Literature DB >> 10395579

Calcium channelopathies in the central nervous system.

J Jen1.   

Abstract

The recent discovery that familial hemiplegic migraine, episodic ataxia type 2, and spinocerebellar ataxia type 6 are allelic disorders caused by different mutations in CACNA1A, a calcium-channel-encoding gene, adds to a growing list of channelopathies causing paroxysmal neurologic disturbance and progressive neurodegeneration. Calcium channelopathies in the central nervous system provide a model to study the important roles that calcium channels play in neuronal function.

Entities:  

Mesh：

Substances：

Year:  1999        PMID： 10395579     DOI： 10.1016/s0959-4388(99)80040-3

Source DB:  PubMed          Journal:  Curr Opin Neurobiol        ISSN： 0959-4388            Impact factor:   6.627


  14 in total

Review 1.  Molecular determinants of inactivation in voltage-gated Ca2+ channels.

Authors:  S Hering; S Berjukow; S Sokolov; R Marksteiner; R G Weiss; R Kraus; E N Timin
Journal:  J Physiol       Date:  2000-10-15       Impact factor: 5.182

2.  Inactivation determinants in segment IIIS6 of Ca(v)3.1.

Authors:  R Marksteiner; P Schurr; S Berjukow; E Margreiter; E Perez-Reyes; S Hering
Journal:  J Physiol       Date:  2001-11-15       Impact factor: 5.182

Review 3.  Targeting mechanisms of high voltage-activated Ca2+ channels.

Authors:  Stefan Herlitze; Mian Xie; Jing Han; Alexander Hümmer; Katya V Melnik-Martinez; Rosa L Moreno; Melanie D Mark
Journal:  J Bioenerg Biomembr       Date:  2003-12       Impact factor: 2.945

Review 4.  In vivo analysis of voltage-dependent calcium channels.

Authors:  Ling Liu; Theresa A Zwingman; Colin F Fletcher
Journal:  J Bioenerg Biomembr       Date:  2003-12       Impact factor: 2.945

5.  Alpha-ketoisocaproic acid increases phosphorylation of intermediate filament proteins from rat cerebral cortex by mechanisms involving Ca2+ and cAMP.

Authors:  Cláudia Funchal; Ariane Zamoner; André Quincozes dos Santos; Samanta Oliveira Loureiro; Moacir Wajner; Regina Pessoa-Pureur
Journal:  Neurochem Res       Date:  2005-09       Impact factor: 3.996

6.  Loss-of-function BK channel mutation causes impaired mitochondria and progressive cerebellar ataxia.

Authors:  Xiaofei Du; Joao L Carvalho-de-Souza; Cenfu Wei; Willy Carrasquel-Ursulaez; Yenisleidy Lorenzo; Naileth Gonzalez; Tomoya Kubota; Julia Staisch; Timothy Hain; Natalie Petrossian; Michael Xu; Ramon Latorre; Francisco Bezanilla; Christopher M Gomez
Journal:  Proc Natl Acad Sci U S A       Date:  2020-03-04       Impact factor: 11.205

7.  Courtship and other behaviors affected by a heat-sensitive, molecularly novel mutation in the cacophony calcium-channel gene of Drosophila.

Authors:  Betty Chan; Adriana Villella; Pablo Funes; Jeffrey C Hall
Journal:  Genetics       Date:  2002-09       Impact factor: 4.562

8.  Paroxysmal dyskinesias in the lethargic mouse mutant.

Authors:  Zubair Khan; H A Jinnah
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

Review 9.  Homeostatic compensation maintains Ca2+ signaling functions in Purkinje neurons in the leaner mutant mouse.

Authors:  David Murchison; Leonard S Dove; Louise C Abbott; William H Griffith
Journal:  Cerebellum       Date:  2002-04       Impact factor: 3.847

10.  The first knockin mouse model of episodic ataxia type 2.

Authors:  Samuel J Rose; Lisa H Kriener; Ann K Heinzer; Xueliang Fan; Robert S Raike; Arn M J M van den Maagdenberg; Ellen J Hess
Journal:  Exp Neurol       Date:  2014-08-08       Impact factor: 5.330
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.