glutamic acid and Glycogen Storage Disease Type II

glutamic acid has been researched along with Glycogen Storage Disease Type II in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chen, CP; Hwu, WL; Lin, SP; Tsai, FJ; Tzen, CY; Wang, W1
de Graaff, E; Hermans, MM; Kroos, MA; Oostra, BA; Reuser, AJ; Willemsen, R; Wisselaar, HA1

Other Studies

2 other study(ies) available for glutamic acid and Glycogen Storage Disease Type II

ArticleYear
Detection of a homozygous D645E mutation of the acid alpha-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II.
    Prenatal diagnosis, 2004, Volume: 24, Issue:3

    Topics: Adult; alpha-Glucosidases; Aspartic Acid; Female; Glutamic Acid; Glycogen; Glycogen Storage Disease Type II; Homozygote; Humans; Lysosomes; Mutation; Pregnancy; Pregnancy Trimester, Second

2004
The conservative substitution Asp-645-->Glu in lysosomal alpha-glucosidase affects transport and phosphorylation of the enzyme in an adult patient with glycogen-storage disease type II.
    The Biochemical journal, 1993, Feb-01, Volume: 289 ( Pt 3)

    Topics: Adult; Alleles; alpha-Glucosidases; Aspartic Acid; Base Sequence; beta-N-Acetylhexosaminidases; Biological Transport; Black People; Cells, Cultured; Codon; DNA Mutational Analysis; Glutamates; Glutamic Acid; Glycogen; Glycogen Storage Disease Type II; Humans; Lysosomes; Microscopy, Immunoelectron; Molecular Sequence Data; Phenotype; Phosphorylation; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Protein Processing, Post-Translational; Regulatory Sequences, Nucleic Acid; Sequence Analysis, DNA; Tunicamycin

1993