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Disease Info Card
Pseudopseudohypoparathyroidism
Information about Pseudopseudohypoparathyroidism: 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 Pseudopseudohypoparathyroidism
Most recent studies have shown that Pseudopseudohypoparathyroidism shares some biological mechanisms with brachydactyly, calcinosis, dwarfism, endocrine-system-diseases, heterotopic-ossification, hypocalcemia, hypoparathyroidism, hypothyroidism, obesity, osteoma, osteoma-cutis, polyostotic-fibrous-dysplasia, pseudohypoparathyroidism, pseudohypoparathyroidism-type-ia, tetany, turner-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Pseudopseudohypoparathyroidism, and have been seen in publications frequently: Bone Remodeling, Bone Resorption, Cell Growth, Cell Proliferation, Diuresis, Excretion, Growth Hormone Secretion, Hormone Secretion, Intracellular Signal Transduction, Localization, Methylation, Ossification, Parathyroid Hormone Secretion, Pathogenesis, Platelet Aggregation, Secretion, Transport
Quite a number of genes have been found to play important roles in Pseudopseudohypoparathyroidism, such as APC, ASAH1, ATP8A2, CALCA, GDI1, GLUL, GNAS, GNL3, PAH, PRKAR1A, PRL, PTH, PTHLH, PTRH1, SOX3, STX16, TRH. 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.