Barbier, Olivier
Université Laval
10 papers on CoChatORCID 0000-0002-3067-1134
Most cited papers
- Verified
Inactivation of androgens by UDP-glucuronosyltransferase enzymes in humans
Bélanger, A., Pelletier, G., Labrie, F., Barbier, O., & Chouinard, S. (2003) · Trends in Endocrinology & Metabolism
Pharmacogenetics and Drug MetabolismProstate Cancer Treatment and Research
Cited by 235
- Verified
UDP-glucuronosyltransferase 2B15 (UGT2B15) and UGT2B17 enzymes are major determinants of the androgen response in prostate cancer LNCaP cells
Chouinard, S., Barbier, O., & Bélanger, A. (2007) · Journal of Biological Chemistry
Prostate Cancer Treatment and ResearchPharmacogenetics and Drug Metabolism
Cited by 109
- Verified
Inactivation by UDP-glucuronosyltransferase enzymes: The end of androgen signaling
Chouinard, S., Yueh, M.-F., Tukey, R. H., Giton, F., Fiet, J., Pelletier, G., Barbier, O., & Bélanger, A. (2008) · The Journal of Steroid Biochemistry and Molecular Biology
Pharmacogenetics and Drug MetabolismProstate Cancer Treatment and Research
Cited by 90
- Verified
Multiple roles for UDP-glucuronosyltransferase (UGT)2B15 and UGT2B17 enzymes in androgen metabolism and prostate cancer evolution
Gauthier-Landry, L., Bélanger, A., & Barbier, O. (2015) · The Journal of Steroid Biochemistry and Molecular Biology
Prostate Cancer Treatment and ResearchPharmacogenetics and Drug Metabolism
Cited by 62
- Verified
The hepatokine Tsukushi is released in response to NAFLD and impacts cholesterol homeostasis
Mouchiroud, M., Camiré, É., Aldow, M., Caron, A., Jubinville, É., Turcotte, L., Kaci, I., Beaulieu, M.-J., Roy, C., Labbé, S. M., et al. (2019) · JCI Insight
Liver Disease Diagnosis and TreatmentCholesterol and Lipid Metabolism
Cited by 57
- Verified
Human uridine diphosphate-glucuronosyltransferase UGT2B7 conjugates mineralocorticoid and glucocorticoid metabolites
Girard, C., Barbier, O., Veilleux, G., El-Alfy, M., & Bélanger, A. (2003) · Endocrinology
Pharmacogenetics and Drug MetabolismHormonal Regulation and Hypertension
Cited by 45
- Verified
PPAR-Mediated Bile Acid Glucuronidation: Therapeutic Targets for the Treatment of Cholestatic Liver Diseases
Gallucci, G. M., Hayes, C. M., Boyer, J. L., Barbier, O., Assis, D. N., & Ghonem, N. S. (2024) · Cells
Liver Diseases and ImmunityDrug Transport and Resistance Mechanisms
Cited by 40
- Verified
PPARα L162V polymorphism alters the potential of n‐3 fatty acids to increase lipoprotein lipase activity
Rudkowska, I., Caron‐Dorval, D., Verreault, M., Couture, P., Deshaies, Y., Barbier, O., & Vohl, M. (2010) · Molecular Nutrition & Food Research
Fatty Acid Research and HealthLipid metabolism and disorders
Cited by 36
- Verified
Adjunct Fenofibrate Up‐regulates Bile Acid Glucuronidation and Improves Treatment Response For Patients With Cholestasis
Gallucci, G. M., Trottier, J., Hemme, C., Assis, D. N., Boyer, J. L., Barbier, O., & Ghonem, N. S. (2021) · Hepatology Communications
Liver Diseases and ImmunityDrug Transport and Resistance Mechanisms
Cited by 26
- Verified
The Hepatokine TSK does not affect brown fat thermogenic capacity, body weight gain, and glucose homeostasis
Mouchiroud, M., Camiré, É., Aldow, M., Caron, A., Jubinville, É., Turcotte, L., Kaci, I., Beaulieu, M.-J., Roy, C., Labbé, S. M., et al. (2019) · Molecular Metabolism
Adipose Tissue and MetabolismAdipokines, Inflammation, and Metabolic Diseases
Cited by 24
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