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ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene.

লেখক

Dan Hu

Angelica López-Izquierdo

Charles Antzelevitch

2000 -

Martin Borggrefe

Rainer Schimpf

Christian Wolpert

Michel Haïssaguerre

1955 -

Hector Barajas-Martinez

Ryan Pfeiffer

Pramod Deshmukh

Christian Veltmann

Elena Burashnikov

José Antonio Sánchez-Chapula

Melvin M Scheinman

1935 -

এতে প্রকাশিত: International Journal of Cardiology

তারিখে প্রকাশিত: 2014-01-04

মূল বিষয়: ATP binding cassette subfamily C member 9, potassium channel activity

Cites articles 40

তারিখ

শিরোনাম

লেখকগণ

2013-06-03

Coronary spasm and acute myocardial infarction due to a mutation (V734I) in the nucleotide binding domain 1 of ABCC9.

Enzo Emanuele
2012-06-22

Association of early repolarization and sudden cardiac death during an acute coronary event
2011-11-03

Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8

Michel Haïssaguerre, Charles Antzelevitch, Martin Borggrefe, Rainer Schimpf, Christian Wolpert, Christian Veltmann, Elena Burashnikov, Hector Barajas-Martinez, Janire Urrutia, José Antonio Sánchez-Chapula
2011-08-01

Advances in cardiac ATP-sensitive K+ channelopathies from molecules to populations
2011-05-01

The early repolarization pattern in the general population: clinical correlates and heritability

Christopher Newton-Cheh, Veikko Salomaa, Antti Jula
2011-01-01

Identification of six novel SCN5A mutations in Japanese patients with Brugada syndrome
2011-10-25

Electrocardiographic characteristics and SCN5A mutations in idiopathic ventricular fibrillation associated with early repolarization
2010-10-14

Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death

Ryan Pfeiffer, Dan Hu, Charles Antzelevitch, Martin Borggrefe, Rainer Schimpf, Christian Wolpert, Mark Marieb, Gi Byoung Nam, Christian Veltmann, Sami Viskin, Guido D Pollevick, Elena Burashnikov, Alejandra Guerchicoff, Mayurika Desai, Hector Barajas-Martinez
2010-10-01

Gain-of-function mutation S422L in the KCNJ8-encoded cardiac K(ATP) channel Kir6.1 as a pathogenic substrate for J-wave syndromes

Argelia Medeiros-domingo, Lia Crotti, Peter J. Schwartz
2009-12-11

J wave syndromes

Charles Antzelevitch
2009-04-21

A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype

Ryan Pfeiffer, Dan Hu, Charles Antzelevitch, Guido D Pollevick, Jonathan M Cordeiro, Elena Burashnikov, Alejandra Guerchicoff, Hector Barajas-Martinez
2009-11-15

Quaternary structure of KATP channel SUR2A nucleotide binding domains resolved by synchrotron radiation X-ray scattering
2009-11-16

Long-term outcome associated with early repolarization on electrocardiography.
2009-01-01

Ventricular fibrillation with prominent early repolarization associated with a rare variant of KCNJ8/KATP channel

Michel Haïssaguerre, Hervé Le Marec, Arthur Wilde
2008-10-01

J-point elevation in survivors of primary ventricular fibrillation and matched control subjects: incidence and clinical significance

Melvin M Scheinman
2008-05-01

Augmentation of J waves and electrical storms in patients with early repolarization

Charles Antzelevitch, Gi Byoung Nam, You Ho Kim
2008-05-01

Sudden cardiac arrest associated with early repolarization

Michel Haïssaguerre, Solena Le Scouarnec, Geneviève Chêne, Isabel Deisenhofer, Mélèze Hocini, Laurence Jesel, Nicolas Derval, Sebastien Knecht, Thomas Rostock, Frederic Sacher, Pierre Bordachar, Jean-Luc Pasquié, Vincent Probst, Dominique Babuty, Akihiko Nogami, Dominique Lamaison, Pascal Defaye, Philippe Mabo, Christian De Chillou, Jacques Clémenty, Sinikka Yli-Mayry, Patrice Scanu, Seiichiro Matsuo, Yoshifusa Aizawa, Kang-Teng Lim, George D Veenhuyzen
2008-06-01

The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome

Lia Crotti, Peter J. Schwartz, Elijah Behr, Naoki Mochizuki, Dan Roden
2008-03-01

Interaction of asymmetric ABCC9-encoded nucleotide binding domains determines KATP channel SUR2A catalytic activity
2006-08-25

Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors

শিনিয়া ইয়ামানাকা, Kazutoshi Takahashi
2006-03-06

A novel Val734Ile variant in the ABCC9 gene associated with myocardial infarction

Enzo Emanuele, Margherita Calcagnino
2005-04-14

ATP-sensitive K+ channel channel/enzyme multimer: metabolic gating in the heart

Amy B. Karger
2005-05-01

Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing

Michael J Ackerman
2004-10-01

The ATP switch model for ABC transporters
2004-04

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

Amy B. Karger, Yuan-Ping Pang
2004-01-01

Nucleotide-gated KATP channels integrated with creatine and adenylate kinases: amplification, tuning and sensing of energetic signals in the compartmentalized cellular environment
2002-03-01

Natural history of Brugada syndrome: insights for risk stratification and management
2002-02-01

Tandem function of nucleotide binding domains confers competence to sulfonylurea receptor in gating ATP-sensitive K+ channels

Amy B. Karger
2000-04-01

Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes
2000-01-01

Ventricular fibrillation in a patient with prominent J (Osborn) waves and ST segment elevation in the inferior electrocardiographic leads: a Brugada syndrome variant?
2000-08-01

The elusive link between LQT3 and Brugada syndrome: the role of flecainide challenge

Carlo Napolitano, Lia Crotti
1999-06-01

Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel.

নিবন্ধ - wd:Q37627289

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