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1
Mutations in MRAP , encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2
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Mutations in MRAP , encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2

Chapple, 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 E

Nature genetics, 2005-02, Vol.37 (2), p.166-170 [Periódico revisado por pares]

London: Nature Publishing Group

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2
Mutant WD-repeat protein in triple-A syndrome
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Mutant WD-repeat protein in triple-A syndrome

Salomon, 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, Jean

Nature genetics, 2000-11, Vol.26 (3), p.332-335 [Periódico revisado por pares]

London: Nature Publishing Group

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3
Identification of Urop11, a novel leptin-modulated gene that is upregulated in the hypothalamus of mice with virus-induced obesity
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Identification of Urop11, a novel leptin-modulated gene that is upregulated in the hypothalamus of mice with virus-induced obesity

Verlaeten, O ; Casery, C ; Cavagna, S ; Naville, D ; Giraudon, P ; Belin, M F ; Begeot, M ; Bernard, A

Journal of molecular endocrinology, 2007, Vol.38 (1), p.3-17 [Periódico revisado por pares]

England: BioScientifica

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4
Expression of the human melanocortin-4 receptor gene is controlled by several members of the Sp transcription factor family
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Expression of the human melanocortin-4 receptor gene is controlled by several members of the Sp transcription factor family

Blondet, A ; Gout, J ; Durand, P ; Bégeot, M ; Naville, D

Journal of molecular endocrinology, 2005-04, Vol.34 (2), p.317-329 [Periódico revisado por pares]

England: BioScientifica

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5
Demonstration by transfection studies that mutations in the adrenocorticotropin receptor gene are one cause of the hereditary syndrome of glucocorticoid deficiency
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Demonstration by transfection studies that mutations in the adrenocorticotropin receptor gene are one cause of the hereditary syndrome of glucocorticoid deficiency

NAVILLE, D ; BARJHOUX, L ; JAILLARD, C ; FAURY, D ; DESPERT, F ; ESTEVA, B ; DURAND, P ; SAEZ, J. M ; BEGEOT, M

The journal of clinical endocrinology and metabolism, 1996-04, Vol.81 (4), p.1442-1448 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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6
Presence of multiple functional polyadenylation signals in the 3′-untranslated region of human corticotropin receptor cDNA
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Presence of multiple functional polyadenylation signals in the 3′-untranslated region of human corticotropin receptor cDNA

Penhoat, Armelle ; Naville, Danielle ; Jaillard, Christine ; Durand, Philippe ; Bégeot, Martine

Biochimica et biophysica acta. Molecular cell research, 1997-05, Vol.1356 (3), p.249-252 [Periódico revisado por pares]

Elsevier B.V

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7
Activator protein‐1 is necessary for angiotensin‐II stimulation of human adrenocorticotropin receptor gene transcription
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Activator protein‐1 is necessary for angiotensin‐II stimulation of human adrenocorticotropin receptor gene transcription

Naville, Danielle ; Bordet, Estelle ; Berthelon, Marie‐Claude ; Durand, Philippe ; Bégeot, Martine

European Journal of Biochemistry, 2001-03, Vol.268 (6), p.1802-1810 [Periódico revisado por pares]

Oxford, UK: Blackwell Science Ltd

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