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Editing TINF2 as a potential therapeutic approach to restore telomere length in dyskeratosis congenita.
Choo, Seunga; Lorbeer, Franziska K; Regalado, Samuel G; Short, Sarah B; Wu, Shannon; Rieser, Gabrielle; Bertuch, Alison A; Hockemeyer, Dirk.
Afiliación
  • Choo S; Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA.
  • Lorbeer FK; Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA.
  • Regalado SG; Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA.
  • Short SB; Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA.
  • Wu S; Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA.
  • Rieser G; Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA.
  • Bertuch AA; Department of Pediatrics, Baylor College of Medicine, Houston, TX.
  • Hockemeyer D; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.
Blood ; 140(6): 608-618, 2022 08 11.
Article en En | MEDLINE | ID: mdl-35421215
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Telomerasa / Disqueratosis Congénita Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Blood Año: 2022 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: 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: Telomerasa / Disqueratosis Congénita Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Blood Año: 2022 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Estados Unidos