| Mitochondrial dysfunction in type 2 diabetes mellitus: an organ-based analysis |
32 |
| Reduced obesity, diabetes, and steatosis upon cinnamon and grape pomace are associated with changes in gut microbiota and markers of gut barrier |
25 |
| ACE2 exerts anti-obesity effect via stimulating brown adipose tissue and induction of browning in white adipose tissue |
17 |
| Circulatory exosomal miRNA following intense exercise is unrelated to muscle and plasma miRNA abundances |
17 |
| Gut bacteria are critical for optimal muscle function: a potential link with glucose homeostasis |
17 |
| Curcumin and other dietary polyphenols: potential mechanisms of metabolic actions and therapy for diabetes and obesity |
16 |
| Berberine alleviates insulin resistance by reducing peripheral branched-chain amino acids |
15 |
| Microbiome potentiates endurance exercise through intestinal acetate production |
15 |
| High-fat, high-fructose, high-cholesterol feeding causes severe NASH and cecal microbiota dysbiosis in juvenile Ossabaw swine |
14 |
| Disruption of glucagon receptor signaling causes hyperaminoacidemia exposing a possible liver-alpha-cell axis |
14 |
| Lipid and glucose metabolism in hepatocyte cell lines and primary mouse hepatocytes: a comprehensive resource for in vitro studies of hepatic metabolism |
13 |
| Evidence for a role for Sestrin1 in mediating leucine-induced activation of mTORC1 in skeletal muscle |
13 |
| Significant improvement in cardiometabolic health in healthy nonobese individuals during caloric restriction-induced weight loss and weight loss maintenance |
13 |
| Intermuscular adipose tissue directly modulates skeletal muscle insulin sensitivity in humans |
13 |
| Considerations for best practices in studies of fiber or other dietary components and the intestinal microbiome |
13 |
| Restricting glycolysis impairs brown adipocyte glucose and oxygen consumption |
12 |
| Fecal transplant from resveratrol-fed donors improves glycaemia and cardiovascular features of the metabolic syndrome in mice |
12 |
| Ketohexokinase knockout mice, a model for essential fructosuria, exhibit altered fructose metabolism and are protected from diet-induced metabolic defects |
12 |
| Low-dose brain estrogen prevents menopausal syndrome while maintaining the diversity of the gut microbiomes in estrogen-deficient rats |
11 |
| Presleep dietary protein-derived amino acids are incorporated in myofibrillar protein during postexercise overnight recovery |
11 |
| Preexercise breakfast ingestion versus extended overnight fasting increases postprandial glucose flux after exercise in healthy men |
11 |
| Physical activity counteracts metabolic syndrome-induced hypogonadotropic hypogonadism and erectile dysfunction in the rabbit |
11 |
| In the absence of UCP1-mediated diet-induced thermogenesis, obesity is augmented even in the obesity-resistant 129S mouse strain |
11 |
| ELABELA, as a potential diagnostic biomarker of preeclampsia, regulates abnormally shallow placentation via APJ |
11 |
| IL-6 release from muscles during exercise is stimulated by lactate-dependent protease activity |
11 |
| Intramuscular triglyceride synthesis: importance in muscle lipid partitioning in humans |
11 |
| Endotoxin-initiated inflammation reduces testosterone production in men of reproductive age |
11 |
| Aging impairs mouse skeletal muscle macrophage polarization and muscle-specific abundance during recovery from disuse |
10 |
| Amelioration of metabolic syndrome by metformin associates with reduced indices of low-grade inflammation independently of the gut microbiota |
10 |
| The pregnane X receptor and its microbiota-derived ligand indole 3-propionic acid regulate endothelium-dependent vasodilation |
10 |
| The PERK-EIF2 alpha-ATF4 signaling branch regulates osteoblast differentiation and proliferation by PTH |
10 |
| HDAC3 inhibition in diabetic mice may activate Nrf2 preventing diabetes-induced liver damage and FGF21 synthesis and secretion leading to aortic protection |
10 |
| NLRP3 inflammasome mediates oxidative stress-induced pancreatic islet dysfunction |
10 |
| Hypoxia exacerbates nonalcoholic fatty liver disease via the HIF-2 alpha/PPAR alpha pathway |
10 |
| Parkin is required for exercise-induced mitophagy in muscle: impact of aging |
10 |
| Evidence of human milk oligosaccharides in maternal circulation already during pregnancy: a pilot study |
10 |
| Intact innervation is essential for diet-induced recruitment of brown adipose tissue |
10 |
| Dietary feeding pattern does not modulate the loss of muscle mass or the decline in metabolic health during short-term bed rest |
10 |
| Increased mast cell abundance in adipose tissue of metabolic syndrome: relevance to the proinflammatory state and increased adipose tissue fibrosis |
10 |
| Pioglitazone improves hepatic mitochondrial function in a mouse model of nonalcoholic steatohepatitis |
9 |
| Nrf2 deletion from adipocytes, but not hepatocytes, potentiates systemic metabolic dysfunction after long-term high-fat diet-induced obesity in mice |
9 |
| Central growth hormone action regulates metabolism during pregnancy |
9 |
| Growth hormone acts along the PPAR gamma-FSP27 axis to stimulate lipolysis in human adipocytes |
9 |
| Metabolic endotoxemia promotes adipose dysfunction and inflammation in human obesity |
9 |
| The gut microbiota is a major regulator of androgen metabolism in intestinal contents |
9 |
| Contractile activity-specific transcriptome response to acute endurance exercise and training in human skeletal muscle |
9 |
| Do skeletal muscle-secreted factors influence the function of pancreatic beta-cells? |
9 |
| Plasma endocannabinoid levels in lean, overweight, and obese humans: relationships to intestinal permeability markers, inflammation, and incretin secretion |
9 |
| Acetyl-CoA from inflammation-induced fatty acids oxidation promotes hepatic malate-aspartate shuttle activity and glycolysis |
9 |
| Mechanistically different effects of fat and sugar on insulin resistance, hypertension, and gut microbiota in rats |
9 |
