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Disease Info Card
Haploinsufficiency
Information about Haploinsufficiency: 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 Haploinsufficiency
Most recent studies have shown that Haploinsufficiency shares some biological mechanisms with carcinoma, cell-transformation-neoplastic, congenital-abnormality, congenital-heart-defects, cytogenetic-abnormality, developmental-delay-(disorder), developmental-disabilities, dwarfism, dysplasia, epilepsy, growth-disorders, hypoplasia, leukemia, malignant-neoplasms, microcephaly, neoplasms, nervousness, turner-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Haploinsufficiency, and have been seen in publications frequently: Aging, Angiogenesis, Brain Development, Cell Cycle, Cell Death, Cell Differentiation, Cell Growth, Cell Proliferation, Dna Repair, Limb Development, Localization, Methylation, Mitosis, Neurogenesis, Ossification, Osteoblast Differentiation, Pathogenesis, Secretion, Translation, Transport
Quite a number of genes have been found to play important roles in Haploinsufficiency, such as ACVRL1, CDKN2A, ELN, ENG, GRN, INS, MB, NF1, NR5A1, PAFAH1B1, PAX6, PTCH1, PTEN, RUNX1, RUNX2, SHH, SHOX, TBX1, TP53, TWIST1. 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.