JP2003530814A5 - - Google Patents

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Publication number
JP2003530814A5
JP2003530814A5 JP2000562396A JP2000562396A JP2003530814A5 JP 2003530814 A5 JP2003530814 A5 JP 2003530814A5 JP 2000562396 A JP2000562396 A JP 2000562396A JP 2000562396 A JP2000562396 A JP 2000562396A JP 2003530814 A5 JP2003530814 A5 JP 2003530814A5
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JP
Japan
Prior art keywords
base
residue
seq
current
kcne1
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
JP2000562396A
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English (en)
Japanese (ja)
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JP2003530814A (ja
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Publication date
Priority claimed from US09/135,020 external-priority patent/US6274332B1/en
Application filed filed Critical
Publication of JP2003530814A publication Critical patent/JP2003530814A/ja
Publication of JP2003530814A5 publication Critical patent/JP2003530814A5/ja
Pending legal-status Critical Current

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JP2000562396A 1998-07-29 1998-10-06 不整脈に関連するヒトmink遺伝子突然変異 Pending JP2003530814A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US9447798P 1998-07-29 1998-07-29
US60/094,477 1998-07-29
US09/135,020 1998-08-17
US09/135,020 US6274332B1 (en) 1995-12-22 1998-08-17 Mutations in the KCNE1 gene encoding human minK which cause arrhythmia susceptibility thereby establishing KCNE1 as an LQT gene
PCT/US1998/017838 WO2000006600A1 (en) 1998-07-29 1998-10-06 Human mink gene mutations associated with arrhythmia

Publications (2)

Publication Number Publication Date
JP2003530814A JP2003530814A (ja) 2003-10-21
JP2003530814A5 true JP2003530814A5 (enExample) 2006-01-05

Family

ID=26788932

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000562396A Pending JP2003530814A (ja) 1998-07-29 1998-10-06 不整脈に関連するヒトmink遺伝子突然変異

Country Status (8)

Country Link
US (6) US6274332B1 (enExample)
EP (1) EP1100825B1 (enExample)
JP (1) JP2003530814A (enExample)
KR (1) KR20010085315A (enExample)
AT (1) ATE359299T1 (enExample)
CA (1) CA2337491C (enExample)
DE (1) DE69837565T2 (enExample)
WO (1) WO2000006600A1 (enExample)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6274332B1 (en) * 1995-12-22 2001-08-14 Univ. Of Utah Research Foundation Mutations in the KCNE1 gene encoding human minK which cause arrhythmia susceptibility thereby establishing KCNE1 as an LQT gene
US6458542B1 (en) * 1999-10-08 2002-10-01 Vanderbilt University Method of screening for susceptibility to drug-induced cardiac arrhythmia
US7115726B2 (en) * 2001-03-30 2006-10-03 Perlegen Sciences, Inc. Haplotype structures of chromosome 21
US7306911B2 (en) * 2001-04-24 2007-12-11 University Of Utah Research Foundation Methods for assessing risk for cardiac dysrythmia in a human subject
US20030073085A1 (en) * 2001-10-05 2003-04-17 Fang Lai Amplifying expressed sequences from genomic DNA of higher-order eukaryotic organisms for DNA arrays
US20040053232A1 (en) * 2001-10-05 2004-03-18 Perlegen Sciences, Inc. Haplotype structures of chromosome 21
US8013133B2 (en) 2003-04-25 2011-09-06 Medtronic, Inc. Genetic modification of targeted regions of the cardiac conduction system
US7537928B2 (en) * 2003-08-22 2009-05-26 Masonic Medical Research Laboratory Mutations in ion channel proteins associated with sudden cardiac death
US7608458B2 (en) * 2004-02-05 2009-10-27 Medtronic, Inc. Identifying patients at risk for life threatening arrhythmias
WO2005078452A1 (en) * 2004-02-05 2005-08-25 Medtronic, Inc. Methods and apparatus for identifying patients at risk for life threatening arrhythmias
US7127355B2 (en) 2004-03-05 2006-10-24 Perlegen Sciences, Inc. Methods for genetic analysis
US20090087854A1 (en) * 2007-09-27 2009-04-02 Perlegen Sciences, Inc. Methods for genetic analysis
US8335652B2 (en) * 2004-06-23 2012-12-18 Yougene Corp. Self-improving identification method
US8027791B2 (en) * 2004-06-23 2011-09-27 Medtronic, Inc. Self-improving classification system
US20050287574A1 (en) * 2004-06-23 2005-12-29 Medtronic, Inc. Genetic diagnostic method for SCD risk stratification
US7833718B2 (en) * 2006-11-06 2010-11-16 Masonic Medical Research Laboratory CACNA1C nucleic acid mutations as indicators of shorter than normal QT interval and ST segment elevation associated with sudden cardiac death
US20110143956A1 (en) * 2007-11-14 2011-06-16 Medtronic, Inc. Diagnostic Kits and Methods for SCD or SCA Therapy Selection
EP2222877A4 (en) * 2007-11-14 2011-10-12 Medtronic Inc GENETIC MARKERS FOR SCD OR SCA THERAPY SELECTION
EP2430184A2 (en) * 2009-05-12 2012-03-21 Medtronic, Inc. Sca risk stratification by predicting patient response to anti-arrhythmics

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5397702A (en) * 1989-03-06 1995-03-14 The Regents Of The University Of California Assay for and treatment of autoimmune diseases
US5387702A (en) * 1993-09-29 1995-02-07 Council Of Scientific And Industrial Research Process for the preparation of cabofuran
US6274332B1 (en) * 1995-12-22 2001-08-14 Univ. Of Utah Research Foundation Mutations in the KCNE1 gene encoding human minK which cause arrhythmia susceptibility thereby establishing KCNE1 as an LQT gene
EP2085478A1 (en) * 1995-12-22 2009-08-05 University Of Utah Research Foundation A long QT syndrome gene which encodes KVLQT1 and its association with minK
US6150104A (en) * 1997-06-13 2000-11-21 University Of Utah Research Foundation Homozygous mutation in KVLQT1 which causes Jervell and Lange Nielsen syndrome
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

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