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A dominant dendrite phenotype caused by the disease-associated G253D mutation in doublecortin (DCX) is not due to its endocytosis defect.
Yap, Chan Choo; Digilio, Laura; Kruczek, Kamil; Roszkowska, Matylda; Fu, Xiao-Qin; Liu, Judy S; Winckler, Bettina.
Afiliación
  • Yap CC; From the Department of Cell Biology, University of Virginia, Charlottesville, Virginia 22908.
  • Digilio L; From the Department of Cell Biology, University of Virginia, Charlottesville, Virginia 22908.
  • Kruczek K; the Program in Biotechnology and.
  • Roszkowska M; the Faculty of Biology and Earth Sciences, Jagiellonian University, 31-007 Cracow, Poland, and.
  • Fu XQ; the Department of Neurology, Brown University, Providence, Rhode Island 02912.
  • Liu JS; the Department of Neurology, Brown University, Providence, Rhode Island 02912.
  • Winckler B; From the Department of Cell Biology, University of Virginia, Charlottesville, Virginia 22908, BWinckler@virginia.edu.
J Biol Chem ; 293(49): 18890-18902, 2018 12 07.
Article en En | MEDLINE | ID: mdl-30291144
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neuropéptidos / Dendritas / Proteínas Asociadas a Microtúbulos / Neuronas Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: J Biol Chem Año: 2018 Tipo del documento: Article
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neuropéptidos / Dendritas / Proteínas Asociadas a Microtúbulos / Neuronas Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: J Biol Chem Año: 2018 Tipo del documento: Article