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Results 1 - 10 of 10
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EC Number Title Organism
Show all pathways known for 2.4.1.265Display the reaction diagram Show all sequences 2.4.1.265A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylation Homo sapiens
Show all pathways known for 2.4.1.265Display the reaction diagram Show all sequences 2.4.1.265A new case of ALG8 deficiency (CDG Ih) Homo sapiens
Show all pathways known for 2.4.1.265Display the reaction diagram Show all sequences 2.4.1.265Alginate polymerization and modification are linked in Pseudomonas aeruginosa Pseudomonas aeruginosa
Show all pathways known for 2.4.1.265Display the reaction diagram Show all sequences 2.4.1.265Alginate polymerization and modification are linked in Pseudomonas aeruginosa Pseudomonas aeruginosa PDO300
Show all pathways known for 2.4.1.265Display the reaction diagram Show all sequences 2.4.1.265Alginate production and alg8 gene expression by Azotobacter vinelandii in continuous cultures Azotobacter vinelandii
Show all pathways known for 2.4.1.265Display the reaction diagram Show all sequences 2.4.1.265Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency) Homo sapiens
Show all pathways known for 2.4.1.265Display the reaction diagram Show all sequences 2.4.1.265Insights into the assembly of the alginate biosynthesis machinery in Pseudomonas aeruginosa Pseudomonas aeruginosa
Show all pathways known for 2.4.1.265Display the reaction diagram Show all sequences 2.4.1.265New phenotype of mutations deficient in glucosylation of the lipid-linked oligosaccharide: cloning of the ALG8 locus Saccharomyces cerevisiae
Show all pathways known for 2.4.1.265Display the reaction diagram Show all sequences 2.4.1.265Novel ALG8 mutations expand the clinical spectrum of congenital disorder of glycosylation type Ih Homo sapiens
Show all pathways known for 2.4.1.265Display the reaction diagram Show all sequences 2.4.1.265Robbins, P.W.: A new yeast mutation in the glucosylation steps of the asparagine-linked glycosylation pathway. Formation of a novel asparagine-linked oligosaccharide containing two glucose residues Saccharomyces cerevisiae
Results 1 - 10 of 10
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