Glycosylation in Congenital Muscular Dystrophies-Reference-Cited by-同舟云学术

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Glycosylation in Congenital Muscular Dystrophies

Published:2003 Issue:12 Volume:26 Page:1641-1647
ISSN:0918-6158
Container-title:Biological and Pharmaceutical Bulletin
language:en
Short-container-title:Biol. Pharm. Bull.

Author:

Endo Tamao¹,Toda Tatsushi²

Affiliation:

1. Glycobiology Research Group, Tokyo Metropolitan Institute of Gerontology, Foundation for Research on Aging and Promotion of Human Welfare

2. Division of Functional Genomics, Department of Post-Genomics and Diseases, Osaka University Graduate School of Medicine

Publisher

Pharmaceutical Society of Japan

Subject

Pharmaceutical Science,Pharmacology,General Medicine

Link

http://www.jstage.jst.go.jp/article/bpb/26/12/26_12_1641/_pdf

Reference53 articles.

1. Structures and functions of the sugar chains of glycoproteins

2. Biological roles of oligosaccharides: all of the theories are correct

3. The muscular dystrophies

4. Muscular Dystrophy—Reason for Optimism?

5. Protein O-mannosylation

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1. Systematic Assessment of Protein C-Termini Mutated in Human Disorders;Biomolecules;2023-02-12

2. The jam session between muscle stem cells and the extracellular matrix in the tissue microenvironment;npj Regenerative Medicine;2022-02-17

3. Cleavage of β-dystroglycan occurs in sarcoglycan-deficient skeletal muscle without MMP-2 and MMP-9;Biochemical and Biophysical Research Communications;2017-10

4. Nonmitochondrial Metabolic Cardioskeletal Myopathies;Cardioskeletal Myopathies in Children and Young Adults;2017

5. Mutations in GDP-Mannose Pyrophosphorylase B Cause Congenital and Limb-Girdle Muscular Dystrophies Associated with Hypoglycosylation of α-Dystroglycan;The American Journal of Human Genetics;2013-07

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