111 results on '"Cero, Cheryl"'
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2. Targeted and selective knockout of the TLQP-21 neuropeptide unmasks its unique role in energy homeostasis
3. The transcriptional co-regulator LDB1 is required for brown adipose function
4. Standardized In Vitro Models of Human Adipose Tissue Reveal Metabolic Flexibility in Brown Adipocyte Thermogenesis
5. Chronic mirabegron treatment increases human brown fat, HDL cholesterol, and insulin sensitivity
6. SAT662 Bone Morphogenetic Protein 7 Induces Transdifferentiation Of Human White Preadipocytes Into Thermogenic Beige Adipocytes
7. Clearance kinetics of the VGF-derived neuropeptide TLQP-21
8. m6A mRNA Methylation in Brown Adipose Tissue Regulates Systemic Insulin Sensitivity via an Inter-Organ Prostaglandin Signaling Axis
9. The neuropeptide TLQP-21 opposes obesity via C3aR1-mediated enhancement of adrenergic-induced lipolysis
10. Targeted and selective knockout of the TLQP-21 neuropeptide unmasks its unique role in energy homeostasis
11. Stress-induced activation of brown adipose tissue prevents obesity in conditions of low adaptive thermogenesis
12. PSUN84 Chronic Adrenergic Stimulation in Humans Increases Plasma Bile Acids and Expression of Bile Acid Synthesis Enzymes in White Adipose Tissue
13. RF36 | PSUN79 Prolonged Stimulation of β-Adrenergic Receptors in Human Brown and White Adipocytes Increases and then Decreases Metabolic Activity
14. How does Stress Affect Energy Balance?
15. Psychosocial stress induces hyperphagia and exacerbates diet-induced insulin resistance and the manifestations of the Metabolic Syndrome
16. Combining a β3 adrenergic receptor agonist with alpha‐lipoic acid reduces inflammation in male mice with diet‐induced obesity
17. VGF-Derived Peptide TLQP-21
18. β3-Adrenergic receptors regulate human brown/beige adipocyte lipolysis and thermogenesis
19. Lipolysis drives expression of the constitutively active receptor GPR3 to induce adipose thermogenesis
20. Lipolysis drives expression of the constitutively active receptor GPR3 to induce adipose thermogenesis
21. Identification and characterization of distinct brown adipocyte subtypes in C57BL/6J mice
22. Epigenetic Signatures of Human Myocardium and Brown Adipose Tissue Revealed with Simultaneous Positron Emission Tomography and Magnetic Resonance of Class I Histone Deacetylases
23. Identification and characterization of distinct brown adipocyte subtypes in C57BL/6J mice
24. Identification and characterization of distinct murine brown adipocyte lineages
25. 232-LB: Chronic Adrenergic Stimulation of Human Brown and White Adipose Tissue Increases Bile Acid Synthesis Enzyme Expression and Plasma Bile Acid Levels
26. 2020-P: ß3-Adrenergic Receptors Regulate Lipolysis and Thermogenesis in Human Brown/Beige Adipocytes
27. 1680-P: A Novel Immunomodulatory Combination That Decreases Adipose Tissue and Systemic Inflammation and Improves Metabolism in Dio Mice
28. 208-LB: Stimulation of the ß3 Adrenergic Receptors Prime Human White and Brown Adipocytes for Increased Lipolysis and Thermogenesis
29. Chronic mirabegron treatment increases human brown fat, HDL cholesterol, and insulin sensitivity
30. Opportunities and challenges in the therapeutic activation of human energy expenditure and thermogenesis to manage obesity
31. Combining a β3 adrenergic receptor agonist with alpha‐lipoic acid reduces inflammation in male mice with diet‐induced obesity.
32. Peptide/Receptor Co-evolution Explains the Lipolytic Function of the Neuropeptide TLQP-21
33. 137-OR: The Selective Human Beta 3 Adrenergic Receptor Mirabegron Potently Activates Lipolysis in Human White Adipocytes
34. Peptide/Receptor Evolution Explains the Lipolytic Function of the Neuropeptide TLQP-21
35. Regulation of Human Adipose Tissue Activation, Gallbladder Size, and Bile Acid Metabolism by a β3-Adrenergic Receptor Agonist
36. Physiological Responses to Daily Use of Beta-Three Adrenergic Receptor Agonist, Mirabegron
37. Stimulation of the ß3-Adrenergic Receptor via Mirabegron Induces Lipolysis and Thermogenesis in Human Adipocytes
38. Functional and Developmental Heterogeneity in Human Adipose Tissue Depots
39. The TLQP‐21 neuropeptide and the complement 3a receptor (C3aR1) regulate a novel prolipolytic pathway
40. Molecular mechanisms and individual vulnerability in an animal model (Mus musculus) of obesity induced by chronic social stress
41. The VGF-derived peptide TLQP-62 modulates insulin secretion and glucose homeostasis
42. The TLQP-21 Peptide Activates the G-Protein-Coupled Receptor C3aR1 via a Folding-upon-Binding Mechanism
43. The granin VGF promotes genesis of secretory vesicles, and regulates circulating catecholamine levels and blood pressure
44. Loss of Gnas Imprinting Differentially Affects REM/NREM Sleep and Cognition in Mice
45. Characterization of a novel peripheral pro-lipolytic mechanism in mice: role of VGF-derived peptide TLQP-21
46. Metabolic Consequences and Vulnerability to Diet-Induced Obesity in Male Mice under Chronic Social Stress
47. Mechanisms of the pro-lipolytic and anti-obesity effects of the VGF-derived peptide TLQP-21
48. Opportunities and challenges in the therapeutic activation of human energy expenditure and thermogenesis to manage obesity.
49. m 6 A mRNA Methylation in Brown Adipose Tissue Regulates Systemic Insulin Sensitivity via an Inter-Organ Prostaglandin Signaling Axis.
50. Targeted and selective knockout of the TLQP-21 neuropeptide unmasks its unique role in energy homeostasis.
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