Compounds > uridine diphosphate glucose
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uridine diphosphate glucose and Glycogen Storage Disease

uridine diphosphate glucose has been researched along with Glycogen Storage Disease in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19901 (33.33)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Anderson, SM; Cleasby, ME; Hingst, JR; Hurley, TD; Mahalingan, KK; Maile, CA; McCue, ME; Mickelson, JR; O'Reilly, AO; Piercy, RJ; Wojtaszewski, JFP1
Carrizo, ME; Curtino, JA; Issoglio, FM; Romero, JM1
Brown, BI; Brown, DH1

Other Studies

3 other study(ies) available for uridine diphosphate glucose and Glycogen Storage Disease

ArticleYear
A highly prevalent equine glycogen storage disease is explained by constitutive activation of a mutant glycogen synthase.
    Biochimica et biophysica acta. General subjects, 2017, Volume: 1861, Issue:1 Pt A

    Topics: Adenylate Kinase; Amino Acid Sequence; Animals; Blotting, Western; Breeding; Enzyme Activation; Glucose Transporter Type 4; Glucose-6-Phosphate; Glycogen; Glycogen Storage Disease; Glycogen Synthase; Glycogen Synthase Kinase 3 beta; Horses; Kinetics; Models, Molecular; Muscle, Skeletal; Mutant Proteins; Mutation; Phosphorylation; Prevalence; Protein Subunits; Structural Homology, Protein; Uridine Diphosphate Glucose

2017
Structural and biochemical insight into glycogenin inactivation by the glycogenosis-causing T82M mutation.
    FEBS letters, 2012, Feb-03, Volume: 586, Issue:3

    Topics: Amino Acid Substitution; Animals; Apoenzymes; Crystallography, X-Ray; Enzyme Activation; Glucosides; Glucosyltransferases; Glycogen Storage Disease; Glycoproteins; Glycosylation; Hydrogen Bonding; Hydrolysis; Models, Molecular; Muscles; Mutant Proteins; Mutation; Protein Conformation; Rabbits; Uridine Diphosphate Glucose

2012
Studies of the residual glycogen branching enzyme activity present in human skin fibroblasts from patients with type IV glycogen storage disease.
    Biochemical and biophysical research communications, 1983, Mar-16, Volume: 111, Issue:2

    Topics: 1,4-alpha-Glucan Branching Enzyme; Cells, Cultured; Cross Reactions; Fibroblasts; Glucosyltransferases; Glycogen Storage Disease; Glycogen Storage Disease Type IV; Glycogen Synthase; Humans; Liver; Skin; Uridine Diphosphate Glucose

1983