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
Publication number Priority date Publication date Assignee Title
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
US20090312410A1 (en) * 2006-04-21 2009-12-17 Applera Corporation Genetic polymorphisms associated with coronary heart disease, methods of detection and uses thereof
DK2471954T3 (en) * 2007-02-21 2016-09-12 Decode Genetics Ehf Susceptibility genetic variants associated with cardiovascular diseases
WO2008132763A2 (en) * 2007-04-30 2008-11-06 Decode Genetics Ehf Genetic variants useful for risk assessment of coronary artery disease and myocardial infarction
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
US10829560B2 (en) 2015-04-20 2020-11-10 Consejo Superior De Investigaciones Cientificas Agents binding specifically to human cadherin-17, human cadherin-5, human cadherin-6 and human cadherin-20 RGD motif
BR112021001878A2 (pt) * 2018-07-31 2021-04-27 Cornell University métodos de terapia genética para o controle da função do órgão
JP2022523564A (ja) 2019-03-04 2022-04-25 アイオーカレンツ， インコーポレイテッド 機械学習を使用するデータ圧縮および通信

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2158479C (en) * 1993-04-05 2009-07-07 Mark T. Keating Diagnosis and treatment of supravalvular aortic stenosis and williams syndrome
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
WO1999055909A1 (en) * 1998-04-27 1999-11-04 Amsterdam Molecular Therapeutics B.V. A FREQUENT MUTATION IN THE CYSTATHIONINE β-SYNTHASE GENE INCREASES RISK FOR CORONARY ARTERY DISEASE
WO2000071753A2 (en) * 1999-05-24 2000-11-30 Interleukin Genetics, Inc. Diagnostics and therapeutics for restenosis
US6297014B1 (en) * 1999-07-02 2001-10-02 Cedars-Sinai Medical Center Genetic test to determine non-responsiveness to statin drug treatment
JP2003527099A (ja) * 1999-11-03 2003-09-16 ザイモジェネティクス，インコーポレイティド フォリスタチン関連タンパク質ｚｆｓｔａ４
AU2001240521A1 (en) * 2000-01-20 2001-07-31 Epidauros Biotechnologie Ag (ca)n polymorphisms in an intron of the endothelial nitric oxide synthase gene and their use in diagnostic and therapeutic applications
JP2004525611A (ja) * 2000-10-31 2004-08-26 アベンティス・ファーマ・ソシエテ・アノニム 多型ヒトａｂｃａ１遺伝子の配列、それらの使用、検出方法およびキット
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
JP2006510341A (ja) * 2002-02-27 2006-03-30 バイエル・ヘルスケア・アクチェンゲゼルシャフト 有害薬剤反応および薬剤効力を予測する単一ヌクレオチド多型
AU2003232034A1 (en) * 2002-05-02 2003-11-17 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
WO2004081186A2 (en) * 2003-03-10 2004-09-23 Applera Corporation Single nucleotide polymorphisms associated with stenosis, methods of detection and uses thereof

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