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Disease Info Card
Extra Unidentified Structurally Abnormal Chromosome (disorder)
Information about Extra Unidentified Structurally Abnormal Chromosome (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.
Overview of Extra Unidentified Structurally Abnormal Chromosome (disorder)
Most recent studies have shown that Extra Unidentified Structurally Abnormal Chromosome (disorder) shares some biological mechanisms with aneuploidy, carcinoma, chromosomal-translocation, chromosome-markers, cytogenetic-abnormality, down-syndrome, embryonic-mosaic, isochromosomes, leukemia, lymphoma, malignant-neoplasms, malignant-paraganglionic-neoplasm, monosomy, myeloid-leukemia, neoplasms, sex-chromosome-aberrations, tetrasomy, trisomy, turner-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Extra Unidentified Structurally Abnormal Chromosome (disorder), and have been seen in publications frequently: Anaphase, Cell Cycle, Cell Division, Cell Growth, Chromosome Breakage, Contact Inhibition, Dna Replication, Fertilization, Interphase, Localization, Meiosis, Meiosis I, Meiosis Ii, Metaphase, Methylation, Mitosis, Mitotic Recombination, Pathogenesis, Pigmentation, Spermatogenesis
Quite a number of genes have been found to play important roles in Extra Unidentified Structurally Abnormal Chromosome (disorder), such as ABL1, ASXL1, CAT, CENPA, CRAT, ENDOU, EXOSC6, GLYAT, INVS, LMLN, MOCOS, MOS, MYC, PAFAH1B1, S100A10, SF3B1, SLC25A10, SRY, TYRO3, YWHAE. 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.