Disease Info Card

Genomic Instability

Information about Genomic Instability: 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 Genomic Instability

Most recent studies have shown that Genomic Instability shares some biological mechanisms with adenocarcinoma, aneuploidy, ataxia-telangiectasia, carcinogenesis, carcinoma, cell-transformation-neoplastic, chromosomal-translocation, colorectal-cancer, colorectal-neoplasms, cytogenetic-abnormality, leukemia, lymphoma, malignant-neoplasm-of-breast, malignant-neoplasms, malignant-paraganglionic-neoplasm, mammary-neoplasms, microsatellite-instability, neoplasm-metastasis, neoplasms, tumor-progression.

Among the many pathways, these few ones have gauged particular interests from scientists studying Genomic Instability, and have been seen in publications frequently: Aging, Cell Cycle, Cell Cycle Arrest, Cell Death, Cell Division, Cell Growth, Cell Proliferation, Chromosome Segregation, Dna Methylation, Dna Repair, Dna Replication, Hypersensitivity, Localization, Methylation, Mismatch Repair, Mitosis, Oncogenesis, Pathogenesis, S Phase, Senescence

Quite a number of genes have been found to play important roles in Genomic Instability, such as ANTXR1, ATM, ATR, BLM, BRCA1, BRCA2, CDKN1A, CDKN2A, CHEK1, CHEK2, MLH1, MMAB, MSH2, MYC, PARP1, PCNA, RAD51, TP53, WRN. 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.