ATE381626T1 - Genetische diagnose zur feststellung von qt- verlängerungen als unerwünschte reaktion auf arzneimittel - Google Patents

Genetische diagnose zur feststellung von qt- verlängerungen als unerwünschte reaktion auf arzneimittel

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Publication number
ATE381626T1
ATE381626T1 AT01926956T AT01926956T ATE381626T1 AT E381626 T1 ATE381626 T1 AT E381626T1 AT 01926956 T AT01926956 T AT 01926956T AT 01926956 T AT01926956 T AT 01926956T AT E381626 T1 ATE381626 T1 AT E381626T1
Authority
AT
Austria
Prior art keywords
genes
prolonged
adverse reaction
genetic
prolongation
Prior art date
Application number
AT01926956T
Other languages
English (en)
Inventor
Raymond Woosley
Original Assignee
Univ Georgetown
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Publication date
Application filed by Univ Georgetown filed Critical Univ Georgetown
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Publication of ATE381626T1 publication Critical patent/ATE381626T1/de

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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING 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
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6883Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING 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
    • C12Q2600/00Oligonucleotides characterized by their use
    • C12Q2600/156Polymorphic or mutational markers

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Organic Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Zoology (AREA)
  • Analytical Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • Molecular Biology (AREA)
  • Biophysics (AREA)
  • Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Immunology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
AT01926956T 2000-04-13 2001-04-13 Genetische diagnose zur feststellung von qt- verlängerungen als unerwünschte reaktion auf arzneimittel ATE381626T1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US19691600P 2000-04-13 2000-04-13

Publications (1)

Publication Number Publication Date
ATE381626T1 true ATE381626T1 (de) 2008-01-15

Family

ID=22727270

Family Applications (1)

Application Number Title Priority Date Filing Date
AT01926956T ATE381626T1 (de) 2000-04-13 2001-04-13 Genetische diagnose zur feststellung von qt- verlängerungen als unerwünschte reaktion auf arzneimittel

Country Status (5)

Country Link
US (1) US7179597B2 (de)
EP (1) EP1290220B1 (de)
AT (1) ATE381626T1 (de)
DE (1) DE60131970T2 (de)
WO (1) WO2001079554A1 (de)

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2449752A1 (en) * 2001-06-05 2002-12-12 Genaissance Pharmaceuticals, Inc. Method of identifying a polymorphism in cyp2d6
US8263375B2 (en) 2002-12-20 2012-09-11 Acea Biosciences Dynamic monitoring of activation of G-protein coupled receptor (GPCR) and receptor tyrosine kinase (RTK) in living cells using real-time microelectronic cell sensing technology
US7192752B2 (en) 2002-12-20 2007-03-20 Acea Biosciences Real time electronic cell sensing systems and applications for cell-based assays
US10215748B2 (en) 2002-12-20 2019-02-26 Acea Biosciences, Inc. Using impedance-based cell response profiling to identify putative inhibitors for oncogene addicted targets or pathways
US10539523B2 (en) 2002-12-20 2020-01-21 Acea Biosciences, Inc. System and method for monitoring cardiomyocyte beating, viability, morphology, and electrophysiological properties
US11346797B2 (en) 2002-12-20 2022-05-31 Agilent Technologies, Inc. System and method for monitoring cardiomyocyte beating, viability, morphology and electrophysiological properties
US10551371B2 (en) 2003-11-10 2020-02-04 Acea Biosciences, Inc. System and method for monitoring cardiomyocyte beating, viability and morphology and for screening for pharmacological agents which may induce cardiotoxicity or modulate cardiomyocyte function
US20100063093A1 (en) * 2007-03-28 2010-03-11 Curt Wolfgang Methods for the administration of iloperidone
CA3113166A1 (en) 2004-09-30 2006-04-13 Vanda Pharmaceuticals Inc. Methods for the administration of iloperidone
AU2006315760A1 (en) * 2005-11-10 2007-05-24 Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services Materials and methods for ABCB1 polymorphic variant screening, diagnosis, and treatment
US20080140371A1 (en) * 2006-11-15 2008-06-12 General Electric Company System and method for treating a patient
WO2009137440A1 (en) 2008-05-05 2009-11-12 Acea Biosciences, Inc. Label-free monitoring of excitation-contraction coupling and excitable cells using impedance based systems with millisecond time resolution
EP2356233A2 (de) * 2008-11-13 2011-08-17 EUCRO European Contract Research GmbH & Co. KG Verfahren zum sammeln von mundschleimhautzellen und/oder -zellfragmenten
US8315815B2 (en) 2008-12-30 2012-11-20 The Invention Science Fund I, Llc Computational methods and systems for suggesting modulators of CYP450 as treatment options
US8321151B2 (en) 2008-12-30 2012-11-27 The Invention Science Fund I, Llc Computational methods and systems for treatment in relation to modulation of CYP450 enzyme activity
US8073633B2 (en) * 2008-12-30 2011-12-06 The Invention Science Fund I, Llc Computational methods and systems for suggesting modulators of CYP450 as treatment options
EP2417266B1 (de) 2009-04-06 2016-03-09 Vanda Pharmaceuticals Inc. Verfahren zur prognose einer prädisposition für qt-verlängerung
CA2757723C (en) 2009-04-06 2018-07-24 Vanda Pharmaceuticals, Inc. Method of predicting a predisposition to qt prolongation based on abcc2 gene sequence or product thereof
HUE037724T2 (hu) 2009-04-06 2018-09-28 Vanda Pharmaceuticals Inc Eljárás a KCNQ1 gén polimorfizmusán alapuló kezelésre
US9072742B2 (en) 2009-04-06 2015-07-07 Vanda Pharmaceuticals, Inc. Method of predicting a predisposition to QT prolongation
KR101251538B1 (ko) 2009-04-17 2013-04-08 (주)아벨리노 아벨리노 각막이상증 진단용 프라이머
WO2011146531A1 (en) * 2010-05-18 2011-11-24 Acea Biosciences, Inc Data analysis of impedance-based cardiomyocyte-beating signals as detected on real-time cell analysis (rtca) cardio instruments
KR101125212B1 (ko) 2010-10-01 2012-03-21 (주)아벨리노 아벨리노 각막이상증 진단용 시스템
WO2012149406A2 (en) * 2011-04-29 2012-11-01 Mayo Foundation For Medical Education And Research Assessing and treating humans with long qt syndrome
KR20220100079A (ko) * 2013-03-15 2022-07-14 아벨리노 랩 유에스에이, 인크. 대립유전자 검출을 위한 게놈 dna 주형의 개선된 단리 방법
US10889850B2 (en) 2013-03-15 2021-01-12 Avellino Lab Usa, Inc. Methods for improved isolation of genomic DNA templates for allele detection
EP3068908B1 (de) 2013-11-15 2021-01-06 Avellino Lab USA, Inc. Verfahren zum multiplexnachweis von mit augenleiden assoziierten allelen
DE102014209627B3 (de) * 2014-05-21 2015-10-29 Cytocentrics Bioscience Gmbh In-Vitro-Diagnostik für die modellgestützte Therapieplanung
EP4036228A1 (de) 2015-11-13 2022-08-03 Avellino Lab USA, Inc. Verfahren zur behandlung von hornhautdystrophien
US12066428B2 (en) 2015-11-20 2024-08-20 Agilent Technologies, Inc. Cell-substrate impedance monitoring of cancer cells
KR101920994B1 (ko) * 2016-06-14 2018-11-21 서울대학교산학협력단 식물의 수액 유속 측정용 마이크로 니들 프로브 장치 및 이를 이용한 식물의 수액 유속 측정 방법
EP4549553A3 (de) 2017-03-03 2025-07-16 Agilent Technologies, Inc. Verfahren und systeme zur funktionellen reifung von kardiomyozyten aus ipsc und esc
US10799138B2 (en) 2018-04-05 2020-10-13 University Of Maryland, Baltimore Method of administering sotalol IV/switch
US11696902B2 (en) 2018-08-14 2023-07-11 AltaThera Pharmaceuticals, LLC Method of initiating and escalating sotalol hydrochloride dosing
US12396970B2 (en) 2021-08-20 2025-08-26 AltaThera Pharmaceuticals LLC Anti-arrhythmic compositions and methods
US11344518B2 (en) 2018-08-14 2022-05-31 AltaThera Pharmaceuticals LLC Method of converting atrial fibrillation to normal sinus rhythm and loading oral sotalol in a shortened time frame
US10512620B1 (en) 2018-08-14 2019-12-24 AltaThera Pharmaceuticals, LLC Method of initiating and escalating sotalol hydrochloride dosing
US11610660B1 (en) 2021-08-20 2023-03-21 AltaThera Pharmaceuticals LLC Antiarrhythmic drug dosing methods, medical devices, and systems
USD941488S1 (en) 2020-02-07 2022-01-18 Agilent Technologies, Inc. Instrument for analyzing biological cells
US20210301245A1 (en) 2020-03-29 2021-09-30 Agilent Technologies, Inc. Systems and methods for electronically and optically monitoring biological samples

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5599673A (en) * 1995-03-09 1997-02-04 University Of Utah Research Foundation Long QT syndrome genes
US6277978B1 (en) 1995-12-22 2001-08-21 University Of Utah Research Foundation KVLQT1—a long QT syndrome gene
US6432639B1 (en) * 1997-09-10 2002-08-13 Dna Sciences Laboratories, Inc. Isolated CYP3A4 nucleic acid molecules and detection methods
US6207383B1 (en) * 1998-07-27 2001-03-27 University Of Utah Research Foundation Mutations in and genomic structure of HERG—a long QT syndrome gene

Also Published As

Publication number Publication date
EP1290220A4 (de) 2004-09-22
DE60131970T2 (de) 2008-12-11
DE60131970D1 (de) 2008-01-31
EP1290220B1 (de) 2007-12-19
WO2001079554A1 (en) 2001-10-25
EP1290220A1 (de) 2003-03-12
US7179597B2 (en) 2007-02-20
US20030211500A1 (en) 2003-11-13

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