Dissection of TMEM165 function in Golgi glycosylation and its Mn(2+) sensitivity

Since 2012, the interest for TMEM165 increased due to its implication in a rare genetic human disease named TMEM165-CDG (Congenital Disorder(s) of Glycosylation). TMEM165 is a Golgi localized protein, highly conserved through evolution and belonging to the uncharacterized protein family 0016 (UPF001...

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Библиографические подробности
Опубликовано в: :Biochimie
Главные авторы: Lebredonchel, Elodie, Houdou, Marine, Potelle, Sven, de Bettignies, Geoffroy, Schulz, Céline, Krzewinski Recchi, Marie-Ange, Lupashin, Vladimir, Legrand, Dominique, Klein, André, Foulquier, François
Формат: Artigo
Язык:Inglês
Опубликовано: 2019
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC6857530/
https://ncbi.nlm.nih.gov/pubmed/31351090
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biochi.2019.07.016
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