Congenital Disorders of Glycosylation Type Ig Is Defined by a Deficiency in Dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl Mannosyltransferase-Reference-Cited by-同舟云学术

Congenital Disorders of Glycosylation Type Ig Is Defined by a Deficiency in Dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl Mannosyltransferase

Published:2002-07 Issue:28 Volume:277 Page:25815-25822
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Chantret Isabelle,Dupré Thierry,Delenda Christophe,Bucher Stéphanie,Dancourt Julia,Barnier Anne,Charollais Aude,Heron Delphine,Bader-Meunier Brigitte,Danos Olivier,Seta Nathalie,Durand Geneviève,Oriol Rafael,Codogno Patrice,Moore Stuart E.H.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference55 articles.

1. Topography of initiation of N-glycosylation reactions.

2. ASSEMBLY OF ASPARAGINE-LINKED OLIGOSACCHARIDES

3. Protein Glucosylation and Its Role in Protein Folding

4. Intracellular Functions of N-Linked Glycans

5. Processing by Endoplasmic Reticulum Mannosidases Partitions a Secretion-impaired Glycoprotein into Distinct Disposal Pathways

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