Your browser doesn't support javascript.
loading
Antisense Transcription in Loci Associated to Hereditary Neurodegenerative Diseases.
Zucchelli, Silvia; Fedele, Stefania; Vatta, Paolo; Calligaris, Raffaella; Heutink, Peter; Rizzu, Patrizia; Itoh, Masayoshi; Persichetti, Francesca; Santoro, Claudio; Kawaji, Hideya; Lassmann, Timo; Hayashizaki, Yoshihide; Carninci, Piero; Forrest, Alistair R R; Gustincich, Stefano.
Afiliación
  • Zucchelli S; Area of Neuroscience, SISSA, Trieste, Italy.
  • Fedele S; Department of Health Sciences and Interdisciplinary Research Center of Autoimmune Diseases (IRCAD), University of Piemonte Orientale (UPO), Novara, Italy.
  • Vatta P; Area of Neuroscience, SISSA, Trieste, Italy.
  • Calligaris R; Area of Neuroscience, SISSA, Trieste, Italy.
  • Heutink P; Department of Neuroscience and Brain Technologies, Istituto Italiano di Tecnologia, Via Morego 30, 16163, Genoa, Italy.
  • Rizzu P; Area of Neuroscience, SISSA, Trieste, Italy.
  • Itoh M; Department of Medical, Surgical and Health Sciences, Clinical Neurology Unit, Cattinara University Hospital, Trieste, Italy.
  • Persichetti F; Section Medical Genomics, Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
  • Santoro C; Genome Biology of Neurodegenerative Diseases, Deutsches Zentrum fur Neurodegenerative Erkrankungen (DZNE), Standort, Tübingen, Germany.
  • Kawaji H; Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, Japan.
  • Lassmann T; RIKEN Omics Science Center, Yokohama, Japan.
  • Hayashizaki Y; Section Medical Genomics, Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
  • Carninci P; Applied Genomics for Neurodegenerative Diseases, Deutsches Zentrum fur Neurodegenerative Erkrankungen (DZNE), Standort, Tübingen, Germany.
  • Forrest ARR; Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, Japan.
  • Gustincich S; RIKEN Preventive Medicine and Diagnosis Innovation Program, Wako, Japan.
Mol Neurobiol ; 56(8): 5392-5415, 2019 Aug.
Article en En | MEDLINE | ID: mdl-30610612
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Transcripción Genética / ARN sin Sentido / Enfermedades Neurodegenerativas / Predisposición Genética a la Enfermedad / Sitios Genéticos Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: Mol Neurobiol Asunto de la revista: BIOLOGIA MOLECULAR / NEUROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Italia
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Transcripción Genética / ARN sin Sentido / Enfermedades Neurodegenerativas / Predisposición Genética a la Enfermedad / Sitios Genéticos Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: Mol Neurobiol Asunto de la revista: BIOLOGIA MOLECULAR / NEUROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Italia