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Transplantation Proceedings|June 15, 2004
Islet of Langerhans allogeneic transplantation at the University of Geneva in the steroid free era in islet after kidney and simultaneous islet-kidney transplantationsT Berney, P Bucher, Z Mathe, et al.
Molecular Brain|August 5, 2016
Sex-dependent adaptive changes in serotonin-1A autoreceptor function and anxiety in Deaf1-deficient miceChristine Luckhart, Tristan J Philippe, Brice Le François, et al.
Endocrinology|September 16, 2022
Corticosteroid-binding Globulin (SERPINA6) Establishes Postpubertal Sex Differences in Rat Adrenal DevelopmentJulia N C Toews, Tristan J Philippe, Lesley A Hill, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|April 14, 2006
Sequential kidney/islet transplantation: efficacy and safety assessment of a steroid-free immunosuppression protocolC Toso, R Baertschiger, P Morel, et al.
American Journal of Human Genetics|June 12, 1999
Characterization of a germline mosaicism in families with Lowe syndrome, and identification of seven novel mutations in the OCRL1 geneV Satre, N Monnier, F Berthoin, et al.
Scientific Reports|April 12, 2018
Loss of MeCP2 in adult 5-HT neurons induces 5-HT1A autoreceptors, with opposite sex-dependent anxiety and depression phenotypesTristan J Philippe, Faranak Vahid-Ansari, Zoe R Donaldson, et al.
Bone Marrow Transplantation|April 9, 2014
Unrelated adult stem cell donor medical suitability: recommendations from the World Marrow Donor Association Clinical Working Group CommitteeR N Lown, J Philippe, W Navarro, et al.
Diabetologia|December 18, 2012
Autonomous and self-sustained circadian oscillators displayed in human islet cellsP Pulimeno, T Mannic, D Sage, et al.
Pflugers Archiv : European Journal of Physiology|September 27, 2013
FXR-induced secretion of FGF15/19 inhibits CYP27 expression in cholangiocytes through p38 kinase pathwayDongju Jung, J Philippe York, Li Wang, et al.
Diabetes & Metabolism|April 9, 2013
Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous familyA Bonnefond, E Vaillant, J Philippe, et al.
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