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Yi Zhu

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Guang-hua Peng; Xiao-wen Tang; Yue Wu; Xiao Yu; Qiong-min Zhang; Bin-jiao Zheng; Jing Zheng; Yi Zhu; Fang Fang; Ling-zhi Liang; Bo-bei Chen
[Mitochondrial 12S rRNA variants studies in 456 subjects with hearing loss in seven schools for deaf and mutes in Zhejiang province].
Bin-Jiao Zheng; Jing Zheng; Yi Zhu; Bo-bei Chen; Fang Fang; Ling-Zhi Liang; Jian-Xin Lu; Ben-Yu Nan; Guang-Hua Peng; Xiao-Wen Tang; Yue Wu; Min-Xin Guan
[Spectrum and frequency of mitochondrial 12S rRNA variants in the Chinese subjects with nonsynrdomic hearing loss in Zhejiang Province].
Zhisen Shen; Jing Zheng; Bobei Chen; Guanghua Peng; Ting Zhang; Shasha Gong; Yi Zhu; Chuqin Zhang; Ronghua Li; Li Yang; Jianjin Zhou; Ting Cai; Lihua Jin; Jianxin Lu; Min-Xin Guan
Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics.

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All Publications

2012: Guang-hua Peng; Xiao-wen Tang; Yue Wu; Xiao Yu; Qiong-min Zhang; Bin-jiao Zheng; Jing Zheng; Yi Zhu; Fang Fang; Ling-zhi Liang; Bo-bei Chen
[Mitochondrial 12S rRNA variants studies in 456 subjects with hearing loss in seven schools for deaf and mutes in Zhejiang province].
Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery 2012;47(12):996-1003.
2012: Bin-Jiao Zheng; Jing Zheng; Yi Zhu; Bo-bei Chen; Fang Fang; Ling-Zhi Liang; Jian-Xin Lu; Ben-Yu Nan; Guang-Hua Peng; Xiao-Wen Tang; Yue Wu; Min-Xin Guan
[Spectrum and frequency of mitochondrial 12S rRNA variants in the Chinese subjects with nonsynrdomic hearing loss in Zhejiang Province].
Yi chuan = Hereditas / Zhongguo yi chuan xue hui bian ji 2012;34(6):695-704.
2011: Zhisen Shen; Jing Zheng; Bobei Chen; Guanghua Peng; Ting Zhang; Shasha Gong; Yi Zhu; Chuqin Zhang; Ronghua Li; Li Yang; Jianjin Zhou; Ting Cai; Lihua Jin; Jianxin Lu; Min-Xin Guan
Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics.
Journal of translational medicine 2011;9():4.
2010: Jianxin Lu; Zhiyuan Li; Yi Zhu; Aifen Yang; Ronghua Li; Jing Zheng; Qin Cai; Guanghua Peng; Wuwei Zheng; Xiaowen Tang; Bobei Chen; Jianfu Chen; Zhisu Liao; Li Yang; Yongyan Li; Junyan You; Yu Ding; Hong Yu; Jindan Wang; Dongmei Sun; Jianyue Zhao; Ling Xue; Jiying Wang; Min-Xin Guan
Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss.
Mitochondrion 2010;10(4):380-90.
2010: Xiaowen Tang; Ronghua Li; Jing Zheng; Qin Cai; Ting Zhang; Shasha Gong; Wuwei Zheng; Xiumei He; Yi Zhu; Ling Xue; Aifen Yang; Li Yang; Jianxin Lu; Min-Xin Guan
Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family.
Molecular genetics and metabolism 2010;100(1):57-64.
2010: Jianxin Lu; Yaping Qian; Zhiyuan Li; Aifen Yang; Yi Zhu; Ronghua Li; Li Yang; Xiaowen Tang; Bobei Chen; Yu Ding; Yongyan Li; Junyan You; Jing Zheng; Zhihua Tao; Fuxin Zhao; Jindan Wang; Dongmei Sun; Jianyue Zhao; Yanzi Meng; Min-Xin Guan
Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.
Mitochondrion 2010;10(1):69-81.
2008: Xiao-Wen Tang; Zhi-Yuan Li; Jian-Xin Lu; Yi Zhu; Rong-Hua Li; Jin-Dan Wang; Min-Xin Guan
[Mitochondrial tRNAThr G15927A mutation may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation.].
Yi chuan = Hereditas / Zhongguo yi chuan xue hui bian ji 2008;30(10):1287-94.
2008: Ai-Fen Yang; Yi Zhu; Jian-Xin Lu; Li Yang; Jian-Yue Zhao; Dong-Mei Sun
[Mitochondrial DNA G7444A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation].
Yi chuan = Hereditas / Zhongguo yi chuan xue hui bian ji 2008;30(6):728-34.
2008: Bobei Chen; Dongmei Sun; Li Yang; Chuqin Zhang; Aifen Yang; Yi Zhu; Jianyue Zhao; Yingying Chen; Minqiang Guan; Xinjian Wang; Ronghua Li; Xiaowen Tang; Jindan Wang; Zhihua Tao; Jianxin Lu; Min-Xin Guan
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.
American journal of medical genetics. Part A 2008;146A(10):1248-58.
2007: Zhisu Liao; Jianyue Zhao; Yi Zhu; Li Yang; Aifen Yang; Dongmei Sun; Zhongnong Zhao; Xinjian Wang; Zhihua Tao; Xiaowen Tang; Jindan Wang; Minqiang Guan; Jiafu Chen; Zhiyuan Li; Jianxin Lu; Min-Xin Guan
The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family.
Biochemical and biophysical research communications 2007;362(3):670-6.
2007: Jianfu Chen; Li Yang; Aifen Yang; Yi Zhu; Jianyue Zhao; Dongmei Sun; Zhihua Tao; Xiaowen Tang; Jindan Wang; Xinjian Wang; Asami Tsushima; Jinshan Lan; Weixing Li; Fangli Wu; Qian Yuan; Jingzhang Ji; Jinbao Feng; Chunli Wu; Zhisu Liao; Zhiyuan Li; John H Greinwald; Jianxin Lu; Min-Xin Guan
Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.
Gene 2007;401(1-2):4-11.
2007: Longjin Jin; Aifen Yang; Yi Zhu; Jianyue Zhao; Xinjian Wang; Li Yang; Dongmei Sun; Zhihua Tao; Asami Tsushima; Guomin Wu; Limin Xu; Chongxi Chen; Boquan Yi; Jianxin Cai; Xiaowen Tang; Jindan Wang; Dong Li; Qian Yuan; Zhisu Liao; Jiafu Chen; Zhiyuan Li; Jianxin Lu; Min-Xin Guan
Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss.
Biochemical and biophysical research communications 2007;361(1):133-9.
2007: Xiaowen Tang; Li Yang; Yi Zhu; Zhisu Liao; Jindan Wang; Yaping Qian; Zhihua Tao; Lenong Hu; Guomin Wu; Jinshan Lan; Xinjian Wang; Jingzhang Ji; Jian Wu; Yu Ji; Jinbao Feng; Jianfu Chen; Zhiyuan Li; Xue Zhang; Jianxin Lu; Min-Xin Guan
Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation.
Gene 2007;393(1-2):11-9.
2006: Jianxin Lu; Dawang Wang; Ronghua Li; Weixing Li; Jingzhang Ji; Jing Zhao; Wei Ye; Li Yang; Yaping Qian; Yi Zhu; Min-Xin Guan
Maternally transmitted diabetes mellitus associated with the mitochondrial tRNA(Leu(UUR)) A3243G mutation in a four-generation Han Chinese family.
Biochemical and biophysical research communications 2006;348(1):115-9.
2006: Yi Zhu; Yaping Qian; Xiaowen Tang; Jindan Wang; Li Yang; Zhisu Liao; Ronghua Li; Jinzhang Ji; Zhiyuan Li; Jianfu Chen; Daniel I Choo; Jianxin Lu; Min-Xin Guan
Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNASer(UCN) genes in two Chinese families.
Biochemical and biophysical research communications 2006;342(3):843-50.
2005: Zhiyuan Li; Ronghua Li; Jianfu Chen; Zhisu Liao; Yi Zhu; Yaping Qian; Sudao Xiong; Selena Heman-Ackah; Jianbo Wu; Daniel I Choo; Min-Xin Guan
Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss.
Human genetics 2005;117(1):9-15.