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TMEM231, mutated in orofaciodigital and Meckel syndromes, organizes the ciliary transition zone.
Roberson, Elle C; Dowdle, William E; Ozanturk, Aysegul; Garcia-Gonzalo, Francesc R; Li, Chunmei; Halbritter, Jan; Elkhartoufi, Nadia; Porath, Jonathan D; Cope, Heidi; Ashley-Koch, Allison; Gregory, Simon; Thomas, Sophie; Sayer, John A; Saunier, Sophie; Otto, Edgar A; Katsanis, Nicholas; Davis, Erica E; Attié-Bitach, Tania; Hildebrandt, Friedhelm; Leroux, Michel R; Reiter, Jeremy F.
Afiliación
  • Roberson EC; Department of Biochemistry and Biophysics and Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158.
  • Dowdle WE; Department of Biochemistry and Biophysics and Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158.
  • Ozanturk A; Center for Human Disease Modeling, Department of Medicine, and Duke Molecular Physiology Institute, Duke University Medical Center, Durham, NC 22710.
  • Garcia-Gonzalo FR; Department of Biochemistry and Biophysics and Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158.
  • Li C; Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, British Columbia, V5A 1S6 Canada.
  • Halbritter J; Division of Nephrology, Department of Medicine, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115.
  • Elkhartoufi N; Département de Génétique, Hôpital Necker-Enfants Malades, Assistance Publique/Hôpitaux de Paris, 75015 Paris, France.
  • Porath JD; Division of Nephrology, Department of Medicine, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115.
  • Cope H; Center for Human Disease Modeling, Department of Medicine, and Duke Molecular Physiology Institute, Duke University Medical Center, Durham, NC 22710.
  • Ashley-Koch A; Center for Human Disease Modeling, Department of Medicine, and Duke Molecular Physiology Institute, Duke University Medical Center, Durham, NC 22710 Center for Human Disease Modeling, Department of Medicine, and Duke Molecular Physiology Institute, Duke University Medical Center, Durham, NC 22710.
  • Gregory S; Center for Human Disease Modeling, Department of Medicine, and Duke Molecular Physiology Institute, Duke University Medical Center, Durham, NC 22710.
  • Thomas S; Institut National de la Santé et de la Recherche Médicale UMR1163, 75015 Paris, France Université Paris Descartes, Sorbonne Paris Cité, Institut Imagine, 75015 Paris, France.
  • Sayer JA; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, England, UK Newcastle Hospitals National Health Service Foundation Trust, Newcastle upon Tyne NE7 7DN, England, UK.
  • Saunier S; Institut National de la Santé et de la Recherche Médicale UMR1163, 75015 Paris, France Université Paris Descartes, Sorbonne Paris Cité, Institut Imagine, 75015 Paris, France.
  • Otto EA; Department of Pediatrics, University of Michigan, Ann Arbor, MI 48109.
  • Katsanis N; Center for Human Disease Modeling, Department of Medicine, and Duke Molecular Physiology Institute, Duke University Medical Center, Durham, NC 22710.
  • Davis EE; Center for Human Disease Modeling, Department of Medicine, and Duke Molecular Physiology Institute, Duke University Medical Center, Durham, NC 22710.
  • Attié-Bitach T; Institut National de la Santé et de la Recherche Médicale UMR1163, 75015 Paris, France Université Paris Descartes, Sorbonne Paris Cité, Institut Imagine, 75015 Paris, France Département de Génétique, Hôpital Necker-Enfants Malades, Assistance Publique/Hôpitaux de Paris, 75015 Paris, France.
  • Hildebrandt F; Division of Nephrology, Department of Medicine, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115 Howard Hughes Medical Institute, Chevy Chase, MD 20815.
  • Leroux MR; Department of Molecular Biology and Biochemistry, Simon Fraser University, Burnaby, British Columbia, V5A 1S6 Canada.
  • Reiter JF; Department of Biochemistry and Biophysics and Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94158 jeremy.reiter@ucsf.edu.
J Cell Biol ; 209(1): 129-42, 2015 Apr 13.
Article en En | MEDLINE | ID: mdl-25869670
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndromes Orofaciodigitales / Cilios / Trastornos de la Motilidad Ciliar / Encefalocele / Enfermedades Renales Poliquísticas / Proteínas de la Membrana Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Cell Biol Año: 2015 Tipo del documento: Article
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndromes Orofaciodigitales / Cilios / Trastornos de la Motilidad Ciliar / Encefalocele / Enfermedades Renales Poliquísticas / Proteínas de la Membrana Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Cell Biol Año: 2015 Tipo del documento: Article