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

Topic mentions per year

Topic mentions per year

1994-2017
012319942017

Papers overview

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2018
2018
Data indicate significant phenotypic and genotypic overlap, plus a common pathogenesis, between two groups of inherited disorders… (More)
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2017
2017
group of genetic disorders characterized by progressive bile duct dilatation and/or the development of >10 liver cysts1. PLDs are… (More)
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Review
2015
Review
2015
BACKGROUND Since 1980, about 100 types of congenital disorders of glycosylation (CDG) have been reported representing an… (More)
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2012
2012
Posttranslationally glycosylated proteins are important in many biological processes in humans and Congenital disorders of… (More)
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2012
2012
In metazoans, miRNAs regulate gene expression primarily through binding to target sites in the 3' UTRs (untranslated regions) of… (More)
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Review
2009
Review
2009
Congenital disorders of glycosylation (CDG) represent an expanding group of inherited diseases. One of them, ALG8 deficiency (CDG… (More)
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2004
2004
In mammals, thyroid hormone responsive Spot 14 (THRSP) is a small acidic protein that is predominately expressed in lipogenic… (More)
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2004
2004
Previously, we have used both biochemical and immunological approaches to determine that the two-component, histidine kinase… (More)
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1994
1994
Glc3Man9GlcNAc2 is the preferred substrate of the oligosaccharyltransferase of N-linked glycosylation of proteins, but… (More)
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