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Disease Info Card
Subcortical Band Heterotopia
Information about Subcortical Band Heterotopia: 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 Subcortical Band Heterotopia
Most recent studies have shown that Subcortical Band Heterotopia shares some biological mechanisms with brain-diseases, classical-lissencephalies-and-subcortical-band-heterotopias, classical-lissencephaly, congenital-neurologic-anomalies, cortical-dysplasia, dysplasia, ectopic-tissue, epilepsies-partial, epilepsy, lissencephaly, neuronal-migration-disorders, pachygyria, periventricular-nodular-heterotopia, polymicrogyria, x-linked-lissencephaly.
Among the many pathways, these few ones have gauged particular interests from scientists studying Subcortical Band Heterotopia, and have been seen in publications frequently: Brain Development, Cell Adhesion, Cell Cycle, Cell Development, Cell Migration, Glycosylation, Localization, Mating, Microtubule Polymerization, Microtubule-based Transport, Nervous System Development, Neuroblast Migration, Neurogenesis, Nuclear Migration, Pathogenesis, Regulation Of Cell Adhesion, Regulation Of Cell Migration, Rna Interference, System Development, Transport
Quite a number of genes have been found to play important roles in Subcortical Band Heterotopia, such as ABL1, ARX, CALM1, CALM2, CP, DCLK1, DCX, EMX2, FLNA, MLYCD, PAFAH1B1, PLA2G7, RELN, SRPX2, TSC1, TSC2, TUBA1A, UBA2. 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.