Your browser doesn't support javascript.
loading
TALPID3 controls centrosome and cell polarity and the human ortholog KIAA0586 is mutated in Joubert syndrome (JBTS23).
Stephen, Louise A; Tawamie, Hasan; Davis, Gemma M; Tebbe, Lars; Nürnberg, Peter; Nürnberg, Gudrun; Thiele, Holger; Thoenes, Michaela; Boltshauser, Eugen; Uebe, Steffen; Rompel, Oliver; Reis, André; Ekici, Arif B; McTeir, Lynn; Fraser, Amy M; Hall, Emma A; Mill, Pleasantine; Daudet, Nicolas; Cross, Courtney; Wolfrum, Uwe; Jamra, Rami Abou; Davey, Megan G; Bolz, Hanno J.
Afiliação
  • Stephen LA; Division of Developmental Biology, The Roslin Institute, University of Edinburgh, Edinburgh, United Kingdom.
  • Tawamie H; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
  • Davis GM; Division of Developmental Biology, The Roslin Institute, University of Edinburgh, Edinburgh, United Kingdom.
  • Tebbe L; Cell and Matrix Biology, Institute of Zoology, Johannes Gutenberg University of Mainz, Mainz, Germany.
  • Nürnberg P; Cologne Center for Genomics, Center for Molecular Medicine Cologne, University of Cologne, Cologne, Germany.
  • Nürnberg G; Cologne Cluster of Excellence, University of Cologne, Cologne, Germany.
  • Thiele H; Cologne Center for Genomics, Center for Molecular Medicine Cologne, University of Cologne, Cologne, Germany.
  • Thoenes M; Cologne Center for Genomics, Center for Molecular Medicine Cologne, University of Cologne, Cologne, Germany.
  • Boltshauser E; Institute of Human Genetics, University Hospital of Cologne, Cologne, Germany.
  • Uebe S; Department of Paediatric Neurology, University Children's Hospital Zurich, Zurich, Switzerland.
  • Rompel O; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
  • Reis A; Institute of Radiology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
  • Ekici AB; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
  • McTeir L; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
  • Fraser AM; Division of Developmental Biology, The Roslin Institute, University of Edinburgh, Edinburgh, United Kingdom.
  • Hall EA; Division of Developmental Biology, The Roslin Institute, University of Edinburgh, Edinburgh, United Kingdom.
  • Mill P; Medical Research Council Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
  • Daudet N; Medical Research Council Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
  • Cross C; UCL Ear Institute, University College London, London, United Kingdom.
  • Wolfrum U; School of Osteopathic Medicine, A.T. Still University, Mesa, United States.
  • Jamra RA; Cell and Matrix Biology, Institute of Zoology, Johannes Gutenberg University of Mainz, Mainz, Germany.
  • Davey MG; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
  • Bolz HJ; Centogene, Rostock, Germany.
Elife ; 42015 Sep 19.
Article em En | MEDLINE | ID: mdl-26386247
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Retina / Cerebelo / Polaridade Celular / Centrossomo / Proteínas de Ciclo Celular / Mutação Limite: Animals / Humans Idioma: En Revista: Elife Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Reino Unido
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Retina / Cerebelo / Polaridade Celular / Centrossomo / Proteínas de Ciclo Celular / Mutação Limite: Animals / Humans Idioma: En Revista: Elife Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Reino Unido