arginine and Gangliosidoses, GM2

arginine has been researched along with Gangliosidoses, GM2 in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	1 (50.00)	2.80

Authors

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

Other Studies

2 other study(ies) available for arginine and Gangliosidoses, GM2

Article	Year
L-Arginine Ameliorates Defective Autophagy in GM2 Gangliosidoses by mTOR Modulation. Cells, 2021, 11-11, Volume: 10, Issue:11 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. Journal of molecular biology, 2006, Jun-16, Volume: 359, Issue:4 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

Article

Year

L-Arginine Ameliorates Defective Autophagy in GM2 Gangliosidoses by mTOR Modulation.

Cells, 2021, 11-11, Volume: 10, Issue:11

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.

Journal of molecular biology, 2006, Jun-16, Volume: 359, Issue:4

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