The rapid-onset dystonia parkinsonism mutation D923N of the Na+, K+-ATPase alpha3 isoform disrupts Na+ interaction at the third Na+ site.
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Managing Brain Extracellular K(+) during Neuronal Activity: The Physiological Role of the Na(+)/K(+)-ATPase Subunit IsoformsAlternating hemiplegia of childhood-related neural and behavioural phenotypes in Na+,K+-ATPase α3 missense mutant mice.Crystal structure of Na+, K(+)-ATPase in the Na(+)-bound stateInhibition of K+ transport through Na+, K+-ATPase by capsazepine: role of membrane span 10 of the α-subunit in the modulation of ion gatingAlternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF RegistryNew insights into behaviour using mouse ENU mutagenesisDistinct neurological disorders with ATP1A3 mutationsMolecular cloning and characterization of porcine Na⁺/K⁺-ATPase isoforms α1, α2, α3 and the ATP1A3 promoter.Mania-like behavior induced by genetic dysfunction of the neuron-specific Na+,K+-ATPase α3 sodium pump.Critical role of a transmembrane lysine in aminophospholipid transport by mammalian photoreceptor P4-ATPase ATP8A2Expression of mutant α1 Na/K-ATPase defective in conformational transition attenuates Src-mediated signal transduction.The genetics of dystonias.The selectivity of the Na(+)/K(+)-pump is controlled by binding site protonation and self-correcting occlusion.Glutamate Water Gates in the Ion Binding Pocket of Na+ Bound Na+, K+-ATPase.Consensus paper: pathological mechanisms underlying neurodegeneration in spinocerebellar ataxias.Route, mechanism, and implications of proton import during Na+/K+ exchange by native Na+/K+-ATPase pumps.Milestones in dystonia.P2C-Type ATPases and Their Regulation.Rescue of Na+ affinity in aspartate 928 mutants of Na+,K+-ATPase by secondary mutation of glutamate 314.Inhibition of phosphorylation of na+,k+-ATPase by mutations causing familial hemiplegic migraine.Importance of a Potential Protein Kinase A Phosphorylation Site of Na+,K+-ATPase and Its Interaction Network for Na+ BindingRelationship between intracellular Na+ concentration and reduced Na+ affinity in Na+,K+-ATPase mutants causing neurological disease.Distinct pH dependencies of Na+/K+-selectivity at the two faces of Na,K-ATPase.Genetic suppression of agrin reduces mania-like behavior in Na+ , K+ -ATPase α3 mutant mice.Crystal structure of a Na+-bound Na+,K+-ATPase preceding the E1P state
P2860
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P2860
The rapid-onset dystonia parkinsonism mutation D923N of the Na+, K+-ATPase alpha3 isoform disrupts Na+ interaction at the third Na+ site.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
The rapid-onset dystonia parki ...... raction at the third Na+ site.
@ast
The rapid-onset dystonia parki ...... raction at the third Na+ site.
@en
The rapid-onset dystonia parki ...... raction at the third Na+ site.
@nl
type
label
The rapid-onset dystonia parki ...... raction at the third Na+ site.
@ast
The rapid-onset dystonia parki ...... raction at the third Na+ site.
@en
The rapid-onset dystonia parki ...... raction at the third Na+ site.
@nl
prefLabel
The rapid-onset dystonia parki ...... raction at the third Na+ site.
@ast
The rapid-onset dystonia parki ...... raction at the third Na+ site.
@en
The rapid-onset dystonia parki ...... raction at the third Na+ site.
@nl
P2093
P2860
P356
P1476
The rapid-onset dystonia parki ...... raction at the third Na+ site.
@en
P2093
Anja Pernille Einholm
Bente Vilsen
Jens Peter Andersen
Mads S Toustrup-Jensen
Rikke Holm
P2860
P304
26245-26254
P356
10.1074/JBC.M110.123976
P407
P577
2010-06-24T00:00:00Z