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A natural non-Watson-Crick base pair in human mitochondrial tRNAThr causes structural and functional susceptibility to local mutations.
Wang, Yong; Zeng, Qi-Yu; Zheng, Wen-Qiang; Ji, Quan-Quan; Zhou, Xiao-Long; Wang, En-Duo.
Afiliación
  • Wang Y; State Key Laboratory of Molecular Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences; University of Chinese Academy of Sciences, 320 Yueyang Road, Shanghai 200031, P.R. China.
  • Zeng QY; School of Life Science and Technology, ShanghaiTech University, 100 Haike Road, Shanghai 201210, P.R. China.
  • Zheng WQ; State Key Laboratory of Molecular Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences; University of Chinese Academy of Sciences, 320 Yueyang Road, Shanghai 200031, P.R. China.
  • Ji QQ; School of Life Science and Technology, ShanghaiTech University, 100 Haike Road, Shanghai 201210, P.R. China.
  • Zhou XL; State Key Laboratory of Molecular Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences; University of Chinese Academy of Sciences, 320 Yueyang Road, Shanghai 200031, P.R. China.
  • Wang ED; State Key Laboratory of Molecular Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences; University of Chinese Academy of Sciences, 320 Yueyang Road, Shanghai 200031, P.R. China.
Nucleic Acids Res ; 46(9): 4662-4676, 2018 05 18.
Article en En | MEDLINE | ID: mdl-29648639
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ARN de Transferencia de Treonina / ARN Mitocondrial / Mutación Tipo de estudio: Etiology_studies Límite: Humans Idioma: En Revista: Nucleic Acids Res Año: 2018 Tipo del documento: Article
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ARN de Transferencia de Treonina / ARN Mitocondrial / Mutación Tipo de estudio: Etiology_studies Límite: Humans Idioma: En Revista: Nucleic Acids Res Año: 2018 Tipo del documento: Article