A long QT mutation substitutes cholesterol for phosphatidylinositol-4,5-bisphosphate in KCNQ1 channel regulation.
about
Molecular pathogenesis of long QT syndrome type 1Regulation of KCNQ/Kv7 family voltage-gated K+ channels by lipids.PIP₂-dependent coupling is prominent in Kv7.1 due to weakened interactions between S4-S5 and S6.bSUM: A bead-supported unilamellar membrane system facilitating unidirectional insertion of membrane proteins into giant vesicles.Voltage-Dependent Gating: Novel Insights from KCNQ1 Channels.A method to control phosphoinositides and to analyze PTEN function in living cells using voltage sensitive phosphatases.
P2860
A long QT mutation substitutes cholesterol for phosphatidylinositol-4,5-bisphosphate in KCNQ1 channel regulation.
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name
A long QT mutation substitutes ...... e in KCNQ1 channel regulation.
@ast
A long QT mutation substitutes ...... e in KCNQ1 channel regulation.
@en
type
label
A long QT mutation substitutes ...... e in KCNQ1 channel regulation.
@ast
A long QT mutation substitutes ...... e in KCNQ1 channel regulation.
@en
prefLabel
A long QT mutation substitutes ...... e in KCNQ1 channel regulation.
@ast
A long QT mutation substitutes ...... e in KCNQ1 channel regulation.
@en
P2093
P2860
P1433
P1476
A long QT mutation substitutes ...... e in KCNQ1 channel regulation.
@en
P2093
Annick Thomas
Céline Marionneau
Céline S Nicolas
Fabien C Coyan
Fayal Abderemane-Ali
Gildas Loussouarn
Jean Mérot
Julien Piron
Jérôme Mordel
Mohamed Yassine Amarouch
P2860
P304
P356
10.1371/JOURNAL.PONE.0093255
P407
P577
2014-03-28T00:00:00Z