ALG9 gene

Known as: DISRUPTED IN BIPOLAR DISORDER 1, ALG9, S. CEREVISIAE, HOMOLOG OF, ALG9, alpha-1,2-mannosyltransferase 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1996-2016
02419962016

Papers overview

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2016
2016
ALG9-CDG is one of the less frequently reported types of CDG. Here, we summarize the features of six patients with ALG9-CDG… (More)
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2016
2016
A rare lethal autosomal recessive syndrome with skeletal dysplasia, polycystic kidneys and multiple malformations was first… (More)
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2010
2010
Normalization of gene expression data refers to the comparison of expression values using reference standards that are consistent… (More)
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Highly Cited
2009
Highly Cited
2009
Real-time RT-PCR is the recommended method for quantitative gene expression analysis. A compulsory step is the selection of good… (More)
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2009
2009
We describe an ALG9-defective (congenital disorders of glycosylation type IL) patient who is homozygous for the p.Y286C (c.860A>G… (More)
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2009
2009
BACKGROUND A more accurate taxonomy of small intestinal (SI) neuroendocrine tumors (NETs) is necessary to accurately predict… (More)
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2005
2005
We describe the second case of congenital disorder of glycosylation type IL (CDG-IL) caused by deficiency of the ALG9 a1,2… (More)
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2005
2005
N-linked protein glycosylation follows a conserved pathway in eukaryotic cells. The assembly of the lipid-linked core… (More)
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2004
2004
Defects of lipid-linked oligosaccharide assembly lead to alterations of N-linked glycosylation known as "type I congenital… (More)
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1996
1996
The core oligosaccharide Glc3Man9GlcNAc2 is assembled at the membrane of the endoplasmic reticulum on the lipid carrier dolichyl… (More)
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