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Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome.
Veeraragavan, Surabi; Wan, Ying-Wooi; Connolly, Daniel R; Hamilton, Shannon M; Ward, Christopher S; Soriano, Sirena; Pitcher, Meagan R; McGraw, Christopher M; Huang, Sharon G; Green, Jennie R; Yuva, Lisa A; Liang, Agnes J; Neul, Jeffrey L; Yasui, Dag H; LaSalle, Janine M; Liu, Zhandong; Paylor, Richard; Samaco, Rodney C.
Afiliação
  • Veeraragavan S; Department of Molecular and Human Genetics.
  • Wan YW; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX, USA.
  • Connolly DR; Department of Molecular and Human Genetics.
  • Hamilton SM; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX, USA.
  • Ward CS; Department of Molecular and Human Genetics.
  • Soriano S; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX, USA.
  • Pitcher MR; Department of Molecular and Human Genetics.
  • McGraw CM; Department of Pediatrics, Section of Neurology.
  • Huang SG; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX, USA.
  • Green JR; Department of Molecular and Human Genetics.
  • Yuva LA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX, USA.
  • Liang AJ; Program in Translational Biology and Molecular Medicine.
  • Neul JL; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX, USA.
  • Yasui DH; Medical Scientist Training Program, Baylor College of Medicine, Houston, TX, USA.
  • LaSalle JM; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX, USA.
  • Liu Z; Department of Molecular and Human Genetics.
  • Paylor R; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX, USA.
  • Samaco RC; Department of Molecular and Human Genetics.
Hum Mol Genet ; 25(15): 3284-3302, 2016 08 01.
Article em En | MEDLINE | ID: mdl-27365498
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Comportamento Animal / Síndrome de Rett / Proteína 2 de Ligação a Metil-CpG / Mutação Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Comportamento Animal / Síndrome de Rett / Proteína 2 de Ligação a Metil-CpG / Mutação Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article