glutamic acid has been researched along with Glycogen Storage Disease Type II in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chen, CP; Hwu, WL; Lin, SP; Tsai, FJ; Tzen, CY; Wang, W | 1 |
de Graaff, E; Hermans, MM; Kroos, MA; Oostra, BA; Reuser, AJ; Willemsen, R; Wisselaar, HA | 1 |
2 other study(ies) available for glutamic acid and Glycogen Storage Disease Type II
Article | Year |
---|---|
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.
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.
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 |