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1 human mitochondria-specific protein and the carnitine palmitoyltransferase 1.
3 l-CoA is a potent inhibitor of mitochondrial carnitine palmitoyltransferase-1, a key enzyme involved
4 reflect a metabolic bottleneck downstream of carnitine palmitoyltransferase-1, a mitochondrial enzyme
5 nthase, acetyl coenzyme A carboxylase 2, and carnitine palmitoyltransferase 1 alpha) in both WT and A
6 lipogenesis and decrease in the activity of carnitine palmitoyltransferase-1 and total energy expend
7 genes of fatty acid oxidation such as Cpt-1 (carnitine palmitoyltransferase-1) as well as Pgc-1alpha
8 tty acid oxidation through the inhibition of carnitine palmitoyltransferase 1 by its product malonyl-
9 cid oxidation by stimulating the activity of carnitine palmitoyltransferase-1 (CPT-1) and inhibiting
11 atty acids (LCFAs) into the mitochondria via carnitine palmitoyltransferase-1 (CPT-1) is inhibited by
13 l downstream effects including inhibition of carnitine palmitoyltransferase-1 (CPT-1) with resultant
14 ns, C75 inhibits FAS activity and stimulates carnitine palmitoyltransferase-1 (CPT-1), consistent wit
15 complex I was associated with a decrease in carnitine palmitoyltransferase 1 (cPT1) and cPT2 levels.
20 Malonyl-CoA is an established inhibitor of carnitine palmitoyltransferase-1 (CPT1), an outer mitoch
21 o this end, we targeted the liver isoform of carnitine palmitoyltransferase-1 (encoded by the CPT1A g
23 quent treatment of mice for 4 weeks with the carnitine palmitoyltransferase-1 inhibitor, oxfenicine (
24 omir) consumed diets containing 0.01% of the carnitine palmitoyltransferase-1 inhibitor, R-etomoxir,
25 of the lipogenic pool but diminution of the carnitine palmitoyltransferase 1 inhibitory pool under c
27 r-activated receptor alpha protein and liver-carnitine palmitoyltransferase-1 (l-CPT-1) mRNA increase
28 lcohol-induced liver injury due to increased carnitine palmitoyltransferase-1, phosphorylated 5'AMP-a
30 ated with changes in ACSL1 (R(2) = 0.39) and carnitine palmitoyltransferase 1 (R(2) = 0.30) expressio
31 ated receptor alpha and induction of hepatic carnitine palmitoyltransferase 1, suggesting increased e
32 unction through its allosteric inhibition of carnitine palmitoyltransferase 1, the enzyme that normal
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