This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Malformations Of Cortical Development
Information about Malformations Of Cortical Development: 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 Malformations Of Cortical Development
Most recent studies have shown that Malformations Of Cortical Development shares some biological mechanisms with brain-diseases, brain-neoplasms, congenital-neurologic-anomalies, cortical-dysplasia, dysplasia, ectopic-tissue, epilepsies-partial, epilepsy, epilepsy-temporal-lobe, hemimegalencephaly, intractable-epilepsy, macular-corneal-dystrophy-type-i, neoplasms, polymicrogyria, schizencephaly, sclerosis, tuberous-sclerosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Malformations Of Cortical Development, and have been seen in publications frequently: Angiogenesis, Brain Development, Cell Migration, Cell Proliferation, Cerebral Cortex Development, Cognition, Glycosylation, Inflammatory Response, Localization, Myelination, Neural Tube Closure, Neuroblast Proliferation, Neurogenesis, Pathogenesis, Reflex, Segmentation, Synaptic Transmission, Transport, Tube Closure, Vasculogenesis
Quite a number of genes have been found to play important roles in Malformations Of Cortical Development, such as CALB2, CR2, DCX, DHRS4, GFAP, MAP2, METAP2, MLYCD, MTOR, NES, PIK3CA, PVALB, RPS6, SLC12A3, SRPX2, TESC, TSC1, TSC2, VEGFA. 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.