Jianyue Zhao

Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss

Jianxin Lü, Zhiyuan Li, Yi Zhu et al. · Mitochondrion · 2010 · 138 citations

Mitochondrial Biogenesis, Mitochondrial Function, Rrna Variants +11

Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation

Jianxin Lü, Yaping Qian, Zhiyuan Li et al. · Mitochondrion · 2009 · 116 citations

Biology, Mendelian Disorder, Rrna 1555A +9

Mitochondrial ND5 T12338C, tRNA^Cys T5802C, and tRNA^Thr G15927A variants may have a modifying role in the phenotypic manifestation of deafness‐associated 12S rRNA A1555G mutation in three Han Chinese pedigrees

Bobei Chen, Dongmei Sun, Li Yang et al. · American Journal of Medical Genetics Part A · 2008 · 51 citations

Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees

Jian‐Fu Chen, Li Yang, Aifen Yang et al. · Gene · 2007 · 44 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +12

Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss

Longjin Jin, Aifen Yang, Yi Zhu et al. · Biochemical and Biophysical Research Communications · 2007 · 44 citations

Non-syndromic Hearing Loss, Mitochondrial Function, Genetic Disorder +8