Genetic inactivation of an inwardly rectifying potassium channel (Kir4.1 subunit) in mice: phenotypic impact in retina
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Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindnessGPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindnessGap junctions couple astrocytes and oligodendrocytesEAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10The Role of MicroRNAs in the Regulation of K(+) Channels in Epithelial TissueRole of astrocytes in epilepsyVascular inward rectifier K+ channels as external K+ sensors in the control of cerebral blood flowPhysiological roles of aquaporin-4 in brainRod and cone function in patients with KCNV2 retinopathyInwardly rectifying potassium channel Kir4.1 is responsible for the native inward potassium conductance of satellite glial cells in sensory gangliaClass 5 transmembrane semaphorins control selective Mammalian retinal lamination and functionContribution of Kir4.1 to the mouse electroretinogramThe light peak of the electroretinogram is dependent on voltage-gated calcium channels and antagonized by bestrophin (best-1)Kir4.1 expression by astrocytes and oligodendrocytes in CNS white matter: a developmental study in the rat optic nerveAquaporin-4 independent Kir4.1 K+ channel function in brain glial cellsThe role of an inwardly rectifying K(+) channel (Kir4.1) in the inner ear and hearing loss.Development and validation of fluorescence-based and automated patch clamp-based functional assays for the inward rectifier potassium channel Kir4.1.The Membrane Properties of Cochlear Root Cells are Consistent with Roles in Potassium Recirculation and Spatial Buffering.Decreased expression of the glial water channel aquaporin-4 in the intrahippocampal kainic acid model of epileptogenesis.Neurological features of epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome.Signalling within the neurovascular unit in the mammalian retina.Functional implication of Dp71 in osmoregulation and vascular permeability of the retinaSmall-molecule modulators of inward rectifier K+ channels: recent advances and future possibilities.The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responsesMolecular diversity and regulation of renal potassium channels.Spinal cord injury causes a wide-spread, persistent loss of Kir4.1 and glutamate transporter 1: benefit of 17 beta-oestradiol treatmentImproved retinal function in RCS rats after suppressing the over-activation of mGluR5Retinal degeneration in a rodent model of Smith-Lemli-Opitz syndrome: electrophysiologic, biochemical, and morphologic featuresLong-Term Safety of Transplanting Human Bone Marrow Stromal Cells into the Extravascular Spaces of the Choroid of Rabbits.Light-evoked responses of the mouse retinal pigment epithelium.Light-evoked responses of the retinal pigment epithelium: changes accompanying photoreceptor loss in the mouse.Celsr3 is required for normal development of GABA circuits in the inner retina.Probing potassium channel function in vivo by intracellular delivery of antibodies in a rat model of retinal neurodegeneration.Differential effects of P2Y1 deletion on glial activation and survival of photoreceptors and amacrine cells in the ischemic mouse retina.Proliferative reactive gliosis is compatible with glial metabolic support and neuronal function.KCNJ10 determines the expression of the apical Na-Cl cotransporter (NCC) in the early distal convoluted tubule (DCT1).Nyctalopin expression in retinal bipolar cells restores visual function in a mouse model of complete X-linked congenital stationary night blindnessKcnj10 is a major type of K+ channel in mouse corneal epithelial cells and plays a role in initiating EGFR signaling.Potassium buffering in the central nervous systemChronic dysfunction of astrocytic inwardly rectifying K+ channels specific to the neocortical epileptic focus after fluid percussion injury in the rat
P2860
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P2860
Genetic inactivation of an inwardly rectifying potassium channel (Kir4.1 subunit) in mice: phenotypic impact in retina
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2000 nî lūn-bûn
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2000 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
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2000 թվականի օգոստոսին հրատարակված գիտական հոդված
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2000年の論文
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2000年学术文章
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2000年学术文章
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2000年学术文章
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2000年学术文章
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2000年学术文章
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Genetic inactivation of an inw ...... e: phenotypic impact in retina
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Genetic inactivation of an inw ...... e: phenotypic impact in retina
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Genetic inactivation of an inw ...... e: phenotypic impact in retina
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label
Genetic inactivation of an inw ...... e: phenotypic impact in retina
@ast
Genetic inactivation of an inw ...... e: phenotypic impact in retina
@en
Genetic inactivation of an inw ...... e: phenotypic impact in retina
@nl
prefLabel
Genetic inactivation of an inw ...... e: phenotypic impact in retina
@ast
Genetic inactivation of an inw ...... e: phenotypic impact in retina
@en
Genetic inactivation of an inw ...... e: phenotypic impact in retina
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P2093
P2860
P3181
P1476
Genetic inactivation of an inw ...... e: phenotypic impact in retina
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P2093
P2860
P304
P3181
P356
10.1523/JNEUROSCI.20-15-05733.2000
P407
P50
P577
2000-08-01T00:00:00Z