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Identification of exosomal muscle-specific miRNAs in serum of myotonic dystrophy patients relating to muscle disease progress.
Koutsoulidou, Andrie; Photiades, Marinos; Kyriakides, Tassos C; Georgiou, Kristia; Prokopi, Marianna; Kapnisis, Konstantinos; Lusakowska, Anna; Nearchou, Marianna; Christou, Yiolanda; Papadimas, George K; Anayiotos, Andreas; Kyriakou, Kyriakos; Kararizou, Evangelia; Zamba Papanicolaou, Eleni; Phylactou, Leonidas A.
Afiliação
  • Koutsoulidou A; Department of Molecular Genetics, Function & Therapy, Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.
  • Photiades M; Department of Molecular Genetics, Function & Therapy, Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.
  • Kyriakides TC; Yale Center for Analytical Sciences, Yale School of Public Health, New Haven, CT, USA.
  • Georgiou K; Department of Molecular Genetics, Function & Therapy, Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.
  • Prokopi M; Department of Mechanical Engineering and Materials Science and Engineering, Cyprus University of Technology, Lemesos, Cyprus.
  • Kapnisis K; Theramir Ltd, Limassol, Cyprus.
  • Lusakowska A; Theramir Ltd, Limassol, Cyprus.
  • Nearchou M; Department of Neurology, Medical University of Warsaw, Warsaw, Poland.
  • Christou Y; Department of Electron Microscopy/Molecular Pathology, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.
  • Papadimas GK; Neurology Clinic D, Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.
  • Anayiotos A; Department of Neurology, Eginitio Hospital, Medical School of Athens, Athens, Greece.
  • Kyriakou K; Department of Mechanical Engineering and Materials Science and Engineering, Cyprus University of Technology, Lemesos, Cyprus.
  • Kararizou E; Department of Electron Microscopy/Molecular Pathology, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.
  • Zamba Papanicolaou E; Department of Neurology, Eginitio Hospital, Medical School of Athens, Athens, Greece.
  • Phylactou LA; Neurology Clinic D, Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.
Hum Mol Genet ; 26(17): 3285-3302, 2017 09 01.
Article em En | MEDLINE | ID: mdl-28637233
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Distrofia Miotônica Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Distrofia Miotônica Idioma: En Ano de publicação: 2017 Tipo de documento: Article