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A screen for deeply conserved non-coding GWAS SNPs uncovers a MIR-9-2 functional mutation associated to retinal vasculature defects in human.
Madelaine, Romain; Notwell, James H; Skariah, Gemini; Halluin, Caroline; Chen, Charles C; Bejerano, Gill; Mourrain, Philippe.
Afiliación
  • Madelaine R; Department of Psychiatry and Behavioral Sciences, Stanford Center for Sleep Sciences and Medicine, Stanford, CA 94305, USA.
  • Notwell JH; Department of Computer Science, Stanford, CA 94305, USA.
  • Skariah G; Department of Psychiatry and Behavioral Sciences, Stanford Center for Sleep Sciences and Medicine, Stanford, CA 94305, USA.
  • Halluin C; Department of Psychiatry and Behavioral Sciences, Stanford Center for Sleep Sciences and Medicine, Stanford, CA 94305, USA.
  • Chen CC; Department of Computer Science, Stanford, CA 94305, USA.
  • Bejerano G; Department of Computer Science, Stanford, CA 94305, USA.
  • Mourrain P; Department of Developmental Biology, Stanford, CA 94305, USA.
Nucleic Acids Res ; 46(7): 3517-3531, 2018 04 20.
Article en En | MEDLINE | ID: mdl-29518216
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Elementos de Facilitación Genéticos / Vasculitis Retiniana / MicroARNs Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Nucleic Acids Res Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Añadir a Mi BVS
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PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Elementos de Facilitación Genéticos / Vasculitis Retiniana / MicroARNs Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Nucleic Acids Res Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos