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Functional assessment of disease-associated regulatory variants in vivo using a versatile dual colour transgenesis strategy in zebrafish.
Bhatia, Shipra; Gordon, Christopher T; Foster, Robert G; Melin, Lucie; Abadie, Véronique; Baujat, Geneviève; Vazquez, Marie-Paule; Amiel, Jeanne; Lyonnet, Stanislas; van Heyningen, Veronica; Kleinjan, Dirk A.
Afiliação
  • Bhatia S; MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
  • Gordon CT; INSERM U781, Hôpital Necker-Enfants Malades and Université Paris Descartes-Sorbonne Paris Cité, Institute Imagine, Paris, France.
  • Foster RG; MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
  • Melin L; INSERM U781, Hôpital Necker-Enfants Malades and Université Paris Descartes-Sorbonne Paris Cité, Institute Imagine, Paris, France.
  • Abadie V; Service de Pédiatrie Générale, Université Paris Descartes, Hôpital Necker-Enfants Malades, Paris, France.
  • Baujat G; Departement de Génétique, Hôpital Necker-Enfants Malades, AP-HP, Paris France.
  • Vazquez MP; Service de Chirurgie Maxillo-Faciale et Plastique, CRMR des Malformations de la Face et de la Cavité Buccale, Hôpital Necker-Enfants Malades, Paris, France.
  • Amiel J; INSERM U781, Hôpital Necker-Enfants Malades and Université Paris Descartes-Sorbonne Paris Cité, Institute Imagine, Paris, France; Departement de Génétique, Hôpital Necker-Enfants Malades, AP-HP, Paris France.
  • Lyonnet S; INSERM U781, Hôpital Necker-Enfants Malades and Université Paris Descartes-Sorbonne Paris Cité, Institute Imagine, Paris, France; Departement de Génétique, Hôpital Necker-Enfants Malades, AP-HP, Paris France.
  • van Heyningen V; MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
  • Kleinjan DA; MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
PLoS Genet ; 11(6): e1005193, 2015 Jun.
Article em En | MEDLINE | ID: mdl-26030420
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Pierre Robin / Transgenes / Elementos Reguladores de Transcrição Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Pierre Robin / Transgenes / Elementos Reguladores de Transcrição Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article