Resultados de procura - Jean‐Pierre Salles

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  1. 1
    Hypophosphatasia: Biological and Clinical Aspects, Avenues for Therapy

    Hypophosphatasia: Biological and Clinical Aspects, Avenues for Therapy por Jean‐Pierre Salles

    Publicado 2020
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  2. 2
    A Novel Role for Gab1 and SHP2 in Epidermal Growth Factor-induced Ras Activation

    A Novel Role for Gab1 and SHP2 in Epidermal Growth Factor-induced Ras Activation por Alexandra Montagner, Armelle Yart, Marie Dance, Bertrand Perret, Jean‐Pierre Salles, Patrick Raynal

    Publicado 2004
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  3. 3
    SHIP-2 and PTEN Are Expressed and Active in Vascular Smooth Muscle Cell Nuclei, but Only SHIP-2 Is Associated with Nuclear Speckles

    SHIP-2 and PTEN Are Expressed and Active in Vascular Smooth Muscle Cell Nuclei, but Only SHIP-2 Is Associated with Nuclear Speckles por Paul Déléris, Daniel Bacqueville, Stéphanie Gayral, Laurent Carrez, Jean‐Pierre Salles, Bertrand Perret, Monique Breton‐Douillon

    Publicado 2003
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  4. 4
    Hyperghrelinemia Precedes Obesity in Prader-Willi Syndrome

    Hyperghrelinemia Precedes Obesity in Prader-Willi Syndrome por Eva Feigerlová, Gwénaëlle Diene, F. Conte-Auriol, Catherine Molinas, Isabelle Gennero, Jean‐Pierre Salles, Catherine Arnaud, Maïthé Tauber

    Publicado 2008
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  5. 5
    Molecular markers of cartilage breakdown and synovitis at baseline as predictors of structural progression of hip osteoarthritis. The ECHODIAH Cohort

    Molecular markers of cartilage breakdown and synovitis at baseline as predictors of structural progression of hip osteoarthritis. The ECHODIAH Cohort por B Mazières, Patrick Garnero, A Guéguen, M. Abbal, Laurent Berdah, M Lequesne, Minh Nguyen, Jean‐Pierre Salles, E. Vignon, Maxime Dougados

    Publicado 2005
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  6. 6
    PLD2 is enriched on exosomes and its activity is correlated to the release of exosomes

    PLD2 is enriched on exosomes and its activity is correlated to the release of exosomes por Karine Laulagnier, David Grand, Arnaud Dujardin, Safouane M. Hamdi, Hélène Vincent-Schneider, Danielle Lankar, Jean‐Pierre Salles, Christian Bonnerot, Bertrand Perret, Michel Record

    Publicado 2004
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  7. 7
    Mast cell- and dendritic cell-derived exosomes display a specific lipid composition and an unusual membrane organization

    Mast cell- and dendritic cell-derived exosomes display a specific lipid composition and an unusual membrane organization por Karine Laulagnier, Claude Motta, Safouane M. Hamdi, Sébastien Roy, Florence Fauvelle, Jean‐François Pageaux, Toshihide Kobayashi, Jean‐Pierre Salles, Bertrand Perret, Christian Bonnerot, Michel Record

    Publicado 2004
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  8. 8
    Pituitary Stalk Interruption Syndrome from Infancy to Adulthood: Clinical, Hormonal, and Radiological Assessment According to the Initial Presentation

    Pituitary Stalk Interruption Syndrome from Infancy to Adulthood: Clinical, Hormonal, and Radiological Assessment According to the Initial Presentation por Céline Bar, Charline Zadro, Gwénaëlle Diene, Isabelle Oliver, Catherine Pienkowski, Béatrice Jouret, Audrey Cartault, Zeina Ajaltouni, Jean‐Pierre Salles, Annick Sévely, Maïthé Tauber, Thomas Édouard

    Publicado 2015
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  9. 9
    Lysophosphatidic acid as a phospholipid mediator: pathways of synthesis

    Lysophosphatidic acid as a phospholipid mediator: pathways of synthesis por Frédérique Gaits‐Iacovoni, Olivier Fourcade, François Le Balle, G. Guéguen, Bernadette Gaigé, Ama Gassama‐Diagne, Josette Fauvel, Jean‐Pierre Salles, Gérard Mauco, Marie‐Françoise Simon, Hugues Chap

    Publicado 1997
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  10. 10
    Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome

    Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome por Éric Bieth, Sanaa Eddiry, Véronique Gaston, F. Lorenzini, Alexandre Buffet, Françoise Auriol, Catherine Molinas, Dorothée Cailley, Caroline Rooryck, Benoı̂t Arveiler, Jérôme Cavaillé, Jean‐Pierre Salles, Maïthé Tauber

    Publicado 2014
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  11. 11
    Functional Effects of <i>PTPN11</i> (SHP2) Mutations Causing LEOPARD Syndrome on Epidermal Growth Factor-Induced Phosphoinositide 3-Kinase/AKT/Glycogen Synthase Kinase 3β Signaling

    Functional Effects of <i>PTPN11</i> (SHP2) Mutations Causing LEOPARD Syndrome on Epidermal Growth Factor-Induced Phosphoinositide 3-Kinase/AKT/Glycogen Synthase Kinase 3β Signaling... por Thomas Édouard, Jean-Philippe Combier, Audrey Nédélec, Sophie Bel-Vialar, Mélanie Metrich, F. Conte-Auriol, Stanislas Lyonnet, Béatrice Parfait, Maïthé Tauber, Jean‐Pierre Salles, Frank Lezoualc’h, Armelle Yart, Patrick Raynal

    Publicado 2010
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  12. 12
    Noonan syndrome-causing SHP2 mutants inhibit insulin-like growth factor 1 release via growth hormone-induced ERK hyperactivation, which contributes to short stature

    Noonan syndrome-causing SHP2 mutants inhibit insulin-like growth factor 1 release via growth hormone-induced ERK hyperactivation, which contributes to short stature por Audrey De Rocca Serra-Nédélec, Thomas Édouard, Karine Tréguer, Mylène Tajan, Toshiyuki Araki, Marie Dance, Marianne Mus, Alexandra Montagner, M. Tauber, Jean‐Pierre Salles, Philippe Valet, Benjamin G. Neel, Patrick Raynal, Armelle Yart

    Publicado 2012
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  13. 13
    Vitamin D and calcium intakes in general pediatric populations: A French expert consensus paper

    Vitamin D and calcium intakes in general pediatric populations: A French expert consensus paper por Justine Bacchetta, Thomas Édouard, Gilles Laverny, Julie Bernardor, Aurélia Bertholet‐Thomas, Mireille Castanet, C. Garnier, Isabelle Gennero, J. Harambat, Alexandre Lapillonne, Arnaud Molin, C. Naud, Jean‐Pierre Salles, Sophie Laborie, Patrick Tounian, Agnès Linglart

    Publicado 2022
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  14. 14
    Absence of the lysophosphatidic acid receptor LPA1 results in abnormal bone development and decreased bone mass

    Absence of the lysophosphatidic acid receptor LPA1 results in abnormal bone development and decreased bone mass por Isabelle Gennero, Sara Laurencin‐Dalicieux, F. Conte-Auriol, Fabienne Briand‐Mésange, Danielle Laurencin, Jackie Rue, Nicolas Beton, Nicole Malet, Marianne Mus, Akira Tokumura, Philippe Bourin, Laurence Vico, G Brunel, Richard O. C. Oreffo, Jerold Chun, Jean‐Pierre Salles

    Publicado 2011
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  15. 15
    Growth patterns of patients with Noonan syndrome: correlation with age and genotype

    Growth patterns of patients with Noonan syndrome: correlation with age and genotype por Catie Cessans, Virginie Ehlinger, Catherine Arnaud, Armelle Yart, Yline Capri, Pascal Barat, B. Cammas, Didier Lacombe, R. Coutant, Albert David, Sabine Baron, Jacques Weill, Bruno Leheup, Marc Nicolino, Jean‐Pierre Salles, Alain Verloès, Maïthé Tauber, Hélène Cavé, Thomas Édouard

    Publicado 2016
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  16. 16
    LEOPARD syndrome-associated SHP2 mutation confers leanness and protection from diet-induced obesity

    LEOPARD syndrome-associated SHP2 mutation confers leanness and protection from diet-induced obesity por Mylène Tajan, Aurélie Batut, Thomas Cadoudal, Simon Deleruyelle, Sophie Le Gonidec, Céline Saint-Laurent, Maëlle Vomscheid, Estelle Wanecq, Karine Tréguer, Audrey De Rocca Serra-Nédélec, Claire Vinel, Marie-Adeline Marquès, Joffrey Pozzo, Oksana Kunduzova, Jean‐Pierre Salles, Maïthé Tauber, Patrick Raynal, Hélène Cavé, Thomas Édouard, Philippe Valet, Armelle Yart

    Publicado 2014
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  17. 17
    The Use of Oxytocin to Improve Feeding and Social Skills in Infants With Prader–Willi Syndrome

    The Use of Oxytocin to Improve Feeding and Social Skills in Infants With Prader–Willi Syndrome por Maïthé Tauber, Kader Boulanouar, Gwénaëlle Diene, Sophie Çabal-Berthoumieu, Virginie Ehlinger, Pascale Fichaux-Bourin, Catherine Molinas, Sandy Faye, Marion Valette, Jeanne Pourrinet, Catie Cessans, Sylvie Viaux‐Savelon, Céline Bascoul, Antoine Guédeney, Patric J. D. Delhanty, Vincent Geenen, Henri Martens, Françoise Muscatelli, David Cohen, Angèle Consoli, Pierre Payoux, Catherine Arnaud, Jean‐Pierre Salles

    Publicado 2017
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  18. 18
    Molecular diagnosis of hypophosphatasia and differential diagnosis by targeted Next Generation Sequencing

    Molecular diagnosis of hypophosphatasia and differential diagnosis by targeted Next Generation Sequencing por A. Taillandier, Christelle Domingues, Clémence De Cazanove, Valérie Porquet‐Bordes, Sophie Monnot, Tina Kiffer-Moreira, Agnès Rothenbuhler, Pascal Guggenbuhl, Catherine Cormier, Geneviève Baujat, Françoise Debiais, Yline Capri, Martine Cohen‐Solal, P. Parent, Jean Chiésa, Anne Dieux, Florence Petit, J. Roume, Monica Isnard, Valérie Cormier‐Daire, Agnès Linglart, José Luís Millán, Jean‐Pierre Salles, Christine Muti, Brigitte Simon‐Bouy, Étienne Mornet

    Publicado 2015
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  19. 19
    Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome

    Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome por Lisa C. Burnett, Charles A. LeDuc, Carlos R. Sulsona, Daniel Paull, Richard Rausch, Sanaa Eddiry, Jayne F. Martin Carli, Michael V. Morabito, Alicja A. Skowronski, Gabriela Hubner, Matthew Zimmer, Liheng Wang, Richard O. Day, Brynn Levy, Ilene Fennoy, B. Dubern, Christine Poitou, Karine Clément, Merlin G. Butler, Michael Rosenbaum, Jean‐Pierre Salles, Maïthé Tauber, Daniel J. Driscoll, Dieter Egli, Rudolph L. Leibel

    Publicado 2016
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  20. 20
    Infigratinib in children with achondroplasia: the PROPEL and PROPEL 2 studies

    Infigratinib in children with achondroplasia: the PROPEL and PROPEL 2 studies por Ravi Savarirayan, Josep Maria De Bergua, Paul Arundel, Helen McDevitt, Valérie Cormier‐Daire, Vrinda Saraff, Mars Skae, Borja Delgado, Antonio Leiva-Gea, Fernando Santos‐Simarro, Jean‐Pierre Salles, Marc Nicolino, Massimiliano Rossi, Pekka Kannus, Michael B. Bober, John A. Phillips, Howard M. Saal, Paul Harmatz, Christine Burren, Garrett Gotway, Terry Cho, Elena Muslimova, Richard Weng, Daniela Rogoff, Julie Hoover‐Fong, Melita Irving

    Publicado 2022
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