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Disease Info Card
Microcephaly
Information about Microcephaly: 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 Microcephaly
Most recent studies have shown that Microcephaly shares some biological mechanisms with atrophy, congenital-abnormality, congenital-heart-defects, cytogenetic-abnormality, developmental-delay-(disorder), developmental-disabilities, dwarfism, dysplasia, epilepsy, fetal-growth-retardation, growth-disorders, growth-retardation, hydrocephalus, hypoplasia, micrognathism, muscle-hypotonia, nervousness, trisomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Microcephaly, and have been seen in publications frequently: Brain Development, Cell Cycle, Cell Death, Cell Division, Cell Proliferation, Dna Repair, Glucose Transport, Glycosylation, Hypersensitivity, Localization, Methylation, Mitosis, Myelination, Neurogenesis, Ossification, Pathogenesis, Pigmentation, Secretion, Translation, Transport
Quite a number of genes have been found to play important roles in Microcephaly, such as ARTN, ASPM, CDK5RAP2, CENPJ, CSF2, IGF1, LAMC2, MB, MCPH1, MECP2, NBN, NLRP2, PAH, PHGDH, SGCG, SHH, SLC2A1, ZEB2. 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.