Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Aurelien Bidaud-Meynard"'
Autor:
Mohammed H. Mosa, Ophélie Nicolle, Sophia Maschalidi, Fernando E. Sepulveda, Aurelien Bidaud-Meynard, Constantin Menche, Birgitta E. Michels, Grégoire Michaux, Geneviève de Saint Basile, Henner F. Farin
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 6, Iss 4, Pp 477-493.e1 (2018)
Background & Aims: Microvillus inclusion disease (MVID) is a congenital intestinal malabsorption disorder caused by defective apical vesicular transport. Existing cellular models do not fully recapitulate this heterogeneous pathology. The aim of this
Externí odkaz:
https://doaj.org/article/ef293e491f7240379703b18ddd4ab05a
Autor:
Aurélien Bidaud-Meynard, Anne Bourdais, Ophélie Nicolle, Maela Duclos, Jad Saleh, Frank M. Ruemmele, Henner F. Farin, Delphine Delacour, Despina Moshous, Grégoire Michaux
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 17, Iss 6, Pp 1072-1075 (2024)
Externí odkaz:
https://doaj.org/article/17e3bd79c7ab45dea4123ebff58c2eeb
Autor:
Guido Veit, Kathryn Oliver, Pirjo M Apaja, Doranda Perdomo, Aurélien Bidaud-Meynard, Sheng-Ting Lin, Jingyu Guo, Mert Icyuz, Eric J Sorscher, John L Hartman, Gergely L Lukacs
Publikováno v:
PLoS Biology, Vol 14, Iss 5, p e1002462 (2016)
The most common cystic fibrosis (CF) causing mutation, deletion of phenylalanine 508 (ΔF508 or Phe508del), results in functional expression defect of the CF transmembrane conductance regulator (CFTR) at the apical plasma membrane (PM) of secretory e
Externí odkaz:
https://doaj.org/article/2e5a3f66228046208e973fd23ba3f520