A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation (Q28115658)

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3 January 2017

D. Bhat

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3 January 2017

M. Faham

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3 January 2017

R. M. Myers

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3 January 2017

A. S. Peterson

https://scigraph.springernature.com/pub.10.1038/ng1095-126

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3 January 2017

language of work or name

English

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publication date

1 October 1995

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126–129

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Cloning provides evidence for a family of inward rectifier and G-protein coupled K+ channels in the brain

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The G-protein-gated atrial K+ channel IKACh is a heteromultimer of two inwardly rectifying K(+)-channel proteins

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Molecular cloning of a mouse G-protein-activated K+ channel (mGIRK1) and distinct distributions of three GIRK (GIRK1, 2 and 3) mRNAs in mouse brain

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Cerebellar granule cell neurogenesis is regulated by cell-cell interactions in vitro.

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The weaver gene encodes a nonautonomous signal for CNS neuronal differentiation.

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Male-sterile phenotype of the neurological mouse mutant weaver.

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Tonic/clonic seizures in a mouse mutant carrying the weaver gene

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Recent advances in the understanding of potassium channel function

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Alteration of ionic selectivity of a K+ channel by mutation of the H5 region

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Sequence of developmental abnormalities leading to granule cell deficit in cerebellar cortex of weaver mutant mice

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Organization of cerebellar cortex secondary to deficit of granule cells in weaver mutant mice

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Weaver Mutant Mouse Cerebellum: Defective Neuronal Migration Secondary to Abnormality of Bergmann Glia

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Abnormal rate of granule cell migration in the cerebellum of “weaver” mutant mice

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In situ labeling of granule cells for apoptosis-associated DNA fragmentation reveals different mechanisms of cell loss in developing cerebellum

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Development and death of external granular layer cells in the weaver mouse cerebellum: a quantitative study

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The weaver granuloprival phenotype is due to intrinsic action of the mutant locus in granule cells: Evidence from homozygous weaver chimeras

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Neuronal differentiation rescued by implantation of Weaver granule cell precursors into wild-type cerebellar cortex.

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Dopamine deficiency in the weaver mutant mouse.

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High-resolution mapping of D16led-1, Gart, Gas-4, Cbr, Pcp-4, and Erg on distal mouse chromosome 16

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7 January 2021

The mouse neurological mutant weaver maps within the region of chromosome 16 that is homologous to human chromosome 21

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A high resolution physical map of 2.5 Mbp of the Down syndrome region on chromosome 21.

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A transcript map of the Down syndrome critical region on chromosome 21.

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Isolation of a cDNA Clone Encoding a KATP Channel-Like Protein Expressed in Insulin-Secreting Cells, Localization of the Human Gene to Chromosome Band 21q22.1, and Linkage Studies With NIDDM

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minibrain: a new protein kinase family involved in postembryonic neurogenesis in Drosophila

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Towards high resolution maps of the mouse and human genomes—a facility for ordering markers to 0.1 cM resolution

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Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

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Exchange of conduction pathways between two related K+ channels.

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A Functional Connection Between the Pores of Distantly Related Ion Channels as Revealed by Mutant K + Channels

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7 January 2021

Rescue of lethal subunits into functional K+ channels

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K+ pore structure revealed by reporter cysteines at inner and outer surfaces.

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Weaver mouse cerebellar granule neurons fail to migrate on wild-type astroglial processes in vitro.

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