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  • WDR34 mutations that cause short-rib polydactyly syndrome type III/severe asphyxiating thoracic dysplasia reveal a role for the NF-κB pathway in cilia.

    Céline Huber, Geneviève Baujat, Kim-Hanh Le Quan Sang, Arnold Munnich, Valérie Cormier-Daire

    Source :

    Am J Hum Genet

    2013 Nov 7

    Pmid / DOI:

    24183449

  • New perspectives on the treatment of skeletal dysplasia.

    Valérie Cormier-Daire

    Source :

    Ther Adv Endocrinol Metab. 2020

    2020 Jan 1

    Pmid / DOI:

    32166011

  • Kawasaki-like-Single_Cell

    Innovation

    Single cell analysis at the service of genetic diseases

  • single-cell

    Imagine Institute

    Inauguration of Single-Cell@Imagine

  • chercheurs scientifique

    Research Acceleration

    SOCS1: a newcomer in autoimmune diseases

  • Imagine Institute

    Group leader positions at Imagine, Institute for Genetic Diseases

  • Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.

    Olivia Boyer, Aude Servais, Olivier Gribouval, Patrick Nitschké, Corinne Antignac, Matias Simons

    Source :

    J Clin Invest

    2020 Jan 2

    Pmid / DOI:

    31613795

  • Research Acceleration

    Collaborative research

  • Coeur_NodalASELacZ

    Research Acceleration

    Where does the asymmetry of the heart come from?

  • Transient Nodal Signaling in Left Precursors Coordinates Opposed Asymmetries Shaping the Heart Loop.

    Audrey Desgrange, Ségolène Bernheim

    Source :

    Dev Cell

    2020 Nov 5

    Pmid / DOI:

    33171097

  • Care

    Achondroplasia: another step forward in treatment

  • Neural and behavioral signature of human social perception.

    Ana Saitovitch, Hervé Lemaître, Elza Rechtman, Alice Vinçon-Leite, Nathalie Boddaert, Monica Zilbovicius

    Source :

    Sci Rep

    2019 Jun 25

    Pmid / DOI:

    31239453