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Gne-Depletion in C2C12 Myoblasts Leads to Alterations in Glycosylation and Myopathogene Expression

GNE myopathy is a rare genetic neuromuscular disorder caused by mutations in the <i>GNE</i> gene. The respective gene product, UDP-<i>N</i>-acetylglucosamine 2-epimerase/<i>N</i>-acetylmannosamine kinase (GNE), is a bifunctional enzyme that initiates endogenous sialic acid biosynthesis. Sialic acids...

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Principais autores: Carolin T. Neu, Aristotelis Antonopoulos, Anne Dell, Stuart M. Haslam, Rüdiger Horstkorte
Format: Artigo
Sprog:Inglês
Udgivet: MDPI AG 2026-01-01
Serier:Cells
Fag:
GNE
GNE-myopathy
myopathogenes
sialic acids
glycosylation
N-glycans
Online adgang:https://www.mdpi.com/2073-4409/15/2/199
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