Your browser doesn't support javascript.
loading
TYROBP genetic variants in early-onset Alzheimer's disease.
Pottier, Cyril; Ravenscroft, Thomas A; Brown, Patricia H; Finch, NiCole A; Baker, Matt; Parsons, Meeia; Asmann, Yan W; Ren, Yingxue; Christopher, Elizabeth; Levitch, Denise; van Blitterswijk, Marka; Cruchaga, Carlos; Campion, Dominique; Nicolas, Gaël; Richard, Anne-Claire; Guerreiro, Rita; Bras, Jose T; Zuchner, Stephan; Gonzalez, Michael A; Bu, Guojun; Younkin, Steven; Knopman, David S; Josephs, Keith A; Parisi, Joseph E; Petersen, Ronald C; Ertekin-Taner, Nilüfer; Graff-Radford, Neill R; Boeve, Bradley F; Dickson, Dennis W; Rademakers, Rosa.
Afiliação
  • Pottier C; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Ravenscroft TA; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Brown PH; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Finch NA; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Baker M; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Parsons M; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Asmann YW; Division of Biomedical Statistics and Informatics, Mayo Clinic, Jacksonville, FL, USA.
  • Ren Y; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Christopher E; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Levitch D; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • van Blitterswijk M; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Cruchaga C; Department of Psychiatry, Washington University School of Medicine, St Louis, MO, USA.
  • Campion D; Inserm U1079, Rouen University, Normandy Center for Genomic Medicine and Personalized Medicine, Normandy University, Rouen, France; CNR-MAJ, Rouen University Hospital, Rouen, France; Department of Research, Rouvray Psychiatric Hospital, Rouen, France.
  • Nicolas G; Inserm U1079, Rouen University, Normandy Center for Genomic Medicine and Personalized Medicine, Normandy University, Rouen, France; CNR-MAJ, Rouen University Hospital, Rouen, France; Department of Genetics, Rouen University Hospital, Rouen, France.
  • Richard AC; Inserm U1079, Rouen University, Normandy Center for Genomic Medicine and Personalized Medicine, Normandy University, Rouen, France; CNR-MAJ, Rouen University Hospital, Rouen, France.
  • Guerreiro R; Department of Molecular Neuroscience, UCL Institute of Neurology, University College London, London, UK.
  • Bras JT; Department of Molecular Neuroscience, UCL Institute of Neurology, University College London, London, UK.
  • Zuchner S; Dr John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami, Miller School of Medicine, Miami, FL, USA.
  • Gonzalez MA; The Genesis Project Inc, Miami, FL, USA.
  • Bu G; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Younkin S; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Knopman DS; Department of Neurology, Mayo Clinic, Rochester, MN, USA.
  • Josephs KA; Department of Neurology, Mayo Clinic, Rochester, MN, USA.
  • Parisi JE; Department of Neurology, Mayo Clinic, Rochester, MN, USA.
  • Petersen RC; Department of Neurology, Mayo Clinic, Rochester, MN, USA.
  • Ertekin-Taner N; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA; Department of Neurology, Mayo Clinic, Jacksonville, FL, USA.
  • Graff-Radford NR; Department of Neurology, Mayo Clinic, Jacksonville, FL, USA.
  • Boeve BF; Department of Neurology, Mayo Clinic, Rochester, MN, USA.
  • Dickson DW; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
  • Rademakers R; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA. Electronic address: Rademakers.rosa@mayo.edu.
Neurobiol Aging ; 48: 222.e9-222.e15, 2016 12.
Article em En | MEDLINE | ID: mdl-27658901
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Proteínas Adaptadoras de Transdução de Sinal / Estudos de Associação Genética / Doença de Alzheimer / Proteínas de Membrana 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: Variação Genética / Proteínas Adaptadoras de Transdução de Sinal / Estudos de Associação Genética / Doença de Alzheimer / Proteínas de Membrana Idioma: En Ano de publicação: 2016 Tipo de documento: Article