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EC Number
BRENDA No.
Title
Journal
Volume
Pages
Year
Organism
PubMed ID
2.4.1.265
708978
A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylation
J. Biol. Chem.
278
9962-9971
2003
Homo sapiens
12480927
2.4.1.265
709391
A new case of ALG8 deficiency (CDG Ih)
J. Inherit. Metab. Dis.
32
259264
2009
Homo sapiens
19688606
2.4.1.265
736726
Alginate polymerization and modification are linked in Pseudomonas aeruginosa
mBio
6
1-17
2015
Pseudomonas aeruginosa
25968647
2.4.1.265
736726
Alginate polymerization and modification are linked in Pseudomonas aeruginosa
mBio
6
1-17
2015
Pseudomonas aeruginosa PDO300
25968647
2.4.1.265
722890
Alginate production and alg8 gene expression by Azotobacter vinelandii in continuous cultures
J. Ind. Microbiol. Biotechnol.
39
613-621
2012
Azotobacter vinelandii
22072437
2.4.1.265
709484
Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency)
J. Med. Genet.
41
550-556
2004
Homo sapiens
15235028
2.4.1.265
735487
Insights into the assembly of the alginate biosynthesis machinery in Pseudomonas aeruginosa
Appl. Environ. Microbiol.
79
3264-3272
2013
Pseudomonas aeruginosa
23503314
2.4.1.265
710441
New phenotype of mutations deficient in glucosylation of the lipid-linked oligosaccharide: cloning of the ALG8 locus
Proc. Natl. Acad. Sci. USA
91
5977-5981
1994
Saccharomyces cerevisiae
8016100
2.4.1.265
709971
Novel ALG8 mutations expand the clinical spectrum of congenital disorder of glycosylation type Ih
Mol. Genet. Metab.
98
305-309
2009
Homo sapiens
19648040
2.4.1.265
708964
Robbins, 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
J. Biol. Chem.
261
15582-15590
1986
Saccharomyces cerevisiae
3536907
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