Search Results - Pu Dai

  • Showing 1 - 14 results of 14
Refine Results
  1. 1

    Outcomes of cochlear implantation in 75 patients with auditory neuropathy by Jie Wu, Jiyue Chen, Zhiwei Ding, Jialin Fan, Qiuquan Wang, Pu Dai, Dongyi Han

    Published in Frontiers in Neuroscience (2023-11-01)
    Get full text
    Article


  2. 2

    A novel PIK3CD C896T mutation detected in bilateral sudden sensorineural hearing loss using next generation sequencing: An indication of primary immunodeficiency by Jing Zou, Xiangqiang Duan, Guiliang Zheng, Zhen Zhao, Shiyue Chen, Pu Dai, Hongliang Zheng

    Published in Journal of Otology (2016-06-01)
    Get full text
    Article


  3. 3

    Analysis of the genotype–phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients by Ying Fu, Shasha Huang, Xue Gao, Mingyu Han, Guojian Wang, Dongyang Kang, Yongyi Yuan, Pu Dai

    Published in BMC Medical Genomics (2022-03-01)
    Get full text
    Article


  4. 4

    Mitochondrial tRNASer(UCN) mutations associated non-syndromic sensorineural hearing loss in Chinese families by Dejun Zhang, Jie Wu, Yongyi Yuan, Xiaohong Li, Xue Gao, Dongyang Kang, Xin Zhang, Sha-sha Huang, Pu Dai

    Published in Heliyon (2024-03-01)
    Get full text
    Article


  5. 5

    Genomic and phenotypic landscapes of X-linked hereditary hearing loss in the Chinese population by Haifeng Feng, Shasha Huang, Ying Ma, Jinyuan Yang, Yijin Chen, Guojian Wang, Mingyu Han, Dongyang Kang, Xin Zhang, Pu Dai, Yongyi Yuan

    Published in Orphanet Journal of Rare Diseases (2024-09-01)
    Get full text
    Article


  6. 6

    Functional characterization of MFSD3 in auditory system and zebrafish embryogenesis by Ying Ma, Ying Ma, Ying Ma, Ying Ma, Ying Ma, Shi-Wei Qiu, Shi-Wei Qiu, Wei-Qian Wang, Hai-Feng Feng, Hai-Feng Feng, Hai-Feng Feng, Hai-Feng Feng, Hai-Feng Feng, Lu Zheng, Lu Zheng, Lu Zheng, Lu Zheng, Lu Zheng, Ge-Ge Wei, Ge-Ge Wei, Ge-Ge Wei, Ge-Ge Wei, Ge-Ge Wei, Hui-Yi Nie, Hui-Yi Nie, Hui-Yi Nie, Hui-Yi Nie, Hui-Yi Nie, Jin-Yuan Yang, Jin-Yuan Yang, Jin-Yuan Yang, Jin-Yuan Yang, Jin-Yuan Yang, Yi-Jin Chen, Yi-Jin Chen, Yi-Jin Chen, Yi-Jin Chen, Yi-Jin Chen, Pu Dai, Pu Dai, Pu Dai, Pu Dai, Pu Dai, Xue Gao, Yong-Yi Yuan, Yong-Yi Yuan, Yong-Yi Yuan, Yong-Yi Yuan, Yong-Yi Yuan

    Published in Frontiers in Genetics (2025-09-01)
    Get full text
    Article


  7. 7

    Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation by Chang Guo, Sha-Sha Huang, Yong-Yi Yuan, Ying Zhou, Ning Wang, Dong-Yang Kang, Su-Yan Yang, Xin Zhang, Xue Gao, Pu Dai

    Published in Neural Plasticity (2020-01-01)
    Get full text
    Article


  8. 8

    Characterization of SH3GLB1 in the auditory system and its potential role in mitophagy by 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

    Published in Genes and Diseases (2024-07-01)
    Get full text
    Article


  9. 9

    Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population by Xue Gao, Sha-Sha Huang, Yong-Yi Yuan, Jin-Cao Xu, Ping Gu, Dan Bai, Dong-Yang Kang, Ming-Yu Han, Guo-Jian Wang, Mei-Guang Zhang, Jia Li, Pu Dai

    Published in Neural Plasticity (2017-01-01)
    Get full text
    Article


  10. 10

    Single Administration of AAV‐mAtp6v1b2 Gene Therapy Rescues Hearing and Vestibular Disorders Caused by Atp6v1b2‐Induced Lysosomal Dysfunction in Hair Cells by Gege Wei, Shiwei Qiu, Xue Gao, Lu Zheng, Yijin Chen, Ying Ma, Haifeng Feng, Jinyuan Yang, Guojie Dong, Huiyi Nie, Weihao Zhao, Xiaoge Li, Guangqin Wang, Wei Xiong, Pu Dai, Yongyi Yuan

    Published in Advanced Science (2025-08-01)
    Get full text
    Article


  11. 11

    Novel autosomal dominant syndromic hearing loss caused by COL4A2-related basement membrane dysfunction of cochlear capillaries and microcirculation disturbance by Jinyuan Yang, Ying Ma, Xue Gao, Shiwei Qiu, Xiaoge Li, Weihao Zhao, Yijin Chen, Guojie Dong, Rongfeng Lin, Gege Wei, Huiyi Nie, Haifeng Feng, Xiaoning Gu, Bo Gao, Pu Dai, Yongyi Yuan, Sihan Zhou

    Published in Chinese Medical Journal (2025-08-01)
    Get full text
    Article


  12. 12

    Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family. by Xue Gao, Yu Su, Yu-Lan Chen, Ming-Yu Han, Yong-Yi Yuan, Jin-Cao Xu, Feng Xin, Mei-Guang Zhang, Sha-Sha Huang, Guo-Jian Wang, Dong-Yang Kang, Li-Ping Guan, Jian-Guo Zhang, Pu Dai

    Published in PLoS ONE (2015-01-01)
    Get full text
    Article


  13. 13

    A novel mutation in the TECTA gene in a Chinese family with autosomal dominant nonsyndromic hearing loss. by Yu Su, Wen-Xue Tang, Xue Gao, Fei Yu, Zhi-Yao Dai, Jian-Dong Zhao, Yu Lu, Fei Ji, Sha-Sha Huang, Yong-Yi Yuan, Ming-Yu Han, Yue-Shuai Song, Yu-Hua Zhu, Dong-Yang Kang, Dong-Yi Han, Pu Dai

    Published in PLoS ONE (2014-01-01)
    Get full text
    Article


  14. 14

    Analysis of influencing factors for prognosis of patients with ventricular septal perforation: A single-center retrospective study by Ming-Xuan Duan, Xi Zhao, Shao-Lin Li, Jun-Zhong Tao, Bo-Yan Li, Xin-Guo Meng, Dong-Pu Dai, Yan-Yu Lu, Zhen-Zhen Yue, Yang Du, Zi-Ao Rui, Shuo Pang, Yuan-Hang Zhou, Guang-Rui Miao, Lin-Peng Bai, Qing-Yang Zhang, Xiao-Yan Zhao

    Published in Frontiers in Cardiovascular Medicine (2022-11-01)
    Get full text
    Article


Search Tools: