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Optimized approach for the identification of highly efficient correctors of nonsense mutations in human diseases.
Benhabiles, Hana; Gonzalez-Hilarion, Sara; Amand, Séverine; Bailly, Christine; Prévotat, Anne; Reix, Philippe; Hubert, Dominique; Adriaenssens, Eric; Rebuffat, Sylvie; Tulasne, David; Lejeune, Fabrice.
Afiliação
  • Benhabiles H; Univ. Lille, CNRS, Institut Pasteur de Lille, UMR 8161-M3T -Mechanisms of Tumorigenesis and Target Therapies, Lille, France.
  • Gonzalez-Hilarion S; Univ. Lille, CNRS, Institut Pasteur de Lille, UMR 8161-M3T -Mechanisms of Tumorigenesis and Target Therapies, Lille, France.
  • Amand S; Muséum National d'Histoire Naturelle, Sorbonne Universités, Centre National de la Recherche Scientifique, Laboratoire Molécules de Communication et Adaptation des Microorganismes (MCAM), UMR 7245 CNRS-MNHN, CP 54, Paris, France.
  • Bailly C; Muséum National d'Histoire Naturelle, Sorbonne Universités, Centre National de la Recherche Scientifique, Laboratoire Molécules de Communication et Adaptation des Microorganismes (MCAM), UMR 7245 CNRS-MNHN, CP 54, Paris, France.
  • Prévotat A; Univ. Lille, Clinique des Maladies Respiratoires, CRCM Hôpital Calmette, CHRU Lille, France.
  • Reix P; Hospices Civils de Lyon, Centre de Référence Mucoviscidose, Lyon, France.
  • Hubert D; Pulmonary Department and Adult CF Centre, Cochin Hospital, AP-HP, Paris, France.
  • Adriaenssens E; INSERM U908, Cell plasticity and Cancer, University of Lille, Villeneuve d'Ascq, France.
  • Rebuffat S; Muséum National d'Histoire Naturelle, Sorbonne Universités, Centre National de la Recherche Scientifique, Laboratoire Molécules de Communication et Adaptation des Microorganismes (MCAM), UMR 7245 CNRS-MNHN, CP 54, Paris, France.
  • Tulasne D; Univ. Lille, CNRS, Institut Pasteur de Lille, UMR 8161-M3T -Mechanisms of Tumorigenesis and Target Therapies, Lille, France.
  • Lejeune F; Univ. Lille, CNRS, Institut Pasteur de Lille, UMR 8161-M3T -Mechanisms of Tumorigenesis and Target Therapies, Lille, France.
PLoS One ; 12(11): e0187930, 2017.
Article em En | MEDLINE | ID: mdl-29131862
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Códon sem Sentido / Predisposição Genética para Doença Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: França
Texto completo
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XML
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Códon sem Sentido / Predisposição Genética para Doença Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: França