bromates has been researched along with Ataxia Telangiectasia Syndrome in 2 studies
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 | Studies |
---|---|
Chessa, L; Cinelli, S; Mosesso, P; Pepe, G; Piane, M | 1 |
Bogliolo, M; Castillo, P; Surralles, J | 1 |
2 other study(ies) available for bromates and Ataxia Telangiectasia Syndrome
Article | Year |
---|---|
Modulation of hypersensitivity to oxidative DNA damage in ATM defective cells induced by potassium bromate by inhibition of the Poly (ADP-ribose) polymerase (PARP).
Topics: Ataxia Telangiectasia; Ataxia Telangiectasia Mutated Proteins; Bromates; Cells, Cultured; DNA Damage; DNA Repair; Humans; Hypersensitivity; Lymphocytes; Oxidative Stress; Phosphorylation; Poly (ADP-Ribose) Polymerase-1; Poly(ADP-ribose) Polymerase Inhibitors | 2018 |
Coordinated action of the Fanconi anemia and ataxia telangiectasia pathways in response to oxidative damage.
Topics: 8-Hydroxy-2'-Deoxyguanosine; Animals; Ataxia Telangiectasia; Ataxia Telangiectasia Mutated Proteins; Bromates; Cell Cycle Proteins; Cell Line; Deoxyguanosine; DNA; DNA Damage; DNA Repair; DNA-Binding Proteins; Fanconi Anemia; Fanconi Anemia Complementation Group D2 Protein; Histones; Humans; Hydrogen Peroxide; Mice; Oxidants; Phosphorylation; Protein Serine-Threonine Kinases; S Phase; Tumor Suppressor Proteins; Ubiquitination | 2011 |