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- Table of Contents
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Disease Info Card
Convulsion Neonatal
Information about Convulsion Neonatal: 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 Convulsion Neonatal
Most recent studies have shown that Convulsion Neonatal shares some biological mechanisms with asphyxia, asphyxia-neonatorum, benign-neonatal-epilepsy, brain-injuries, cerebral-palsy, convulsions, encephalopathies, epilepsies-myoclonic, epilepsy, epilepsy-generalized, familial-benign-neonatal-epilepsy, febrile-convulsions, hemorrhage, hypoxia, hypoxic-ischaemic-encephalopathy, infantile-spasms, nervousness, status-epilepticus.
Among the many pathways, these few ones have gauged particular interests from scientists studying Convulsion Neonatal, and have been seen in publications frequently: Brain Development, Cell Death, Cell Proliferation, Coagulation, Cognition, Excretion, Fatty Acid Oxidation, Localization, Myelination, Neurogenesis, Neuroprotection, Pathogenesis, Reflex, Response To Anticonvulsant, Segmentation, Swimming, Synaptic Transmission, Translation, Transport, Vasodilation
Quite a number of genes have been found to play important roles in Convulsion Neonatal, such as ADSL, AGA, CA1, CA3, CHRNA4, CP, CSF2, EXOSC2, EXOSC9, IKBKG, KCNQ1, KCNQ2, KCNQ3, KCNQ5, LAMC2, S100A10, SCN1A, SCN2A, SLC10A7. 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.