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DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism.
Maresca, Alessandra; Del Dotto, Valentina; Capristo, Mariantonietta; Scimonelli, Emanuela; Tagliavini, Francesca; Morandi, Luca; Tropeano, Concetta Valentina; Caporali, Leonardo; Mohamed, Susan; Roberti, Marina; Scandiffio, Letizia; Zaffagnini, Mirko; Rossi, Jacopo; Cappelletti, Martina; Musiani, Francesco; Contin, Manuela; Riva, Roberto; Liguori, Rocco; Pizza, Fabio; La Morgia, Chiara; Antelmi, Elena; Loguercio Polosa, Paola; Mignot, Emmanuel; Zanna, Claudia; Plazzi, Giuseppe; Carelli, Valerio.
Afiliación
  • Maresca A; IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna 40139, Italy.
  • Del Dotto V; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40139, Italy.
  • Capristo M; IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna 40139, Italy.
  • Scimonelli E; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40139, Italy.
  • Tagliavini F; IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna 40139, Italy.
  • Morandi L; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40139, Italy.
  • Tropeano CV; IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna 40139, Italy.
  • Caporali L; IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna 40139, Italy.
  • Mohamed S; IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna 40139, Italy.
  • Roberti M; Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari "Aldo Moro", Bari 70126, Italy.
  • Scandiffio L; Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari "Aldo Moro", Bari 70126, Italy.
  • Zaffagnini M; Department of Pharmacy and Biotechnology, University of Bologna, Bologna 40126, Italy.
  • Rossi J; Department of Pharmacy and Biotechnology, University of Bologna, Bologna 40126, Italy.
  • Cappelletti M; Department of Pharmacy and Biotechnology, University of Bologna, Bologna 40126, Italy.
  • Musiani F; Department of Pharmacy and Biotechnology, University of Bologna, Bologna 40126, Italy.
  • Contin M; IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna 40139, Italy.
  • Riva R; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40139, Italy.
  • Liguori R; IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna 40139, Italy.
  • Pizza F; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40139, Italy.
  • La Morgia C; IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna 40139, Italy.
  • Antelmi E; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40139, Italy.
  • Loguercio Polosa P; IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna 40139, Italy.
  • Mignot E; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40139, Italy.
  • Zanna C; IRCCS Istituto delle Scienze Neurologiche di Bologna, UOC Clinica Neurologica, Bologna 40139, Italy.
  • Plazzi G; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40139, Italy.
  • Carelli V; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40139, Italy.
Hum Mol Genet ; 29(11): 1864-1881, 2020 07 21.
Article en En | MEDLINE | ID: mdl-31984424
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neuropatías Hereditarias Sensoriales y Autónomas / Predisposición Genética a la Enfermedad / Ataxias Espinocerebelosas / ADN (Citosina-5-)-Metiltransferasa 1 / Degeneración Nerviosa Límite: Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido
Texto completo
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neuropatías Hereditarias Sensoriales y Autónomas / Predisposición Genética a la Enfermedad / Ataxias Espinocerebelosas / ADN (Citosina-5-)-Metiltransferasa 1 / Degeneración Nerviosa Límite: Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido