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Fetal Bovine Serum impacts the observed N-glycosylation defects in TMEM165 KO HEK cells

TMEM165 is involved in a rare genetic human disease named TMEM165-CDG (Congenital Disorders of Glycosylation). It is Golgi localized, highly conserved through evolution and belongs to the uncharacterized protein family 0016 (UPF0016). The use of isogenic TMEM165 KO HEK cells was crucial in decipheri...

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Bibliografiske detaljer
Udgivet i:J Inherit Metab Dis
Main Authors: Vicogne, Dorothée, Houdou, Marine, Garat, Anne, Climer, Leslie, Lupashin, Vladimir, Morelle, Willy, Foulquier, François
Format: Artigo
Sprog:Inglês
Udgivet: 2019
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7021577/
https://ncbi.nlm.nih.gov/pubmed/31415112
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jimd.12161
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