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Material Type: Artigo
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Mutations in MRAP , encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2Chapple, J Paul ; Naville, Danielle ; Cooray, Sadani ; Metherell, Louise A ; Begeot, Martine ; Clark, Adrian J L ; Khoo, Bernard ; Nürnberg, Peter ; Rüschendorf, Franz ; David, Alessia ; Becker, Christian ; Huebner, Angela ; Cheetham, Michael ENature genetics, 2005-02, Vol.37 (2), p.166-170 [Periódico revisado por pares]London: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Metabolic Phenotyping of Adipose-Derived Stem Cells Reveals a Unique Signature and Intrinsic Differences between Fat PadsLefevre, Camille ; Panthu, Baptiste ; Naville, Danielle ; Guibert, Sylvie ; Pinteur, Claudie ; Elena-Herrmann, Bénédicte ; Vidal, Hubert ; Rautureau, Gilles J. P. ; Mey, Anne Harvey, Alexandra ; Alexandra HarveyStem cells international, 2019-01, Vol.2019, p.9323864-16 [Periódico revisado por pares]United States: HindawiTexto completo disponível |
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Material Type: Artigo
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Nonclassic Lipoid Congenital Adrenal Hyperplasia Masquerading as Familial Glucocorticoid DeficiencyMetherell, Louise A ; Naville, Danielle ; Halaby, George ; Begeot, Martine ; Huebner, Angela ; Nürnberg, Gudrun ; Nürnberg, Peter ; Green, Jane ; Tomlinson, Jeremy W ; Krone, Nils P ; Lin, Lin ; Racine, Michael ; Berney, Dan M ; Achermann, John C ; Arlt, Wiebke ; Clark, Adrian J. LThe journal of clinical endocrinology and metabolism, 2009-10, Vol.94 (10), p.3865-3871 [Periódico revisado por pares]Bethesda, MD: Endocrine SocietyTexto completo disponível |
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Material Type: Artigo
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Mutant WD-repeat protein in triple-A syndromeSalomon, Rémi ; Cattolico, Laurence ; Penet, Clothilde ; Bégeot, Martine ; Bakiri, Fawzi ; Munnich, Arnold ; Hadj-Rabia, Smaïl ; Naville, Danielle ; de Laet, Marc-Henri ; Nicolino, Marc ; Chaussain, Jean-Louis ; Chaouachi, Beji ; Brottier, Philippe ; Tullio-Pelet, Anna ; Mugnier, Claude ; Lyonnet, Stanislas ; Weissenbach, JeanNature genetics, 2000-11, Vol.26 (3), p.332-335 [Periódico revisado por pares]London: Nature Publishing GroupTexto completo disponível |
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Material Type: Artigo
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Study of the Alteration of Gene Expression in Adipose Tissue of Diet-Induced Obese Mice by Microarray and Reverse Transcription-Polymerase Chain Reaction AnalysesMoraes, R. C ; Blondet, A ; Birkenkamp-Demtroeder, K ; Tirard, J ; Orntoft, T. F ; Gertler, A ; Durand, P ; Naville, D ; Bégeot, MEndocrinology (Philadelphia), 2003-11, Vol.144 (11), p.4773-4782 [Periódico revisado por pares]Bethesda, MD: Endocrine SocietyTexto completo disponível |
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Material Type: Artigo
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Agouti-Related Protein Antagonizes Glucocorticoid Production Induced through Melanocortin 4 Receptor Activation in Bovine Adrenal Cells: A Possible Autocrine ControlDoghman, Mabrouka ; Delagrange, Philippe ; Blondet, Antonine ; Berthelon, Marie-Claude ; Durand, Philippe ; Naville, Danielle ; Bégeot, MartineEndocrinology (Philadelphia), 2004-02, Vol.145 (2), p.541-547 [Periódico revisado por pares]Bethesda, MD: Endocrine SocietyTexto completo disponível |
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Material Type: Artigo
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Relacion Entre La Densidad Óptima Agronomica Y El Número De Granos Por Planta En Maíz (Zea Maysl.)Cerliani, Cecilia ; Esposito, Gabriel P. ; Morla, Federico D. ; Balboa, Guillermo R. ; Naville, Rafael A.European Scientific Journal (Kocani), 2018-03, Vol.14 (9), p.29Texto completo disponível |
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Material Type: Artigo
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Linkage of one gene for familial glucocorticoid deficiency type 2 (FGD2) to chromosome 8q and further evidence of heterogeneityGENIN, Emmanuelle ; HUEBNER, Angela ; JAILLARD, Christine ; FAURE, Armelle ; HALABY, Georges ; SAKA, Nurcin ; CLARK, Adrian J. L ; DURAND, Philippe ; BEGEOT, Martine ; NAVILLE, DanielleHuman genetics, 2002-10, Vol.111 (4-5), p.428-434 [Periódico revisado por pares]Heidelberg: SpringerTexto completo disponível |
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Material Type: Artigo
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Demonstration by transfection studies that mutations in the adrenocorticotropin receptor gene are one cause of the hereditary syndrome of glucocorticoid deficiencyNAVILLE, D ; BARJHOUX, L ; JAILLARD, C ; FAURY, D ; DESPERT, F ; ESTEVA, B ; DURAND, P ; SAEZ, J. M ; BEGEOT, MThe journal of clinical endocrinology and metabolism, 1996-04, Vol.81 (4), p.1442-1448 [Periódico revisado por pares]Bethesda, MD: Endocrine SocietyTexto completo disponível |
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Material Type: Artigo
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Familial Glucocorticoid Deficiency Type 2 in Two NeonatesRamachandran, Pallath ; Penhoat, Armelle ; Naville, Danielle ; Begeot, Martine ; Osama Abdel-Wareth, Laila ; Reza Sedaghatian, MohamadJournal of Perinatology, 2003-01, Vol.23 (1), p.62-66 [Periódico revisado por pares]United States: Nature Publishing GroupTexto completo disponível |