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Epigenetic changes as a common trigger of muscle weakness in congenital myopathies.
Rokach, Ori; Sekulic-Jablanovic, Marijana; Voermans, Nicol; Wilmshurst, Jo; Pillay, Komala; Heytens, Luc; Zhou, Haiyan; Muntoni, Francesco; Gautel, Mathias; Nevo, Yoram; Mitrani-Rosenbaum, Stella; Attali, Ruben; Finotti, Alessia; Gambari, Roberto; Mosca, Barbara; Jungbluth, Heinz; Zorzato, Francesco; Treves, Susan.
Afiliação
  • Rokach O; Department of Biomedicine and Anesthesia, Basel University Hospital, Basel, Switzerland.
  • Sekulic-Jablanovic M; Department of Biomedicine and Anesthesia, Basel University Hospital, Basel, Switzerland.
  • Voermans N; Department of Neurology, Roadboud University Medical Center, Nijmegen, The Netherlands.
  • Wilmshurst J; Department of Paediatric Neurology and Child Health.
  • Pillay K; Department of Paediatric Pathology, NHLS, Cape Town, South Africa, Department of Paediatrics and Child Health, University of Cape Town, Red Cross Children's Hospital, Cape Town, South Africa.
  • Heytens L; Department of Anesthesiology and Neurology, Antwerp University Hospital, Antwerp, Belgium.
  • Zhou H; Dubowitz Neuromuscular Centre and MRC Centre for Neuromuscular Diseases, Institute of Child Health, London, UK.
  • Muntoni F; Dubowitz Neuromuscular Centre and MRC Centre for Neuromuscular Diseases, Institute of Child Health, London, UK.
  • Gautel M; Randall Division of Cell and Molecular Biophysics and Cardiovascular Division, King's College London, London, UK.
  • Nevo Y; The Unit of Neuropediatrics and Child Development, Division of Pediatrics.
  • Mitrani-Rosenbaum S; Goldyne Savad Institute of Gene Therapy, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
  • Attali R; Goldyne Savad Institute of Gene Therapy, Hadassah Hebrew University Medical Center, Jerusalem, Israel.
  • Finotti A; Department of Life Sciences, Section of Biochemistry and Molecular Biology.
  • Gambari R; Department of Life Sciences, Section of Biochemistry and Molecular Biology.
  • Mosca B; Department of Life Sciences, General Pathology Section, University of Ferrara, Ferrara, Italy.
  • Jungbluth H; Department of Paediatric Neurology, Neuromuscular Service, Evelina Children's Hospital, St. Thomas' Hospital, London, UK and Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience (IoPPN), King's College London, London, UK.
  • Zorzato F; Department of Biomedicine and Anesthesia, Basel University Hospital, Basel, Switzerland, Department of Life Sciences, General Pathology Section, University of Ferrara, Ferrara, Italy.
  • Treves S; Department of Biomedicine and Anesthesia, Basel University Hospital, Basel, Switzerland, Department of Life Sciences, General Pathology Section, University of Ferrara, Ferrara, Italy, susan.treves@unibas.ch.
Hum Mol Genet ; 24(16): 4636-47, 2015 Aug 15.
Article em En | MEDLINE | ID: mdl-26019235
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Debilidade Muscular / Canal de Liberação de Cálcio do Receptor de Rianodina / Epigênese Genética / Histona Desacetilases / Miotonia Congênita Limite: Animals Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Suíça
Texto completo
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XML
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Debilidade Muscular / Canal de Liberação de Cálcio do Receptor de Rianodina / Epigênese Genética / Histona Desacetilases / Miotonia Congênita Limite: Animals Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Suíça