Compounds > adenosine diphosphate ribose

adenosine diphosphate ribose and Cerebellar Ataxia

adenosine diphosphate ribose has been researched along with Cerebellar Ataxia 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	0 (0.00)	29.6817
2010's	2 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Alhaddad, B; Berutti, R; Bonnen, PE; Bültmann, E; Danhauser, K; Das, AM; Fang, F; Feichtinger, RG; Gomez-Ospina, N; Graf, E; Gusic, M; Haack, TB; Haberlandt, E; Hartmann, H; Hoffmann, GF; Karall, D; Kostera-Pruszczyk, A; Kovács-Nagy, R; Krahn-Peper, C; Laugwitz, L; Makowski, C; Manning, MA; Mayr, JA; Meitinger, T; Morlot, S; Piekutowska-Abramczuk, D; Prokisch, H; Pronicki, M; Płoski, R; Röblitz, M; Schatz, UA; Strom, TM; Syrbe, S; Wroblewski, A; Xu, M; Zellner, H	1
Caldecott, KW; Gittens, W; Hanzlikova, H; Hoch, NC; Hornyak, P; Ju, L; Komulainen, E; Mancini, GM; McKinnon, PJ; Rey, SA; Rulten, SL; Staras, K; Tétreault, M; Wagner, JD; Wang, ZQ; Yoon, G; Zeng, Z	1

Studies

Alhaddad, B; Berutti, R; Bonnen, PE; Bültmann, E; Danhauser, K; Das, AM; Fang, F; Feichtinger, RG; Gomez-Ospina, N; Graf, E; Gusic, M; Haack, TB; Haberlandt, E; Hartmann, H; Hoffmann, GF; Karall, D; Kostera-Pruszczyk, A; Kovács-Nagy, R; Krahn-Peper, C; Laugwitz, L; Makowski, C; Manning, MA; Mayr, JA; Meitinger, T; Morlot, S; Piekutowska-Abramczuk, D; Prokisch, H; Pronicki, M; Płoski, R; Röblitz, M; Schatz, UA; Strom, TM; Syrbe, S; Wroblewski, A; Xu, M; Zellner, H

Caldecott, KW; Gittens, W; Hanzlikova, H; Hoch, NC; Hornyak, P; Ju, L; Komulainen, E; Mancini, GM; McKinnon, PJ; Rey, SA; Rulten, SL; Staras, K; Tétreault, M; Wagner, JD; Wang, ZQ; Yoon, G; Zeng, Z

Other Studies

2 other study(ies) available for adenosine diphosphate ribose and Cerebellar Ataxia

Article	Year
Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal Neuropathy. American journal of human genetics, 2018, 11-01, Volume: 103, Issue:5 Topics: Adenosine Diphosphate Ribose; Adolescent; ADP-Ribosylation; Alleles; Cerebellar Ataxia; Child; Child, Preschool; Developmental Disabilities; Exome; Female; Glycoside Hydrolases; Humans; Infant; Male; Mutation; Nervous System Malformations; Neurodegenerative Diseases; Protein Processing, Post-Translational	2018
XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia. Nature, 2017, 01-05, Volume: 541, Issue:7635 Topics: Adenosine Diphosphate Ribose; Alleles; Animals; Apraxias; Ataxia; Axons; Cerebellar Ataxia; Cerebellum; Chromatin; Cogan Syndrome; DNA Breaks, Single-Stranded; DNA Repair; DNA Repair Enzymes; DNA-Binding Proteins; Female; Humans; Interneurons; Male; Mice; Mutation; Pedigree; Phenotype; Phosphotransferases (Alcohol Group Acceptor); Poly (ADP-Ribose) Polymerase-1; X-ray Repair Cross Complementing Protein 1	2017

Article

Year

Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal Neuropathy.

American journal of human genetics, 2018, 11-01, Volume: 103, Issue:5

Topics: Adenosine Diphosphate Ribose; Adolescent; ADP-Ribosylation; Alleles; Cerebellar Ataxia; Child; Child, Preschool; Developmental Disabilities; Exome; Female; Glycoside Hydrolases; Humans; Infant; Male; Mutation; Nervous System Malformations; Neurodegenerative Diseases; Protein Processing, Post-Translational

2018

XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia.

Nature, 2017, 01-05, Volume: 541, Issue:7635

Topics: Adenosine Diphosphate Ribose; Alleles; Animals; Apraxias; Ataxia; Axons; Cerebellar Ataxia; Cerebellum; Chromatin; Cogan Syndrome; DNA Breaks, Single-Stranded; DNA Repair; DNA Repair Enzymes; DNA-Binding Proteins; Female; Humans; Interneurons; Male; Mice; Mutation; Pedigree; Phenotype; Phosphotransferases (Alcohol Group Acceptor); Poly (ADP-Ribose) Polymerase-1; X-ray Repair Cross Complementing Protein 1

2017