Stilbenes and fenamates rescue the loss of I(KS) channel function induced by an LQT5 mutation and other IsK mutants

EMBO Journal

Volumn 18, Issue 15, 1999, Pages 4137-4148

  Abitbol, Ilane ^a   Peretz, Asher ^a   Lerche, Christian ^b   Busch, Andreas E ^c   Attali, Bernard ^a  

^a WEIZMANN INSTITUTE OF SCIENCE   (Israel)

^b UNIVERSITY OF TÜBINGEN   (Germany)

^c SANOFI   (France)

Author keywords

I(KS); IsK; LQT; Mink; Potassium channels

Indexed keywords

FENAMIC ACID DERIVATIVE; MEMBRANE PROTEIN; MUTANT PROTEIN; POTASSIUM CHANNEL; STILBENE DERIVATIVE;

ALLOSTERISM; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CHANNEL GATING; CONTROLLED STUDY; HUMAN; LONG QT SYNDROME; MOUSE; NONHUMAN; PRIORITY JOURNAL;

4,4'-DIISOTHIOCYANOSTILBENE-2,2'-DISULFONIC ACID; ANIMALS; BINDING SITES; HUMANS; MEFENAMIC ACID; MEMBRANE POTENTIALS; MUTAGENESIS, SITE-DIRECTED; POTASSIUM CHANNELS; XENOPUS;

ANIMALIA; MUSTELA VISON;

EID: 0033517136     PISSN: 02614189     EISSN: None     Source Type: Journal    
DOI: 10.1093/emboj/18.15.4137     Document Type: Article

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