Etude de la régulation du canal CFTR impliqué dans la mucoviscidose par un analogue de la GnRHet le Mg2+

Etude de la régulation du canal CFTR impliqué dans la mucoviscidose par un analogue de la GnRHet le Mg2+

La mucoviscidose est la maladie héréditaire autosomique récessive, rare, létale, la plus fréquente dans la population caucasienne. Cette maladie est causée par des mutations du gène CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) codant la protéine CFTR. Cette protéine est principalement...

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Bibliographic Details
Main Author:	Calvez, Marie-Laure
Other Authors:	Brest
Language:	fr
Published:	2017
Subjects:	CFTR Mutation F508del GnRH Cellules nasales humaines Analogue R-GnRH Mg2+ TRPM7 F508del mutation Human nasal epithelial cells GnRHR 616.372
Online Access:	http://www.theses.fr/2017BRES0048/document

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