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2. Pharmacological activation of constitutive androstane receptor induces female-specific modulation of hepatic metabolism

3. Obesity promotes fumonisin B1 hepatotoxicity

7. The pregnane X receptor drives sexually dimorphic hepatic changes in lipid and xenobiotic metabolism in response to gut microbiota in mice

9. Dietary Amino Acid Source Elicits Sex‐Specific Metabolic Response to Diet‐Induced NAFLD in Mice

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

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

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

14. Haem iron reshapes colonic luminal environment: impact on mucosal homeostasis and microbiome through aldehyde formation

15. Obesity promotes fumonisin B1 hepatotoxicity

16. Dietary Amino Acid Source Elicits Sex‐Specific Metabolic Response to Diet‐Induced NAFLD in Mice.

18. Pharmacological activation of constitutive androstane receptor induces female-specific modulation of hepatic metabolism

19. Obesity promotes Fumonisin B1 toxicity and induces hepatitis

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

21. Tissular Genomic Responses to Oral FB1 Exposure in Pigs

23. Additional file 14 of The pregnane X receptor drives sexually dimorphic hepatic changes in lipid and xenobiotic metabolism in response to gut microbiota in mice

24. Additional file 3 of The pregnane X receptor drives sexually dimorphic hepatic changes in lipid and xenobiotic metabolism in response to gut microbiota in mice

25. Additional file 8 of The pregnane X receptor drives sexually dimorphic hepatic changes in lipid and xenobiotic metabolism in response to gut microbiota in mice

26. Additional file 5 of The pregnane X receptor drives sexually dimorphic hepatic changes in lipid and xenobiotic metabolism in response to gut microbiota in mice

27. The brlA Gene Deletion Reveals That Patulin Biosynthesis Is Not Related to Conidiation in Penicillium expansum

28. The GMO90+ Project: Absence of Evidence for Biologically Meaningful Effects of Genetically Modified Maize-based Diets on Wistar Rats After 6-Months Feeding Comparative Trial

29. Statistical Integration of ‘Omics Data Increases Biological Knowledge Extracted from Metabolomics Data: Application to Intestinal Exposure to the Mycotoxin Deoxynivalenol

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

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

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

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

36. Sex dimorphic role of estrogen receptor a in physiological regulation of hepatic metabolism

37. Gene Expression Profiling Reveals that PXR Activation Inhibits Hepatic PPARα Activity and Decreases FGF21 Secretion in Male C57Bl6/J Mice

39. Impact of veA on the development, aggressiveness, dissemination and secondary metabolism of Penicillium expansum

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

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

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

44. Time course study of the response to LPS targeting the pig immune gene networks

45. Intestinal toxicity of the type B trichothecene mycotoxin fusarenon-X: whole transcriptome profiling reveals new signaling pathways

46. The GMO90+ Project: Absence of Evidence for Biologically Meaningful Effects of Genetically Modified Maize-based Diets on Wistar Rats After 6-Months Feeding Comparative Trial.

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

49. The GeT-TRiX facility: automated processing of expression microarrays - from samples to data analysis reports

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