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Disease Info Card
Congenital Neurologic Anomalies
Information about Congenital Neurologic Anomalies: 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 Congenital Neurologic Anomalies
Most recent studies have shown that Congenital Neurologic Anomalies shares some biological mechanisms with atrophy, brain-diseases, congenital-abnormality, congenital-absence, congenital-heart-defects, cortical-dysplasia, cytogenetic-abnormality, dysplasia, ectopic-tissue, epilepsy, eye-abnormalities, fetal-diseases, hydrocephalus, hypoplasia, lissencephaly, microcephaly, nervousness, polymicrogyria.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Neurologic Anomalies, and have been seen in publications frequently: Axon Guidance, Brain Development, Cell Adhesion, Cell Cycle, Cell Death, Cell Migration, Cell Proliferation, Central Nervous System Development, Cognition, Innervation, Localization, Locomotion, Myelination, Nervous System Development, Neurogenesis, Pathogenesis, Reflex, Segmentation, System Development, Transport
Quite a number of genes have been found to play important roles in Congenital Neurologic Anomalies, such as AFP, BDNF, CALB1, CALB2, CSF2, DCX, GFAP, IKBKG, INS, LAMC2, MLYCD, PAFAH1B1, PLA2G7, RELN, SS18L1, TH, TMEM67, TREX1. 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.