UNC45A deficiency causes microvillus inclusion disease–like phenotype by impairing myosin VB–dependent apical trafficking-Reference-Cited by-同舟云学术

UNC45A deficiency causes microvillus inclusion disease–like phenotype by impairing myosin VB–dependent apical trafficking

Published:2022-05-16 Issue:10 Volume:132 Page:
ISSN:1558-8238
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:

Author:

Duclaux-Loras Rémi,Lebreton Corinne,Berthelet Jérémy,Charbit-Henrion Fabienne^ORCID,Nicolle Ophelie,Revenu de Courtils Céline,Waich Stephanie,Valovka Taras^ORCID,Khiat Anis,Rabant Marion,Racine Caroline,Guerrera Ida Chiara^ORCID,Baptista Júlia,Mahe Maxime M.^ORCID,Hess Michael W.,Durel Béatrice,Lefort Nathalie^ORCID,Banal Céline,Parisot Mélanie,Talbotec Cecile,Lacaille Florence,Ecochard-Dugelay Emmanuelle,Demir Arzu Meltem,Vogel Georg F.^ORCID,Faivre Laurence,Rodrigues Astor,Fowler Darren,Janecke Andreas R.^ORCID,Müller Thomas^ORCID,Huber Lukas A.^ORCID,Rodrigues-Lima Fernando,Ruemmele Frank M.^ORCID,Uhlig Holm H.^ORCID,Del Bene Filippo^ORCID,Michaux Grégoire^ORCID,Cerf-Bensussan Nadine^ORCID,Parlato Marianna

Funder

Agence nationale de la recherche

H2020 European Research Council

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Link

https://www.jci.org/articles/view/154997/files/pdf

Reference39 articles.

1. Congenital diarrhoeal disorders: advances in this evolving web of inherited enteropathies

2. Intestinal immunoregulation: lessons from human mendelian diseases