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Pflugers Archiv European Journal of Physiology

Volumn 457, Issue 2, 2008, Pages 315-326

The S218L familial hemiplegic migraine mutation promotes deinhibition of Cav2.1 calcium channels during direct G-protein regulation

(5) Weiss, Norbert a,b,f Sandoval, Alejandro c,d Felix, Ricardo c Van Den Maagdenberg, Arn e De Waard, Michel a,b

a GRENOBLE INSTITUT DES NEUROSCIENCES (France)

b UNIV GRENOBLE ALPES (France)

c DEPARTAMENTO DE FÍSICA (Mexico)

d UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO (Mexico)

e LEIDEN UNIVERSITY MEDICAL CENTER (Netherlands)

f Laboratoire de Physiologie Int&EACUTE grative Cellulaire et Mol&EACUTE culaire Villeurbanne (France)

Author keywords

Ca v2.1 type calcium channel; Cav2.1 subunit; Familial hemiplegic migraine; G protein; G protein coupled receptor; P Q current; R192Q mutation; S218L mutation; subunit; Opioid receptor

Indexed keywords

ENKEPHALIN[2 DEXTRO ALANINE 4 METHYLPHENYLALANINE 5 GLYCINE]; G PROTEIN COUPLED RECEPTOR; GUANINE NUCLEOTIDE BINDING PROTEIN; OPIATE RECEPTOR; VOLTAGE GATED CALCIUM CHANNEL;

AMPLITUDE MODULATION; ARTICLE; BIOPHYSICS; CONTROLLED STUDY; DISSOCIATION; EMBRYO; FAMILIAL DISEASE; GENE MUTATION; HEMIPLEGIC MIGRAINE; HUMAN; HUMAN CELL; HYPERACTIVITY; MEMBRANE POTENTIAL; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; WILD TYPE;

EID: 56649086752 PISSN: 00316768 EISSN: 14322013 Source Type: Journal
DOI: 10.1007/s00424-008-0541-2 Document Type: Article

Times cited : (48)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.