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Disease Info Card
Homocystinuria
Information about Homocystinuria: 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 Homocystinuria
Most recent studies have shown that Homocystinuria shares some biological mechanisms with 510-methylenetetrahydrofolate-reductase-deficiency, anemia, arteriosclerosis, atherosclerosis, cardiovascular-diseases, cystathionine-beta-synthase-deficiency-disease, ectopia-lentis, galactosemias, hyperhomocysteinemia, inborn-errors-of-metabolism, maple-syrup-urine-disease, marfan-syndrome, metabolic-diseases, methylmalonic-acidemia, phenylketonurias, thromboembolism, thrombosis, vascular-diseases.
Among the many pathways, these few ones have gauged particular interests from scientists studying Homocystinuria, and have been seen in publications frequently: Aging, Blood Coagulation, Cell Proliferation, Coagulation, Cognition, Dna Repair, Excretion, Fatty Acid Oxidation, Fibrinolysis, Glycosylation, Hemostasis, Methylation, Pathogenesis, Platelet Activation, Platelet Aggregation, Secretion, Translation, Transport, Transsulfuration, Urea Cycle
Quite a number of genes have been found to play important roles in Homocystinuria, such as BTD, CBL, CBLC, CBS, F5, MMACHC, MTHFR, MTR, MTRR, PAH, PDXP, PLP1, PRDX5, PTHLH, SDS, SERPINC1, SRR. 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.