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Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|October 4, 2014
Recruited metastasis suppressor NM23-H2 attenuates expression and activity of peroxisome proliferator-activated receptor δ (PPARδ) in human cholangiocarcinomaFang He, J Philippe York, Sherilyn Gordon Burroughs, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|December 23, 2003
Prenatal diagnosis of a cleidocranial dysplasia-like phenotype associated with a de novo balanced t(2q;6q)(q36;q16) translocationN Winer, C Le Caignec, M P Quere, et al.
International Journal of Obesity (2005)|June 4, 2014
A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesityJ Philippe, P Stijnen, D Meyre, et al.
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.
Molecular Metabolism|November 27, 2019
Glucagon-like peptide 1 (GLP-1)T D Müller, B Finan, S R Bloom, 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.
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