tyrosine and Spinocerebellar Ataxias

tyrosine has been researched along with Spinocerebellar Ataxias in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Lin, D; Snider, A; Takemoto, DJ; Willard, L; Zhang, Y1
Brice, A; Durr, A; Dussert, C; Faivre, L; Forlani, S; Klebe, S; Stevanin, G; Tourbah, A1
Baron, R; Deuschl, G; Klebe, S; Müller, U; Nolte, D1

Other Studies

3 other study(ies) available for tyrosine and Spinocerebellar Ataxias

ArticleYear
Loss of Purkinje cells in the PKCgamma H101Y transgenic mouse.
    Biochemical and biophysical research communications, 2009, Jan-16, Volume: 378, Issue:3

    Topics: Amino Acid Substitution; Animals; Caspase 12; Connexins; Disease Models, Animal; Enzyme Activation; Histidine; Humans; Mice; Mice, Transgenic; Phosphorylation; Protein Kinase C; Purkinje Cells; Spinocerebellar Ataxias; Tyrosine

2009
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
Codon 101 of PRKCG, a preferential mutation site in SCA14.
    Movement disorders : official journal of the Movement Disorder Society, 2007, Sep-15, Volume: 22, Issue:12

    Topics: Codon; DNA Mutational Analysis; Exons; Family Health; Histidine; Humans; Male; Middle Aged; Mutation; Protein Kinase C; Spinocerebellar Ataxias; Tyrosine

2007