C Silve

Summary

Country: France

Publications

  1. ncbi request reprint Methylation and transcripts expression at the imprinted GNAS locus in human embryonic and induced pluripotent stem cells and their derivatives
    Virginie Grybek
    INSERM U986, Hopital Bicetre, Le Kremlin Bicêtre 94276, France
    Stem Cell Reports 3:432-43. 2014
  2. ncbi request reprint Acrodysostosis
    C Silve
    INSERM U986, Centre de Référence des Maladies Rares du Métabolisme du Calcium et du Phosphore, Hopital de Bicetre, Le Kremlin Bicetre, France
    Horm Metab Res 44:749-58. 2012
  3. ncbi request reprint PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistance
    Agnes Linglart
    Institut National de la Santé et de la Recherche Médicale Unité 986 et Centre de Reference des Maladies Rares du Phosphate et du Calcium, Hopital de Bicetre, 94276 Le Kremlin Bicetre Cedex, France
    J Clin Endocrinol Metab 97:E2328-38. 2012

Collaborators

  • Agnes Linglart
  • Virginie Grybek
  • Mathilde Girard
  • Laetitia Aubry
  • Catherine Le Stunff
  • Cécile Denis
  • Stéphanie Maupetit-Méhouas
  • Bruno LeHeup
  • Annette Richter-Unruh
  • Jesus Argente
  • Dorothée Schmidt
  • Guylene Bertrand
  • Paul Martin Holterhus
  • Giovanna Mantovani
  • Virginie Chassot
  • Emese Boros
  • Claudine Heinrichs
  • Marco Castori
  • Philippe Wicart
  • Eric Clauser
  • Arrate Pereda
  • Sara Berrade
  • Yasemin Gunes
  • Alma Kuechler
  • Guiomar Perez de Nanclares
  • Helena Fryssira
  • María Teresa Muñoz-Calvo
  • Oscar Rubio-Cabezas
  • Olaf Hiort
  • Pierre Bougneres

Detail Information

Publications3

  1. ncbi request reprint Methylation and transcripts expression at the imprinted GNAS locus in human embryonic and induced pluripotent stem cells and their derivatives
    Virginie Grybek
    INSERM U986, Hopital Bicetre, Le Kremlin Bicêtre 94276, France
    Stem Cell Reports 3:432-43. 2014
    ....
  2. ncbi request reprint Acrodysostosis
    C Silve
    INSERM U986, Centre de Référence des Maladies Rares du Métabolisme du Calcium et du Phosphore, Hopital de Bicetre, Le Kremlin Bicetre, France
    Horm Metab Res 44:749-58. 2012
    ....
  3. ncbi request reprint PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistance
    Agnes Linglart
    Institut National de la Santé et de la Recherche Médicale Unité 986 et Centre de Reference des Maladies Rares du Phosphate et du Calcium, Hopital de Bicetre, 94276 Le Kremlin Bicetre Cedex, France
    J Clin Endocrinol Metab 97:E2328-38. 2012
    ..Acrodysostosis is genetically heterogeneous because it results from heterozygous mutations in PRKAR1A or PDE4D, two key actors in the GPCR-cAMP-protein kinase A pathway...