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Motor, Somatosensory, Viscerosensory and Metabolic Impairments in a Heterozygous Female Rat Model of Rett Syndrome.
Bhattacherjee, Aritra; Winter, Michelle K; Eggimann, Linda S; Mu, Ying; Gunewardena, Sumedha; Liao, Zhaohui; Christianson, Julie A; Smith, Peter G.
Afiliação
  • Bhattacherjee A; Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS 66160, USA. Aritra.Bhattacherjee@childrens.harvard.edu.
  • Winter MK; Kansas Intellectual and Developmental Disabilities Research Center, University of Kansas Medical Center, Kansas City, KS 66160, USA. Aritra.Bhattacherjee@childrens.harvard.edu.
  • Eggimann LS; Kansas Intellectual and Developmental Disabilities Research Center, University of Kansas Medical Center, Kansas City, KS 66160, USA. mwinter2@kumc.edu.
  • Mu Y; Kansas Intellectual and Developmental Disabilities Research Center, University of Kansas Medical Center, Kansas City, KS 66160, USA. leggimann@kumc.edu.
  • Gunewardena S; Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS 66160, USA. mu2@uthsc.edu.
  • Liao Z; Kansas Intellectual and Developmental Disabilities Research Center, University of Kansas Medical Center, Kansas City, KS 66160, USA. mu2@uthsc.edu.
  • Christianson JA; Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, KS 66160, USA. sgunewardena@kumc.edu.
  • Smith PG; Kansas Intellectual and Developmental Disabilities Research Center, University of Kansas Medical Center, Kansas City, KS 66160, USA. sgunewardena@kumc.edu.
Int J Mol Sci ; 19(1)2017 Dec 29.
Article em En | MEDLINE | ID: mdl-29286317
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Psicomotores / Ataxia / Síndrome de Rett / Proteína 2 de Ligação a Metil-CpG / Mutação Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Psicomotores / Ataxia / Síndrome de Rett / Proteína 2 de Ligação a Metil-CpG / Mutação Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article