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Disease Info Card
Cerebral Palsy
Information about Cerebral Palsy: 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 Cerebral Palsy
Most recent studies have shown that Cerebral Palsy shares some biological mechanisms with asphyxia-neonatorum, brain-injuries, congenital-abnormality, developmental-disabilities, diplegia, epilepsy, hemiplegia, hemorrhage, impairment-(finding), leukomalacia-periventricular, littles-disease, movement-disorders, muscle-spasticity, nervous-system-disorder, pain, quadriplegia, spastic-cerebral-palsy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cerebral Palsy, and have been seen in publications frequently: Aging, Brain Development, Cell Death, Coagulation, Cognition, Inflammatory Response, Innervation, Localization, Locomotion, Muscle Contraction, Myelination, Neuroprotection, Ossification, Pathogenesis, Reflex, Secretion, Translation, Transport, Transposition, Visual Perception
Quite a number of genes have been found to play important roles in Cerebral Palsy, such as AGA, CP, CSF2, DMD, F2, GLS2, GRIP1, IL6, LAMC2, MARCKS, MAS1, NDUFB6, PES1, RANGAP1, RIN2, SLC17A5, TNF. 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.