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Endocrinology|September 10, 2003
Differential regulation of two 3' end variants of P450 aromatase transcripts and of a new truncated aromatase protein in rabbit preovulatory granulosa cellsVincent Hanoux, Hélène Bouraima, Hervé Mittre, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 6, 2022
Local aromatase excess with recruitment of unusual promoters of CYP19A1 gene in prepubertal patients with gynecomastiaEmilie Deberles, Isabelle Durand, Hervé Mittre, et al.
The Journal of Steroid Biochemistry and Molecular Biology|August 12, 2006
The absence of a functional nuclear receptor element A (NREA) in the promoter II of the aromatase P450 gene in rabbit granulosa cellsThomas Andrieu, Colette Féral, Michael Joubert, et al.
European Journal of Endocrinology|August 20, 2009
Cushing's syndrome associated with a nested stromal epithelial tumor of the liver: hormonal, immunohistochemical, and molecular studiesAnne Rod, Manuela Voicu, Laurence Chiche, et al.
European Journal of Endocrinology|November 1, 2008
Aromatase expression in the normal human adult adrenal and in adrenocortical tumors: biochemical, immunohistochemical, and molecular studiesFrançois Moreau, Hervé Mittre, Annie Benhaim, et al.
European Journal of Medical Genetics|April 19, 2019
Unusual clinical description of adult with Timothy syndrome, carrier of a new heterozygote mutation of CACNA1CCindy Colson, Hervé Mittre, Adeline Busson, et al.
Prenatal Diagnosis|October 26, 2011
Array CGH analysis in high-risk pregnancies: comparing DNA from cultured cells and cell-free fetal DNANicolas Gruchy, Matthieu Decamp, Nicolas Richard, et al.
The Journal of Steroid Biochemistry and Molecular Biology|May 23, 2009
cAMP-dependent regulation of CYP19 gene in rabbit preovulatory granulosa cells and corpus luteumThomas Andrieu, Vincenzo Pezzi, Rosa Sirianni, et al.
European Journal of Endocrinology|December 18, 2012
BMP system expression in GCs from polycystic ovary syndrome women and the in vitro effects of BMP4, BMP6, and BMP7 on GC steroidogenesisMohamad Khalaf, Julia Morera, Antoine Bourret, et al.
The Journal of Clinical Endocrinology and Metabolism|March 2, 2012
A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type IbNicolas Richard, Genevieve Abeguilé, Nadia Coudray, et al.
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