phenylalanine and Spinocerebellar Ataxias

phenylalanine has been researched along with Spinocerebellar Ataxias 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	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Gatchel, JR; Lee, Y; Orr, HT; Samaco, RC; Thaller, C; Zoghbi, HY	1
Hiramoto, K; Inoue, K; Kawakami, H; Kurisu, K; Maruyama, H; Matsumoto, M; Morino, H; Sakai, N; Seki, T	1

Other Studies

2 other study(ies) available for phenylalanine and Spinocerebellar Ataxias

Article	Year
miR-19, miR-101 and miR-130 co-regulate ATXN1 levels to potentially modulate SCA1 pathogenesis. Nature neuroscience, 2008, Volume: 11, Issue:10 Topics: Animals; Ataxin-1; Ataxins; Cell Line, Transformed; Cerebellum; Disease Models, Animal; Gene Expression Regulation; Glutamine; Green Fluorescent Proteins; Humans; Mice; Mice, Transgenic; MicroRNAs; Nerve Tissue Proteins; Nuclear Proteins; Phenylalanine; Purkinje Cells; RNA, Small Interfering; Spinocerebellar Ataxias; Time Factors; Transfection; Trinucleotide Repeat Expansion	2008
Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4. Movement disorders : official journal of the Movement Disorder Society, 2006, Volume: 21, Issue:9 Topics: Adult; Aged; Amino Acid Substitution; Brain; DNA Mutational Analysis; Exons; Female; Genetic Testing; Humans; Introns; Japan; Magnetic Resonance Imaging; Male; Middle Aged; Mutation, Missense; Pedigree; Phenylalanine; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Protein Kinase C; Serine; Spinocerebellar Ataxias	2006

Article

Year

miR-19, miR-101 and miR-130 co-regulate ATXN1 levels to potentially modulate SCA1 pathogenesis.

Nature neuroscience, 2008, Volume: 11, Issue:10

Topics: Animals; Ataxin-1; Ataxins; Cell Line, Transformed; Cerebellum; Disease Models, Animal; Gene Expression Regulation; Glutamine; Green Fluorescent Proteins; Humans; Mice; Mice, Transgenic; MicroRNAs; Nerve Tissue Proteins; Nuclear Proteins; Phenylalanine; Purkinje Cells; RNA, Small Interfering; Spinocerebellar Ataxias; Time Factors; Transfection; Trinucleotide Repeat Expansion

2008

Identification of a new family of spinocerebellar ataxia type 14 in the Japanese spinocerebellar ataxia population by the screening of PRKCG exon 4.

Movement disorders : official journal of the Movement Disorder Society, 2006, Volume: 21, Issue:9

Topics: Adult; Aged; Amino Acid Substitution; Brain; DNA Mutational Analysis; Exons; Female; Genetic Testing; Humans; Introns; Japan; Magnetic Resonance Imaging; Male; Middle Aged; Mutation, Missense; Pedigree; Phenylalanine; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Protein Kinase C; Serine; Spinocerebellar Ataxias

2006