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The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder.
Barish, Scott; Senturk, Mumine; Schoch, Kelly; Minogue, Amanda L; Lopergolo, Diego; Fallerini, Chiara; Harland, Jake; Seemann, Jacob H; Stong, Nicholas; Kranz, Peter G; Kansagra, Sujay; Mikati, Mohamad A; Jasien, Joan; El-Dairi, Mays; Galluzzi, Paolo; Ariani, Francesca; Renieri, Alessandra; Mari, Francesca; Wangler, Michael F; Arur, Swathi; Jiang, Yong-Hui; Yamamoto, Shinya; Shashi, Vandana; Bellen, Hugo J.
Afiliação
  • Barish S; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
  • Senturk M; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030, USA.
  • Schoch K; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
  • Minogue AL; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030, USA.
  • Lopergolo D; Howard Hughes Medical Institute, BCM, Houston, TX 77030, USA.
  • Fallerini C; Program in Developmental Biology, Baylor College of Medicine, Houston, TX 77030, USA.
  • Harland J; Division of Medical Genetics, Department of Pediatrics, Duke University School of Medicine, Durham, NC 27710, USA.
  • Seemann JH; Program in Developmental Biology, Baylor College of Medicine, Houston, TX 77030, USA.
  • Stong N; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
  • Kranz PG; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena 53100, Italy.
  • Kansagra S; Medical Genetics, University of Siena, Siena 53100, Italy.
  • Mikati MA; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena 53100, Italy.
  • Jasien J; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena 53100, Italy.
  • El-Dairi M; Medical Genetics, University of Siena, Siena 53100, Italy.
  • Galluzzi P; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
  • Ariani F; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
  • Renieri A; Institute for Genomic Medicine, Columbia University, New York, NY 10032, USA.
  • Mari F; Division of Neuroradiology, Department of Radiology, Duke Health, Durham, NC 27710, USA.
  • Wangler MF; Division of Pediatric Neurology, Department of Pediatrics, Duke Health, Durham, NC 27710, USA.
  • Arur S; Division of Pediatric Neurology, Department of Pediatrics, Duke Health, Durham, NC 27710, USA.
  • Jiang YH; Division of Pediatric Neurology, Department of Pediatrics, Duke Health, Durham, NC 27710, USA.
  • Yamamoto S; Department of Ophthalmology, Duke Health, Durham, NC 27710, USA.
  • Shashi V; Department of Medical Genetics, NeuroImaging and NeuroInterventional Unit, Azienda Ospedaliera e Universitaria, Senese, Siena 53100, Italy.
Hum Mol Genet ; 31(17): 2934-2950, 2022 08 25.
Article em En | MEDLINE | ID: mdl-35405010
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: MicroRNAs / Epilepsia / Deficiência Intelectual / Microcefalia / Malformações do Sistema Nervoso Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Hum Mol Genet Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: MicroRNAs / Epilepsia / Deficiência Intelectual / Microcefalia / Malformações do Sistema Nervoso Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Hum Mol Genet Ano de publicação: 2022 Tipo de documento: Article