Disease Info Card

Periodic Paralysis (finding)

Information about Periodic Paralysis (finding): 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 Periodic Paralysis (finding)

Most recent studies have shown that Periodic Paralysis (finding) shares some biological mechanisms with acidosis, andersen-syndrome, cardiac-arrhythmia, channelopathies, familial-periodic-paralysis, graves-disease, horse-diseases, hyperkalemic-periodic-paralysis, hyperthyroidism, hypokalemic-periodic-paralysis, malignant-hyperpyrexia-due-to-anesthesia, malignant-paraganglionic-neoplasm, muscle-weakness, myopathy, myotonia-congenita, paramyotonia-congenita-(disorder), renal-tubular-acidosis, thyrotoxic-periodic-paralysis, thyrotoxicosis, weakness.

Among the many pathways, these few ones have gauged particular interests from scientists studying Periodic Paralysis (finding), and have been seen in publications frequently: Aging, Cation Transport, Cell Adhesion, Cell Death, Cell Migration, Excretion, Glomerular Filtration, Insulin Secretion, Ion Transport, Localization, Mating, Membrane Depolarization, Membrane Hyperpolarization, Muscle Atrophy, Muscle Contraction, Pathogenesis, Regulation Of Cell Migration, Secretion, Skeletal Muscle Contraction, Transport

Quite a number of genes have been found to play important roles in Periodic Paralysis (finding), such as CACNA1S, CST7, DBNL, DPYD, DPYS, INS, KCNE3, KCNJ2, KCNQ1, POMC, PSMC1, REN, RPS4X, RPS4Y1, RYR1, SCN4A, SPTA1. 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.