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Disease Info Card
Chromosome Break
Information about Chromosome Break: 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.
Overview of Chromosome Break
Most recent studies have shown that Chromosome Break shares some biological mechanisms with anemia, aneuploidy, ataxia, ataxia-telangiectasia, carcinoma, cell-transformation-neoplastic, chromosomal-translocation, chromosome-breakage, chromosome-fragility, cytogenetic-abnormality, fanconi-anemia, genomic-instability, leukemia, leukemia-myelocytic-acute, lymphoma, malignant-neoplasms, malignant-paraganglionic-neoplasm, myeloid-leukemia, neoplasms.
Among the many pathways, these few ones have gauged particular interests from scientists studying Chromosome Break, and have been seen in publications frequently: Aging, Anaphase, Cell Cycle, Cell Death, Cell Division, Cell Proliferation, Chromosome Breakage, Chromosome Condensation, Dna Repair, Dna Replication, Double-strand Break Repair, Gene Conversion, Hypersensitivity, Interphase, Localization, Metaphase, Mitosis, Pathogenesis, S Phase, V(d)j Recombination
Quite a number of genes have been found to play important roles in Chromosome Break, such as AICDA, ATM, BCR, BLM, BRCA1, BRCA2, CA9, CCND1, CDKN1A, FANCA, FXN, GYPA, MYC, NBN, PRKDC, RAD51, RAD52, TP53, XRCC5. 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.