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ALG8 gene

Known as: DOLICHYL-P-GLUCOSE:Glc-1-Man-9-GlcNAc-2-PP-DOLICHYL-ALPHA-3-GLUCOSYLTRANSFERASE, ALG8, S. CEREVISIAE, HOMOLOG OF, ALG8 
National Institutes of Health

Papers overview

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2018
2018
ABSTRACTBackgroundCongenital disorders of glycosylation (CDG) includes ALG8 deficiency, a protein N-glycosylation defect with a… 
Highly Cited
2017
Highly Cited
2017
Dominantly inherited isolated polycystic liver disease (PCLD) consists of liver cysts that are radiologically and pathologically… 
2017
2017
Dominantly inherited isolated polycystic liver disease (PCLD) consists of liver cysts that are radiologically and pathologically… 
2017
2017
A new study identifies heterozygous loss-of-function mutations in three additional genes (ALG8, SEC61B and PKHD1) as causative… 
Review
2015
Review
2015
BackgroundSince 1980, about 100 types of congenital disorders of glycosylation (CDG) have been reported representing an expanding… 
2012
2012
In metazoans, miRNAs regulate gene expression primarily through binding to target sites in the 3′ UTRs (untranslated regions) of… 
Review
2009
Review
2009
SummaryCongenital disorders of glycosylation (CDG) represent an expanding group of inherited diseases. One of them, ALG8… 
Highly Cited
2006
Highly Cited
2006
ABSTRACT An enzymatic in vitro alginate polymerization assay was developed by using 14C-labeled GDP-mannuronic acid as a… 
Highly Cited
1994
Highly Cited
1994
Glc3Man9GlcNAc2 is the preferred substrate of the oligosaccharyltransferase of N-linked glycosylation of proteins, but…