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phosphotyrosine and Autosomal Dominant Cerebellar Ataxia, Type II

phosphotyrosine has been researched along with Autosomal Dominant Cerebellar Ataxia, Type II in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Akopiants, K; Hawkins, AJ; Povirk, LF; Rice, AC; Subler, MA; Taylor, SM; Valerie, K; Wiley, JL; Windle, JJ	1

Other Studies

1 other study(ies) available for phosphotyrosine and Autosomal Dominant Cerebellar Ataxia, Type II

Article	Year
In vitro complementation of Tdp1 deficiency indicates a stabilized enzyme-DNA adduct from tyrosyl but not glycolate lesions as a consequence of the SCAN1 mutation. DNA repair, 2009, May-01, Volume: 8, Issue:5 Topics: Animals; Blotting, Southern; Blotting, Western; Catalysis; DNA Adducts; DNA Breaks, Double-Stranded; DNA Breaks, Single-Stranded; Embryo, Mammalian; Female; Fibroblasts; Genetic Complementation Test; Glycolates; Male; Mice; Mice, Knockout; Mutagenesis, Site-Directed; Mutation; Phosphoric Diester Hydrolases; Phosphotyrosine; Polymerase Chain Reaction; Spinocerebellar Ataxias	2009

Article

Year

In vitro complementation of Tdp1 deficiency indicates a stabilized enzyme-DNA adduct from tyrosyl but not glycolate lesions as a consequence of the SCAN1 mutation.

DNA repair, 2009, May-01, Volume: 8, Issue:5

Topics: Animals; Blotting, Southern; Blotting, Western; Catalysis; DNA Adducts; DNA Breaks, Double-Stranded; DNA Breaks, Single-Stranded; Embryo, Mammalian; Female; Fibroblasts; Genetic Complementation Test; Glycolates; Male; Mice; Mice, Knockout; Mutagenesis, Site-Directed; Mutation; Phosphoric Diester Hydrolases; Phosphotyrosine; Polymerase Chain Reaction; Spinocerebellar Ataxias

2009