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Disease Info Card
Spina Bifida Cystica
Information about Spina Bifida Cystica: 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 Spina Bifida Cystica
Most recent studies have shown that Spina Bifida Cystica shares some biological mechanisms with anencephaly, arnold-chiari-malformation, congenital-abnormality, congenital-cerebral-hernia, congenital-failure-of-fusion, epilepsy, exencephaly, fetal-diseases, hydrocephalus, malnutrition, meningocele, meningomyelocele, nervousness, neurogenic-urinary-bladder, pregnancy-complications, scoliosis-unspecified, spina-bifida, spina-bifida-occulta, urinary-incontinence.
Among the many pathways, these few ones have gauged particular interests from scientists studying Spina Bifida Cystica, and have been seen in publications frequently: Brain Development, Cell Adhesion, Cell Cycle, Cell Proliferation, Coagulation, Fertilization, Hatching, Hypersensitivity, Neural Tube Closure, Neurogenesis, Ossification, Pathogenesis, Reflex, Sensitization, Translation, Transport, Transposition, Tube Closure, Tube Formation, Tube Fusion
Quite a number of genes have been found to play important roles in Spina Bifida Cystica, such as AFP, CERS2, CSF2, DHFR, FANCA, FUZ, FXN, LAMC2, MTHFR, NOG, PAX3, RARA, RPL3, RPL5, SS18L1, TFF2, TRIM26. 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.