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Disease Info Card
Disorders Of Peroxisome Biogenesis
Information about Disorders Of Peroxisome Biogenesis: 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 Disorders Of Peroxisome Biogenesis
Most recent studies have shown that Disorders Of Peroxisome Biogenesis shares some biological mechanisms with adrenoleukodystrophy, adrenoleukodystrophy-neonatal, aortic-aneurysm-abdominal, chondrodysplasia-punctata, chondrodysplasia-punctata-rhizomelic, hepatomegaly, hereditary-diseases, hyperoxaluria, inborn-errors-of-metabolism, infantile-refsum-disease-(disorder), liver-diseases, metabolic-diseases, muscle-hypotonia, nervousness, peroxisomal-disorders, protein-deficiency, refsum-disease, retinal-diseases, zellweger-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Disorders Of Peroxisome Biogenesis, and have been seen in publications frequently: Aging, Cell Differentiation, Cytokinesis, Fatty Acid Beta-oxidation, Fatty Acid Oxidation, Lipid Storage, Localization, Membrane Assembly, Membrane Biogenesis, Organelle Assembly, Ossification, Oxidative Phosphorylation, Pathogenesis, Protein Import, Protein Targeting, Receptor Recycling, Spermatogenesis, Translation, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Disorders Of Peroxisome Biogenesis, such as AAAS, APP, CAT, EPB41L4B, GNPAT, MAMLD1, PEX1, PEX10, PEX12, PEX13, PEX14, PEX2, PEX26, PEX5, PEX6, PEX7, PHEX, ZNF260. 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.