Resultats de la cerca - Clauser, Eric

Systematic identification of mutations that constitutively activate the angiotensin II type 1A receptor by screening a randomly mutated cDNA library with an original pharmacologica... per Parnot, Charles, Bardin, Sabine, Miserey-Lenkei, Stéphanie, Guedin, Denis, Corvol, Pierre, Clauser, Eric

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Severe Arterial Hypertension from Cullin 3 Mutations Is Caused by Both Renal and Vascular Effects per Abdel Khalek, Waed, Rafael, Chloé, Loisel-Ferreira, Irmine, Kouranti, Ilektra, Clauser, Eric, Hadchouel, Juliette, Jeunemaitre, Xavier

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Cullin 3 Exon 9 Deletion in Familial Hyperkalemic Hypertension Impairs Cullin3-Ring-E3 Ligase (CRL3) Dynamic Regulation and Cycling per Kouranti, Ilektra, Abdel Khalek, Waed, Mazurkiewicz, Stephani, Loisel-Ferreira, Irmine, Gautreau, Alexis M., Pintard, Lionel, Jeunemaitre, Xavier, Clauser, Eric

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Systematic Analysis of G Protein-Coupled Receptor Gene Expression in Adrenocorticotropin-Independent Macronodular Adrenocortical Hyperplasia Identifies Novel Targets for Pharmacolo... per Assie, Guillaume, Louiset, Estelle, Sturm, Nathalie, Rénée-Corail, Fernande, Groussin, Lionel, Bertherat, Jerôme, Thomas, Michaël, Lefebvre, Hervé, Feige, Jean-Jacques, Clauser, Eric, Chabre, Olivier, Cherradi, Nadia

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ACTH-Independent Cushing’s Syndrome with Bilateral Micronodular Adrenal Hyperplasia and Ectopic Adrenocortical Adenoma per Louiset, Estelle, Gobet, Françoise, Libé, Rossella, Horvath, Anelia, Renouf, Sylvie, Cariou, Juliette, Rothenbuhler, Anya, Bertherat, Jérôme, Clauser, Eric, Grise, Philippe, Stratakis, Constantine A., Kuhn, Jean-Marc, Lefebvre, Hervé

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Gain-of-function mutant of angiotensin II receptor, type 1A, causes hypertension and cardiovascular fibrosis in mice per Billet, Sandrine, Bardin, Sabine, Verp, Sonia, Baudrie, Véronique, Michaud, Annie, Conchon, Sophie, Muffat-Joly, Martine, Escoubet, Brigitte, Souil, Evelyne, Hamard, Ghislaine, Bernstein, Kenneth E., Gasc, Jean Marie, Elghozi, Jean-Luc, Corvol, Pierre, Clauser, Eric

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Mutations and Polymorphisms in the Gene Encoding Regulatory Subunit Type 1-alpha of Protein Kinase A (PRKAR1A): An Update per Horvath, Anélia, Bertherat, Jérôme, Groussin, Lionel, Guillaud-Bataille, Marine, Tsang, Kitman, Cazabat, Laure, Libe, Rosella, Remmers, Elaine, René-Corail, Fernande, Faucz, Fabio Rueda, Clauser, Eric, Calender, Alain, Bertagna, Xavier, Carney, J Aidan, Stratakis, Constantine A.

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Mutations in Regulatory Subunit Type 1A of Cyclic Adenosine 5′-Monophosphate-Dependent Protein Kinase (PRKAR1A): Phenotype Analysis in 353 Patients and 80 Different Genotypes per Bertherat, Jérôme, Horvath, Anélia, Groussin, Lionel, Grabar, Sophie, Boikos, Sosipatros, Cazabat, Laure, Libe, Rosella, René-Corail, Fernande, Stergiopoulos, Sotirios, Bourdeau, Isabelle, Bei, Thalia, Clauser, Eric, Calender, Alain, Kirschner, Lawrence S., Bertagna, Xavier, Carney, J. Aidan, Stratakis, Constantine A.

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IGF2 Promotes Growth of Adrenocortical Carcinoma Cells, but Its Overexpression Does Not Modify Phenotypic and Molecular Features of Adrenocortical Carcinoma per Guillaud-Bataille, Marine, Ragazzon, Bruno, de Reyniès, Aurélien, Chevalier, Claire, Francillard, Isabelle, Barreau, Olivia, Steunou, Virginie, Guillemot, Johann, Tissier, Frédérique, Rizk-Rabin, Marthe, René-Corail, Fernande, Ghuzlan, Abir Al, Assié, Guillaume, Bertagna, Xavier, Baudin, Eric, Le Bouc, Yves, Bertherat, Jérôme, Clauser, Eric

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Frequent Phosphodiesterase 11A Gene (PDE11A) Defects in Patients with Carney Complex (CNC) Caused by PRKAR1A Mutations: PDE11A May Contribute to Adrenal and Testicular Tumors in CN... per Libé, Rossella, Horvath, Anelia, Vezzosi, Delphine, Fratticci, Amato, Coste, Joel, Perlemoine, Karine, Ragazzon, Bruno, Guillaud-Bataille, Marine, Groussin, Lionel, Clauser, Eric, Raffin-Sanson, Marie-Laure, Siegel, Jennifer, Moran, Jason, Drori-Herishanu, Limor, Faucz, Fabio Rueda, Lodish, Maya, Nesterova, Maria, Bertagna, Xavier, Bertherat, Jerome, Stratakis, Constantine A.

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TREM-1 orchestrates angiotensin II–induced monocyte trafficking and promotes experimental abdominal aortic aneurysm per Vandestienne, Marie, Zhang, Yujiao, Santos-Zas, Icia, Al-Rifai, Rida, Joffre, Jeremie, Giraud, Andreas, Laurans, Ludivine, Esposito, Bruno, Pinet, Florence, Bruneval, Patrick, Raffort, Juliette, Lareyre, Fabien, Vilar, Jose, Boufenzer, Amir, Guyonnet, Lea, Guerin, Coralie, Clauser, Eric, Silvestre, Jean-Sébastien, Lang, Sylvie, Soulat-Dufour, Laurie, Tedgui, Alain, Mallat, Ziad, Taleb, Soraya, Boissonnas, Alexandre, Derive, Marc, Chinetti, Giulia, Ait-Oufella, Hafid

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Adrenal GIPR expression and chromosome 19q13 microduplications in GIP-dependent Cushing’s syndrome per Lecoq, Anne-Lise, Stratakis, Constantine A., Viengchareun, Say, Chaligné, Ronan, Tosca, Lucie, Deméocq, Vianney, Hage, Mirella, Berthon, Annabel, Faucz, Fabio R., Hanna, Patrick, Boyer, Hadrien-Gaël, Servant, Nicolas, Salenave, Sylvie, Tachdjian, Gérard, Adam, Clovis, Benhamo, Vanessa, Clauser, Eric, Guiochon-Mantel, Anne, Young, Jacques, Lombès, Marc, Bourdeau, Isabelle, Maiter, Dominique, Tabarin, Antoine, Bertherat, Jérôme, Lefebvre, Hervé, de Herder, Wouter, Louiset, Estelle, Lacroix, André, Chanson, Philippe, Bouligand, Jérôme, Kamenický, Peter

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Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosis per Louis-Dit-Picard, Hélène, Kouranti, Ilektra, Rafael, Chloé, Loisel-Ferreira, Irmine, Chavez-Canales, Maria, Abdel-Khalek, Waed, Argaiz, Eduardo R., Baron, Stéphanie, Vacle, Sarah, Migeon, Tiffany, Coleman, Richard, Do Cruzeiro, Marcio, Hureaux, Marguerite, Thurairajasingam, Nirubiah, Decramer, Stéphane, Girerd, Xavier, O’Shaugnessy, Kevin, Mulatero, Paolo, Roussey, Gwenaëlle, Tack, Ivan, Unwin, Robert, Vargas-Poussou, Rosa, Staub, Olivier, Grimm, Richard, Welling, Paul A., Gamba, Gerardo, Clauser, Eric, Hadchouel, Juliette, Jeunemaitre, Xavier

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