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Disease Info Card
Stiff-person Syndrome
Information about Stiff-person Syndrome: 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 Stiff-person Syndrome
Most recent studies have shown that Stiff-person Syndrome shares some biological mechanisms with ataxia, autoimmune-diseases, autoimmune-reaction, autoimmunity, cerebellar-ataxia, cns-disorder, diabetes-mellitus, diabetes-mellitus-insulin-dependent, encephalomyelitis, epilepsy, malignant-neoplasms, muscle-rigidity, myasthenia-gravis, myoclonus, nervous-system-disorder, nervousness, pain, paraneoplastic-syndromes, spasm.
Among the many pathways, these few ones have gauged particular interests from scientists studying Stiff-person Syndrome, and have been seen in publications frequently: Cell Activation, Cell Adhesion, Cell Proliferation, Cytokine Secretion, Endocytosis, Exocytosis, Immune Response, Insulin Secretion, Keratinization, Localization, Muscle Contraction, Pathogenesis, Reflex, Secretion, Startle Response, Synaptic Transmission, T Cell Activation, T Cell Proliferation, T Cell Selection, Transport
Quite a number of genes have been found to play important roles in Stiff-person Syndrome, such as AMPH, CSF2, GAD1, GAD2, GLRA1, GLUL, GPHN, ICA, INS, LAMC2, MS4A1, PDSS1, POMC, PTPRN, RAI1, SEPHS1, SMS, TBX4. 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.