arginine has been researched along with Tay-Sachs Disease in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alcocer-Gómez, E; Cachón-González, MB; Castejón-Vega, B; Cordero, MD; Cox, TM; Fernández-Domínguez, B; Lane, JD; Martín-Ruiz, C; Pérez-Pulido, AJ; Quiles, JL; Rubio, A; Sanz, A | 1 |
| Cherney, MM; James, MN; Lemieux, MJ; Mahuran, DJ; Mark, BL; Withers, SG | 1 |
| Brown, CA; Mahuran, DJ | 1 |
| dos Santos, MR; Maia, M; Ribeiro, MG; sá Miranda, MC; Suzuki, K; Tanaka, A | 1 |
4 other study(ies) available for arginine and Tay-Sachs Disease
| Article | Year |
|---|---|
L-Arginine Ameliorates Defective Autophagy in GM2 Gangliosidoses by mTOR Modulation.
Topics: Arginine; Autophagosomes; Autophagy; Cathepsins; Fibroblasts; Gangliosidoses, GM2; Hexosaminidase A; Hexosaminidase B; Humans; Lysosomes; Mutation; Permeability; Proto-Oncogene Proteins c-akt; Sandhoff Disease; Signal Transduction; Tay-Sachs Disease; TOR Serine-Threonine Kinases; Transcriptome | 2021 |
Crystallographic structure of human beta-hexosaminidase A: interpretation of Tay-Sachs mutations and loss of GM2 ganglioside hydrolysis.
Topics: Acetylglucosamine; Amino Acid Substitution; Arginine; Aspartic Acid; beta-N-Acetylhexosaminidases; Binding Sites; Crystallography, X-Ray; Dimerization; Gangliosidoses, GM2; Glycine; Glycosylation; Hexosaminidase A; Humans; Hydrolysis; Models, Molecular; Mutation; Protein Conformation; Protein Subunits; Tay-Sachs Disease; Thiazoles | 2006 |
Active arginine residues in beta-hexosaminidase. Identification through studies of the B1 variant of Tay-Sachs disease.
Topics: Arginine; Base Sequence; beta-N-Acetylhexosaminidases; Blotting, Western; Catalysis; Cell Line; Diacetyl; Hexosaminidase A; Hexosaminidase B; Humans; Hydrogen-Ion Concentration; Isoenzymes; Kinetics; Lysosomes; Molecular Sequence Data; Mutation; Phenylglyoxal; Tay-Sachs Disease; Transfection | 1991 |
GM2-gangliosidosis B1 variant: analysis of beta-hexosaminidase alpha gene mutations in 11 patients from a defined region in Portugal.
Topics: Adolescent; Arginine; beta-N-Acetylhexosaminidases; Blotting, Southern; Cell Line, Transformed; Child; Child, Preschool; Female; G(M2) Ganglioside; Humans; Male; Mutation; Oligonucleotides; Polymerase Chain Reaction; Portugal; Tay-Sachs Disease | 1991 |