(Q44683600)

5 December 2017

entla, a novel epileptic and ataxic Cacna2d2 mutant of the mouse (English)

1 reference

5 December 2017

4

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5 December 2017

Julia Brill

1

1 reference

5 December 2017

Rainer Klocke

2

1 reference

5 December 2017

Dieter Paul

3

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5 December 2017

Nicolette Gouder

5

1 reference

5 December 2017

Norbert Klugbauer

6

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5 December 2017

Franz Hofmann

7

1 reference

5 December 2017

Cord-Michael Becker

8

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5 December 2017

Kristina Becker

9

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5 December 2017

language of work or name

English

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publication date

2 December 2003

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Journal of Biological Chemistry

5 December 2017

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5 December 2017

279

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5 December 2017

8

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5 December 2017

7322-7330

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Structure and regulation of voltage-gated Ca2+ channels

5 December 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Insights from mouse models of absence epilepsy into Ca2+ channel physiology and disease etiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

The effect of alpha2-delta and other accessory subunits on expression and properties of the calcium channel alpha1G.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Neuronal distribution and functional characterization of the calcium channel alpha2delta-2 subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Gabapentin inhibits calcium currents in isolated rat brain neurons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

The neuropathology of ducky, a neurological mutation of the mouse. A pathological and preliminary histochemical study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

The ducky mutation in Cacna2d2 results in altered Purkinje cell morphology and is associated with the expression of a truncated alpha 2 delta-2 protein with abnormal function

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

A comprehensive genetic map of the mouse genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Functional chloride channels by mammalian cell expression of rat glycine receptor subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

The NMDA receptor subunit NR2B of neonatal rat brain: complex formation and enrichment in axonal growth cones.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Transient expression of NMDA receptor subunit NR2B in the developing rat heart.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Solubilization of the glycine receptor from rat spinal cord

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

P-type calcium channels in rat central and peripheral neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Novel myosin heavy chain encoded by murine dilute coat colour locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Stargazer: a new neurological mutant on chromosome 15 in the mouse with prolonged cortical seizures.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

The C57BL/10Bg sps/sps mouse: a mutant with absence-like seizures; neurochemical and behavioral correlates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Tissue-specific expression and gabapentin-binding properties of calcium channel alpha2delta subunit subtypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Recent duplication, domain accretion and the dynamic mutation of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Common exon duplication in animals and its role in alternative splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Cloning and deletion mutagenesis of the alpha2 delta calcium channel subunit from porcine cerebral cortex. Expression of a soluble form of the protein that retains [3H]gabapentin binding activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Cortical and subcortical generators of normal and abnormal rhythmicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Decrease in calbindin content significantly alters LTP but not NMDA receptor and calcium channel properties

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M308778200

21 January 2018

Identifiers

DOI

10.1074/JBC.M308778200

1 reference

5 December 2017

1 reference