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Dongyang Kang

Research Profile

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China

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DNA Mutational Analysis

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Vestibular Aqueduct

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Publications

TOP 3
Shasha Huang; Dongyang Kang; Jun Liu; Xiaofei Yan; Yongyi Yuan; Xin Zhang; Min Dong; Dongyi Han; Pu Dai
De novo dominant mutation of GJB2 in two Chinese families with nonsyndromic hearing loss.
Guojian Wang; Yongyi Yuan; Xin Zhang; Pu Dai; Min Dong; Mingyu Han; Shasha Huang; Dongyang Kang; Rong Li; Dongyi Han
[Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype].
Shasha Huang; Dongyang Kang; Xiaoxiao Meng; Guojian Wang; Xiaofei Yan; Yongyi Yuan; Xin Zhang; Min Dong; Dongyi Han; Pu Dai
Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct.

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All Publications

2011: Shasha Huang; Dongyang Kang; Jun Liu; Xiaofei Yan; Yongyi Yuan; Xin Zhang; Min Dong; Dongyi Han; Pu Dai
De novo dominant mutation of GJB2 in two Chinese families with nonsyndromic hearing loss.
International journal of pediatric otorhinolaryngology 2011;75(10):1333-6.
2011: Guojian Wang; Yongyi Yuan; Xin Zhang; Pu Dai; Min Dong; Mingyu Han; Shasha Huang; Dongyang Kang; Rong Li; Dongyi Han
[Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype].
Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery 2011;25(10):445-8.
2011: Shasha Huang; Dongyang Kang; Xiaoxiao Meng; Guojian Wang; Xiaofei Yan; Yongyi Yuan; Xin Zhang; Min Dong; Dongyi Han; Pu Dai
Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct.
Journal of translational medicine 2011;9():167.
2010: Jianzhong Li; Jing Cheng; Yanping Lu; Yu Lu; Aiting Chen; Yi Sun; Dongyang Kang; Xin Zhang; Pu Dai; Dongyi Han; Huijun Yuan
Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss.
Journal of genetics and genomics = Yi chuan xue bao 2010;37(12):787-93.
2009: Pu Dai; Andrew K Stewart; Fouad Chebib; Ann Hsu; Julia Rozenfeld; Deliang Huang; Dongyang Kang; Va Lip; Hong Fang; Hong Shao; Xin Liu; Fei Yu; Huijun Yuan; Margaret Kenna; David T Miller; Yiping Shen; Weiyan Yang; Israel Zelikovic; Orah S Platt; Dongyi Han; Seth L Alper; Bai-Lin Wu
Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.
Physiological genomics 2009;38(3):281-90.
2009: Yongyi Yuan; Yiwen You; Deliang Huang; Jinghong Cui; Yong Wang; Qiang Wang; Fei Yu; Dongyang Kang; Huijun Yuan; Dongyi Han; Pu Dai
Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China.
Journal of translational medicine 2009;7():79.
2008: Jing Chen; Huijun Yuan; Jianxin Lu; Xin Liu; Guojian Wang; Yi Zhu; Jing Cheng; Xinjian Wang; Bing Han; Li Yang; Shuzhi Yang; Aifeng Yang; Qing Sun; Dongyang Kang; Xin Zhang; Pu Dai; Suoqiang Zhai; Dongyi Han; Wie-Yen Young; Min-Xin Guan
Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss.
Mitochondrion 2008;8(4):285-92.
2007: Huijun Yuan; Jing Chen; Xin Liu; Jing Cheng; Xinjian Wang; Li Yang; Shuzhi Yang; Juyang Cao; Dongyang Kang; Pu Dai; Suoqiang Zhai; Dongyi Han; Wie-Yen Young; Min-Xin Guan
Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss.
Biochemical and biophysical research communications 2007;362(1):94-100.
2007: Qingwen Zhu; Xin Liu; Dongyi Han; Dongyang Kang; Xin Zhang; Zhengce Jin; Mei Li; Pu Dai
[Molecular etiology of 573 patients with nonsyndromic hearing loss in 5 provinces of northwest region of China].
Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery 2007;21(10):460-2.
2006: Pu Dai; Xin Liu; Dongyi Han; Yaping Qian; Deliang Huang; Huijun Yuan; Weiming Li; Fei Yu; Ruining Zhang; Hongyan Lin; Yong He; Youjun Yu; Quanzhu Sun; Huaiyi Qin; Ronghua Li; Xin Zhang; Dongyang Kang; Juyang Cao; Wie-Yen Young; Min-Xin Guan
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness.
Biochemical and biophysical research communications 2006;340(1):194-9.
2006: Pu Dai; Dongyi Han; Juyang Cao; Suoqiang Zhai; Dongyang Kang; Xin Liu; Huijun Yuan; Xin Zhang; Mei Li; Lixian Liu; Bo Feng; Weiyan Yang; Bailin Wu
[Genotypic analysis of familial dilated vestibular aqueduct syndrome].
Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology 2006;20(4):147-50.
2005: Huijun Yuan; Yaping Qian; Yanjun Xu; Juyang Cao; Linna Bai; Weidong Shen; Fei Ji; Xin Zhang; Dongyang Kang; Jun Qin Mo; John H Greinwald; Dongyi Han; Suoqiang Zhai; Wie-Yen Young; Min-Xin Guan
Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss.
American journal of medical genetics. Part A 2005;138A(2):133-40.