Differential cerebellar GABAA receptor expression in mice with mutations in CaV2.1 (P/Q-type) calcium channels-Reference-Cited by-同舟云学术

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Differential cerebellar GABAA receptor expression in mice with mutations in CaV2.1 (P/Q-type) calcium channels

Published:2015-09 Issue: Volume:304 Page:198-208
ISSN:0306-4522
Container-title:Neuroscience
language:en
Short-container-title:Neuroscience

Author:

Kaja S.^ORCID,Payne A.J.,Nielsen E.Ø.,Thompson C.L.,van den Maagdenberg A.M.J.M.,Koulen P.,Snutch T.P.

Funder

European Molecular Biology Organization

Michael Smith Foundation

National Headache Foundation

Canadian Institutes of Health Research

Tier 1 Canada Research Chair in Biotechnology and Genomics-Neurobiology

Wellcome Trust

Biotechnology and Biological Sciences Research Council

NIH/NEI

NIH/NCRR

NIH/NIA

Publisher

Elsevier BV

Subject

General Neuroscience

Reference59 articles.

1. KCa channels as therapeutic targets in episodic ataxia type-2;Alvina;J Neurosci,2010

2. The therapeutic mode of action of 4-aminopyridine in cerebellar ataxia;Alvina;J Neurosci,2010

3. The MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments;Bustin;Clin Chem,2009

4. GABA transporter deficiency causes tremor, ataxia, nervousness, and increased GABA-induced tonic conductance in cerebellum;Chiu;J Neurosci,2005

5. Molecular genetics of migraine;de Vries;Hum Genet,2009

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2. Prioritizing Suggestive Candidate Genes in Migraine: An Opinion;Frontiers in Neurology;2022-06-15

3. Gimmicks of gamma‐aminobutyric acid (GABA) in pancreatic β‐cell regeneration through transdifferentiation of pancreatic α‐ to β‐cells;Cell Biology International;2020-01-16

4. Neonatal brain injury causes cerebellar learning deficits and Purkinje cell dysfunction;Nature Communications;2018-08-13

5. Using the shared genetics of dystonia and ataxia to unravel their pathogenesis;Neuroscience & Biobehavioral Reviews;2017-04

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