Hasil Pencarian - Cécile Ged

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  1. 1
    Xeroderma Pigmentosum C (XPC) Mutations in Primary Fibroblasts Impair Base Excision Repair Pathway and Increase Oxidative DNA Damage

    Xeroderma Pigmentosum C (XPC) Mutations in Primary Fibroblasts Impair Base Excision Repair Pathway and Increase Oxidative DNA Damage oleh Nour Fayyad, Farah Kobaisi, Farah Kobaisi, Farah Kobaisi, David Beal, Walid Mahfouf, Cécile Ged, Cécile Ged, Fanny Morice-Picard, Mohammad Fayyad-Kazan, Hussein Fayyad-Kazan, Bassam Badran, Hamid R. Rezvani, Hamid R. Rezvani, Walid Rachidi, Walid Rachidi

    Diterbitkan 2020-11-01
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  2. 2
    Xeroderma pigmentosum: clues to understanding cancer initiation

    Xeroderma pigmentosum: clues to understanding cancer initiation oleh Hamid Reza Rezvani, Frédéric Mazurier, Fanny Morice-Picard, Thomas Jouary, Muriel Cario-André, Cécile Ged, Hubert de Verneuil, Alain Taïeb

    Diterbitkan 2010-09-01
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  3. 3
    Identification of novel UROS mutations in a patient with congenital erythropoietic porphyria and efficient treatment by phlebotomy

    Identification of novel UROS mutations in a patient with congenital erythropoietic porphyria and efficient treatment by phlebotomy oleh Jean-Marc Blouin, Cécile Ged, Ganeko Bernardo-Seisdedos, Txomin Cabantous, Benoît Pinson, Antoine Poli, Hervé Puy, Oscar Millet, Laurent Gouya, Fanny Morice-Picard, Emmanuel Richard

    Diterbitkan 2021-06-01
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  4. 4
    Severe Perinatal Presentations of Günther’s Disease: Series of 20 Cases and Perspectives

    Severe Perinatal Presentations of Günther’s Disease: Series of 20 Cases and Perspectives oleh Claire Goudet, Cécile Ged, Audrey Petit, Chloe Desage, Perrine Mahe, Aicha Salhi, Ines Harzallah, Jean-Marc Blouin, Patrick Mercie, Caroline Schmitt, Antoine Poli, Laurent Gouya, Vincent Barlogis, Emmanuel Richard

    Diterbitkan 2024-01-01
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  5. 5
    The SLC40A1 R178Q mutation is a recurrent cause of hemochromatosis and is associated with a novel pathogenic mechanism

    The SLC40A1 R178Q mutation is a recurrent cause of hemochromatosis and is associated with a novel pathogenic mechanism oleh Chandran Ka, Julie Guellec, Xavier Pepermans, Caroline Kannengiesser, Cécile Ged, Wim Wuyts, David Cassiman, Victor de Ledinghen, Bruno Varet, Caroline de Kerguenec, Claire Oudin, Isabelle Gourlaouen, Thibaud Lefebvre, Claude Férec, Isabelle Callebaut, Gérald Le Gac

    Diterbitkan 2018-11-01
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  6. 6
    Phlebotomy as an efficient long-term treatment of congenital erythropoietic porphyria

    Phlebotomy as an efficient long-term treatment of congenital erythropoietic porphyria oleh Arienne Mirmiran, Antoine Poli, Cecile Ged, Caroline Schmitt, Thibaud Lefebvre, Hana Manceau, Raêd Daher, Boualem Moulouel, Katell Peoc'h, Sylvie Simonin, Jean-Marc Blouin, Jean-Charles Deybach, Gaël Nicolas, Hervé Puy, Emmanuel Richard, Laurent Gouya

    Diterbitkan 2020-01-01
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  7. 7
    Hemolytic anemia repressed hepcidin level without hepatocyte iron overload: lesson from Günther disease model

    Hemolytic anemia repressed hepcidin level without hepatocyte iron overload: lesson from Günther disease model oleh Sarah Millot, Constance Delaby, Boualem Moulouel, Thibaud Lefebvre, Nathalie Pilard, Nicolas Ducrot, Cécile Ged, Philippe Lettéron, Lucia de Franceschi, Jean Charles Deybach, Carole Beaumont, Laurent Gouya, Hubert De Verneuil, Saïd Lyoumi, Hervé Puy, Zoubida Karim

    Diterbitkan 2017-02-01
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  8. 8
    CRISPR-Cas9 genome editing induces megabase-scale chromosomal truncations

    CRISPR-Cas9 genome editing induces megabase-scale chromosomal truncations oleh Grégoire Cullot, Julian Boutin, Jérôme Toutain, Florence Prat, Perrine Pennamen, Caroline Rooryck, Martin Teichmann, Emilie Rousseau, Isabelle Lamrissi-Garcia, Véronique Guyonnet-Duperat, Alice Bibeyran, Magalie Lalanne, Valérie Prouzet-Mauléon, Béatrice Turcq, Cécile Ged, Jean-Marc Blouin, Emmanuel Richard, Sandrine Dabernat, François Moreau-Gaudry, Aurélie Bedel

    Diterbitkan 2019-03-01
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