Results 221 to 230 of about 21,879 (258)

Novel therapeutic strategies for targeting fatty acid oxidation in cancer. [PDF]

open access: yesBiomark Res
Wang Y   +10 more
europepmc   +1 more source

Pancreatic expression of CPT1A is essential for whole body glucose homeostasis by supporting glucose-stimulated insulin secretion. [PDF]

open access: yesJ Biol Chem
Ducote MP   +10 more
europepmc   +1 more source

Human Hepatocytes in Experimental Steatosis: Influence of Donor Sex and Sex Hormones. [PDF]

open access: yesBiomedicines
Seidemann L   +6 more
europepmc   +1 more source

Inhibition of systemic mammalian metabolism by carnitine mimics from the gut microbiota

open access: yes
Thümmler K   +20 more
europepmc   +1 more source

Carnitine palmitoyltransferase I [PDF]

open access: bronzeEuropean Journal of Biochemistry, 1983
Palmitate oxidation by liver mitochondria from rats treated with d‐galactosamine (GalN) was markedly inhibited, 3 h after administration. The mitochondrial defect responsible for this inhibition was shown to be an inhibition of the activity of palmitoylcarnitine transferase I (EC 2.3.1.21). Apparent Km of the enzyme remained unchanged whereas apparent
O, Sire   +4 more
openaire   +3 more sources

(+)-Hemipalmitoylcarnitinium strongly inhibits carnitine palmitoyltransferase-I in intact mitochondria

open access: greenJournal of Medicinal Chemistry, 1993
The reaction of the methyl ester of (R)-norcarnitine with 1-bromo-2-heptadecanone produces (+)-6-[(methoxycarbonyl)methyl]-2-pentadecyl-4,4-dimethylmorpholinium bromide, 3, which hydrolyzes to (+)-6-(carboxylatomethyl)-2-pentadecyl-4,4-dimethylmorpholinium (hemipalmitoylcarnitinium, HPC) upon treatment with aqueous sodium hydroxide.
R D, Gandour   +7 more
openaire   +3 more sources
Some of the next articles are maybe not open access.

Related searches:

Deficiency of Carnitine Palmitoyltransferase I

Journal of Child Neurology, 1989
Defective activity of carnitine palmitoyltransferase I was demonstrated in fibroblasts derived from a patient with hypoketotic hypoglycemia. The level of activity observed was approximately 10% of the control mean. Oxidation of palmitate by intact fibroblasts was reduced to 5% of control values. The patient presented at age 14 months with seizures and
J P, Bonnefont   +8 more
openaire   +2 more sources

Hyperlipidaemia due to carnitine palmitoyltransferase I deficiency

Journal of Inherited Metabolic Disease, 2006
SummaryWe report a patient with carnitine palmitoyltransferase I (CPT I) deficiency, who presented with acute encephalopathy at 6 months of age. This was precipitated by an episode of gastroenteritis. No hypoglycaemia was documented, but there was hepatomegaly; blood tests revealed raised transaminases, a coagulopathy and severe hypertriglyceridaemia ...
H, Worthington   +3 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy