耳鼻喉科学

30728030
2007
H1403.耳及侧颅底疾病
陈正一
海外或港、澳青年学者合作研究基金
副教授
中国人民解放军总医院
40万元
耳聋;基因;功能基因组学;cDNA微阵列;毛细胞再生
2008-01至2010-12
  • 中英文摘要
  • 结题摘要
  • 结题报告
  • 项目成果
  • 项目参与人
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序号 标题 类型 作者
1 GJB2 mutation spectrum in 2,063 Chinese patients with nonsyndromic hearing impairment. 期刊 Dai. Pu;Yu Fei;Han Bing;Liu Xuezhong;Wang Guojian;Li Qi;Yuan Yongyi;Liu Xin;Huang Deliang;Kang Dongyang;Zhang Xin;Yuan Huijun;Yao Kun;Hao Jinsheng;He Jia;He Yong;Wang Youqin;Ye Qing;Yu Youjun;Lin Hongyan;Liu Lijia;Deng Wei;Zhu Xiuhui;You Yiwen;Cui Jinghong;Hou Nongsheng;Xu Xuehai;Zhang Jin;Tang Liang;Song Rendong;Lin Yongjun;Sun Shuanzhu;Zhang Ruining;Wu Hao;Ma Yuebing;Zhu Shanxiang...
2 Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss 期刊 Dai. Pu;Stewart Andrew K;Chebib Fouad;Hsu Ann;Rozenfeld Julia;Huang Deliang;Kang Dongyang;Lip Va;Fang Hong;Shao Hong;Liu Xin;Yu Fei;Yuan Huijun;Kenna Margaret;Miller David T;Shen Yiping;Yang Weiyan;Zelikovic Israel;Platt Orah S;Han Dongyi;Alper Seth L;Wu Bailin
3 Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2 期刊 Xuezhong Liu;Dongyi Han;Jianzhong Li;Bing Han;Xiaomei Ouyang;Jing Cheng;Xu Li;Zhanguo Jin;Youqin Wang;Maria Bitner-Glindzicz;Xiangyin Kong;Heng Xu;Albena Kantardzhieva;Roland D. Eavey;Christine E. Seidman;Jonathan G. Seidman;Li L. Du;Zheng-Yi Chen;Pu Dai;Maikun Teng;Denise Yan;Huijun Yuan
4 Prevalence of the GJB2 IVS1+ 1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2 期刊 Yuan Yongyi;Yu Fei;Wang Guojian;Huang Shasha;Yu Ruili;Zhang Xin;Huang Deliang;Han Dongyi;Dai Pu
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