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Disease Info Card
Cystathionine Beta-synthase Deficiency Disease
Information about Cystathionine Beta-synthase Deficiency Disease: 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 Cystathionine Beta-synthase Deficiency Disease
Most recent studies have shown that Cystathionine Beta-synthase Deficiency Disease shares some biological mechanisms with 510-methylenetetrahydrofolate-reductase-deficiency, arteriosclerosis, atherosclerosis, cardiovascular-diseases, cerebrovascular-accident, congenital-ectopia, ectopia-lentis, hepatic-methionine-adenosyltransferase-deficiency, homocystinuria, hyperhomocysteinemia, inborn-errors-of-metabolism, infarction, metabolic-diseases, myocardial-infarction, osteoporosis, thromboembolism, thrombosis, vascular-diseases, vitamin-b-12-deficiency.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cystathionine Beta-synthase Deficiency Disease, and have been seen in publications frequently: Adaptive Immune Response, Aging, Cardiac Muscle Hypertrophy, Cellular Homeostasis, Cholesterol Transport, Cognition, Excretion, Immune Response, Lipid Homeostasis, Methylation, Muscle Cell Proliferation, Ossification, Pathogenesis, Platelet Activation, Platelet Aggregation, Secretory Pathway, Smooth Muscle Cell Proliferation, Translation, Transport, Transsulfuration
Quite a number of genes have been found to play important roles in Cystathionine Beta-synthase Deficiency Disease, such as ALB, APOA1, APOA4, CAT, CBS, CTH, F5, GNMT, HTT, LRP2, MAT1A, MCF2L, MTHFR, PDXP, PLP1, PRDX5, PTHLH. 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.