9 results on '"Freeze, H H"'
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2. Mutations in STT3A and STT3B cause two congenital disorders of glycosylation
3. A "Glyconutrient Sham"
4. Molecular cloning, gene organization, and expression of mouse Mpi encoding phosphomannose isomerase
5. Update and perspectives on congenital disorders of glycosylation
6. Mannose supplementation corrects GDP-mannose deficiency in cultured fibroblasts from some patients with Congenital Disorders of Glycosylation (CDG)
7. Characterization of mammalian UDP-GalNAc:glucuronide 1-4-N-acetylgalactosaminyltransferase
8. Fucose -1-P-Ser is a new type of glycosylation: using antibodies to identify a novel structure in Dictyostelium discoideum and study multiple types of fucosylation during growth and development
9. -N-Acetylgalactosamine-capping of chondroitin sulfate core region oligosaccharides primed on xylosides
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