Martine Bégeot

Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2

Louise Metherell, J. Paul Chapple, Sadani N. Cooray et al. · Nature Genetics · 2005 · 446 citations

Life Sciences, Endocrinology, Genetics +13

Mutant WD-repeat protein in triple-A syndrome

A Tullio-Pelet, Rémi Salomon, S. Hadj‐Rabia et al. · Nature Genetics · 2000 · 320 citations

Life Sciences, Genetics, Molecular Genetics +9

Nonclassic Lipoid Congenital Adrenal Hyperplasia Masquerading as Familial Glucocorticoid Deficiency

Louise Metherell, Danielle Naville, G Halaby et al. · The Journal of Clinical Endocrinology & Metabolism · 2009 · 159 citations · Full text

Medicine, Endocrinology, Genetics +17

Regulation of corticotropin receptor number and messenger RNA in cultured human adrenocortical cells by corticotropin and angiotensin II.

M C Lebrethon, Danielle Naville, Martine Bégeot et al. · Journal of Clinical Investigation · 1994 · 155 citations · Full text

Life Sciences, Endocrinology, Physiology +15

Study of the Alteration of Gene Expression in Adipose Tissue of Diet-Induced Obese Mice by Microarray and Reverse Transcription-Polymerase Chain Reaction Analyses

Ricardo Moraes, Antonine Blondet, J. Tirard et al. · Endocrinology · 2003 · 141 citations · Full text

Life Sciences, Molecular Biology, Physiology +17