has output has result has context hypofunction of mitochondrial fatty acid beta-oxidation [Lipidosis] dysfunction of peroxisomal fatty acid beta-oxidation [NASH] lipidosis (course) PPARalpha inactivation PPAR alpha inactivation [Lipidosis] PMID:25450203 PMID:25703085 PPARalpha inactivation is a subtype of inactivation: A process that changes the activity of the activating PPAR alpha (Peroxisome Proliferator Activated Receptor Alpha) with a nuclear receptor role to be lower. This entity is a specific course-dependent process. This process can constitute the course of Lipidosis. Reactome The set of genes regulated by PPAR-alpha is not fully known in humans, however many examples have been found in mice. Genes directly activated by PPAR-alpha contain peroxisome proliferator receptor elements (PPREs) in their promoters and include: 1) genes involved in fatty acid oxidation and ketogenesis (Acox1, Cyp4a, Acadm, Hmgcs2); 2) genes involved in fatty acid transport (Cd36, , Slc27a1, Fabp1, Cpt1a, Cpt2); 3) genes involved in producing fatty acids and very low density lipoproteins (Me1, Scd1); 4) genes encoding apolipoproteins (Apoa1, Apoa2, Apoa5); 5) genes involved in triglyceride clearance ( Angptl4); 6) genes involved in glycerol metabolism (Gpd1 in mouse); hepatic steatosis dependent process hypofunction of PPARa regulated gene expression [NASH] PPARA - inactivated (canonical)[lipidosis]