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1. The interplay between dietary fatty acids and gut microbiota influences host metabolism and hepatic steatosis

2. Membrane estrogen receptor-α contributes to female protection against high-fat diet-induced metabolic disorders

3. The interplay between dietary fatty acids and gut microbiota influences host metabolism and hepatic steatosis

4. Ephrin-B1 regulates the adult diastolic function through a late postnatal maturation of cardiomyocyte surface crests

5. Author response: Ephrin-B1 regulates the adult diastolic function through a late postnatal maturation of cardiomyocyte surface crests

7. ATGL-dependent white adipose tissue lipolysis controls hepatocyte PPARα activity

8. The hepatocyte insulin receptor is required to program the liver clock and rhythmic gene expression

9. Nuclear HMGB1 protects from nonalcoholic fatty liver disease through negative regulation of liver X receptor

10. Crest maturation at the cardiomyocyte surface contributes to a new late postnatal development stage that controls the diastolic function of the adult heart

12. Integrative study of diet-induced mouse models of NAFLD identifies PPARα as a sexually dimorphic drug target

13. Dual regulation of TxNIP by ChREBP and FoxO1 in liver

14. Nuclear HMGB1 protects from non-alcoholic fatty liver diseases through negative regulation of liver X receptor

15. The hepatocyte insulin receptor is required to program rhythmic gene expression and the liver clock

16. ATGL-dependent white adipose tissue lipolysis controls hepatocyte PPARα activity

18. Hepatocyte-specific deletion of Pparα promotes NAFLD in the context of obesity

19. Author Correction: Dimorphic metabolic and endocrine disorders in mice lacking the constitutive androstane receptor

20. Dimorphic metabolic and endocrine disorders in mice lacking the constitutive androstane receptor

23. Hepatic PPARα is critical in the metabolic adaptation to sepsis

24. Selective Liver Estrogen Receptor α Modulation Prevents Steatosis, Diabetes, and Obesity Through the Anorectic Growth Differentiation Factor 15 Hepatokine in Mice

25. The class 3 PI3K coordinates autophagy and mitochondrial lipid catabolism by controlling nuclear receptor PPARα

26. Hepatocyte-specific deletion of Pparα promotes NASH in the context of obesity

27. The protective role of liver X receptor (LXR) during fumonisin B1-induced hepatotoxicity

30. Insights into the role of hepatocyte PPARα activity in response to fasting

32. Metabolic Effects of a Chronic Dietary Exposure to a Low-Dose Pesticide Cocktail in Mice: Sexual Dimorphism and Role of the Constitutive Androstane Receptor

33. Dual extraction of mRNA and lipids from a single biological sample

34. A Specific ChREBP and PPARα Cross-Talk Is Required for the Glucose-Mediated FGF21 Response

35. Dietary oleic acid regulates hepatic lipogenesis through a liver X receptor-dependent signaling

36. Selective Activation of Estrogen Receptor α Activation Function-1 Is Sufficient to Prevent Obesity, Steatosis, and Insulin Resistance in Mouse

37. L’hépatokine FGF21 est unique dans sa réponse nutrionnelle au glucose et au jeûne dans le foie : interdépendence des facteurs de transcription ChREBP et PPARα

38. Identification des fonctions physiologiques de PPARbeta hépatocytaire : rôle possible dans le diabète de type 2

39. L’absence du récepteur CAR induit une obésité et un diabète qui dépendent du genre

40. L’exposition à un mélange de pesticides à faible dose induit obésité et intolérance au glucose in vivo

41. Rôle spécifique de la PI3kinase alpha hépatocytaire : influence sur le diabète et la stéatose hépatique

42. Perilipin 5 fine-tunes lipid oxidation to metabolic demand and protects against lipotoxicity in skeletal muscle

46. Activation of the Constitutive Androstane Receptor induces hepatic lipogenesis and regulates Pnpla3 gene expression in a LXR-independent way

48. Identification of a novel PPAR β/δ/miR‐21‐3p axis in UV ‐induced skin inflammation

49. Erratum: Hepatic circadian clock oscillators and nuclear receptors integrate microbiome-derived signals

50. Hepatic circadian clock oscillators and nuclear receptors integrate microbiome-derived signals

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