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Disease Info Card
Partial Trisomy
Information about Partial Trisomy: 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 Partial Trisomy
Most recent studies have shown that Partial Trisomy shares some biological mechanisms with aneuploidy, chromosomal-deletion, chromosomal-translocation, congenital-abnormality, congenital-heart-defects, cytogenetic-abnormality, developmental-delay-(disorder), down-syndrome, embryonic-mosaic, growth-retardation, leukemia, microcephaly, monosomy, multiple-congenital-anomalies, neoplasms, trisomy, unbalanced-translocation.
Among the many pathways, these few ones have gauged particular interests from scientists studying Partial Trisomy, and have been seen in publications frequently: Aging, Cell Proliferation, Fertilization, Interphase, Localization, Mating, Meiosis, Meiosis I, Meiosis Ii, Metaphase, Methylation, Mitosis, Mitotic Recombination, Neural Tube Development, Neurogenesis, Pachytene, Pathogenesis, Regulation Of Gene Expression, Transposition, Tube Development
Quite a number of genes have been found to play important roles in Partial Trisomy, such as CDK5R1, CDKN2B, CHP1, DCTN3, DYNC1H1, ENDOU, EXOSC6, INVS, LMLN, MRPL28, NXT1, PHB2, PTER, PTGES3, RRAS, S100A10, SUB1, TMED10, TPT1. 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.