EC Number   |
Title |
Organism |
|---|
    2.4.1.142 | Association studies of WD repeat domain 3 and chitobiosyldiphosphodolichol beta-mannosyltransferase genes with schizophrenia in a Japanese population |
Rattus norvegicus |
| 2.4.1.142 | Association studies of WD repeat domain 3 and chitobiosyldiphosphodolichol beta-mannosyltransferase genes with schizophrenia in a Japanese population |
Homo sapiens |
| 2.4.1.142 | Chemo-enzymatic synthesis of lipid-linked GlcNAc2Man5 oligosaccharides using recombinant Alg1, Alg2 and Alg11 proteins |
Saccharomyces cerevisiae |
| 2.4.1.142 | Chemo-enzymatic synthesis of lipid-linked GlcNAc2Man5 oligosaccharides using recombinant Alg1, Alg2 and Alg11 proteins |
Saccharomyces cerevisiae ATCC 204508 |
| 2.4.1.142 | Structural and functional analysis of Alg1 beta-1,4 mannosyltransferase reveals the physiological importance of its membrane topology |
Saccharomyces cerevisiae |
| 2.4.1.142 | Structural and functional analysis of Alg1 beta-1,4 mannosyltransferase reveals the physiological importance of its membrane topology |
Saccharomyces cerevisiae ATCC 204508 |
| 2.4.1.142 | Cloning of the human cDNA which can complement the defect of the yeast mannosyltransferase I-deficient mutant alg 1 |
Homo sapiens |
| 2.4.1.142 | Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I |
Homo sapiens |
| 2.4.1.142 | Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik |
Homo sapiens |
| 2.4.1.142 | Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik |
Homo sapiens |
