This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Syringomyelia
Information about Syringomyelia: 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 Syringomyelia
Most recent studies have shown that Syringomyelia shares some biological mechanisms with arachnoiditis, arnold-chiari-malformation, arthropathy, compression-of-spinal-cord, congenital-abnormality, headache, hernia, hydrocephalus, multiple-sclerosis, neoplasms, nervousness, neurogenic-arthropathy, pain, post-traumatic-syrinx, scoliosis-unspecified, spina-bifida, spinal-cord-diseases, spinal-cord-injuries, spinal-cord-neoplasms, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Syringomyelia, and have been seen in publications frequently: Bone Resorption, Cell Death, Coagulation, Excretion, Innervation, Localization, Micturition, Muscle Atrophy, Neural Tube Closure, Ossification, Pathogenesis, Proprioception, Reflex, Regeneration, Secretion, Segmentation, Translation, Transport, Transposition, Tube Closure
Quite a number of genes have been found to play important roles in Syringomyelia, such as AQP4, ARHGAP4, C2, C3, C5, C6, C7, CFD, CFP, CSF2, CXCL10, FLNA, HNRNPC, LAMC2, MMEL1, NLRP5, PFDN4, PLXNB1, PSMA7, PTS. 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.