Hasil Pencarian - Delphine Chamousset

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  1. 1
    Taperin (c9orf75), a mutated gene in nonsyndromic deafness, encodes a vertebrate specific, nuclear localized protein phosphatase one alpha (PP1α) docking protein

    Taperin (c9orf75), a mutated gene in nonsyndromic deafness, encodes a vertebrate specific, nuclear localized protein phosphatase one alpha (PP1α) docking protein oleh Tony Ferrar, Delphine Chamousset, Veerle De Wever, Mhairi Nimick, Jens Andersen, Laura Trinkle-Mulcahy, Greg B. G. Moorhead

    Diterbitkan 2012-02-01
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  2. 2
    Diagnosis of Fanconi anemia in patients with bone marrow failure

    Diagnosis of Fanconi anemia in patients with bone marrow failure oleh Fernando O. Pinto, Thierry Leblanc, Delphine Chamousset, Gwenaelle Le Roux, Benoit Brethon, Bruno Cassinat, Jérôme Larghero, Jean-Pierre de Villartay, Dominique Stoppa-Lyonnet, André Baruchel, Gérard Socié, Eliane Gluckman, Jean Soulier

    Diterbitkan 2009-04-01
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  3. 3
    Single-cell absolute contact probability detection reveals chromosomes are organized by multiple low-frequency yet specific interactions

    Single-cell absolute contact probability detection reveals chromosomes are organized by multiple low-frequency yet specific interactions oleh Diego I. Cattoni, Andrés M. Cardozo Gizzi, Mariya Georgieva, Marco Di Stefano, Alessandro Valeri, Delphine Chamousset, Christophe Houbron, Stephanie Déjardin, Jean-Bernard Fiche, Inma González, Jia-Ming Chang, Thomas Sexton, Marc A. Marti-Renom, Frédéric Bantignies, Giacomo Cavalli, Marcelo Nollmann

    Diterbitkan 2017-11-01
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