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Disease Info Card
Polymicrogyria
Information about Polymicrogyria: 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 Polymicrogyria
Most recent studies have shown that Polymicrogyria shares some biological mechanisms with brain-diseases, congenital-abnormality, congenital-absence, congenital-anomaly-of-brain, congenital-neurologic-anomalies, cortical-dysplasia, developmental-delay-(disorder), dysplasia, ectopic-tissue, epilepsy, hypoplasia, lissencephaly, malformations-of-cortical-development, microcephaly, muscular-dystrophy, nervousness, pachygyria, schizencephaly.
Among the many pathways, these few ones have gauged particular interests from scientists studying Polymicrogyria, and have been seen in publications frequently: Axon Guidance, Brain Development, Cell Adhesion, Cell Division, Cell Migration, Cell Proliferation, Cognition, Developmental Process, Glycosylation, Localization, Mitochondrial Translation, Myelination, Nervous System Development, Neural Tube Closure, Neuroblast Migration, Neurogenesis, Neuron Migration, Pathogenesis, Reflex, System Development
Quite a number of genes have been found to play important roles in Polymicrogyria, such as CALB2, DCX, FKTN, FLNA, GFAP, GPR151, GPRC6A, LGR6, LPAR3, MLYCD, MRGPRX1, OXER1, PAFAH1B1, RELN, SRPX2, TUBA1A, TUBB2B, VN1R17P. 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.