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HDAC4: a key factor underlying brain developmental alterations in CDKL5 disorder.
Trazzi, Stefania; Fuchs, Claudia; Viggiano, Rocchina; De Franceschi, Marianna; Valli, Emanuele; Jedynak, Paulina; Hansen, Finn K; Perini, Giovanni; Rimondini, Roberto; Kurz, Thomas; Bartesaghi, Renata; Ciani, Elisabetta.
Afiliación
  • Trazzi S; Department of Biomedical and Neuromotor Sciences, University of Bologna, Italy.
  • Fuchs C; Department of Biomedical and Neuromotor Sciences, University of Bologna, Italy.
  • Viggiano R; Department of Biomedical and Neuromotor Sciences, University of Bologna, Italy.
  • De Franceschi M; Department of Biomedical and Neuromotor Sciences, University of Bologna, Italy.
  • Valli E; Department of Pharmacy and Biotechnology, and CIRI Health Sciences and Technologies.
  • Jedynak P; Department of Biomedical and Neuromotor Sciences, University of Bologna, Italy.
  • Hansen FK; Institut für Pharmazeutische und Medizinische Chemie, Heinrich Heine Universität, Düsseldorf, Germany.
  • Perini G; Department of Pharmacy and Biotechnology, and CIRI Health Sciences and Technologies.
  • Rimondini R; Department of Medical and Clinical Sciences, University of Bologna, Italy.
  • Kurz T; Institut für Pharmazeutische und Medizinische Chemie, Heinrich Heine Universität, Düsseldorf, Germany.
  • Bartesaghi R; Department of Biomedical and Neuromotor Sciences, University of Bologna, Italy.
  • Ciani E; Department of Biomedical and Neuromotor Sciences, University of Bologna, Italy elisabetta.ciani@unibo.it.
Hum Mol Genet ; 25(18): 3887-3907, 2016 09 15.
Article en En | MEDLINE | ID: mdl-27466189
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Espasmos Infantiles / Síndrome de Rett / Proteínas Serina-Treonina Quinasas / Histona Desacetilasas / Discapacidad Intelectual Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Italia
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Espasmos Infantiles / Síndrome de Rett / Proteínas Serina-Treonina Quinasas / Histona Desacetilasas / Discapacidad Intelectual Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Italia