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- Table of Contents
Information about Dna Repair Disorder: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Most recent studies have shown that Dna Repair Disorder shares some biological mechanisms with anemia, ataxia-telangiectasia, carcinogenesis, carcinoma, cockayne-syndrome, cytogenetic-abnormality, dna-repair-deficiency-disorders, fanconi-anemia, genomic-instability, hereditary-diseases, leukemia, malignant-neoplasm-of-breast, malignant-neoplasm-of-skin, malignant-neoplasms, malignant-squamous-cell-neoplasm, neoplasms, premature-aging-syndrome, skin-neoplasms, xeroderma, xeroderma-pigmentosum.
Among the many pathways, these few ones have gauged particular interests from scientists studying Dna Repair Disorder, and have been seen in publications frequently: Aging, Cell Cycle, Cell Death, Cell Killing, Cell Proliferation, Chromosome Breakage, Dna Excision, Dna Repair, Dna Replication, Double-strand Break Repair, G2 Phase, Hypersensitivity, Localization, Meiosis, Metaphase, Mismatch Repair, Oncogenesis, Pathogenesis, System Development, Translesion Synthesis
Quite a number of genes have been found to play important roles in Dna Repair Disorder, such as BRCA1, BRCA2, CDKN1A, ERCC1, ERCC2, ERCC3, ERCC4, ERCC5, ERCC6, ERCC8, FANCA, GTF2H5, LIG4, NBN, PARP1, PRKDC, TP53, XPA, XPC, XRCC1. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.