Compounds > arginine

arginine and Spinocerebellar Ataxias

arginine has been researched along with Spinocerebellar Ataxias in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (25.00)29.6817
2010's5 (62.50)24.3611
2020's1 (12.50)2.80

Authors

AuthorsStudies
Adachi, H; Fujita, H; Ito, C; Katsuno, M; Minakawa, EN; Mochizuki, H; Nagai, Y; Okamoto, Y; Onodera, O; Ozawa, D; Popiel, HA; Saito, Y; Saitoh, Y; Shiraki, K; Sobue, G; Suzuki, M; Tada, M; Takahashi, T; Takahashi, Y; Takeda, A; Takeuchi, T; Toda, T; Wada, K; Watase, K; Yagihara, H; Yamamoto, K; Yamane, H1
Advincula, J; Ashizawa, T; Lee, LV; Perlman, S; Rosales, RL; Subramony, SH; Waters, MF1
Bannykh, S; Bickford, JS; Fernandez-Funez, P; Gallego-Iradi, C; Hall, A; Huynh, DP; Khare, S; Nick, HS; Nick, JA; Pulst, SM; Rincon-Limas, DE; Salmasinia, D; Waters, MF; Wawrowsky, K1
Bindoff, LA; Engelsen, BE; Ersland, L; Moen, G; Mørk, SJ; Neckelmann, G; Tzoulis, C; Viscomi, C; Zeviani, M1
Ding, J; Federoff, HJ; Gibbs, JR; Hardy, J; Hernandez, D; Houlden, H; Hummerich, H; Johnson, JO; Plagnol, V; Sailer, A; Scholz, SW; Singleton, AB; Traynor, BJ; Tucci, A; Wood, NW1
Annesi, G; Bruno, E; Cavalcanti, F; Dibilio, V; Gagliardi, M; Gambardella, A; Mostile, G; Nicoletti, A; Quattrone, A; Tarantino, P; Zappia, M1
Bird, TD; Chen, DH; Kikuchi, S; Raskind, WH; Sasaki, H; Tashiro, K; Tsuji, S; Yabe, I; Yamashita, I1
Bassi, MT; Bresolin, N; D'Angelo, MG; Frattini, T; Germinasi, C; Meola, G; Salati, R; Tonelli, A; Turconi, AC; Villa, L1

Other Studies

8 other study(ies) available for arginine and Spinocerebellar Ataxias

ArticleYear
Arginine is a disease modifier for polyQ disease models that stabilizes polyQ protein conformation.
    Brain : a journal of neurology, 2020, 06-01, Volume: 143, Issue:6

    Topics: Animals; Arginine; Caenorhabditis elegans; Disease Models, Animal; Drosophila; Female; Heredodegenerative Disorders, Nervous System; Huntington Disease; Male; Mice; Mice, Inbred Strains; Molecular Chaperones; Peptides; Protein Aggregation, Pathological; Protein Conformation; Protein Folding; Spinocerebellar Ataxias

2020
Comprehensive phenotype of the p.Arg420his allelic form of spinocerebellar ataxia type 13.
    Cerebellum (London, England), 2013, Volume: 12, Issue:6

    Topics: Adult; Arginine; Cerebellum; Family Health; Female; Genetic Linkage; Genotype; Histidine; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Phenotype; Philippines; Shaw Potassium Channels; Spinocerebellar Ataxias; Spinocerebellar Degenerations

2013
KCNC3(R420H), a K(+) channel mutation causative in spinocerebellar ataxia 13 displays aberrant intracellular trafficking.
    Neurobiology of disease, 2014, Volume: 71

    Topics: Animals; Animals, Genetically Modified; Arginine; Biotinylation; Cadherins; Chlorocebus aethiops; COS Cells; Cytoplasm; Drosophila; Drosophila Proteins; Endoplasmic Reticulum; Female; Histidine; Humans; Intracellular Fluid; Male; Mutation; Oocytes; Protein Processing, Post-Translational; Protein Transport; Shaw Potassium Channels; Spinocerebellar Ataxias; Spinocerebellar Degenerations; Transfection

2014
Localized cerebral energy failure in DNA polymerase gamma-associated encephalopathy syndromes.
    Brain : a journal of neurology, 2010, Volume: 133, Issue:Pt 5

    Topics: Arginine; Brain; Brain Diseases; Cerebellum; Cysteine; Diffuse Cerebral Sclerosis of Schilder; Diffusion Magnetic Resonance Imaging; Disease Progression; DNA Polymerase gamma; DNA-Directed DNA Polymerase; DNA, Mitochondrial; Electroencephalography; Energy Metabolism; Epilepsy; Glycine; Humans; Magnetic Resonance Angiography; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Mitochondrial Diseases; Mutation; Neocortex; Sensitivity and Specificity; Spinocerebellar Ataxias; Stroke; Syndrome; Thalamus; Tomography, X-Ray Computed

2010
Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases.
    Neurology, 2012, Jul-10, Volume: 79, Issue:2

    Topics: Adolescent; Adult; Aged; Arginine; Exome; Genetic Testing; Glycine; Humans; Middle Aged; Mutation; Pedigree; Protein Kinase C; Spinocerebellar Ataxias; Young Adult

2012
Sacsin-related spastic ataxia caused by a novel missense mutation p.Arg272His in a patient from Sicily, southern Italy.
    Cerebellum (London, England), 2013, Volume: 12, Issue:4

    Topics: Adult; Arginine; Female; Heat-Shock Proteins; Histidine; Humans; Intellectual Disability; Italy; Muscle Spasticity; Mutation, Missense; Optic Atrophy; Sicily; Spinocerebellar Ataxias

2013
Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma.
    Archives of neurology, 2003, Volume: 60, Issue:12

    Topics: Adult; Aged; Arginine; Base Sequence; Case-Control Studies; Glycine; Heterozygote; Humans; Male; Middle Aged; Mutation, Missense; Pedigree; Protein Kinase C; Spinocerebellar Ataxias

2003
Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene.
    Journal of the neurological sciences, 2006, Feb-15, Volume: 241, Issue:1-2

    Topics: Age of Onset; Arginine; Calcium Channels; Child, Preschool; DNA Mutational Analysis; Glutamic Acid; Humans; Male; Mutation, Missense; Spinocerebellar Ataxias

2006