about
Genetic basis of hyperlysinemiaAcyl-CoA dehydrogenase 9 is required for the biogenesis of oxidative phosphorylation complex IA general introduction to the biochemistry of mitochondrial fatty acid β-oxidationAdaptive reciprocity of lipid and glucose metabolism in human short-term starvationAcylcarnitines: reflecting or inflicting insulin resistance?Biochemical and genetic aspects of mevalonate kinase and its deficiencyFood withdrawal lowers energy expenditure and induces inactivity in long-chain fatty acid oxidation-deficient mouse modelsFasting-induced myocardial lipid accumulation in long-chain acyl-CoA dehydrogenase knockout mice is accompanied by impaired left ventricular functionMitochondrial long chain fatty acid beta-oxidation in man and mouseCarnitine supplementation attenuates myocardial lipid accumulation in long-chain acyl-CoA dehydrogenase knockout miceBile acids induce energy expenditure by promoting intracellular thyroid hormone activationMyocardial energy shortage and unmet anaplerotic needs in the fasted long-chain acyl-CoA dehydrogenase knockout mouseMitochondrial protein acetylation is driven by acetyl-CoA from fatty acid oxidationBiochemical competition makes fatty-acid β-oxidation vulnerable to substrate overloadChanges in the Metabolome in Response to Low-Dose Exposure to Environmental Chemicals Used in Personal Care Products during Different Windows of SusceptibilityOverexpression of PLIN5 in skeletal muscle promotes oxidative gene expression and intramyocellular lipid content without compromising insulin sensitivityIdentification and characterization of Eci3, a murine kidney-specific Δ3,Δ2-enoyl-CoA isomeraseThe small heterodimer partner is a gonadal gatekeeper of sexual maturation in male mice.Pioglitazone treatment restores in vivo muscle oxidative capacity in a rat model of diabetes.Critical assessment of human metabolic pathway databases: a stepping stone for future integration.Nonorthologous gene displacement of phosphomevalonate kinase.Fasting serum taurine-conjugated bile acids are elevated in type 2 diabetes and do not change with intensification of insulinGlutamine synthetase in muscle is required for glutamine production during fasting and extrahepatic ammonia detoxification.Multilayered genetic and omics dissection of mitochondrial activity in a mouse reference population.Bile acid binding resin improves metabolic control through the induction of energy expenditureMitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia.PARP-2 regulates SIRT1 expression and whole-body energy expenditureLowering bile acid pool size with a synthetic farnesoid X receptor (FXR) agonist induces obesity and diabetes through reduced energy expenditure.Post-natal myogenic and adipogenic developmental: defects and metabolic impairment upon loss of A-type lamins.Cholesterol-induced hepatic inflammation does not underlie the predisposition to insulin resistance in dyslipidemic female LDL receptor knockout miceIn vivo proton T1 relaxation times of mouse myocardial metabolites at 9.4 T.The metabolic footprint of aging in miceMuscle or liver-specific Sirt3 deficiency induces hyperacetylation of mitochondrial proteins without affecting global metabolic homeostasis.Peroxisomal L-bifunctional enzyme (Ehhadh) is essential for the production of medium-chain dicarboxylic acidsIn vivo mouse myocardial (31)P MRS using three-dimensional image-selected in vivo spectroscopy (3D ISIS): technical considerations and biochemical validations.Compromised intestinal lipid absorption in mice with a liver-specific deficiency of liver receptor homolog 1.Serum bile acids are higher in humans with prior gastric bypass: potential contribution to improved glucose and lipid metabolismPeroxisomes and bile acid biosynthesis.Homing in on bile acid physiology.Metabolomics: unraveling the chemical individuality of common human diseases.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Sander M Houten
@nl
Sander M Houten
@sl
Sander M. Houten
@en
Sander M. Houten
@es
type
label
Sander M Houten
@nl
Sander M Houten
@sl
Sander M. Houten
@en
Sander M. Houten
@es
altLabel
Sander Houten
@en
prefLabel
Sander M Houten
@nl
Sander M Houten
@sl
Sander M. Houten
@en
Sander M. Houten
@es
P106
P1153
6603900835
P21
P31
P496
0000-0002-6167-9147