High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation
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A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylationMolecular pathogenesis of long QT syndrome type 1KCNQ1 variants associate with hypertension in type 2 diabetes and affect smooth muscle contractility in vitro.Molecular Pathophysiology of Congenital Long QT Syndrome.Identification of KCNQ1 compound heterozygous mutations in three Chinese families with Jervell and Lange-Nielsen Syndrome.
P2860
High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation
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2012 nî lūn-bûn
@nan
2012 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
High-risk long QT syndrome mut ...... asis for rapid K(+) permeation
@ast
High-risk long QT syndrome mut ...... asis for rapid K(+) permeation
@en
type
label
High-risk long QT syndrome mut ...... asis for rapid K(+) permeation
@ast
High-risk long QT syndrome mut ...... asis for rapid K(+) permeation
@en
prefLabel
High-risk long QT syndrome mut ...... asis for rapid K(+) permeation
@ast
High-risk long QT syndrome mut ...... asis for rapid K(+) permeation
@en
P2093
P2860
P50
P356
P1433
P1476
High-risk long QT syndrome mut ...... asis for rapid K(+) permeation
@en
P2093
Allison R Reloj
Arthur J Moss
Daniel C Bartos
David J Tester
Don E Burgess
Isabelle Denjoy
Jonathan N Johnson
Michael J Ackerman
Minoru Horie
Seiko Ohno
P2860
P304
P356
10.1021/BI3009449
P407
P577
2012-11-02T00:00:00Z