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Oncogene|November 21, 2019
Aberrant granulosa cell-fate related to inactivated p53/Rb signaling contributes to granulosa cell tumors and to FOXL2 downregulation in the mouse ovaryVictoria Cluzet, Marie M Devillers, Florence Petit, et al.Human Reproduction (Oxford, England)|February 13, 2025
Reduction in minipubertal gonadotropin levels alters reproductive lifespan and ovarian follicular loss in female miceMélanie Chester, Marie M Devillers, Raphaël Corre, et al.Molecular Cancer Therapeutics|April 1, 2025
Pharmacological inhibition of SIRT1 limits the growth of tumoral and metastatic granulosa cells by impacting mTOR, Myc and E2F pathwaysVictoria Cluzet, Eloïse Airaud, Arnaud Tete, et al.The Journal of Clinical Investigation|October 14, 1998
Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasiaV Verkarre, J C Fournet, P de Lonlay, et al.Journal of Medical Genetics|August 19, 2008
A PCSK9 variant and familial combined hyperlipidaemiaM Abifadel, L Bernier, G Dubuc, et al.European Journal of Human Genetics : EJHG|August 22, 2000
Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defectsB Saint-Jore, M Varret, C Dachet, et al.The American Journal of Pathology|June 8, 2001
Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11J C Fournet, C Mayaud, P de Lonlay, et al.The Journal of Pathology|December 3, 2021
Estradiol promotes cell survival and induces Greb1 expression in granulosa cell tumors of the ovary through an ERα-dependent mechanismVictoria Cluzet, Marie M Devillers, Florence Petit, et al.American Journal of Human Genetics|April 17, 1999
A third major locus for autosomal dominant hypercholesterolemia maps to 1p34.1-p32M Varret, J P Rabès, B Saint-Jore, et al.Neurology|August 6, 2008
Dehydroepiandrosterone for myotonic dystrophy type 1I Pénisson-Besnier, M Devillers, R Porcher, et al.Pageof 2