Results 281 to 290 of about 691,764 (342)
Adipose Tissue as a Target for Precision Medicine Approaches in Childhood Obesity. [PDF]
Cartwright BR, Scherer PE.
europepmc +1 more source
Chronic PET‐Microplastic Exposure: Disruption of Gut–Liver Homeostasis and Risk of Hepatic Steatosis
Chronic exposure to environmentally relevant PET microplastics disrupts gut–liver homeostasis, leading to hepatic steatosis, early fibrosis, and altered gut microbiota. These effects signal metabolic imbalance and gut–liver axis impairment, emphasizing chronic microplastic ingestion as an emerging environmental health risk linked to non‐communicable ...
Surye Park +5 more
wiley +1 more source
Propionate Induces Energy Expenditure via Browning in Mesenteric Adipose Tissue.
Lu B +9 more
europepmc +1 more source
Gut-Adipose Tissue Axis and Metabolic Health. [PDF]
Borozan S +3 more
europepmc +1 more source
The loss of Ubiquitin Specific Peptidase 26 (USP26) in osteoblasts results in decreased bone formation, as well as multi‐organ fibrosis associated with insulin resistance (IR). Mechanistically, the absence of USP26 reduces glycolysis and lactate accumulation, leading to decreased histone H3 lysine 18 lactylation (H3K18LA) in the promoter region of KH ...
Jiyuan Tang +9 more
wiley +1 more source
Proangiogenic effects of peritumoral adipose tissue in kidney cancer. [PDF]
Ferrando M +8 more
europepmc +1 more source
Targeting Endothelial KDM5A to Attenuate Aging and Ameliorate Age‐Associated Metabolic Abnormalities
This study identifies endothelial KDM5A as a key regulator of aging. KDM5A deficiency accelerates aging by enhancing H3K4me3‐mediated FABP4 expression, disrupting fatty acid metabolism, and promoting multi‐organ senescence. KDM5A restoration or FABP4 inhibition reverses these adverse effects and extends lifespan, positioning the KDM5A/FABP4 axis as a ...
Rifeng Gao +21 more
wiley +1 more source
Reduced Growth and Inflammation in Lrp5<sup>-/-</sup> Mice Adipose Tissue. [PDF]
Luquero A +4 more
europepmc +1 more source
Extracellular Matrix Viscoelasticity Regulates Mammary Branching Morphogenesis
This study shows that mammary branching morphogenesis is regulated by extracellular matrix (ECM) stress relaxation. Slow stress‐relaxing matrices promote branching through focal adhesion signaling, collagen fiber alignment, and cell contractions, whereas fast stress‐relaxing matrices impair branching and collagen alignment.
Daniella I. Walter +3 more
wiley +1 more source

