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ALG9 gene

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

Papers overview

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2019
2019
BACKGROUND Mutations in PKD1 or PKD2 cause typical autosomal dominant polycystic kidney disease (ADPKD), the most common… Expand
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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… Expand
2014
2014
Abstract Background: We have developed a PCR-based tool that measures a 51-gene panel for identification of… Expand
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Highly Cited
2007
Highly Cited
2007
Accurate quantitation of target genes depends on correct normalization. Use of genes with variable tissue transcription (GAPDH… Expand
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2006
2006
BackgroundA mannosyltransferase gene (ALG9, DIBD1) at chromosome band 11q23 was previously identified to be disrupted by a… Expand
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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… Expand
Highly Cited
2005
Highly Cited
2005
N-linked protein glycosylation follows a conserved pathway in eukaryotic cells. The assembly of the lipid-linked core… Expand
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Highly Cited
2004
Highly Cited
2004
Defects of lipid-linked oligosaccharide assembly lead to alterations of N-linked glycosylation known as "type I congenital… Expand
2001
2001
Bipolar affective disorder (BPAD) is a complex neuropsychiatric disease characterized by extreme mood swings. Genetic influences… Expand
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Highly Cited
1996
Highly Cited
1996
The core oligosaccharide Glc3Man9GlcNAc2 is assembled at the membrane of the endoplasmic reticulum on the lipid carrier dolichyl… Expand