Variable loss of Kir4.1 channel function in SeSAME syndrome mutations.
about
Mislocalization of K+ channels causes the renal salt wasting in EAST/SeSAME syndromeEAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10New Insights on Astrocyte Ion Channels: Critical for Homeostasis and Neuron-Glia SignalingPotassium channel KIR4.1 as an immune target in multiple sclerosisMajor channels involved in neuropsychiatric disorders and therapeutic perspectivesThe role of an inwardly rectifying K(+) channel (Kir4.1) in the inner ear and hearing loss.Genetic deletion of laminin isoforms β2 and γ3 induces a reduction in Kir4.1 and aquaporin-4 expression and function in the retinaMolecular mechanisms of EAST/SeSAME syndrome mutations in Kir4.1 (KCNJ10)Systems genetics of the lateral septal nucleus in mouse: heritability, genetic control, and covariation with behavioral and morphological traits.Molecular basis of decreased Kir4.1 function in SeSAME/EAST syndrome.Molecular aspects of structure, gating, and physiology of pH-sensitive background K2P and Kir K+-transport channels.Basolateral membrane K+ channels in renal epithelial cellsElevated GFAP induces astrocyte dysfunction in caudal brain regions: A potential mechanism for hindbrain involved symptoms in type II Alexander disease.Novel KCNJ10 Gene Variations Compromise Function of Inwardly Rectifying Potassium Channel 4.1.The salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channel.Astrocyte dysfunction in temporal lobe epilepsy: K+ channels and gap junction coupling.The role of glial-specific Kir4.1 in normal and pathological states of the CNS.Role and mechanisms of regulation of the basolateral Kir 4.1/Kir 5.1K+ channels in the distal tubules.Founder mutation in KCNJ10 in Pakistani patients with EAST syndrome.Expressional analysis of the astrocytic Kir4.1 channel in a pilocarpine-induced temporal lobe epilepsy model.Inhibition of Inwardly Rectifying Potassium (Kir) 4.1 Channels Facilitates Brain-Derived Neurotrophic Factor (BDNF) Expression in Astrocytes.Lethal digenic mutations in the K+ channels Kir4.1 (KCNJ10) and SLACK (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay.Distal convoluted tubule.
P2860
Q24338162-59104A9A-172A-4972-86CE-EA3526B68403Q26738592-0544D465-BB4F-4D2F-B51B-6787C07C5254Q26782952-B4BC6902-58AD-426C-AE6E-3F0494B4F0A1Q28270799-B9DE8E61-F4F5-47D7-AB35-9A094772BD07Q28290639-D0C8CE55-3D32-4E4A-8B65-8F7F00756C17Q30414096-000172C6-A743-41D4-8E8C-A4C43440CD39Q33809095-168D45A3-2445-4BF8-8417-62FE23BE33F8Q34285417-94985C10-1356-4C5E-A82B-63E52AFE1230Q34406487-E45D9F52-BAED-4D83-A6DC-C211CB6D69FDQ34457174-EEB8B97F-27B8-42D8-A97D-B10AB0F06D6EQ34800154-77851718-50A3-45A4-A71C-AC7D7C1252D4Q35994501-7D3A6E78-9ECB-461B-8FEE-6D4263467E1DQ36014767-5B8203B6-8210-4353-9D02-D9EF5DF9935AQ36755104-5E3BA264-1CBA-492F-91B3-17C59850283FQ37827380-51FDAAD4-9911-451D-A276-D7D26AEE4DEAQ37983519-E7D570CA-3588-410A-ADDA-92438FCA62F8Q38767547-18B6262E-3AA1-4D6C-9FD8-49D164D7B513Q38821145-4A6FED04-5A01-4ECE-AE13-5AA0BB6C9C53Q39367404-31B45B39-9AE3-45AB-92F6-BD8531A9998AQ42094622-F38C72CF-B8E9-4CE4-A061-687166DFFD39Q47846065-0980E5A0-C7F8-4172-954C-72A979B65895Q48023962-3772C9AA-0C0C-48F0-A912-69CE299C6574Q52975643-B8B78AEA-0E21-4499-A83F-4A7AD4E90BBE
P2860
Variable loss of Kir4.1 channel function in SeSAME syndrome mutations.
description
2010 nî lūn-bûn
@nan
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
2010年论文
@zh
2010年论文
@zh-cn
name
Variable loss of Kir4.1 channel function in SeSAME syndrome mutations.
@en
Variable loss of Kir4.1 channel function in SeSAME syndrome mutations.
@nl
type
label
Variable loss of Kir4.1 channel function in SeSAME syndrome mutations.
@en
Variable loss of Kir4.1 channel function in SeSAME syndrome mutations.
@nl
prefLabel
Variable loss of Kir4.1 channel function in SeSAME syndrome mutations.
@en
Variable loss of Kir4.1 channel function in SeSAME syndrome mutations.
@nl
P2093
P2860
P1476
Variable loss of Kir4.1 channel function in SeSAME syndrome mutations
@en
P2093
Andrea Sand
Darwin Hang
Xiaofang Tang
P2860
P304
P356
10.1016/J.BBRC.2010.07.105
P407
P50
P577
2010-08-03T00:00:00Z