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Disease Info Card
Nijmegen Breakage Syndrome
Information about Nijmegen Breakage Syndrome: 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 Nijmegen Breakage Syndrome
Most recent studies have shown that Nijmegen Breakage Syndrome shares some biological mechanisms with anemia, ataxia, ataxia-telangiectasia, cell-transformation-neoplastic, chromosome-breakage, cytogenetic-abnormality, fanconi-anemia, genomic-instability, growth-retardation, hereditary-diseases, immunologic-deficiency-syndromes, instabilities-chromosomal, leukemia, lymphoma, malignant-neoplasm-of-breast, malignant-neoplasms, microcephaly, neoplasms, telangiectasis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Nijmegen Breakage Syndrome, and have been seen in publications frequently: Cell Cycle, Cell Cycle Arrest, Cell Cycle Checkpoint, Cell Death, Chromosome Breakage, Dna Damage Checkpoint, Dna Repair, Dna Replication, Double-strand Break Repair, G2 Phase, Hypersensitivity, Localization, Metaphase, Pathogenesis, Response To Ionizing Radiation, Response To Radiation, S Phase, Telomere Maintenance, Translation, V(d)j Recombination
Quite a number of genes have been found to play important roles in Nijmegen Breakage Syndrome, such as ANTXR1, ARTN, ATM, ATR, BRCA1, CDKN1A, CHEK2, LIG4, MMAB, NBN, NLRP2, NME1, PRKDC, RAD50, RAD51, SMC1A, TP53, TP53BP1. 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.