FGF21 Lowers Plasma Triglycerides by Accelerating Lipoprotein Catabolism in White and Brown Adipose Tissues

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Items 201–252 of 252

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  11. Hepatic lipogenesis marked by GCKR ‐modulated triglycerides increases serum FGF21 in children/teens with obesity
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  13. Hepatic FGF21 Deletion Improves Glucose Metabolism, Alters Lipogenic and Chrna4 Gene Expression, and Enhances Telomere Maintenance in Aged Female Mice
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  14. The elevation of fibroblast growth factor 21 is associated with generalized periodontitis in patients with treated metabolic syndrome
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  15. FGF21 Improves Glycolipid Metabolism in Rainbow Trout ( Oncorhynchus mykiss ) Fed a High-Carbohydrate Diet by Inhibiting Inflammatory Responses and Activating Autophagy
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  16. Novel FGF21 analogues through structure-based optimization for therapeutic development
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  17. Anatomy and Physiology of Adipose Tissue
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  19. FGF21 and its Relationship with Inflammatory and Metabolic Parameters in HIV Patients after Antiretroviral Treatment
    Alan Joel Ruiz-Padilla, Yeniley Ruíz‐Noa, Lorena del Rocío Ibarra‐Reynoso, María-Luisa Lazo-de-la-Vega-Monroy, Ángel Josabad Alonso‐Castro, Mauricio Sánchez-Barajas, Rosa Margarita Alvarez-Alvarez, Mónica del Carmen Preciado‐Puga · 2020 · Current HIV Research
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  23. Hepatocyte PPARα Is Essential for Triglyceride-Lowering Effect of Pemafibrate
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  26. Inflammatory and Non-Inflammatory Risk Factors in Acquired Aortic Valve Stenosis. Doctoral Thesis
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  28. Author response: FGF21 protects against hepatic lipotoxicity and macrophage activation to attenuate fibrogenesis in nonalcoholic steatohepatitis
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  31. Brown Adipose Tissue in Obesity and Diabetes
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  38. Transgenic female mice producing trans 10, cis 12-conjugated linoleic acid present excessive prostaglandin E2, adrenaline, corticosterone, glucagon, and FGF21
    Yu Rao, Lu-Wen Liang, Meijuan Li, Yangyang Wang, Baozhu Wang, Kemian Gou · 2023 · bioRxiv (Cold Spring Harbor Laboratory)
  39. Pemafibrate
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  43. Limiting De Novo Lipogenesis Unlocks the Thermogenic Potential of Glucose in Brown Fat
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  47. Emerging metabolic hormone therapeutics for metabolic dysfunction-associated steatohepatitis: incretin-based drugs, fibroblast growth factor analogs, and liver-targeting strategies
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