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Disease Info Card
Isaacs Syndrome
Information about Isaacs 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 Isaacs Syndrome
Most recent studies have shown that Isaacs Syndrome shares some biological mechanisms with ataxia, autoimmune-diseases, autoimmune-reaction, encephalitis, muscle-cramp, muscular-fasciculation, myasthenia-gravis, myasthenias, myokymia, myopathy, neoplasms, nervous-system-disorder, nervousness, neuromuscular-diseases, peripheral-neuropathy, spasm, thymoma.
Among the many pathways, these few ones have gauged particular interests from scientists studying Isaacs Syndrome, and have been seen in publications frequently: Cell Adhesion, Cell Maturation, Cell Motility, Hypersensitivity, Immune Response, Ion Transport, Localization, Muscle Atrophy, Muscle Contraction, Muscle Hypertrophy, Myelination, Pathogenesis, Reflex, Regeneration, Secretion, Short-term Memory, Synaptic Transmission, Transport
Quite a number of genes have been found to play important roles in Isaacs Syndrome, such as ATP2A1, CAMP, CD69, CNTN2, CNTNAP2, CSF2, GAD1, GLUL, KCNA1, KCNA2, KCNA6, KCNQ2, LAMC2, LGI1, NMT1, PMP22, PSMD1, PXMP2. 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.