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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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2020
2020
The development of drug resistance is the main obstacle for successful treatment in acute myeloid leukemia (AML). Noncoding RNAs… 
Highly Cited
2019
Highly Cited
2019
BACKGROUND Mutations in PKD1 or PKD2 cause typical autosomal dominant polycystic kidney disease (ADPKD), the most common… 
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… 
Highly Cited
2007
Highly Cited
2007
Accurate quantitation of target genes depends on correct normalization. Use of genes with variable tissue transcription (GAPDH… 
Highly Cited
2005
Highly Cited
2005
N-linked protein glycosylation follows a conserved pathway in eukaryotic cells. The assembly of the lipid-linked core… 
2005
2005
We describe the second case of congenital disorder of glycosylation type IL (CDG‐IL) caused by deficiency of the ALG9 a1,2… 
Highly Cited
2004
Highly Cited
2004
Defects of lipid-linked oligosaccharide assembly lead to alterations of N-linked glycosylation known as "type I congenital… 
2002
2002
Bipolar affective disorder (BPAD) is a complex neuropsychiatric disease characterized by extreme mood swings. Genetic influences… 
Highly Cited
1996
Highly Cited
1996
The core oligosaccharide Glc3Man9GlcNAc2 is assembled at the membrane of the endoplasmic reticulum on the lipid carrier dolichyl…