Literature DB >> 4212176

Molecular studies on glycogen storage diseases.

J C Dreyfus, D Proux, Y Alexandre.   

Abstract

Mesh:

Substances:

Year:  1974        PMID: 4212176     DOI: 10.1159/000459414

Source DB:  PubMed          Journal:  Enzyme        ISSN: 0013-9432


× No keyword cloud information.
  5 in total

Review 1.  Animal models of glycogen storage conditions. Their relation to human disease.

Authors:  S R Gross
Journal:  West J Med       Date:  1975-09

2.  Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts.

Authors:  N G Beratis; G U LaBadie; K Hirschhorn
Journal:  J Clin Invest       Date:  1978-12       Impact factor: 14.808

3.  McArdle's disease heterozygotes. Metabolic adaptation assessed using 31P-nuclear magnetic resonance.

Authors:  R T Bogusky; R G Taylor; L J Anderson; K L Angelos; J S Lieberman; D A Walsh
Journal:  J Clin Invest       Date:  1986-06       Impact factor: 14.808

4.  The polymorphic locus for glycogen storage disease VI (liver glycogen phosphorylase) maps to chromosome 14.

Authors:  C B Newgard; R J Fletterick; L A Anderson; R V Lebo
Journal:  Am J Hum Genet       Date:  1987-04       Impact factor: 11.025

5.  Skeletal-muscle alpha-glucosidases in bovine generalized glycogenosis type II.

Authors:  P R Dorling; J M Howell; J M Gawthorne
Journal:  Biochem J       Date:  1981-08-15       Impact factor: 3.857

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.