Effects of mutations causing hypokalaemic periodic paralysis on the skeletal muscle L-type Ca2+ channel expressed in Xenopus laevis oocytes.
about
Muscle channelopathies and critical points in functional and genetic studies.Channelopathies of skeletal muscle excitabilitySkeletal muscle sodium current is reduced in hypokalemic periodic paralysisChannelopathies: ion channel defects linked to heritable clinical disorders.Genetic disorders of neuromuscular ion channels.Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family.Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current.A rare case of unilateral adrenal hyperplasia accompanied by hypokalaemic periodic paralysis caused by a novel dominant mutation in CACNA1S: features and prognosis after adrenalectomy.Hypokalemic periodic paralysis; two different genes responsible for similar clinical manifestations.Pathophysiological role of omega pore current in channelopathiesThe L-type voltage-dependent Ca2+ channel EGL-19 controls body wall muscle function in Caenorhabditis elegansA calcium channel mutant mouse model of hypokalemic periodic paralysisHypokalemic periodic paralysis: a model for a clinical and research approach to a rare disorder.Gating pore currents in DIIS4 mutations of NaV1.4 associated with periodic paralysis: saturation of ion flux and implications for disease pathogenesisHow voltage-gated calcium channels gate forms of homeostatic synaptic plasticityMuscle channelopathies: does the predicted channel gating pore offer new treatment insights for hypokalaemic periodic paralysis?Voltage-sensor mutations in channelopathies of skeletal muscle.Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels.Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.Pathophysiologic and anesthetic considerations for patients with myotonia congenita or periodic paralyses.Elevated resting H(+) current in the R1239H type 1 Hypokalemic Periodic Paralysis mutated Ca(2+) channel.Stac3 enhances expression of human CaV1.1 in Xenopus oocytes and reveals gating pore currents in HypoPP mutant channels.When muscle Ca2+ channels carry monovalent cations through gating pores: insights into the pathophysiology of type 1 hypokalaemic periodic paralysis.
P2860
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P2860
Effects of mutations causing hypokalaemic periodic paralysis on the skeletal muscle L-type Ca2+ channel expressed in Xenopus laevis oocytes.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh-hant
name
Effects of mutations causing h ...... sed in Xenopus laevis oocytes.
@en
Effects of mutations causing h ...... sed in Xenopus laevis oocytes.
@nl
type
label
Effects of mutations causing h ...... sed in Xenopus laevis oocytes.
@en
Effects of mutations causing h ...... sed in Xenopus laevis oocytes.
@nl
prefLabel
Effects of mutations causing h ...... sed in Xenopus laevis oocytes.
@en
Effects of mutations causing h ...... sed in Xenopus laevis oocytes.
@nl
P2860
P1476
Effects of mutations causing h ...... sed in Xenopus laevis oocytes.
@en
P2093
J A Morrill
S C Cannon
P2860
P304
P356
10.1111/J.1469-7793.1999.00321.X
P407
P478
P577
1999-10-01T00:00:00Z