Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
Alle Spezies anzeigen
Weitere Synonyme anzeigen
Select your species
the fatty acid oxidation pathway and LCAD are factors contributing to the pathophysiology of pulmonary disease
Sirtuin 3 (SIRT3 (zeige SIRT3 ELISA Kits)) protein regulates long-chain acyl-CoA dehydrogenase by deacetylating conserved lysines near the active site.
LCAD is minimally expressed in human skeletal muscle and likely does not play a significant role in long-chain fatty acid oxidation.
SIRT3 (zeige SIRT3 ELISA Kits) may play an essential role in attenuating lipid accumulation in the heart through the deacetylation of LCAD
Carnitine supplementation lowered myocardial triglycerides, normalizing myocardial triglycerides levels in LCAD Knock-out mice.
LCAD KO mice are ineffective in maintaining metabolic homeostasis during fasting, which is reflected by an impaired myocardial energy status in fasted LCAD KO mice.
mice with an inherited deficiency of very long-chain acyl-CoA dehydrogenase (VLCAD (zeige ACADVL ELISA Kits)), were protected from high-fat diet-induced obesity and liver and muscle insulin (zeige INS ELISA Kits) resistance.
LCAD is deacetylated in wild-type mice under fasted conditions and by SIRT3 (zeige SIRT3 ELISA Kits) in vitro and in vivo; hyperacetylation of LCAD reduces its enzymatic activity
These data demonstrate that primary defects in mitochondrial fatty acid oxidation capacity can lead to diacylglycerol accumulation, PKCepsilon (zeige PRKCE ELISA Kits) activation, and hepatic insulin (zeige INS ELISA Kits) resistance.
Novel candidate genes in T1D CD55 (zeige CD55 ELISA Kits) and Acadl were identified.
substantial cardiac hypertrophy in LCAD-deficient mice
The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.
, long-chain specific acyl-CoA dehydrogenase, mitochondrial
, acyl-Coenzyme A dehydrogenase, long chain
, long-chain acyl-CoA dehydrogenase
, Acyl Coenzyme A dehydrogenase, long chain
, LCAD long chain acyl-CoA dehydrogenase
, acetyl-Coenzyme A dehydrogenase, long-chain
, acyl-Coenzyme A dehydrogenase, long-chain