E G Berger Selected Research

Congenital disorder of glycosylation type 1E

1/2000

Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie.

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E G Berger Research Topics

Disease

1	Vesicular Stomatitis 12/2001
1	Congenital Disorders of Glycosylation 12/2001
1	Leukemia 09/2000
1	Teratocarcinoma 07/2000
1	Neoplasms (Cancer) 01/2000
1	Congenital disorder of glycosylation type 1E 01/2000

Drug/Important Bio-Agent (IBA)

2	Polysaccharides (Glycans)IBA 12/2001 - 09/2000
1	GTP-Binding Proteins (G-Protein)IBA 12/2001
1	Proteins (Proteins, Gene)FDA Link 12/2001
1	phorbolIBA 09/2000
1	GalactosyltransferasesIBA 09/2000
1	Phorbol EstersIBA 09/2000
1	UDP-galactose N- acetylglucosaminyl- 1- 3- N- acetylgalactosamine beta-1,3-galactosyltransferaseIBA 07/2000
1	stage-specific embryonic antigen-3 (GL-X)IBA 07/2000
1	Monoclonal AntibodiesIBA 07/2000
1	GlycolipidsIBA 07/2000
1	DolicholsIBA 01/2000
1	EnzymesIBA 01/2000
1	Mannose (D-Mannose)IBA 01/2000
1	Phosphates (Orthophosphate)IBA 01/2000