Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells (Q28591132)

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English	Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells	scientific journal article

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31 January 2017

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11487633%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells (English)

2 references

PubMed publication ID

31 January 2017

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11487633%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

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Calcium channel, voltage-dependent, alpha 2/delta subunit 2

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GOA release 2020-03-11

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J Barclay

1

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10 November 2019

N Balaguero

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10 November 2019

M Mione

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10 November 2019

S L Ackerman

4

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10 November 2019

V A Letts

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10 November 2019

J Brodbeck

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10 November 2019

C Canti

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A Meir

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K M Page

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10 November 2019

K Kusumi

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10 November 2019

E Perez-Reyes

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E S Lander

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10 November 2019

W N Frankel

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10 November 2019

R M Gardiner

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10 November 2019

A C Dolphin

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10 November 2019

M Rees

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publication date

1 August 2001

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10 November 2019

Journal of Neuroscience

2 references

PubMed publication ID

31 January 2017

Europe PubMed Central

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10 November 2019

21

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PubMed publication ID

31 January 2017

Europe PubMed Central

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10 November 2019

16

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PubMed publication ID

31 January 2017

Europe PubMed Central

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10 November 2019

6095-6104

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10 November 2019

Whole-cell and single-channel analysis of P-type calcium currents in cerebellar Purkinje cells of leaner mutant mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic organization of the mouse and human alpha2delta2 voltage-dependent calcium channel subunit genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular diversity of the calcium channel alpha2delta subunit

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Seizure disorders in mutant mice: relevance to human epilepsies

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Subunit interaction sites in voltage-dependent Ca2+ channels: role in channel function.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nomenclature of voltage-gated calcium channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purkinje cell loss from alternating sagittal zones in the cerebellum of leaner mutant mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A YAC-based physical map of the mouse genome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered calcium channel currents in Purkinje cells of the neurological mutant mouse leaner

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Excitatory but not inhibitory synaptic transmission is reduced in lethargic (Cacnb4(lh)) and tottering (Cacna1atg) mouse thalami

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Basic mechanisms of generalized absence seizures

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Calcium - a life and death signal

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure and function of neuronal Ca2+ channels and their role in neurotransmitter release

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human semaphorins A(V) and IV reside in the 3p21.3 small cell lung cancer deletion region and demonstrate distinct expression patterns

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal localization of genes encoding guanine nucleotide-binding protein subunits in mouse and human

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of residues in the N terminus of alpha1B critical for inhibition of the voltage-dependent calcium channel by Gbeta gamma.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The novel anticonvulsant drug, gabapentin (Neurontin), binds to the alpha2delta subunit of a calcium channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Presynaptic Ca(2+) influx at a mouse central synapse with Ca(2+) channel subunit mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DLX-1, DLX-2, and DLX-5 expression define distinct stages of basal forebrain differentiation

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dystonia associated with mutation of the neuronal sodium channel Scn8a and identification of the modifier locus Scnm1 on mouse chromosome 3

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of Ca2+ channel currents in cultured rat cerebellar granule neurones

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cluster of three novel Ca2+ channel gamma subunit genes on chromosome 19q13.4: evolution and expression profile of the gamma subunit gene family

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence epilepsy in tottering mutant mice is associated with calcium channel defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional properties of a new voltage-dependent calcium channel alpha(2)delta auxiliary subunit gene (CACNA2D2)

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

P-type calcium channels in rat central and peripheral neurons

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neural network of structures in which GABAB receptors regulate absence seizures in the lethargic (lh/lh) mouse model

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of the mouse neuromuscular mutation kyphoscoliosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning of CISH, chromosome assignment to 3p21.3, and analysis of expression in fetal and adult tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single tottering mutations responsible for the neuropathic phenotype of the P-type calcium channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of GABAB receptor activation in absence seizures of lethargic (lh/lh) mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comprehensive large-insert yeast artificial chromosome library for physical mapping of the mouse genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited epilepsy: spike-wave and focal motor seizures in the mutant mouse tottering

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Calcium channel beta subunit promotes voltage-dependent modulation of alpha 1 B by G beta gamma.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11487633

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1523/JNEUROSCI.21-16-06095.2001

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Europe PubMed Central

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10 November 2019

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

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10 November 2019

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2 references

Consolidated OpenCitations Corpus – April 2017

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Europe PubMed Central

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10 November 2019

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