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Extensive cryptic splicing upon loss of RBM17 and TDP43 in neurodegeneration models.
Tan, Qiumin; Yalamanchili, Hari Krishna; Park, Jeehye; De Maio, Antonia; Lu, Hsiang-Chih; Wan, Ying-Wooi; White, Joshua J; Bondar, Vitaliy V; Sayegh, Layal S; Liu, Xiuyun; Gao, Yan; Sillitoe, Roy V; Orr, Harry T; Liu, Zhandong; Zoghbi, Huda Y.
Afiliación
  • Tan Q; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.
  • Yalamanchili HK; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • Park J; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.
  • De Maio A; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • Lu HC; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.
  • Wan YW; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • White JJ; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • Bondar VV; Program in Developmental Biology.
  • Sayegh LS; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • Liu X; Program in Developmental Biology.
  • Gao Y; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.
  • Sillitoe RV; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • Orr HT; Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas 77030, USA.
  • Liu Z; Department of Neuroscience.
  • Zoghbi HY; Department of Pathology and Immunology, Baylor College of Medicine, Houston, Texas 77030, USA.
Hum Mol Genet ; 25(23): 5083-5093, 2016 12 01.
Article en En | MEDLINE | ID: mdl-28007900

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas de Unión al ADN / Demencia Frontotemporal / Factores de Empalme de ARN / Esclerosis Amiotrófica Lateral / Degeneración Nerviosa / Proteínas del Tejido Nervioso Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas de Unión al ADN / Demencia Frontotemporal / Factores de Empalme de ARN / Esclerosis Amiotrófica Lateral / Degeneración Nerviosa / Proteínas del Tejido Nervioso Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos