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Disease Info Card
Thyrotoxic Periodic Paralysis
Information about Thyrotoxic Periodic Paralysis: 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 Thyrotoxic Periodic Paralysis
Most recent studies have shown that Thyrotoxic Periodic Paralysis shares some biological mechanisms with acidosis, adenoma, cardiac-arrhythmia, familial-periodic-paralysis, goiter, graves-disease, hyperthyroidism, hypokalemic-periodic-paralysis, hypophosphatemia, muscle-weakness, myopathy, paralysis-flaccid, periodic-paralysis-(finding), quadriparesis, quadriplegia, thyroid-crisis, thyroid-diseases, thyrotoxicosis, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Thyrotoxic Periodic Paralysis, and have been seen in publications frequently: Cation Transport, Conjugation, Excretion, Innervation, Insulin Secretion, Ion Transport, Pathogenesis, Secretion, Transport
Quite a number of genes have been found to play important roles in Thyrotoxic Periodic Paralysis, such as ADAMTS13, CACNA1S, CST7, DBNL, HLA-A, HLA-B, INS, KCNE3, KCNJ18, KCNJ2, MSX2, POMC, SCN4A, SH3BP4, SLC25A5, SPTA1, THPO, TSHR, ZFP36. 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.
Pathways Related to Thyrotoxic Periodic Paralysis
This information is being compiled and will come in a future update
| Cation Transport | Conjugation | Excretion |
| Innervation | Insulin Secretion | Ion Transport |
| Pathogenesis | Secretion | Transport |