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Xinjian Wang

Research Profile

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Chemicals & Drugs

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China

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Asian Continental Ancestry Group

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DNA Mutational Analysis

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TOP 3
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.
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.
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.

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All Publications

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: Yi Tong; Yijian Mao; Zhou Xiangtian; Li Yang; Juanjuan Zhang; Wanshi Cai; Fuxing Zhao; Xinjian Wang; Fan Lu; Jia Qu; Min-Xin Guan
The mitochondrial tRNA(Glu) A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber's hereditary optic neuropathy.
Biochemical and biophysical research communications 2007;357(2):524-30.
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.