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2-deoxyribose 5-phosphate and Ataxia Telangiectasia

2-deoxyribose 5-phosphate has been researched along with Ataxia Telangiectasia in 1 studies

*Ataxia Telangiectasia: An autosomal recessive inherited disorder characterized by choreoathetosis beginning in childhood, progressive CEREBELLAR ATAXIA; TELANGIECTASIS of CONJUNCTIVA and SKIN; DYSARTHRIA; B- and T-cell immunodeficiency, and RADIOSENSITIVITY to IONIZING RADIATION. Affected individuals are prone to recurrent sinobronchopulmonary infections, lymphoreticular neoplasms, and other malignancies. Serum ALPHA-FETOPROTEINS are usually elevated. (Menkes, Textbook of Child Neurology, 5th ed, p688) The gene for this disorder (ATM) encodes a cell cycle checkpoint protein kinase and has been mapped to chromosome 11 (11q22-q23). [MeSH]

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Calsou, P; Franklin, WA; Karam, LR; Lindahl, T; Olsson, M; Painter, RB1

Other Studies

1 other study(ies) available for 2-deoxyribose 5-phosphate and Ataxia Telangiectasia

ArticleYear
Modification of deoxyribose-phosphate residues by extracts of ataxia telangiectasia cells.
    Mutation research, 1990, Volume: 236, Issue:1

    Topics: Ataxia Telangiectasia; Cell Division; Cell Line; DNA Damage; DNA Repair; Humans; Pentosephosphates; Ribosemonophosphates; Tissue Extracts

1990