Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Selma Angèlica Serra"'
Autor:
Maria Isabel Bahamonde, Selma Angèlica Serra, Oliver Drechsel, Rubayte Rahman, Anna Marcé-Grau, Marta Prieto, Stephan Ossowski, Alfons Macaya, José M Fernández-Fernández
Publikováno v:
PLoS ONE, Vol 10, Iss 12, p e0146035 (2015)
Mutations in the CACNA1A gene, encoding the pore-forming CaV2.1 (P/Q-type) channel α1A subunit, result in heterogeneous human neurological disorders, including familial and sporadic hemiplegic migraine along with episodic and progressive forms of at
Externí odkaz:
https://doaj.org/article/86c62683d5e547b387afc1ff9cb87119
Publikováno v:
Physiological Reports
Modulation of CaV2.1 channel activity plays a key role in interneuronal communication and synaptic plasticity. SNAREs interact with a specific synprint site at the second intracellular loop (LII‐III) of the CaV2.1 pore‐forming α 1A subunit to op
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f00c5b4de7eefb2c08f414707940b89
https://pubmed.ncbi.nlm.nih.gov/29380539
https://pubmed.ncbi.nlm.nih.gov/29380539
Autor:
Oriel, Carreño, Roser, Corominas, Selma Angèlica, Serra, Cèlia, Sintas, Noèlia, Fernández-Castillo, Marta, Vila-Pueyo, Claudio, Toma, Gemma G, Gené, Roser, Pons, Miguel, Llaneza, María-Jesús, Sobrido, Daniel, Grinberg, Miguel Ángel, Valverde, José Manuel, Fernández-Fernández, Alfons, Macaya, Bru, Cormand
Publikováno v:
Molecular Genetics & Genomic Medicine
Hemiplegic migraine (HM) is a rare and severe subtype of autosomal dominant migraine, characterized by a complex aura including some degree of motor weakness. Mutations in four genes (CACNA1A, ATP1A2, SCN1A and PRRT2) have been detected in familial a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7c48b25bc93d12847ea1f92e0bf6cb71
https://pubmed.ncbi.nlm.nih.gov/24498617
https://pubmed.ncbi.nlm.nih.gov/24498617