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Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephaly.
Sgourdou, Paraskevi; Mishra-Gorur, Ketu; Saotome, Ichiko; Henagariu, Octavian; Tuysuz, Beyhan; Campos, Cynthia; Ishigame, Keiko; Giannikou, Krinio; Quon, Jennifer L; Sestan, Nenad; Caglayan, Ahmet O; Gunel, Murat; Louvi, Angeliki.
Afiliação
  • Sgourdou P; Departments of Neurosurgery and Neuroscience, Program on Neurogenetics, Yale School of Medicine, New Haven, CT, 06520, USA.
  • Mishra-Gorur K; Departments of Neurosurgery and Neuroscience, Program on Neurogenetics, Yale School of Medicine, New Haven, CT, 06520, USA.
  • Saotome I; Departments of Neurosurgery and Neuroscience, Program on Neurogenetics, Yale School of Medicine, New Haven, CT, 06520, USA.
  • Henagariu O; Departments of Neurosurgery and Neuroscience, Program on Neurogenetics, Yale School of Medicine, New Haven, CT, 06520, USA.
  • Tuysuz B; Department of Pediatric Genetics, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey.
  • Campos C; Departments of Neurosurgery and Neuroscience, Program on Neurogenetics, Yale School of Medicine, New Haven, CT, 06520, USA.
  • Ishigame K; Departments of Neurosurgery and Neuroscience, Program on Neurogenetics, Yale School of Medicine, New Haven, CT, 06520, USA.
  • Giannikou K; Departments of Neurosurgery and Neuroscience, Program on Neurogenetics, Yale School of Medicine, New Haven, CT, 06520, USA.
  • Quon JL; Departments of Neurosurgery and Neuroscience, Program on Neurogenetics, Yale School of Medicine, New Haven, CT, 06520, USA.
  • Sestan N; Departments of Neuroscience, Genetics and Psychiatry, Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT, 06520, USA.
  • Caglayan AO; Departments of Neurosurgery and Neuroscience, Program on Neurogenetics, Yale School of Medicine, New Haven, CT, 06520, USA.
  • Gunel M; Department of Medical Genetics, School of Medicine, Istanbul Bilim University, Istanbul, Turkey.
  • Louvi A; Departments of Neurosurgery and Neuroscience, Program on Neurogenetics, Yale School of Medicine, New Haven, CT, 06520, USA.
Sci Rep ; 7: 43708, 2017 03 08.
Article em En | MEDLINE | ID: mdl-28272472
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Centrossomo / Padrões de Herança / Epistasia Genética / Aurora Quinase B / Microcefalia / Proteínas do Tecido Nervoso Tipo de estudo: Prognostic_studies Limite: Animals / Humans / Male Idioma: En Revista: Sci Rep Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Centrossomo / Padrões de Herança / Epistasia Genética / Aurora Quinase B / Microcefalia / Proteínas do Tecido Nervoso Tipo de estudo: Prognostic_studies Limite: Animals / Humans / Male Idioma: En Revista: Sci Rep Ano de publicação: 2017 Tipo de documento: Article