Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutations identified in sporadic or familial hemiplegic migraine.
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ATP1A2 Mutations in Migraine: Seeing through the Facets of an Ion Pump onto the Neurobiology of DiseaseIncreased susceptibility to cortical spreading depression in the mouse model of familial hemiplegic migraine type 2.Sodium and proton effects on inward proton transport through Na/K pumps.Control of gastric H,K-ATPase activity by cations, voltage and intracellular pH analyzed by voltage clamp fluorometry in Xenopus oocytes.Defective glutamate and K+ clearance by cortical astrocytes in familial hemiplegic migraine type 2.Neuronal calcium signaling: function and dysfunction.The α2β2 isoform combination dominates the astrocytic Na(+) /K(+) -ATPase activity and is rendered nonfunctional by the α2.G301R familial hemiplegic migraine type 2-associated mutation.Stabilization of the α2 isoform of Na,K-ATPase by mutations in a phospholipid binding pocket.Functional analysis of human Na(+)/K(+)-ATPase familial or sporadic hemiplegic migraine mutations expressed in Xenopus oocytes.Measuring cation transport by Na,K- and H,K-ATPase in Xenopus oocytes by atomic absorption spectrophotometry: an alternative to radioisotope assays.Clinical spectrum in three families with familial hemiplegic migraine type 2 including a novel mutation in the ATP1A2 gene.A new Italian FHM2 family: clinical aspects and functional analysis of the disease-associated mutation.Génétique de la migraine
P2860
Q26738318-1B3D0105-BD22-418B-A0B2-98B01305E95FQ31022226-C242E2A6-7C91-4B3B-BCE0-D1405A77F5EAQ33803674-38F83F0B-D3E9-42E5-9AB5-A63164946A13Q35842488-07540BC3-59E8-4A85-93EF-C270DDFCF25FQ36063681-1B8759CE-A755-43E3-8420-B4895B524184Q38179996-7BF8D55A-7A4B-4B31-83E8-34FC69F50DABQ38634878-901C1646-563F-47D3-9638-A4FD220CA728Q39708587-1A244F16-F68F-4623-B021-AEF8A4B111CAQ40464255-0CDA5EF7-DFE1-4186-9011-987A5D69F7C7Q41827662-458E769B-5CBD-4F0E-AC5C-260885BBE740Q50687547-3437AA7C-9DF5-488D-9662-9AA51CAD765BQ54383380-D32AE55E-C776-42E7-A9A4-25E7AC1C46E8Q57811709-2AECAC45-907A-434D-867F-6A4156C8DA31
P2860
Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutations identified in sporadic or familial hemiplegic migraine.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Impaired plasma membrane targe ...... familial hemiplegic migraine.
@en
Impaired plasma membrane targe ...... familial hemiplegic migraine.
@nl
type
label
Impaired plasma membrane targe ...... familial hemiplegic migraine.
@en
Impaired plasma membrane targe ...... familial hemiplegic migraine.
@nl
prefLabel
Impaired plasma membrane targe ...... familial hemiplegic migraine.
@en
Impaired plasma membrane targe ...... familial hemiplegic migraine.
@nl
P2093
P921
P356
P1433
P1476
Impaired plasma membrane targe ...... familial hemiplegic migraine.
@en
P2093
Ernst Bamberg
Jan B Koenderink
Katharina L Dürr
Neslihan N Tavraz
Thomas Friedrich
Tobias Freilinger
P356
10.4161/CHAN.3.2.8085
P577
2009-03-03T00:00:00Z