Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome.
about
Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysisFunctional expression of inward rectifier potassium channels in cultured human pulmonary smooth muscle cells: evidence for a major role of Kir2.4 subunitsChannelopathies of skeletal muscle excitabilityFunctional expression of Kir2.x in human aortic endothelial cells: the dominant role of Kir2.2The function and molecular identity of inward rectifier channels in vestibular hair cells of the mouse inner earFluid flow facilitates inward rectifier K+ current by convectively restoring [K+] at the cell membrane surface.Whole genome and exome sequencing realignment supports the assignment of KCNJ12, KCNJ17, and KCNJ18 paralogous genes in thyrotoxic periodic paralysis locus: functional characterization of two polymorphic Kir2.6 isoforms.Pregnenolone sulfate potentiates the inwardly rectifying K channel Kir2.3.Discovery of Selective Small Molecule ROMK Inhibitors as Potential New Mechanism Diuretics.Separation of heteromeric potassium channel Kcv towards probing subunit composition-regulated ion permeation and gating.Coordinating heart morphogenesis: A novel role for hyperpolarization-activated cyclic nucleotide-gated (HCN) channels during cardiogenesis in Xenopus laevisUnraveling monogenic channelopathies and their implications for complex polygenic diseaseExtracellular potassium homeostasis: insights from hypokalemic periodic paralysis.Functional consequences of Kir2.1/Kir2.2 subunit heteromerization.Cholesterol sensitivity and lipid raft targeting of Kir2.1 channels.Roles of the Drosophila SK channel (dSK) in courtship memory.A voltage-driven switch for ion-independent signaling by ether-à-go-go K+ channels.Molecular dissection of the inward rectifier potassium current (IK1) in rabbit cardiomyocytes: evidence for heteromeric co-assembly of Kir2.1 and Kir2.2.Management and treatment of Andersen-Tawil syndrome (ATS).Kir2.6 regulates the surface expression of Kir2.x inward rectifier potassium channelsAndersen-Tawil syndromeCalcium-activated K+ channels increase cell proliferation independent of K+ conductance.Functional role of inward rectifier current in heart probed by Kir2.1 overexpression and dominant-negative suppression.The inward rectifier potassium channel Kir2.1 is expressed in mouse neutrophils from bone marrow and liver.Potassium channels in epithelial transport.Upregulation of the inwardly rectifying potassium channel Kir2.1 (KCNJ2) modulates multidrug resistance of small-cell lung cancer under the regulation of miR-7 and the Ras/MAPK pathway.Characterization of a novel, dominant negative KCNJ2 mutation associated with Andersen-Tawil syndrome.Regional variation of the inwardly rectifying potassium current in the canine heart and the contributions to differences in action potential repolarizationAndersen syndrome: the newest variant of the hereditary-familial long QT syndrome.Kir2.3 isoform confers pH sensitivity to heteromeric Kir2.1/Kir2.3 channels in HEK293 cells.Inhibition of Cardiac Kir Current (IK1) by Protein Kinase C Critically Depends on PKCβ and Kir2.2.Inhibition of inwardly rectifying Kir2.x channels by the novel anti-cancer agent gambogic acid depends on both pore block and PIP2 interference.The short QT syndrome as a paradigm to understand the role of potassium channels in ventricular fibrillation.Functional and clinical characterization of a mutation in KCNJ2 associated with Andersen-Tawil syndromeInward-rectifying potassium (Kir) channels regulate pacemaker activity in spinal nociceptive circuits during early life.Neonatal tissue injury reduces the intrinsic excitability of adult mouse superficial dorsal horn neuronsCardiac strong inward rectifier potassium channels.The mechanosensitive channel of small conductance (MscS) superfamily: not just mechanosensitive channels anymore.K(+) channels: function-structural overview.Potassium channels: structures, diseases, and modulators.
P2860
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P2860
Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome.
description
2002 nî lūn-bûn
@nan
2002 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Heteromerization of Kir2.x pot ...... enotype of Andersen's syndrome
@nl
Heteromerization of Kir2.x pot ...... notype of Andersen's syndrome.
@ast
Heteromerization of Kir2.x pot ...... notype of Andersen's syndrome.
@en
Heteromerization of Kir2.x pot ...... notype of Andersen's syndrome.
@en-gb
type
label
Heteromerization of Kir2.x pot ...... enotype of Andersen's syndrome
@nl
Heteromerization of Kir2.x pot ...... notype of Andersen's syndrome.
@ast
Heteromerization of Kir2.x pot ...... notype of Andersen's syndrome.
@en
Heteromerization of Kir2.x pot ...... notype of Andersen's syndrome.
@en-gb
prefLabel
Heteromerization of Kir2.x pot ...... enotype of Andersen's syndrome
@nl
Heteromerization of Kir2.x pot ...... notype of Andersen's syndrome.
@ast
Heteromerization of Kir2.x pot ...... notype of Andersen's syndrome.
@en
Heteromerization of Kir2.x pot ...... notype of Andersen's syndrome.
@en-gb
P2093
P2860
P3181
P356
P1476
Heteromerization of Kir2.x pot ...... notype of Andersen's syndrome.
@en
P2093
Andrea Brüggemann
Christian Derst
Günter Schlichthörl
Jürgen Daut
Regina Preisig-Müller
Rüdiger W Veh
Sindhu Rajan
Steffen Heinen
Tobias Goerge
P2860
P304
P3181
P356
10.1073/PNAS.102609499
P407
P577
2002-05-01T00:00:00Z