Publications scientifiques

Publications

• 1998

  • Mutation analysis of the RSK2 gene in Coffin-Lowry patients: extensive allelic heterogeneity and a high rate of de novo mutations

    • Sylvie Jacquot
    • Karine Merienne
    • Dario de Cesare
    • S. Pannetier
    • Jean-Louis Mandel
    • Paolo Sassone-Corsi
    • Andre Hanauer

    American Journal of Human Genetics ; Volume: 63 ; Page: 1631-1640

    HAL DOI

  • Natural dietary polyphenolic compounds cause endothelium-dependent vasorelaxation in rat thoracic aorta.

    • E Andriambeloson
    • C Magnier
    • Gisele Haan-Archipoff
    • Annelise Lobstein
    • R Anton
    • Alain Beretz
    • Jc Stoclet
    • R Andriantsitohaina

    The Journal of Nutrition

    HAL DOI

  • Visual sensations produced by optic nerve stimulation using an implanted self-sizing spiral cuff electrode.

    • C. Veraart
    • C. Raftopoulos
    • J. T. Mortimer
    • J. Delbeke
    • D. Pins
    • G. Michaux
    • A. Vanlierde
    • S. Parrini
    • M. C. Wanet-Defalque

    Brain Research ; Volume: 813 ; Page: 181-6

    HAL

  • Positive autoregulation of the glial promoting factor glide/gcm

    • Alita Miller
    • Roberto Bernardoni
    • Angela Giangrande

    The EMBO Journal ; Volume: 17 ; Page: 6316-6326

    HAL DOI

  • Exon organisation of the mouse gene encoding the Adrenoleukodystrophy related protein (ALDRP)

    • Cyril Broccardo
    • Nathalie Troffer-Charlier
    • Stephane Savary
    • Jean-Louis Mandel
    • Giovanna Chimini

    European Journal of Human Genetics ; Volume: 6 ; Page: 638-641

    HAL DOI

  • Spatio-temporally-controlled somatic mutations in the mouse

    • Jacques Brocard Brocard
    • Xavier Warot
    • Olivia Wendling
    • Nadia Messaddeq
    • Jean-Luc Vonesch
    • Pierre Chambon
    • Daniel Metzger

    Pathologie Biologie ; Volume: 46 ; Page: 671-673

    HAL

  • Mutations in XPD helicase prevent its interaction and regulation by p44, another subunit of TFIIH, resulting in Xeroderma pigmentosum (XP) and trichothiodystrophy (TTD) phenotypes

    • Frédéric Coin
    • J. C. Marinoni
    • Jean-Marc Egly

    Pathologie Biologie ; Volume: 46 ; Page: 679-680

    HAL

  • Rapid immunoblot and kinase assay tests for a syndromal form of X linked mental retardation: Coffin-Lowry syndrome

    • Karine Merienne
    • Sylvie Jacquot
    • E. Trivier
    • S. Pannetier
    • A. Rossi
    • C. Scott
    • A. Schinzel
    • C. Castellan
    • W. Kress
    • Andre Hanauer

    Journal of Medical Genetics ; Volume: 35 ; Page: 890-894

    HAL DOI

  • CD4+ T cell responses in mice lacking MHC class II molecules specifically on B cells

    • G. Stuart Williams
    • Annette Oxenius
    • Hans Hengartner
    • Christophe Benoist
    • Diane Mathis

    European Journal of Immunology ; Volume: 28 ; Page: 3763-3772

    HAL DOI

  • Tetraspanin CD9 is associated with very late-acting integrins in human vascular smooth muscle cells and modulates collagen matrix reorganization.

    • A Scherberich
    • Sylvie Moog
    • Gisele Haan-Archipoff
    • D Azorsa
    • Francois Lanza
    • Alain Beretz

    Arteriosclerosis, Thrombosis, and Vascular Biology

    HAL DOI