DE69628758D1 - Identifikation von mutationen, die mit menschlicher alpha-thalassämie assoziiert sind, und ihre verwendung für die vorhersage von blutkrankheiten. - Google Patents
Identifikation von mutationen, die mit menschlicher alpha-thalassämie assoziiert sind, und ihre verwendung für die vorhersage von blutkrankheiten.Info
- Publication number
- DE69628758D1 DE69628758D1 DE69628758T DE69628758T DE69628758D1 DE 69628758 D1 DE69628758 D1 DE 69628758D1 DE 69628758 T DE69628758 T DE 69628758T DE 69628758 T DE69628758 T DE 69628758T DE 69628758 D1 DE69628758 D1 DE 69628758D1
- Authority
- DE
- Germany
- Prior art keywords
- prediction
- identification
- human alpha
- mutations associated
- blood diseases
- 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.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/156—Polymorphic or mutational markers
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/16—Primer sets for multiplex assays
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Analytical Chemistry (AREA)
- Zoology (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- Pathology (AREA)
- Immunology (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Biophysics (AREA)
- Physics & Mathematics (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/550,715 US5750345A (en) | 1995-10-31 | 1995-10-31 | Detection of human α-thalassemia mutations and their use as predictors of blood-related disorders |
PCT/US1996/017565 WO1997016568A1 (en) | 1995-10-31 | 1996-10-30 | DETECTION OF HUMAN α-THALASSEMIA MUTATIONS AND THEIR USE AS PREDICTORS OF BLOOD-RELATED DISORDERS |
Publications (1)
Publication Number | Publication Date |
---|---|
DE69628758D1 true DE69628758D1 (de) | 2003-07-24 |
Family
ID=24198323
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE69628758T Expired - Lifetime DE69628758D1 (de) | 1995-10-31 | 1996-10-30 | Identifikation von mutationen, die mit menschlicher alpha-thalassämie assoziiert sind, und ihre verwendung für die vorhersage von blutkrankheiten. |
Country Status (5)
Country | Link |
---|---|
US (1) | US5750345A (de) |
EP (1) | EP0859863B1 (de) |
JP (1) | JP2000501923A (de) |
DE (1) | DE69628758D1 (de) |
WO (1) | WO1997016568A1 (de) |
Families Citing this family (50)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998007884A1 (en) * | 1996-08-23 | 1998-02-26 | The Council Of The Queensland Institute Of Medical Research | A method of diagnosing autosomal recessive disorders and agents useful for same |
US6322981B1 (en) | 1996-11-27 | 2001-11-27 | The United States Of America As Represented By The Department Of Health And Human Services | Rapid method for diagnosing the various forms of alpha-thalassemia |
US7395158B2 (en) * | 2000-05-30 | 2008-07-01 | Sensys Medical, Inc. | Method of screening for disorders of glucose metabolism |
IL156746A0 (en) * | 2001-01-02 | 2004-02-08 | Stemron Inc | A method for producing a population of homozygous stem cells having a pre-selected immunotype and/or genotype, cells suitable for transplant derived therefrom and materials and method using same |
US20020187483A1 (en) * | 2001-04-20 | 2002-12-12 | Cerner Corporation | Computer system for providing information about the risk of an atypical clinical event based upon genetic information |
US6905827B2 (en) | 2001-06-08 | 2005-06-14 | Expression Diagnostics, Inc. | Methods and compositions for diagnosing or monitoring auto immune and chronic inflammatory diseases |
US7235358B2 (en) * | 2001-06-08 | 2007-06-26 | Expression Diagnostics, Inc. | Methods and compositions for diagnosing and monitoring transplant rejection |
US20030162174A1 (en) * | 2001-06-11 | 2003-08-28 | Sutherland John W. | Detecting nucleic acid deletion sequences |
US20040142403A1 (en) * | 2001-08-13 | 2004-07-22 | Donald Hetzel | Method of screening for disorders of glucose metabolism |
AU2002343417A1 (en) * | 2001-09-24 | 2003-04-14 | Nuvelo | Novel nucleic acids and polypeptides |
EP2277532A1 (de) * | 2002-09-11 | 2011-01-26 | Genentech, Inc. | Neuartige Zusammensetzung und Verfahren zur Behandlung von Immunerkrankungen |
JP5392980B2 (ja) * | 2003-03-27 | 2014-01-22 | チルドレンズ ホスピタル メディカル センター | 早発型の腎尿細管細胞障害を検出するための方法およびキット |
EP1519194A1 (de) | 2003-09-24 | 2005-03-30 | Roche Diagnostics GmbH | Die Verwendung von GFAP zur Identifizierung einer Intrazerebralblutung |
US20050272101A1 (en) * | 2004-06-07 | 2005-12-08 | Prasad Devarajan | Method for the early detection of renal injury |
DE602005024850D1 (de) * | 2004-09-24 | 2010-12-30 | Beth Israel Hospital | Verfahren zur diagnose und behandlung von schwangerschaftsskomplikationen |
PL1831699T3 (pl) * | 2004-12-20 | 2010-04-30 | Antibodyshop As | Oznaczanie lipokaliny neutrofilowej związanej z żelatynazą (NGAL) jako markera diagnostycznego dla zaburzeń nerek |
US20070037232A1 (en) * | 2005-03-31 | 2007-02-15 | Barasch Jonathan M | Detection of NGAL in chronic renal disease |
US20080090304A1 (en) * | 2006-10-13 | 2008-04-17 | Barasch Jonathan Matthew | Diagnosis and monitoring of chronic renal disease using ngal |
EP1975614A4 (de) * | 2005-12-22 | 2010-06-09 | Shionogi & Co | Verfahren für die vorhersage bzw. prognose von akutem koronarsyndrom |
WO2007116779A1 (ja) * | 2006-03-31 | 2007-10-18 | Mochida Pharmaceutical Co., Ltd. | 新規血小板活性化マーカー及びその測定方法 |
WO2007116975A1 (ja) * | 2006-04-06 | 2007-10-18 | Eisai R & D Management Co., Ltd. | チトクロムcの定量による非アルコール性脂肪性肝炎の非侵襲的な検査方法及び検査キット |
US20090197280A1 (en) | 2006-05-30 | 2009-08-06 | Kristian Bangert | Methods and Devices for Rapid Assessment of Severity of Injury |
US20090286271A1 (en) * | 2006-05-31 | 2009-11-19 | Karumanchi Ananth S | Methods of Diagnosing and Treating Complications of Pregnancy |
EP2064553B2 (de) * | 2006-08-07 | 2023-06-07 | Antibodyshop A/S | Diagnostischer test zum ausschliessen einer signifikanten nierenverletzung |
US20080050749A1 (en) * | 2006-08-17 | 2008-02-28 | Ildiko Amann-Zalan | Use of bnp-type peptides for the stratification of therapy with erythropoietic stimulating agents |
US20080124712A1 (en) * | 2006-10-26 | 2008-05-29 | Hantash Feras M | Alpha globin gene dosage assay |
AU2007328206B2 (en) * | 2006-12-04 | 2013-08-01 | Promedior, Inc. | Conjoint therapy for treating fibrotic diseases |
ES2430290T3 (es) * | 2007-03-06 | 2013-11-19 | F. Hoffmann-La Roche Ag | Utilización de péptidos de tipo PNC para predecir la necesidad de diálisis |
JP5081930B2 (ja) * | 2007-03-08 | 2012-11-28 | エフ.ホフマン−ラ ロシュ アーゲー | 心不全の評価におけるslim−1の使用 |
EP2137538B1 (de) * | 2007-03-21 | 2014-04-09 | Bioporto Diagnostics A/s | Diagnostischer test auf nierenverletzung |
US9884899B2 (en) * | 2007-07-06 | 2018-02-06 | Promedior, Inc. | Methods for treating fibrosis using CRP antagonists |
US8497243B2 (en) * | 2007-07-06 | 2013-07-30 | Promedior, Inc. | Methods and compositions useful in the treatment of mucositis |
WO2009062520A1 (en) * | 2007-11-15 | 2009-05-22 | Bioporto Diagnostics A/S | Diagnostic use of individual molecular forms of a biomarker |
HUE036780T2 (hu) | 2008-04-09 | 2018-07-30 | Genentech Inc | Új kompozíciók és eljárások immunológiai vonatkozású betegségek kezelésére |
TWI354789B (en) * | 2008-07-18 | 2011-12-21 | Univ Kaohsiung Medical | Il-8 as biomarker for the detection of urolithiasi |
SI2384368T1 (sl) * | 2009-01-30 | 2016-04-29 | Kantonsspital Aarau Ag | Analiza genskega odmerjanja |
DK2405928T3 (en) * | 2009-03-11 | 2017-01-30 | Promedior Inc | Treatment and diagnosis procedure for hypersensitive diseases |
ES2684493T3 (es) * | 2009-03-11 | 2018-10-03 | Promedior Inc. | Un polipéptido SAP para uso en el tratamiento de trastornos autoinmunitarios y enfermedad del injerto contra el huésped |
UA110323C2 (en) * | 2009-06-04 | 2015-12-25 | Promedior Inc | Derivative of serum amyloid p and their receipt and application |
US8329659B2 (en) | 2009-06-17 | 2012-12-11 | Promedior, Inc. | SAP variants and their use |
US20120135425A1 (en) * | 2010-08-23 | 2012-05-31 | The Ohio State University Research Foundation | ELISA for Haptoglobin-Matrix Metalloproteinase 9 Complex as a Diagnostic Test for Conditions Including Acute Inflammation |
US20120045778A1 (en) * | 2010-08-23 | 2012-02-23 | The Ohio State University Research Foundation | Elisa for haptoglobin-matrix metalloproteinase 9 complex as a diagnostic test for conditions including acute inflammation |
WO2014191981A1 (en) * | 2013-05-28 | 2014-12-04 | Ramot At Tel-Aviv University Ltd. | Detection of hydroxymethylcytosine bases |
PT3021869T (pt) | 2013-07-16 | 2020-09-10 | Hoffmann La Roche | Métodos de tratamento do cancro com antagonistas da ligação ao eixo pd-1 e inibidores do tigit |
RU2732591C2 (ru) | 2015-09-25 | 2020-09-21 | Дженентек, Инк. | Анти-tigit антитела и способы применения |
CN106399478A (zh) | 2016-08-31 | 2017-02-15 | 桂林优利特医疗电子有限公司 | 一种荧光探针PCR 法快速检测α/β‑地中海贫血的试剂盒 |
CN112080558B (zh) * | 2019-06-13 | 2024-03-12 | 杭州贝瑞和康基因诊断技术有限公司 | 同时检测hba1/2和hbb基因突变的试剂盒和方法 |
EP4323513A2 (de) * | 2021-04-12 | 2024-02-21 | Graphite Bio, Inc. | Verfahren und zusammensetzungen zur herstellung genetisch modifizierter primärzellen |
CN113755568B (zh) * | 2021-08-26 | 2023-09-15 | 广东省妇幼保健院 | 利用微滴数字PCR检测α珠蛋白基因拷贝数的引物探针、试剂盒及应用 |
WO2023058100A1 (ja) * | 2021-10-04 | 2023-04-13 | 国立大学法人 東京大学 | 構造多型の検出方法、プライマーセット及びプライマーセットの設計方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5075216A (en) * | 1988-09-23 | 1991-12-24 | Cetus Corporation | Methods for dna sequencing with thermus aquaticus dna polymerase |
AU7855991A (en) * | 1990-04-11 | 1991-10-30 | United States of America, as represented by the Secretary, U.S. Department of Commerce, The | A simple, rapid and reliable method for detecting thalassemia |
US5374525A (en) * | 1992-09-30 | 1994-12-20 | University Of Utah Research Foundation | Methods to determine predisposition to hypertension and association of variant angiotensinogen gene and hypertension |
-
1995
- 1995-10-31 US US08/550,715 patent/US5750345A/en not_active Expired - Lifetime
-
1996
- 1996-10-30 DE DE69628758T patent/DE69628758D1/de not_active Expired - Lifetime
- 1996-10-30 WO PCT/US1996/017565 patent/WO1997016568A1/en active IP Right Grant
- 1996-10-30 EP EP96937870A patent/EP0859863B1/de not_active Expired - Lifetime
- 1996-10-30 JP JP9517585A patent/JP2000501923A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
WO1997016568A1 (en) | 1997-05-09 |
EP0859863B1 (de) | 2003-06-18 |
EP0859863A1 (de) | 1998-08-26 |
JP2000501923A (ja) | 2000-02-22 |
US5750345A (en) | 1998-05-12 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
8332 | No legal effect for de |