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Haploinsufficiency of BAZ1B contributes to Williams syndrome through transcriptional dysregulation of neurodevelopmental pathways.
Lalli, Matthew A; Jang, Jiwon; Park, Joo-Hye C; Wang, Yidi; Guzman, Elmer; Zhou, Hongjun; Audouard, Morgane; Bridges, Daniel; Tovar, Kenneth R; Papuc, Sorina M; Tutulan-Cunita, Andreea C; Huang, Yadong; Budisteanu, Magdalena; Arghir, Aurora; Kosik, Kenneth S.
Afiliación
  • Lalli MA; Department of Molecular, Cellular, and Developmental Biology, Neuroscience Research Institute, Biomolecular Science and Engineering Program.
  • Jang J; Department of Molecular, Cellular, and Developmental Biology, Neuroscience Research Institute.
  • Park JH; Department of Molecular, Cellular, and Developmental Biology, Neuroscience Research Institute.
  • Wang Y; Department of Molecular, Cellular, and Developmental Biology, Neuroscience Research Institute.
  • Guzman E; Department of Molecular, Cellular, and Developmental Biology, Neuroscience Research Institute.
  • Zhou H; Department of Molecular, Cellular, and Developmental Biology, Neuroscience Research Institute.
  • Audouard M; Department of Molecular, Cellular, and Developmental Biology, Neuroscience Research Institute.
  • Bridges D; Department of Molecular, Cellular, and Developmental Biology, Neuroscience Research Institute, Department of Physics, University of California, Santa Barbara, CA, USA.
  • Tovar KR; Department of Molecular, Cellular, and Developmental Biology, Neuroscience Research Institute.
  • Papuc SM; Victor Babes National Institute of Pathology, Clinical Cytogenetics, Bucharest, Romania.
  • Tutulan-Cunita AC; Victor Babes National Institute of Pathology, Clinical Cytogenetics, Bucharest, Romania.
  • Huang Y; Gladstone Institute of Neurological Disease, University of California, San Francisco, CA, USA and.
  • Budisteanu M; Victor Babes National Institute of Pathology, Clinical Cytogenetics, Bucharest, Romania, Alexandru Obregia Clinical Hospital of Psychiatry, Neuropediatric Pathology, Bucharest, Romania.
  • Arghir A; Victor Babes National Institute of Pathology, Clinical Cytogenetics, Bucharest, Romania.
  • Kosik KS; Department of Molecular, Cellular, and Developmental Biology, Neuroscience Research Institute, Biomolecular Science and Engineering Program, kosik@lifesci.ucsb.edu.
Hum Mol Genet ; 25(7): 1294-306, 2016 Apr 01.
Article en En | MEDLINE | ID: mdl-26755828
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Regulación del Desarrollo de la Expresión Génica / Síndrome de Williams / Neurogénesis / Células Madre Pluripotentes Inducidas / Haploinsuficiencia / Neuronas Límite: Female / Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2016 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Factores de Transcripción / Regulación del Desarrollo de la Expresión Génica / Síndrome de Williams / Neurogénesis / Células Madre Pluripotentes Inducidas / Haploinsuficiencia / Neuronas Límite: Female / Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2016 Tipo del documento: Article