Functional analysis of the Kv1.1 N255D mutation associated with autosomal dominant hypomagnesemia.
about
The renal channelopathiesProtein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfacesPhysiological and pathological functions of mechanosensitive ion channels.Distal convoluted tubuleRegulation of magnesium balance: lessons learned from human genetic diseasePDB_REDO: constructive validation, more than just looking for errors.Role of renal TRP channels in physiology and pathologyClinical heterogeneity associated with KCNA1 mutations include cataplexy and nonataxic presentationsThe salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channel.Inherited disorders of renal hypomagnesaemia.Familial Paroxysmal Kinesigenic Dyskinesia is associated with mutations in the KCNA1 gene.Distal convoluted tubule.
P2860
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P2860
Functional analysis of the Kv1.1 N255D mutation associated with autosomal dominant hypomagnesemia.
description
2009 nî lūn-bûn
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2009年の論文
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年学术文章
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2009年学术文章
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name
Functional analysis of the Kv1 ...... somal dominant hypomagnesemia.
@en
Functional analysis of the Kv1 ...... somal dominant hypomagnesemia.
@nl
type
label
Functional analysis of the Kv1 ...... somal dominant hypomagnesemia.
@en
Functional analysis of the Kv1 ...... somal dominant hypomagnesemia.
@nl
prefLabel
Functional analysis of the Kv1 ...... somal dominant hypomagnesemia.
@en
Functional analysis of the Kv1 ...... somal dominant hypomagnesemia.
@nl
P2093
P2860
P356
P1476
Functional analysis of the Kv1 ...... osomal dominant hypomagnesemia
@en
P2093
Anil V Nair
Anna-Lena Forst
Bob Glaudemans
Joost G J Hoenderop
René J M Bindels
P2860
P304
P356
10.1074/JBC.M109.041517
P407
P577
2009-11-10T00:00:00Z