B. Zheng

Mitochondrial haplogroup B increases the risk for hearing loss among the Eastern Asian pedigrees carrying 12S rRNA 1555A>G mutation

M. Guan, Yi Zhu, Xiao-wen Tang, 2015, Protein & Cell.

A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function

Taosheng Huang, Meng Wang, M. Guan, 2016, Nucleic acids research.

[Mitochondrial tRNAIle A4317G mutation may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation].

M. Guan, Jianxin Lu, Yi Zhu, 2013, Yi chuan = Hereditas.

Mitochondrial haplogroup B increases the risk for hearing loss among the Eastern Asian pedigrees carrying 12S rRNA 1555A>G mutation

M. Guan, Yi Zhu, Xiao-wen Tang, 2015, Protein & Cell.

[Spectrum and frequency of mitochondrial 12S rRNA variants in the Chinese subjects with nonsynrdomic hearing loss in Zhejiang Province].

M. Guan, Bobei Chen, Jianxin Lu, 2012, Yi chuan = Hereditas.

[Mitochondrial 12S rRNA A1555G mutation associated with nonsyndromic hearing loss in twenty-five Han Chinese pedigrees].

Jing Zheng, Min-Xin Guan, Jian-Xin Lu, 2013, Yi chuan = Hereditas.

[Molecular mechanisms underlying function of hair bundle: study on genetic deafness in mouse models].

M. Guan, Jing Zheng, B. Zheng, 2012, Sheng li xue bao : [Acta physiologica Sinica].