Comparative expression of the inward rectifier K+ channel GIRK2 in the cerebellum of normal and weaver mutant mice (Q48730820)

15 February 2018

title

Comparative expression of the inward rectifier K+ channel GIRK2 in the cerebellum of normal and weaver mutant mice (English)

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15 February 2018

author

Florian Lesage

4

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15 February 2018

author name string

Lauritzen I

1

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15 February 2018

De Weille J

2

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Adelbrecht C

3

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15 February 2018

Murer G

5

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Raisman-Vozari R

6

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Lazdunski M

7

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language of work or name

English

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publication date

1 April 1997

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15 February 2018

published in

Brain Research

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15 February 2018

volume

753

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issue

1

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15 February 2018

page(s)

8-17

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15 February 2018

Postnatal development of the cerebellar cortex in the rat. 3. Maturation of the components of the granular layer.

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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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Cloning of a Xenopus laevis inwardly rectifying K+ channel subunit that permits GIRK1 expression of IKACh currents in oocytes

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Identification of the weaver mouse mutation: the end of the beginning

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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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Evidence that neuronal G-protein-gated inwardly rectifying K+ channels are activated by G beta gamma subunits and function as heteromultimers

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Functional analysis of the weaver mutant GIRK2 K+ channel and rescue of weaver granule cells

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Primary structure and functional expression of a mouse inward rectifier potassium channel

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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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Assessment of a mutation in the H5 domain of Girk2 as a candidate for the weaver mutation.

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Nonselective and G betagamma-insensitive weaver K+ channels

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

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Morphological abnormalities in the hippocampus of the weaver mutant mouse

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Purkinje cell loss is due to a direct action of the weaver gene in Purkinje cells: evidence from chimeric mice.

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The weaver mutation of GIRK2 results in a loss of inwardly rectifying K+ current in cerebellar granule cells

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The weaver mutation changes the ion selectivity of the affected inwardly rectifying potassium channel GIRK2.

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Heteromeric channel formation and Ca(2+)-free media reduce the toxic effect of the weaver Kir 3.2 allele.

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The abnormal cerebellar organization of Weaver and reeler mice does not affect the cellular distribution of three neuronal mRNAs

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Apoptotic cell death in the cerebellum of mutant weaver and lurcher mice

7 January 2021

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10.1016/S0006-8993(96)01491-6

7 January 2021

Identifiers

DOI

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15 February 2018

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15 February 2018