Gait analysis in a Mecp2 knockout mouse model of Rett syndrome reveals early-onset and progressive motor deficits.

Gadalla, Kamal K E; Ross, Paul D; Riddell, John S; Bailey, Mark E S; Cobb, Stuart R

Gadalla, Kamal K E; Ross, Paul D; Riddell, John S; Bailey, Mark E S; Cobb, Stuart R.

Afiliação

Gadalla KK; Institute of Neuroscience and Psychology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom; Pharmacology Department, Faculty of Medicine, Tanta University, Egypt.
Ross PD; Institute of Neuroscience and Psychology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.
Riddell JS; Institute of Neuroscience and Psychology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.
Bailey ME; School of Life Sciences, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.
Cobb SR; Institute of Neuroscience and Psychology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.

PLoS One ; 9(11): e112889, 2014.

Article em En | MEDLINE | ID: mdl-25392929

Assuntos

Marcha Atáxica/fisiopatologia; Proteína 2 de Ligação a Metil-CpG/deficiência; Transtornos Motores/fisiopatologia; Síndrome de Rett/fisiopatologia; Animais; Modelos Animais de Doenças; Marcha Atáxica/genética; Masculino; Camundongos; Camundongos Knockout; Transtornos Motores/genética; Síndrome de Rett/genética

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Rett / Marcha Atáxica / Proteína 2 de Ligação a Metil-CpG / Transtornos Motores Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2014 Tipo de documento: Article

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