DPM3 gene

Known as: DOLICHYL-PHOSPHATE MANNOSYLTRANSFERASE 3, dolichyl-phosphate mannosyltransferase subunit 3, MGC34275 
 

Topic mentions per year

Topic mentions per year

2000-2017
01220002017

Papers overview

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2017
2017
Defects of O-linked glycosylation of alpha-dystroglycan cause a wide spectrum of muscular dystrophies ranging from severe… (More)
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2015
2015
Dystroglycanopathies are neuromuscular disorders due to abnormal glycosylation of dystroglycan which is a cell-surface… (More)
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2013
2013
Congenital disorders of glycosylation (CDG) are rare genetic defects mainly in the post-translational modification of proteins… (More)
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2012
2012
OBJECTIVE Congenital disorders of glycosylation (CDG) are a group of metabolic diseases due to defects in protein and lipid… (More)
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2011
2011
Dystroglycanopathies are a heterogeneous group of muscular dystrophies with autosomal recessive inheritance characterized by… (More)
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Highly Cited
2009
Highly Cited
2009
Alpha-dystroglycanopathies such as Walker Warburg syndrome represent an important subgroup of the muscular dystrophies that have… (More)
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Review
2009
Review
2009
Defects in the biosynthesis of the oligosaccharide precursor for N-glycosylation lead to decreased occupancy of glycosylation… (More)
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2006
2006
Dolichol-phosphate mannose (DPM) synthase is required for synthesis of the glycosylphosphatidylinositol (GPI) anchor, N-glycan… (More)
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2004
2004
Summary: CDG Ie is caused by a deficiency of dolichol-phosphate-mannose synthase 1 (DPM1), an enzyme involved in N-glycan… (More)
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2000
2000
Dolichol-phosphate-mannose (DPM) synthase generates mannosyl donors for glycosylphosphatidylinositols, N-glycan and protein O… (More)
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