Interaction of Aminoglycosides with Human Mitochondrial 12S rRNA Carrying the Deafness-Associated Mutation

Liknande verk

• Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss
  av: Li, Zhiyuan, et al.
  Publicerad: (2005)
• Maternally Inherited Aminoglycoside-Induced and Nonsyndromic Deafness Is Associated with the Novel C1494T Mutation in the Mitochondrial 12S rRNA Gene in a Large Chinese Family
  av: Zhao, Hui, et al.
  Publicerad: (2004)
• Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation
  av: Lu, Jianxin, et al.
  Publicerad: (2009)
• A Human Mitochondrial GTP Binding Protein Related to tRNA Modification May Modulate Phenotypic Expression of the Deafness-Associated Mitochondrial 12S rRNA Mutation
  av: Li, Xiaoming, et al.
  Publicerad: (2002)
• Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss
  av: Zhao, Hui, et al.
  Publicerad: (2005)