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Specific ZNF274 binding interference at SNORD116 activates the maternal transcripts in Prader-Willi syndrome neurons.
Langouët, Maéva; Gorka, Dea; Orniacki, Clarisse; Dupont-Thibert, Clémence M; Chung, Michael S; Glatt-Deeley, Heather R; Germain, Noelle; Crandall, Leann J; Cotney, Justin L; Stoddard, Christopher E; Lalande, Marc; Chamberlain, Stormy J.
Afiliación
  • Langouët M; Department of Genetics and Genome Sciences, University of Connecticut School of Medicine, Farmington, CT 06030, USA.
  • Gorka D; Department of Genetics and Genome Sciences, University of Connecticut School of Medicine, Farmington, CT 06030, USA.
  • Orniacki C; Department of Genetics and Genome Sciences, University of Connecticut School of Medicine, Farmington, CT 06030, USA.
  • Dupont-Thibert CM; Department of Genetics and Genome Sciences, University of Connecticut School of Medicine, Farmington, CT 06030, USA.
  • Chung MS; Department of Genetics and Genome Sciences, University of Connecticut School of Medicine, Farmington, CT 06030, USA.
  • Glatt-Deeley HR; Department of Genetics and Genome Sciences, University of Connecticut School of Medicine, Farmington, CT 06030, USA.
  • Germain N; Department of Genetics and Genome Sciences, University of Connecticut School of Medicine, Farmington, CT 06030, USA.
  • Crandall LJ; Department of Genetics and Genome Sciences, University of Connecticut School of Medicine, Farmington, CT 06030, USA.
  • Cotney JL; Department of Genetics and Genome Sciences, University of Connecticut School of Medicine, Farmington, CT 06030, USA.
  • Stoddard CE; Institute for Systems Genomics, University of Connecticut, Farmington, CT 06030, USA.
  • Lalande M; Department of Genetics and Genome Sciences, University of Connecticut School of Medicine, Farmington, CT 06030, USA.
  • Chamberlain SJ; Department of Genetics and Genome Sciences, University of Connecticut School of Medicine, Farmington, CT 06030, USA.
Hum Mol Genet ; 29(19): 3285-3295, 2020 11 25.
Article en En | MEDLINE | ID: mdl-32977341
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi / ARN Nucleolar Pequeño / ARN Mensajero Almacenado / Factores de Transcripción de Tipo Kruppel / Células Madre Pluripotentes Inducidas / Neuronas Límite: Female / Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi / ARN Nucleolar Pequeño / ARN Mensajero Almacenado / Factores de Transcripción de Tipo Kruppel / Células Madre Pluripotentes Inducidas / Neuronas Límite: Female / Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido