Aifen Yang

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 · 140 citations

Medicine, Genetics, Molecular Genetics +15

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 · 117 citations

Medicine, Genetics, Molecular Genetics +15

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

Life Sciences, Genetics, Molecular Genetics +17

S100B is selectively expressed by gray matter protoplasmic astrocytes and myelinating oligodendrocytes in the developing CNS

Junqing Du, Min Yi, Fang Zhou et al. · Molecular Brain · 2021 · 50 citations · Full text

Medicine, Neurobiology, Neuroscience +17

Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families

Xinjian Wang, Jianxin Lü, Yi Zhu et al. · Pharmacogenetics and Genomics · 2008 · 49 citations · Full text

Medicine, Genetics, Molecular Genetics +15