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Disease Info Card
Phenylketonurias
Information about Phenylketonurias: 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 Phenylketonurias
Most recent studies have shown that Phenylketonurias shares some biological mechanisms with classical-phenylketonuria, congenital-abnormality, congenital-hypothyroidism, cystic-fibrosis, down-syndrome, fibrosis, galactosemias, genetic-diseases-inborn, hereditary-diseases, homocystinuria, hyperphenylalaninemia, hypothyroidism, inborn-errors-of-metabolism, maple-syrup-urine-disease, metabolic-diseases, microcephaly, phenylketonuria-ii, phenylketonuria-maternal, pregnancy-complications.
Among the many pathways, these few ones have gauged particular interests from scientists studying Phenylketonurias, and have been seen in publications frequently: Aging, Amino Acid Transport, Bone Resorption, Brain Development, Cognition, Dna Amplification, Excretion, Fatty Acid Oxidation, Immune Response, Intestinal Absorption, Localization, Myelination, Pathogenesis, Phenylalanine Transport, Pigmentation, Regeneration, Secretion, Translation, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Phenylketonurias, such as BLMH, BTD, CFTR, CSF2, G6PD, GCH1, HPSE, LAMC2, NBN, NME1, PAH, PAM, PTS, QDPR, SHCBP1, TH, TYR. 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.