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The presence of highly disruptive 16S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human disease.
Elson, Joanna L; Smith, Paul M; Greaves, Laura C; Lightowlers, Robert N; Chrzanowska-Lightowlers, Zofia M A; Taylor, Robert W; Vila-Sanjurjo, Antón.
Afiliação
  • Elson JL; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, United Kingdom; Centre for Human Metabonomics, North-West University, Potchefstroom, South Africa.
  • Smith PM; Institute of Medical Sciences, Ninewells Hospital and Medical School, Dundee University, Dundee DD1 9SY, Scotland, UK; Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, The Medical School, Newcastle upon Tyne NE2 4HH, United Kingdom.
  • Greaves LC; Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, The Medical School, Newcastle upon Tyne NE2 4HH, United Kingdom.
  • Lightowlers RN; Newcastle University Institute for Cell and Molecular Biosciences, Newcastle University, The Medical School, Newcastle upon Tyne NE2 4HH, United Kingdom.
  • Chrzanowska-Lightowlers ZM; Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, The Medical School, Newcastle upon Tyne NE2 4HH, United Kingdom.
  • Taylor RW; Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, The Medical School, Newcastle upon Tyne NE2 4HH, United Kingdom.
  • Vila-Sanjurjo A; Grupo GIBE, Bioloxía Celular e Molecular, Facultade de Ciencias, Universidade da Coruña (UDC), Campus Zapateira s/n, 15071 A Coruña, Spain. Electronic address: antonvila.s@gmail.com.
Mitochondrion ; 25: 17-27, 2015 Nov.
Article em En | MEDLINE | ID: mdl-26349026

Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA Ribossômico 16S / RNA Ribossômico 23S / Doenças Mitocondriais / Ribossomos Mitocondriais / Mutação Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA Ribossômico 16S / RNA Ribossômico 23S / Doenças Mitocondriais / Ribossomos Mitocondriais / Mutação Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article