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Disease Info Card
Isodisomies, Uniparental
Information about Isodisomies, Uniparental: 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 Isodisomies, Uniparental
Most recent studies have shown that Isodisomies, Uniparental shares some biological mechanisms with aneuploidy, angelman-syndrome, beckwith-wiedemann-syndrome, cytogenetic-abnormality, diabetes-mellitus, diabetes-mellitus-insulin-dependent, down-syndrome, dwarfism, embryonic-mosaic, fetal-growth-retardation, hereditary-diseases, isochromosomes, monosomy, muscle-hypotonia, prader-willi-syndrome, trisomy, uniparental-disomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Isodisomies, Uniparental, and have been seen in publications frequently: Bone Development, Cell Cycle, Cell Cycle Arrest, Cell Division, Complement Activation, Dna Methylation, Fertilization, Gene Conversion, Insulin Secretion, Interphase, Meiosis, Meiosis I, Meiosis Ii, Metaphase, Methylation, Mitosis, Mrna Splicing, Pathogenesis, Pigmentation, Secretion
Quite a number of genes have been found to play important roles in Isodisomies, Uniparental, such as ABCB11, ABCC8, CD46, CDKN1C, CDKN2A, CFH, CFTR, ETV6, FH, FOXE1, GNAS, IFNGR1, INS, KCNJ11, PAX5, PLAGL1, PLEC, PTH, UROD. 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.