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Exclusive expression of MeCP2 in the nervous system distinguishes between brain and peripheral Rett syndrome-like phenotypes.
Ross, Paul D; Guy, Jacky; Selfridge, Jim; Kamal, Bushra; Bahey, Noha; Tanner, K Elizabeth; Gillingwater, Thomas H; Jones, Ross A; Loughrey, Christopher M; McCarroll, Charlotte S; Bailey, Mark E S; Bird, Adrian; Cobb, Stuart.
Afiliação
  • Ross PD; Institute of Neuroscience and Psychology, College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow, UK.
  • Guy J; Wellcome Trust Centre for Cell Biology, University of Edinburgh, Michael Swann Building, Edinburgh, UK.
  • Selfridge J; Wellcome Trust Centre for Cell Biology, University of Edinburgh, Michael Swann Building, Edinburgh, UK.
  • Kamal B; Institute of Neuroscience and Psychology, College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow, UK.
  • Bahey N; Institute of Neuroscience and Psychology, College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow, UK.
  • Tanner KE; Histology Department, Faculty of Medicine, Tanta University, Tanta, Egypt
  • Gillingwater TH; School of Engineering, University of Glasgow, Glasgow, UK.
  • Jones RA; Edinburgh Medical School: Biomedical Sciences, University of Edinburgh, Hugh Robson Building, Edinburgh, UK.
  • Loughrey CM; Edinburgh Medical School: Biomedical Sciences, University of Edinburgh, Hugh Robson Building, Edinburgh, UK.
  • McCarroll CS; Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK and.
  • Bailey ME; Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK and.
  • Bird A; School of Life Sciences, College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow, UK.
  • Cobb S; Wellcome Trust Centre for Cell Biology, University of Edinburgh, Michael Swann Building, Edinburgh, UK.
Hum Mol Genet ; 25(20): 4389-4404, 2016 10 15.
Article em En | MEDLINE | ID: mdl-28173151
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Encéfalo / Síndrome de Rett / Proteína 2 de Ligação a Metil-CpG Limite: Animals Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Reino Unido
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Encéfalo / Síndrome de Rett / Proteína 2 de Ligação a Metil-CpG Limite: Animals Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Reino Unido