/04 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
  • C40B 30/04 - Methods of screening libraries by measuring the ability to specifically bind a target molecule, e.g. antibody-antigen binding, receptor-ligand binding
  • G01N 33/48 - Biological material, e.g. blood, urineHaemocytometers
  • G01N 35/00 - Automatic analysis not limited to methods or materials provided for in any single one of groups Handling materials therefor

67.

SINGLE NUCLEOTIDE POLYMORPHISMS ASSOCIATED WITH CARDIOVASCULAR DISORDERS AND STATIN RESPONSE, METHODS OF DETECTION AND USES THEREOF

      
Document Number 02921196
Status In Force
Filing Date 2004-11-24
Open to Public Date 2005-06-23
Grant Date 2019-03-05
Owner
  • CELERA CORPORATION (USA)
  • BRISTOL-MYERS SQUIBB COMPANY (USA)
Inventor
  • Cargill, Michele
  • Iakoubova, Olga
  • Devlin, James J.
  • Tsuchihashi, Zenta
  • Shaw, Peter
  • Ploughman, Lynn Marie
  • Zerba, Kim E.
  • Koustubh, Ranade
  • Kirchgessner, Todd

Abstract


A method is provided for indicating whether a human has an increased risk for
a
myocardial infarction (MI), or whether a human's risk for MI is reduced by
treatment with an
HMG-CoA reductase inhibitor, e.g. a statin such as pravastatin, atorvastatin,
simvastatin,
cerevastatin, or lovastatin. The method comprises testing nucleic acid from
the human for
presence or absence of a single nucleotide polymorphism at position 101 of SEQ
ID NO:191 or
its complement. Presence of G at position 101 of SEQ ID NO:191 or C at
position 101 of the
complement indicates that the human has increased risk for MI and that the
risk is reduced by
such treatment. Also provided are polynucleotides useful for such testing.

IPC Classes  ?

  • A61K 31/22 - Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
  • A61K 31/366 - Lactones having six-membered rings, e.g. delta-lactones
  • A61K 31/40 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
  • A61K 31/4418 - Non-condensed pyridinesHydrogenated derivatives thereof having a carbocyclic ring directly attached to the heterocyclic ring, e.g. cyproheptadine
  • C07K 14/47 - Peptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from animalsPeptides having more than 20 amino acidsGastrinsSomatostatinsMelanotropinsDerivatives thereof from humans from vertebrates from mammals
  • C07K 16/18 - Immunoglobulins, e.g. monoclonal or polyclonal antibodies against material from animals or humans
  • C12N 15/12 - Genes encoding animal proteins
  • C12Q 1/6827 - Hybridisation assays for detection of mutation or polymorphism
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
  • C40B 30/04 - Methods of screening libraries by measuring the ability to specifically bind a target molecule, e.g. antibody-antigen binding, receptor-ligand binding
  • C40B 40/06 - Libraries containing nucleotides or polynucleotides, or derivatives thereof
  • G01N 33/48 - Biological material, e.g. blood, urineHaemocytometers
  • G01N 33/50 - Chemical analysis of biological material, e.g. blood, urineTesting involving biospecific ligand binding methodsImmunological testing
  • G01N 33/53 - ImmunoassayBiospecific binding assayMaterials therefor

68.

SINGLE NUCLEOTIDE POLYMORPHISMS ASSOCIATED WITH CARDIOVASCULAR DISORDERS AND STATIN RESPONSE, METHODS OF DETECTION AND USES THEREOF

      
Document Number 02991249
Status In Force
Filing Date 2004-11-24
Open to Public Date 2005-06-23
Grant Date 2020-07-07
Owner
  • CELERA CORPORATION (USA)
  • BRISTOL-MYERS SQUIBB COMPANY (USA)
Inventor
  • Cargill, Michele
  • Iakoubova, Olga
  • Devlin, James J.
  • Tshuchihashi, Zenta
  • Shaw, Peter
  • Ploughman, Lynn Marie
  • Zerba, Kim E.
  • Koustubh, Ranade
  • Kirchgessner, Todd

Abstract


A method is provided for indicating whether a human has an increased risk for
a
myocardial infarction (MI), or whether a human's risk for MI is reduced by
treatment with an
HMG-CoA reductase inhibitor, e.g. a statin such as pravastatin, atorvastatin,
simvastatin,
cerevastatin, or lovastatin. The method comprises testing nucleic acid from
the human for
presence or absence of a single nucleotide polymorphism at position 101 of SEQ
ID NO:200 or
its complement. Presence of G at position 101 of SEQ ID NO:200 or C at
position 101 of the
complement indicates that the human has increased risk for MI and that the
risk is reduced by
such treatment. Also provided are polynucleotides useful for such testing.

IPC Classes  ?

  • C12Q 1/68 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving nucleic acids
  • C12Q 1/6827 - Hybridisation assays for detection of mutation or polymorphism
  • C12Q 1/6876 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
  • C12Q 1/6883 - Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material

69.

CELERA

      
Application Number 001062876
Status Registered
Filing Date 1999-02-02
Registration Date 2010-03-08
Owner Celera Corporation (USA)
NICE Classes  ?
  • 01 - Chemical and biological materials for industrial, scientific and agricultural use
  • 05 - Pharmaceutical, veterinary and sanitary products
  • 09 - Scientific and electric apparatus and instruments
  • 42 - Scientific, technological and industrial services, research and design

Goods & Services

Synthetic materials for scientific or medical research use, synthetic DNA, tissues and proteins; biological materials for scientific or medical research use, tissues, cells and natural DNA; reagents and other materials for scientific or medical research use. Medical diagnostic reagents, assays and assay systems; clinical medical reagents, assays and assay systems. Computer software and software tools for analysis and management of data and information in the fields of science, technology, medicine, health and their related business, law and public policy areas; computer software and software tools for analysis and management of genomic databases; proteonomic databases and disease databases; CD-ROMS, interactive software and computer programs, compact discs, pre-recorded audio and video tapes and cassettes on the subjects of science, technology, medicine, health and their related business, law and public policy areas; CD -ROMS, compact discs and audio and video tapes and cassettes on the subject of science, technology, medicine, health and related business, law and public policy issues; reports and publications, in electronic format, concerning the subjects of science, technology, medicine, health and related business, law and public policy issues. Consultation and research in the fields of science, technology, medicine, health and their related business, law and public policy areas; providing databases and information in the fields of science, technology, medicine, health and their related business, law and public policy areas; providing computer service in the fields of science, technology, medicine, health and their related business, law and public policy areas; providing diagnostic service and assay systems in the fields of medicine and health; providing biological materials including tissues, cells and natural DNA to the specifications of others; providing synthetic materials including tissues, proteins and DNA to the specification of others; developing, producing, distributing and licensing all above products and databases.