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Disease Info Card
Proline Dehydrogenase Deficiency
Information about Proline Dehydrogenase Deficiency: 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 Proline Dehydrogenase Deficiency
Most recent studies have shown that Proline Dehydrogenase Deficiency shares some biological mechanisms with complete-hearing-loss, deficiency-of-pyrroline-5-carboxylate-reductase, digeorge-syndrome, epilepsy, homocystinuria, hydroxyprolinaemia, inborn-errors-of-metabolism, kidney-diseases, malignant-neoplasms, malnutrition, metabolic-diseases, phenylketonurias, schizophrenia, sjogren-larsson-syndrome, succinate-semialdehyde-dehydrogenase-deficiency, vitamin-b-6-deficiency.
Among the many pathways, these few ones have gauged particular interests from scientists studying Proline Dehydrogenase Deficiency, and have been seen in publications frequently: Aspartate Transport, Cell Death, Cognition, Energy Homeostasis, Excretion, Flight, Gluconeogenesis, Glycosylation, Habituation, Intestinal Absorption, Light Absorption, Localization, Proline Transport, Synaptic Transmission, Translation, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Proline Dehydrogenase Deficiency, such as ACHE, ACP5, ALDH4A1, CA1, CAT, CD40LG, COMT, CYCS, F2, OAT, PEPD, PRODH, PYCR1, SCYL1, TBX1, TDRD7, TRAF2. 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.