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A novel pathogenic mutation of MeCP2 impairs chromatin association independent of protein levels.
Zhou, Jian; Cattoglio, Claudia; Shao, Yingyao; Tirumala, Harini P; Vetralla, Carlo; Bajikar, Sameer S; Li, Yan; Chen, Hu; Wang, Qi; Wu, Zhenyu; Tang, Bing; Zahabiyon, Mahla; Bajic, Aleksandar; Meng, Xiangling; Ferrie, Jack J; LaGrone, Anel; Zhang, Ping; Kim, Jean J; Tang, Jianrong; Liu, Zhandong; Darzacq, Xavier; Heintz, Nathaniel; Tjian, Robert; Zoghbi, Huda Y.
Afiliación
  • Zhou J; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.
  • Cattoglio C; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • Shao Y; Department of Molecular and Cell Biology, Li Ka Shing Center for Biomedical and Health Sciences, California Institute for Regenerative Medicine (CIRM) Center of Excellence, University of California, Berkeley, Berkeley, California 94720, USA.
  • Tirumala HP; Howard Hughes Medical Institute, Berkeley, California 94720, USA.
  • Vetralla C; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.
  • Bajikar SS; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • Li Y; Program in Developmental Biology, Baylor College of Medicine, Houston, Texas 77030, USA.
  • Chen H; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.
  • Wang Q; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • Wu Z; Department of Molecular and Cell Biology, Li Ka Shing Center for Biomedical and Health Sciences, California Institute for Regenerative Medicine (CIRM) Center of Excellence, University of California, Berkeley, Berkeley, California 94720, USA.
  • Tang B; Howard Hughes Medical Institute, Berkeley, California 94720, USA.
  • Zahabiyon M; School of Medicine and Surgery, University of Milan-Bicocca, Milano 20126, Italy.
  • Bajic A; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.
  • Meng X; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • Ferrie JJ; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.
  • LaGrone A; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • Zhang P; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • Kim JJ; Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030, USA.
  • Tang J; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • Liu Z; Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030, USA.
  • Darzacq X; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • Heintz N; Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030, USA.
  • Tjian R; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • Zoghbi HY; Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030, USA.
Genes Dev ; 37(19-20): 883-900, 2023 10 01.
Article en En | MEDLINE | ID: mdl-37890975
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cromatina / Síndrome de Rett Idioma: En Revista: Genes Dev Asunto de la revista: BIOLOGIA MOLECULAR Año: 2023 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Cromatina / Síndrome de Rett Idioma: En Revista: Genes Dev Asunto de la revista: BIOLOGIA MOLECULAR Año: 2023 Tipo del documento: Article