Your browser doesn't support javascript.
loading
Functional regulatory variants implicate distinct transcriptional networks in dementia.
Cooper, Yonatan A; Teyssier, Noam; Dräger, Nina M; Guo, Qiuyu; Davis, Jessica E; Sattler, Sydney M; Yang, Zhongan; Patel, Abdulsamie; Wu, Sarah; Kosuri, Sriram; Coppola, Giovanni; Kampmann, Martin; Geschwind, Daniel H.
Afiliación
  • Cooper YA; Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA.
  • Teyssier N; Medical Scientist Training Program, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA.
  • Dräger NM; Center for Neurobehavioral Genetics, Jane and Terry Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA 90095, USA.
  • Guo Q; Institute for Neurodegenerative Diseases, University of California, San Francisco, CA 94158, USA.
  • Davis JE; Institute for Neurodegenerative Diseases, University of California, San Francisco, CA 94158, USA.
  • Sattler SM; Center for Neurobehavioral Genetics, Jane and Terry Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA 90095, USA.
  • Yang Z; Department of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095, USA.
  • Patel A; Institute for Neurodegenerative Diseases, University of California, San Francisco, CA 94158, USA.
  • Wu S; Center for Neurobehavioral Genetics, Jane and Terry Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA 90095, USA.
  • Kosuri S; Center for Neurobehavioral Genetics, Jane and Terry Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA 90095, USA.
  • Coppola G; Center for Neurobehavioral Genetics, Jane and Terry Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA 90095, USA.
  • Kampmann M; Department of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095, USA.
  • Geschwind DH; Center for Neurobehavioral Genetics, Jane and Terry Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles, CA 90095, USA.
Science ; 377(6608): eabi8654, 2022 08 19.
Article en En | MEDLINE | ID: mdl-35981026
Asunto(s)
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Variación Genética / Cromosomas Humanos Par 17 / Regiones no Traducidas / Redes Reguladoras de Genes / Enfermedad de Alzheimer Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Science Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Variación Genética / Cromosomas Humanos Par 17 / Regiones no Traducidas / Redes Reguladoras de Genes / Enfermedad de Alzheimer Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Science Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos