JP2009523006A5 - - Google Patents

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Publication number
JP2009523006A5
JP2009523006A5 JP2007511679A JP2007511679A JP2009523006A5 JP 2009523006 A5 JP2009523006 A5 JP 2009523006A5 JP 2007511679 A JP2007511679 A JP 2007511679A JP 2007511679 A JP2007511679 A JP 2007511679A JP 2009523006 A5 JP2009523006 A5 JP 2009523006A5
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JP
Japan
Prior art keywords
seq
snp
risk
polynucleotide
individual
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2007511679A
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English (en)
Japanese (ja)
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JP2009523006A (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/US2005/016076 external-priority patent/WO2005110039A2/en
Publication of JP2009523006A publication Critical patent/JP2009523006A/ja
Publication of JP2009523006A5 publication Critical patent/JP2009523006A5/ja
Pending legal-status Critical Current

Links

JP2007511679A 2004-05-07 2005-05-09 脈管疾患に関連する遺伝的多型、その検出方法および使用 Pending JP2009523006A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US56884504P 2004-05-07 2004-05-07
US62593604P 2004-11-09 2004-11-09
PCT/US2005/016076 WO2005110039A2 (en) 2004-05-07 2005-05-09 Genetic polymorphisms associated with vascular diseases, methods of detection and uses thereof

Publications (2)

Publication Number Publication Date
JP2009523006A JP2009523006A (ja) 2009-06-18
JP2009523006A5 true JP2009523006A5 (enExample) 2009-07-30

Family

ID=35394601

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007511679A Pending JP2009523006A (ja) 2004-05-07 2005-05-09 脈管疾患に関連する遺伝的多型、その検出方法および使用

Country Status (5)

Country Link
US (1) US20050287559A1 (enExample)
EP (1) EP1753875A2 (enExample)
JP (1) JP2009523006A (enExample)
CA (1) CA2566257A1 (enExample)
WO (1) WO2005110039A2 (enExample)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
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WO2007028147A2 (en) * 2005-09-01 2007-03-08 Philadelphia Health & Education Corporation D.B.A. Drexel University College Of Medicin Identification of a prostatic intraepithelial neoplasia (pin)-specific gene and protein (pin-1) useful as a diagnostic treatment for prostate cancer
EP2016197A4 (en) * 2006-04-21 2009-09-16 Celera GENETIC POLYMORPHISMS ASSOCIATED WITH CORONARY DISEASE, DETECTION METHODS AND JOBS
KR101571523B1 (ko) * 2007-02-21 2015-11-24 디코드 제네틱스 이에이치에프 심혈관 질환과 연관된 유전적 감수성 변이
DK2155907T3 (da) * 2007-04-30 2015-08-31 Decode Genetics Ehf Genetiske varianter nyttige til risikovurdering af koronararteriesygdom og myokardieinfarkt
WO2008140776A1 (en) 2007-05-09 2008-11-20 The Brigham And Women's Hospital, Inc. Polymorphism in the apo (a) gene predict responsiveness to acetylsalicylic acid treatment
GB2453173A (en) 2007-09-28 2009-04-01 Dxs Ltd Polynucleotide primers
WO2015100300A2 (en) * 2013-12-23 2015-07-02 Duke University Methods for diagnosing and treating copper-dependent diseases
JP2018513141A (ja) * 2015-04-20 2018-05-24 コンセジョ スペリオール デ インベスティガショネス シエンティフィカス ヒトカドヘリン−１７、ヒトカドヘリン−５、ヒトカドヘリン−６およびヒトカドヘリン−２０のｒｇｄモチーフに特異的に結合する薬剤
CA3108324A1 (en) * 2018-07-31 2020-02-06 Cornell University Gene therapy methods to control organ function
EP3935581A4 (en) 2019-03-04 2022-11-30 Iocurrents, Inc. DATA COMPRESSION AND COMMUNICATION USING MACHINE LEARNING

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08512198A (ja) * 1993-04-05 1996-12-24 ユニバーシティ・オブ・ユタ・リサーチ・ファウンデーション 大動脈弁上部狭窄およびウィリアムズ症候群の診断および治療
US5658729A (en) * 1994-10-11 1997-08-19 The University Of British Columbia Method, reagent and kit for evaluating susceptibility to premature atherosclerosis
US6210877B1 (en) * 1997-03-10 2001-04-03 Interleukin Genetics, Inc. Prediction of coronary artery disease
US6524795B1 (en) * 1997-03-10 2003-02-25 Interleukin Genetics, Inc. Diagnostics for cardiovascular disorders
EP0939136A1 (en) * 1998-01-07 1999-09-01 Academisch Ziekenhuis bij de Universiteit van Amsterdam Assay for predicting the angiographic response to lipid-lowering therapy in patients
AU7350598A (en) * 1998-04-27 1999-11-16 Amsterdam Molecular Therapeutics B.V. A frequent mutation in the cystathionine beta-synthase gene increases risk for coronary artery disease
JP2003500069A (ja) * 1999-05-24 2003-01-07 インタールーキン ジェネティックス インク 再狭窄の診断及び治療薬
US6297014B1 (en) * 1999-07-02 2001-10-02 Cedars-Sinai Medical Center Genetic test to determine non-responsiveness to statin drug treatment
AU1356401A (en) * 1999-11-03 2001-05-14 Zymogenetics Inc. Follistatin-related protein zfsta4
WO2001053522A2 (en) * 2000-01-20 2001-07-26 Epidauros Biotechnologie Ag (CA)n POLYMORPHISMS IN AN INTRON OF THE ENDOTHELIAL NITRIC OXIDE SYNTHASE GENE AND THEIR USE IN DIAGNOSTIC AND THERAPEUTIC APPLICATIONS
WO2002036770A2 (fr) * 2000-10-31 2002-05-10 Aventis Pharma S.A. Sequences polymorphes du gene humain abca1, leurs utilisations, les methodes et kits de detection
EP1217080A3 (en) * 2000-12-22 2004-01-28 Pfizer Products Inc. Methods, compositions and kits relating to cardiovascular disease
US20050075283A1 (en) * 2001-07-13 2005-04-07 Applera Corporation Isolated human secreted proteins, nucleic acid molecules encoding human secreted proteins, and uses thereof
EP1293569A3 (en) * 2001-09-14 2004-03-31 Research Association for Biotechnology Full-length cDNAs
AU2003210276A1 (en) * 2002-02-27 2003-09-09 Bayer Aktiengesellschaft Single nucleotide polymorphisms predicting adverse drug reactions and medication efficacy
WO2003093432A2 (en) * 2002-05-02 2003-11-13 Curagen Corporation Therapeutic polypeptides, nucleic acids encoding same, and methods of use
US7306913B2 (en) * 2002-12-20 2007-12-11 Applera Corporation Genetic polymorphisms associated with coronary stenosis, methods of detection and uses thereof
US7625699B2 (en) * 2003-03-10 2009-12-01 Celera Corporation Genetic polymorphisms associated with coronary stenosis, methods of detection and uses thereof

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