Hasil Pencarian - Yongyi Yuan
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1
The Relationship between the p.V37I Mutation in GJB2 and Hearing Phenotypes in Chinese Individuals. oleh Shasha Huang, Bangqing Huang, Guojian Wang, Yongyi Yuan, Pu Dai
Diterbitkan 2015-01-01
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2
Calibrating FY4A QPE using CMPA over Yunnan–Kweichow Plateau in summer 2019 oleh Hanyu Lu, Ziyue Huang, Leiding Ding, Tianjian Lu, Yongyi Yuan
Diterbitkan 2021-01-01
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Editorial: Hearing Loss: Mechanisms and Prevention oleh Renjie Chai, Hongzhe Li, Tao Yang, Shan Sun, Yongyi Yuan
Diterbitkan 2022-02-01
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Integrated Evaluation and error decomposition of four gridded precipitation products using dense rain gauge observations over the Yunnan-Kweichow Plateau, China oleh Tianjian Lu, Qingquan Xiao, Hanyu Lu, Jintong Ren, Yongyi Yuan, Xiaoshan Luo, Zhijie Zhang
Diterbitkan 2024-12-01
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Mitochondrial tRNASer(UCN) mutations associated non-syndromic sensorineural hearing loss in Chinese families oleh Dejun Zhang, Jie Wu, Yongyi Yuan, Xiaohong Li, Xue Gao, Dongyang Kang, Xin Zhang, Sha-sha Huang, Pu Dai
Diterbitkan 2024-03-01
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A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disabilityResearch in context oleh Weihao Zhao, Xue Gao, Shiwei Qiu, Bo Gao, Song Gao, Xin Zhang, Dongyang Kang, Weiju Han, Pu Dai, Yongyi Yuan
Diterbitkan 2019-07-01
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9
Molecular epidemiology and functional assessment of novel allelic variants of SLC26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct in China. oleh Yongyi Yuan, Weiwei Guo, Jie Tang, Guozheng Zhang, Guojian Wang, Mingyu Han, Xun Zhang, Shiming Yang, David Z Z He, Pu Dai
Diterbitkan 2012-01-01
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10
Establishment of an iPSC line (CPGHi005-A) from a patient with Waardenburg syndrome carrying a heterozygous SVA-F retrotransposon insertion into SOX10 oleh Xiaohong Li, Xue Gao, Shasha Huang, Mingyu Han, Dongyang Kang, Jinyuan Yang, Xiedong Wu, Qiuchen Zheng, Yongyi Yuan, Pu Dai, Guojian Wang
Diterbitkan 2022-07-01
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11
Genomic and phenotypic landscapes of X-linked hereditary hearing loss in the Chinese population oleh Haifeng Feng, Shasha Huang, Ying Ma, Jinyuan Yang, Yijin Chen, Guojian Wang, Mingyu Han, Dongyang Kang, Xin Zhang, Pu Dai, Yongyi Yuan
Diterbitkan 2024-09-01
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12
Common molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairment. oleh Yongyi Yuan, Xun Zhang, Shasha Huang, Lujie Zuo, Guozheng Zhang, Yueshuai Song, Guojian Wang, Hongtian Wang, Deliang Huang, Dongyi Han, Pu Dai
Diterbitkan 2012-01-01
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13
Syndromic Deafness Gene ATP6V1B2 Controls Degeneration of Spiral Ganglion Neurons Through Modulating Proton Flux oleh Shiwei Qiu, Shiwei Qiu, Weihao Zhao, Weihao Zhao, Xue Gao, Dapeng Li, Weiqian Wang, Bo Gao, Weiju Han, Shiming Yang, Pu Dai, Peng Cao, Yongyi Yuan
Diterbitkan 2021-10-01
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14
Characterization of SH3GLB1 in the auditory system and its potential role in mitophagy oleh Xue Gao, Weiqian Wang, Jincao Xu, Shasha Huang, Kun Yang, Jinyuan Yang, Yijin Chen, Guojian Wang, Mingyu Han, Zhendong Wang, Dongyang Kang, Yongyi Yuan, Pu Dai
Diterbitkan 2024-07-01
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15
Gene4HL: An Integrated Genetic Database for Hearing Loss oleh Shasha Huang, Shasha Huang, Shasha Huang, Guihu Zhao, Guihu Zhao, Jie Wu, Jie Wu, Jie Wu, Kuokuo Li, Kuokuo Li, Qiuquan Wang, Qiuquan Wang, Qiuquan Wang, Ying Fu, Ying Fu, Ying Fu, Honglei Zhang, Honglei Zhang, Honglei Zhang, Qingling Bi, Qingling Bi, Qingling Bi, Xiaohong Li, Xiaohong Li, Xiaohong Li, Weiqian Wang, Weiqian Wang, Weiqian Wang, Chang Guo, Chang Guo, Chang Guo, Dejun Zhang, Dejun Zhang, Dejun Zhang, Lihua Wu, Lihua Wu, Lihua Wu, Xiaoge Li, Xiaoge Li, Xiaoge Li, Huiyan Xu, Huiyan Xu, Huiyan Xu, Mingyu Han, Mingyu Han, Mingyu Han, Xin Wang, Chen Lei, Xiaofang Qiu, Yang Li, Jinchen Li, Jinchen Li, Pu Dai, Pu Dai, Pu Dai, Yongyi Yuan, Yongyi Yuan, Yongyi Yuan
Diterbitkan 2021-10-01
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