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Disease Info Card
Loss Of Chromosome 17
Information about Loss Of Chromosome 17: 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 Loss Of Chromosome 17
Most recent studies have shown that Loss Of Chromosome 17 shares some biological mechanisms with adenocarcinoma, aneuploidy, carcinoma, chromosomal-translocation, chronic-lymphocytic-leukemia, congenital-abnormality, cytogenetic-abnormality, del(13q14), del(17p13), leukemia, loss-of-chromosome-11, loss-of-chromosome-13, lymphoid-leukemia, malignant-neoplasms, monosomy, neoplasms, smith-magenis-syndrome, trisomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Loss Of Chromosome 17, and have been seen in publications frequently: Anaphase, Cell Adhesion, Cell Cycle, Cell Division, Cell Proliferation, Coagulation, Dna Amplification, Dna Methylation, Interphase, Localization, Metaphase, Methylation, Pathogenesis, Reverse Transcription, S Phase
Quite a number of genes have been found to play important roles in Loss Of Chromosome 17, such as ANXA2, BRCA1, CD38, CDKN1A, CDKN2A, CHP1, ENDOU, EXOSC1, EXOSC6, MID1, MYO15A, POLD4, POLE4, RAI1, S100A10, SUB1, TP53. 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.