Page last updated: 2024-08-17

adenosine monophosphate and Ataxia

adenosine monophosphate has been researched along with Ataxia in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	3 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Caldecott, KW; El-Khamisy, SF; Reynolds, JJ	1
Bieganowski, P; Brenner, C; Seidle, HF	1
Date, H; Igarashi, S; Koyama, A; Nishizawa, M; Onodera, O; Shiga, A; Tada, M; Takahashi, T; Tsuji, S; Yokoseki, A; Yoshida, Y	1

Reviews

1 review(s) available for adenosine monophosphate and Ataxia

Article	Year
Short-patch single-strand break repair in ataxia oculomotor apraxia-1. Biochemical Society transactions, 2009, Volume: 37, Issue:Pt 3 Topics: Adenosine Monophosphate; Animals; Apraxias; Ataxia; DNA Breaks, Single-Stranded; DNA Repair; DNA-Binding Proteins; Humans; Mutation; Nuclear Proteins	2009

Other Studies

2 other study(ies) available for adenosine monophosphate and Ataxia

Article	Year
Disease-associated mutations inactivate AMP-lysine hydrolase activity of Aprataxin. The Journal of biological chemistry, 2005, Jun-03, Volume: 280, Issue:22 Topics: Adenosine Monophosphate; Alleles; Apraxias; Ataxia; Binding Sites; Blotting, Western; Cations; DNA Damage; DNA-Binding Proteins; Electrophoresis, Polyacrylamide Gel; Escherichia coli; Eye Diseases; Humans; Hydrogen-Ion Concentration; Hydrolases; Kinetics; Lysine; Metals; Motor Neuron Disease; Mutagenesis, Site-Directed; Mutation; Nuclear Proteins; Phenotype; Plasmids; Protein Binding; Protein Structure, Tertiary; RNA, Messenger; Substrate Specificity; Syndrome; Temperature; Zinc Fingers	2005
Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3'-phosphate and 3'-phosphoglycolate ends. Nucleic acids research, 2007, Volume: 35, Issue:11 Topics: Adenosine Monophosphate; Apraxias; Ataxia; DNA; DNA Breaks, Single-Stranded; DNA Ligase ATP; DNA Ligases; DNA Polymerase beta; DNA Repair; DNA-Binding Proteins; Glycolates; Guanosine Monophosphate; Humans; Mutation; Nuclear Proteins; Phosphates; Phosphoric Monoester Hydrolases; Poly-ADP-Ribose Binding Proteins; Protein Structure, Tertiary; Substrate Specificity; Xenopus Proteins	2007

Article

Year

Disease-associated mutations inactivate AMP-lysine hydrolase activity of Aprataxin.

The Journal of biological chemistry, 2005, Jun-03, Volume: 280, Issue:22

Topics: Adenosine Monophosphate; Alleles; Apraxias; Ataxia; Binding Sites; Blotting, Western; Cations; DNA Damage; DNA-Binding Proteins; Electrophoresis, Polyacrylamide Gel; Escherichia coli; Eye Diseases; Humans; Hydrogen-Ion Concentration; Hydrolases; Kinetics; Lysine; Metals; Motor Neuron Disease; Mutagenesis, Site-Directed; Mutation; Nuclear Proteins; Phenotype; Plasmids; Protein Binding; Protein Structure, Tertiary; RNA, Messenger; Substrate Specificity; Syndrome; Temperature; Zinc Fingers

2005

Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3'-phosphate and 3'-phosphoglycolate ends.

Nucleic acids research, 2007, Volume: 35, Issue:11

Topics: Adenosine Monophosphate; Apraxias; Ataxia; DNA; DNA Breaks, Single-Stranded; DNA Ligase ATP; DNA Ligases; DNA Polymerase beta; DNA Repair; DNA-Binding Proteins; Glycolates; Guanosine Monophosphate; Humans; Mutation; Nuclear Proteins; Phosphates; Phosphoric Monoester Hydrolases; Poly-ADP-Ribose Binding Proteins; Protein Structure, Tertiary; Substrate Specificity; Xenopus Proteins

2007