glutamine has been researched along with Ataxia in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (25.00) | 29.6817 |
2010's | 2 (50.00) | 24.3611 |
2020's | 1 (25.00) | 2.80 |
Authors | Studies |
---|---|
Araki, A; Huang, S; Ito, Y; Mitaki, S; Nagai, A; Omura, K; Sheikh, AM; Tabassum, S; Yano, S | 1 |
Brand-Arzamendi, K; Dobritzsch, D; Dolzhenko, E; Drögemöller, BI; Eberle, MA; Geraghty, MT; Hayward, B; Jones, MJ; Karbassi, F; Kobor, MS; Koster, J; Kumari, D; Leen, R; Li, M; MacIsaac, J; McDonald, C; Meijer, J; Nguyen, C; Pouladi, MA; Rajan-Babu, IS; Richmond, PA; Ross, CJ; Santra, S; Scherer, SW; Sim, B; Tarailo-Graovac, M; Trost, B; Tseng, LA; Turkenburg, M; Usdin, K; van Karnebeek, CDM; van Kuilenburg, ABP; van Vugt, JJFA; van Weeghel, M; Veldink, JH; Walia, JS; Wanders, RJA; Wang, Y; Wasserman, WW; Waterham, HR; Wen, XY; Wright, GEB; Xu, X; Yuen, RKC; Zhang, J | 1 |
Bersano, A; Di Cristofori, A; Fusi, L; Gomitoni, A; Grampa, G | 1 |
Goellner, GM; Rechsteiner, M | 1 |
2 review(s) available for glutamine and Ataxia
Article | Year |
---|---|
R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update.
Topics: Arginine; Ataxia; Calcium Channels; Cerebellum; DNA Mutational Analysis; Female; Glutamine; Humans; Middle Aged; Migraine with Aura; Radiography; Tomography Scanners, X-Ray Computed | 2012 |
Are Huntington's and polyglutamine-based ataxias proteasome storage diseases?
Topics: Animals; Ataxia; Autoantigens; Cysteine Endopeptidases; Glutamine; Huntington Disease; Mice; Multienzyme Complexes; Nuclear Proteins; Proteasome Endopeptidase Complex; Proteins; Ubiquitin | 2003 |
2 other study(ies) available for glutamine and Ataxia
Article | Year |
---|---|
Alteration of Neural Stem Cell Functions in Ataxia and Male Sterility Mice: A Possible Role of β-Tubulin Glutamylation in Neurodegeneration.
Topics: Animals; Ataxia; Female; Glutamine; Heredodegenerative Disorders, Nervous System; Infertility, Male; Male; Mice; Mice, Mutant Strains; NAD(P)H Dehydrogenase (Quinone); Neural Stem Cells; Tubulin | 2021 |
Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in
Topics: Amino Acid Metabolism, Inborn Errors; Ataxia; Atrophy; Cerebellum; Child, Preschool; Developmental Disabilities; Female; Genotype; Glutaminase; Glutamine; Humans; Male; Microsatellite Repeats; Mutation; Phenotype; Polymerase Chain Reaction; Whole Genome Sequencing | 2019 |