CN102998458B - 通过测定半乳糖苷凝集素-3或者血小板反应蛋白-2的水平鉴定具有发生心力衰竭风险的受试者的方法 - Google Patents
通过测定半乳糖苷凝集素-3或者血小板反应蛋白-2的水平鉴定具有发生心力衰竭风险的受试者的方法 Download PDFInfo
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| EP03078161.1 | 2003-10-09 | ||
| CN2004800332637A CN1879022B (zh) | 2003-10-09 | 2004-09-27 | 通过测定半乳糖苷凝集素-3或者血小板反应蛋白-2的水平鉴定具有发生心力衰竭风险的受试者的方法 |
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| CN2004800332637A Expired - Fee Related CN1879022B (zh) | 2003-10-09 | 2004-09-27 | 通过测定半乳糖苷凝集素-3或者血小板反应蛋白-2的水平鉴定具有发生心力衰竭风险的受试者的方法 |
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| EP2067042A2 (en) * | 2006-09-25 | 2009-06-10 | Universiteit Maastricht | Means and methods for diagnosing and/or treating a subject at risk of developing heart failure |
| EP2109688A4 (en) * | 2007-01-23 | 2010-02-17 | Univ Virginia | GALECTIN-3 BINDING PROTEIN AS BIOMARKER FOR HEART CIRCULATION DISEASES |
| WO2009039078A1 (en) * | 2007-09-17 | 2009-03-26 | Bg Medicine, Inc. | Assessing congestive heart risk in patients treated or potentially to be treated with a peroxisome-proliferator-activator-receptor-gamma agonist or a thiazolidinedione |
| CA2742265C (en) * | 2008-10-29 | 2014-07-15 | Bg Medicine, Inc. | Galectin-3 immunoassay |
| KR20120104167A (ko) * | 2009-08-25 | 2012-09-20 | 비쥐 메디신, 인코포레이티드 | 갈렉틴―3 및 심장 재동기화 요법 |
| WO2012003475A1 (en) | 2010-07-02 | 2012-01-05 | Bg Medicine, Inc. | Statin therapy monitored by galectin- 3 measurement |
| JP5787895B2 (ja) * | 2010-10-18 | 2015-09-30 | 原 英彰 | 筋萎縮性側索硬化症マーカー及びその利用 |
| EP2460890A1 (en) * | 2010-12-01 | 2012-06-06 | Max-Delbrück-Centrum für Molekulare Medizin (MDC) | Gpnmb/Osteoactivin as a drug target and biomarker in cardiac diseases |
| JP2014505256A (ja) * | 2011-01-31 | 2014-02-27 | ビージー メディシン， インコーポレイテッド | 急性冠動脈症候群後の心不全を検出し、予後を判定するためのガレクチン−３の使用 |
| CN103718046B (zh) | 2011-03-17 | 2016-10-12 | 重症监护诊断股份有限公司 | 预测不良临床结果的风险的方法 |
| AR086543A1 (es) | 2011-05-25 | 2014-01-08 | Bg Medicine Inc | Inhibidores de galectina-3 y metodos de uso de los mismos, composicion farmaceutica |
| EP2788761B1 (en) * | 2011-12-08 | 2018-02-28 | Eliaz Therapeutics, Inc. | Reduction of galectin-3 levels by plasmapheresis |
| WO2014052803A2 (en) * | 2012-09-27 | 2014-04-03 | Siemens Healthcare Diagnostics Inc. | Cystatin c and galectin-3 as biomarkers for pulmonary arterial hypertension |
| JP6366598B2 (ja) * | 2012-11-15 | 2018-08-01 | タフツ ユニバーシティー | ガレクチンタンパク質阻害剤を用いて被験体の眼の血管新生または繊維症を処置し、調節し、または、予防する方法、組成物、およびキット |
| CA2973653A1 (en) | 2015-01-18 | 2016-07-21 | Diasorin S.P.A. | Use of 1,25-dihydroxyvitamin d values in ratio with pth as a prognostic biomarker |
| CN107614168B (zh) * | 2015-05-28 | 2019-10-25 | 京瓷株式会社 | 切削工具 |
| CN112553335A (zh) * | 2020-12-17 | 2021-03-26 | 核工业总医院 | 肾细胞癌生物标志物及其应用 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1283269A (zh) * | 1997-10-24 | 2001-02-07 | 盐野义制药株式会社 | 利尿钠肽分解抑制方法及其用该方法分析利尿钠肽的改良方法 |
| CN1339107A (zh) * | 1999-01-29 | 2002-03-06 | 罗赫诊断器材股份有限公司 | 鉴定n－末端前bnp的方法 |
Family Cites Families (46)
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|---|---|---|---|---|
| US4632901A (en) | 1984-05-11 | 1986-12-30 | Hybritech Incorporated | Method and apparatus for immunoassays |
| US4946778A (en) | 1987-09-21 | 1990-08-07 | Genex Corporation | Single polypeptide chain binding molecules |
| US4704692A (en) | 1986-09-02 | 1987-11-03 | Ladner Robert C | Computer based system and method for determining and displaying possible chemical structures for converting double- or multiple-chain polypeptides to single-chain polypeptides |
| US5132405A (en) | 1987-05-21 | 1992-07-21 | Creative Biomolecules, Inc. | Biosynthetic antibody binding sites |
| US5091513A (en) | 1987-05-21 | 1992-02-25 | Creative Biomolecules, Inc. | Biosynthetic antibody binding sites |
| AU2684488A (en) | 1988-06-27 | 1990-01-04 | Carter-Wallace, Inc. | Test device and method for colored particle immunoassay |
| US20010051350A1 (en) | 1995-05-02 | 2001-12-13 | Albert Nazareth | Diagnostic detection device and method |
| BE1010935A7 (nl) * | 1997-02-19 | 1999-03-02 | Delanghe Joris Richard Siegfri | Fenotypering van humaan haptoglobine in serum of plasma door middel van quantitatieve agglutinatie met streptococcus antigenen. |
| CA2293718A1 (en) | 1997-06-10 | 1998-12-17 | Medlyte Diagnostics, Inc. | Methods for early detection of heart disease |
| US20060166276A1 (en) * | 1997-09-05 | 2006-07-27 | Lung Health Diagnostics Pty Ltd | Method of diagnosis and agents useful for same |
| DE69841804D1 (de) * | 1997-09-05 | 2010-09-16 | Southern Medical Diagnostics P | Diagnoseverfahren |
| ES2314786T3 (es) * | 1998-04-02 | 2009-03-16 | Genentech, Inc. | Uso de interferon gamma para el tratamiento de la hipertrofia cardiaca. |
| WO2001006262A1 (en) * | 1999-02-19 | 2001-01-25 | University Of Iowa Research Foundation | Diagnostics and therapeutics for macular degeneration |
| WO2001014581A2 (en) * | 1999-08-20 | 2001-03-01 | Board Of Regents, The University Of Texas System | Hdac4 and hdac5 in the regulation of cardiac gene expression |
| GB2373500B (en) | 2000-02-04 | 2004-12-15 | Aeomica Inc | Methods and apparatus for predicting, confirming, and displaying functional information derived from genomic sequence |
| EP1358347A2 (en) | 2000-04-05 | 2003-11-05 | Incyte Genomics, Inc. | Genes expressed in foam cell differentiation |
| KR100395254B1 (ko) | 2000-10-30 | 2003-08-21 | (주)자리타 바이오텍 | 종양 발생 예측 키트 |
| AU2002220266A1 (en) * | 2000-11-09 | 2002-05-21 | Millennium Pharmaceuticals, Inc. | Methods for the identification and the treatment of cardiovascular disease |
| WO2002038794A2 (en) * | 2000-11-09 | 2002-05-16 | The Brigham And Women's Hospital, Inc. | Cardiovascular disease diagnostic and therapeutic targets |
| ATE506075T1 (de) * | 2000-12-08 | 2011-05-15 | Curagen Corp | Verfahren zur bestimmung und behandlung von tuberöse-sklerose komplex assoziierten erkrankungen |
| JP4035562B2 (ja) * | 2001-01-31 | 2008-01-23 | 国立大学法人富山大学 | ガレクチン−３誘導能を利用した物質のスクリーニング方法、肝の状態の診断方法およびこれらの方法を利用したキット |
| WO2002074911A2 (en) | 2001-03-19 | 2002-09-26 | Wisconsin Alumni Research Foundation | Identification of gene expression alterations underlying the aging process in mammals |
| US20060019235A1 (en) | 2001-07-02 | 2006-01-26 | The Board Of Trustees Of The Leland Stanford Junior University | Molecular and functional profiling using a cellular microarray |
| US7447594B2 (en) | 2001-07-10 | 2008-11-04 | Ocimum Biosolutions, Inc. | Molecular cardiotoxicology modeling |
| US20030099958A1 (en) * | 2001-09-05 | 2003-05-29 | Vitivity, Inc. | Diagnosis and treatment of vascular disease |
| GB0124145D0 (en) | 2001-10-08 | 2001-11-28 | Bayer Ag | Genes and proteins for prevention,prediction,prognosis and therapy of cardiovascular disease |
| US20060141493A1 (en) | 2001-11-09 | 2006-06-29 | Duke University Office Of Science And Technology | Atherosclerotic phenotype determinative genes and methods for using the same |
| DE60323091D1 (de) * | 2002-05-13 | 2008-10-02 | Arexis Ab | Autoimmunerkrankungen und nadph-oxidase-defekte |
| AU2003290537A1 (en) | 2002-10-24 | 2004-05-13 | Duke University | Binary prediction tree modeling with many predictors and its uses in clinical and genomic applications |
| JP2006514554A (ja) | 2002-11-21 | 2006-05-11 | ワイス | 腎細胞癌および他の固形腫瘍の診断法 |
| EP1431399A1 (en) * | 2002-12-20 | 2004-06-23 | Clinigenetics | Methods and composition for identifying therapeutic agents of atherosclerotic plaque lesions |
| US6889083B2 (en) | 2003-04-21 | 2005-05-03 | Medtronic, Inc. | Atrial tracking recovery to restore cardiac resynchronization therapy in dual chamber tracking modes |
| WO2005020784A2 (en) | 2003-05-23 | 2005-03-10 | Mount Sinai School Of Medicine Of New York University | Surrogate cell gene expression signatures for evaluating the physical state of a subject |
| WO2004111654A2 (en) | 2003-06-06 | 2004-12-23 | Ciphergen Biosystems, Inc. | Serum biomarkers in ischaemic heart disease |
| US20050106100A1 (en) | 2003-09-03 | 2005-05-19 | Harris Thomas D. | Compounds containing matrix metalloproteinase substrates and methods of their use |
| EP1560025A3 (en) * | 2003-10-03 | 2011-09-07 | F. Hoffmann-La Roche AG | Specific markers for diabetes |
| EP1522857A1 (en) * | 2003-10-09 | 2005-04-13 | Universiteit Maastricht | Method for identifying a subject at risk of developing heart failure by determining the level of galectin-3 or thrombospondin-2 |
| DE10347436B4 (de) | 2003-10-13 | 2007-08-02 | Johann Wolfgang Goethe-Universität Frankfurt am Main | In vitro Verfahren zur Diagnose der kardiovaskulären Funktionalität von Blut-abgeleiteter zirkulierender Vorläuferzellen (BDP) |
| US20060019890A1 (en) | 2004-01-15 | 2006-01-26 | Kapoun Ann M | Method for treating cardiac remodeling following myocardial injury |
| WO2006026074A2 (en) | 2004-08-04 | 2006-03-09 | Duke University | Atherosclerotic phenotype determinative genes and methods for using the same |
| CA2596469A1 (en) | 2005-02-01 | 2006-08-10 | Government Of The U.S.A, As Represented By The Secretary Department Of H Ealth & Human Services | Biomarkers for tissue status |
| US20070092886A1 (en) | 2005-03-22 | 2007-04-26 | Raymond Tabibiazar | Methods and compositions for diagnosis, monitoring and development of therapeutics for treatment of atherosclerotic disease |
| US7632634B2 (en) | 2005-04-15 | 2009-12-15 | University Of Maryland Biotechnology Institute | Method and assay for early diagnosis of prostate cancer |
| US9592970B2 (en) | 2008-07-17 | 2017-03-14 | Toby D. Henderson | Robotic gantry with end effector for product lifting |
| CA2742265C (en) | 2008-10-29 | 2014-07-15 | Bg Medicine, Inc. | Galectin-3 immunoassay |
| KR20120104167A (ko) | 2009-08-25 | 2012-09-20 | 비쥐 메디신, 인코포레이티드 | 갈렉틴―3 및 심장 재동기화 요법 |
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Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1283269A (zh) * | 1997-10-24 | 2001-02-07 | 盐野义制药株式会社 | 利尿钠肽分解抑制方法及其用该方法分析利尿钠肽的改良方法 |
| CN1339107A (zh) * | 1999-01-29 | 2002-03-06 | 罗赫诊断器材股份有限公司 | 鉴定n－末端前bnp的方法 |
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