Compounds > cysteine

cysteine and Autosomal Dominant Cerebellar Ataxia, Type II

cysteine has been researched along with Autosomal Dominant Cerebellar Ataxia, Type II in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (33.33)29.6817
2010's2 (33.33)24.3611
2020's2 (33.33)2.80

Authors

AuthorsStudies
Hikida, M; Ito, S; Kanuka, M; Kato, N; Katsuki, R; Miura, K; Ouchi, F; Tamura, T1
Hirai, H; Hisatsune, A; Katsuki, H; Konno, A; Kurauchi, Y; Morikawa, Y; Ohta, T; Sato, M; Seki, T1
Becker, EBE; Chelban, V; Efthymiou, S; Fabian-Jessing, BK; Giunti, P; Gregersen, PA; Haridy, NA; Hersheson, J; Hojland, AT; Houlden, H; Khan, A; Lindquist, SG; Newland, K; Nielsen, JE; Nielsen, M; O'Connor, E; Petersen, MB; Wiethoff, S; Wood, NW1
Bindoff, LA; Engelsen, BE; Ersland, L; Moen, G; Mørk, SJ; Neckelmann, G; Tzoulis, C; Viscomi, C; Zeviani, M1
Alonso, I; Barros, J; Coelho, J; Coutinho, P; Sequeiros, J; Silveira, I; Tuna, A1
Brice, A; Durr, A; Dussert, C; Faivre, L; Forlani, S; Klebe, S; Stevanin, G; Tourbah, A1

Other Studies

6 other study(ies) available for cysteine and Autosomal Dominant Cerebellar Ataxia, Type II

ArticleYear
Endoplasmic Reticulum Associated Degradation of Spinocerebellar Ataxia-Related CD10 Cysteine Mutant.
    International journal of molecular sciences, 2020, Jun-14, Volume: 21, Issue:12

    Topics: Cell Membrane; Cysteine; Disulfides; Endoplasmic Reticulum; Endoplasmic Reticulum-Associated Degradation; HeLa Cells; Humans; Mutation; Neprilysin; Oligopeptides; Proteolysis; Spinocerebellar Ataxias

2020
Therapeutic potential of d-cysteine against in vitro and in vivo models of spinocerebellar ataxia.
    Experimental neurology, 2021, Volume: 343

    Topics: Animals; Ataxin-1; Cells, Cultured; Cerebellum; Cysteine; Female; Male; Mice; Mice, Inbred ICR; Mice, Transgenic; Pregnancy; Rats; Rats, Wistar; Spinocerebellar Ataxias

2021
Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14.
    Movement disorders : official journal of the Movement Disorder Society, 2018, Volume: 33, Issue:7

    Topics: Adult; Age of Onset; Aged; Child, Preschool; Cohort Studies; Cysteine; Disease Progression; Dystonia; Family Health; Female; Genetic Association Studies; Genetic Testing; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Mutation, Missense; Peptides; Phenotype; Protein Kinase C; Spinocerebellar Ataxias; Young Adult

2018
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
Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family.
    Archives of neurology, 2003, Volume: 60, Issue:4

    Topics: Adolescent; Adult; Alanine; Child; Cysteine; Female; Genetic Linkage; Glycine; Hemiplegia; Humans; Lod Score; Male; Microsatellite Repeats; Middle Aged; Migraine Disorders; Mutation, Missense; Phenotype; Polymorphism, Single-Stranded Conformational; Spinocerebellar Ataxias

2003
Another mutation in cysteine 131 in protein kinase C gamma as a cause of spinocerebellar ataxia type 14.
    Archives of neurology, 2007, Volume: 64, Issue:6

    Topics: Adenine; Amino Acid Substitution; Cysteine; Guanine; Humans; Magnetic Resonance Imaging; Male; Mutation, Missense; Protein Kinase C; Spinocerebellar Ataxias; Tyrosine

2007