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Disease Info Card
Neuronal Migration Disorders
Information about Neuronal Migration Disorders: 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 Neuronal Migration Disorders
Most recent studies have shown that Neuronal Migration Disorders shares some biological mechanisms with brain-diseases, congenital-abnormality, congenital-neurologic-anomalies, cortical-dysplasia, dysplasia, ectopic-tissue, epilepsies-partial, epilepsy, intractable-epilepsy, lissencephaly, nervousness, pachygyria, periventricular-nodular-heterotopia, polymicrogyria, schizencephaly, sclerosis, subcortical-band-heterotopia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Neuronal Migration Disorders, and have been seen in publications frequently: Anaphase, Blood Vessel Development, Brain Development, Cell Adhesion, Cell Cycle, Cell Division, Cell Migration, Cell-cell Adhesion, Developmental Process, Glycosylation, Localization, Myelination, Nervous System Development, Neurogenesis, Pathogenesis, Protein Glycosylation, Regionalization, Synaptic Transmission, System Development, Transport
Quite a number of genes have been found to play important roles in Neuronal Migration Disorders, such as ARX, CA1, CDK5, DAG1, DCX, FKTN, FLNA, GFAP, PAFAH1B1, PLA2G7, POMGNT1, PSEN1, RELN, TUBA1A, UBA2, VIM, VLDLR, YWHAE. 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.