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Loss of FTO antagonises Wnt signaling and leads to developmental defects associated with ciliopathies.
Osborn, Daniel P S; Roccasecca, Rosa Maria; McMurray, Fiona; Hernandez-Hernandez, Victor; Mukherjee, Sriparna; Barroso, Inês; Stemple, Derek; Cox, Roger; Beales, Philip L; Christou-Savina, Sonia.
Afiliación
  • Osborn DP; Biomedical Sciences, St George's University of London, London, United Kingdom.
  • Roccasecca RM; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, United Kingdom.
  • McMurray F; Harwell Science and Innovation Campus, MRC Harwell, Harwell, United Kingdom.
  • Hernandez-Hernandez V; Molecular Medicine Unit, Institute of Child Health, University College London, London, United Kingdom.
  • Mukherjee S; Molecular Medicine Unit, Institute of Child Health, University College London, London, United Kingdom.
  • Barroso I; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, United Kingdom ; University of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, United Kingdom.
  • Stemple D; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, United Kingdom.
  • Cox R; Harwell Science and Innovation Campus, MRC Harwell, Harwell, United Kingdom.
  • Beales PL; Molecular Medicine Unit, Institute of Child Health, University College London, London, United Kingdom.
  • Christou-Savina S; Molecular Medicine Unit, Institute of Child Health, University College London, London, United Kingdom.
PLoS One ; 9(2): e87662, 2014.
Article en En | MEDLINE | ID: mdl-24503721
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Congénitas / Proteínas / Cilios / Vía de Señalización Wnt Tipo de estudio: Risk_factors_studies Límite: Animals / Female / Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2014 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
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XML
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Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Congénitas / Proteínas / Cilios / Vía de Señalización Wnt Tipo de estudio: Risk_factors_studies Límite: Animals / Female / Humans Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2014 Tipo del documento: Article País de afiliación: Reino Unido