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Progressive neuroanatomical changes caused by Grin1 loss-of-function mutation.
Intson, Katheron; van Eede, Matthijs C; Islam, Rehnuma; Milenkovic, Marija; Yan, Yuanye; Salahpour, Ali; Henkelman, R Mark; Ramsey, Amy J.
Afiliação
  • Intson K; Department of Pharmacology & Toxicology, University of Toronto, 1 King's College Circle, Medical Sciences Building, Toronto, ON, Canada.
  • van Eede MC; Mouse Imaging Centre, Hospital for Sick Children, 25 Orde Street, Toronto, ON, Canada.
  • Islam R; Department of Physiology, University of Toronto, Toronto, ON, Canada.
  • Milenkovic M; Department of Pharmacology & Toxicology, University of Toronto, 1 King's College Circle, Medical Sciences Building, Toronto, ON, Canada.
  • Yan Y; Department of Pharmacology & Toxicology, University of Toronto, 1 King's College Circle, Medical Sciences Building, Toronto, ON, Canada.
  • Salahpour A; Department of Pharmacology & Toxicology, University of Toronto, 1 King's College Circle, Medical Sciences Building, Toronto, ON, Canada.
  • Henkelman RM; Mouse Imaging Centre, Hospital for Sick Children, 25 Orde Street, Toronto, ON, Canada.
  • Ramsey AJ; Department of Pharmacology & Toxicology, University of Toronto, 1 King's College Circle, Medical Sciences Building, Toronto, ON, Canada; Department of Physiology, University of Toronto, Toronto, ON, Canada. Electronic address: a.ramsey@utoronto.ca.
Neurobiol Dis ; 132: 104527, 2019 12.
Article em En | MEDLINE | ID: mdl-31299220
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Receptores de N-Metil-D-Aspartato / Mutação com Perda de Função / Proteínas do Tecido Nervoso Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encéfalo / Receptores de N-Metil-D-Aspartato / Mutação com Perda de Função / Proteínas do Tecido Nervoso Idioma: En Ano de publicação: 2019 Tipo de documento: Article