Hasil Pencarian - Ming-Yu Han

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  1. 1
    How the enhanced East Asian summer monsoon regulates total gross primary production in eastern China

    How the enhanced East Asian summer monsoon regulates total gross primary production in eastern China oleh Ming-Yu Han, Yong Zhang, Jing Peng

    Diterbitkan 2024-04-01
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  2. 2
    Establishment of human induced pluripotent stem cell line (CPGHi002-A) from a 10-month-old female patient with DDOD syndrome carrying a heterozygous c.1516 C > T mutation in ATP6V1B2

    Establishment of human induced pluripotent stem cell line (CPGHi002-A) from a 10-month-old female patient with DDOD syndrome carrying a heterozygous c.1516 C > T mutation in ATP6V1... oleh Xue Gao, Shi–Wei Qiu, Meng-Long Feng, Sha-Sha Huang, Dong-Yang Kang, Ming-Yu Han, Pu Dai, Yong–Yi Yuan

    Diterbitkan 2020-10-01
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  3. 3
    MPZL2—a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population

    MPZL2—a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population oleh Lang Zhang, Jin-Yuan Yang, Qiu-Quan Wang, Xue Gao, Guo-Jian Wang, Ming-Yu Han, Dong-Yang Kang, Dong-Yi Han, Sha-Sha Huang, Yong-Yi Yuan

    Diterbitkan 2024-01-01
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  4. 4
    A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3–4

    A newborn male with Myhre syndrome, hearing loss, and complete syndactyly of fingers 3–4 oleh Kun Yang, Xi Wang, Wei‐Qian Wang, Ming‐Yu Han, Li‐Min Hu, Dong‐Yang Kang, Jin‐Yuan Yang, Min Liu, Xue Gao, Yong‐Yi Yuan, Jin‐Cao Xu

    Diterbitkan 2023-03-01
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  5. 5
    Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population

    Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population oleh 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

    Diterbitkan 2017-01-01
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  6. 6
    Novel compound heterozygous mutations in MYO7A Associated with Usher syndrome 1 in a Chinese family.

    Novel compound heterozygous mutations in MYO7A Associated with Usher syndrome 1 in a Chinese family. oleh Xue Gao, Guo-Jian Wang, Yong-Yi Yuan, Feng Xin, Ming-Yu Han, Jing-Qiao Lu, Hui Zhao, Fei Yu, Jin-Cao Xu, Mei-Guang Zhang, Jiang Dong, Xi Lin, Pu Dai

    Diterbitkan 2014-01-01
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  7. 7
    Correction: Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family.

    Correction: Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family. oleh Xue Gao, Guo-Jian Wang, Yong-Yi Yuan, Feng Xin, Ming-Yu Han, Jing-Qiao Lu, Hui Zhao, Fei Yu, Jin-Cao Xu, Mei-Guang Zhang, Jiang Dong, Xi Lin, Pu Dai

    Diterbitkan 2015-01-01
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  8. 8
    Novel compound heterozygous TMC1 mutations associated with autosomal recessive hearing loss in a Chinese family.

    Novel compound heterozygous TMC1 mutations associated with autosomal recessive hearing loss in a Chinese family. oleh Xue Gao, Yu Su, Li-Ping Guan, Yong-Yi Yuan, Sha-Sha Huang, Yu Lu, Guo-Jian Wang, Ming-Yu Han, Fei Yu, Yue-Shuai Song, Qing-Yan Zhu, Jing Wu, Pu Dai

    Diterbitkan 2013-01-01
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  9. 9
    Genetic Analysis of the LOXHD1 Gene in Chinese Patients With Non-Syndromic Hearing Loss

    Genetic Analysis of the LOXHD1 Gene in Chinese Patients With Non-Syndromic Hearing Loss oleh Wei-Qian Wang, Wei-Qian Wang, Xue Gao, Xue Gao, Sha-Sha Huang, Dong-Yang Kang, Jin-Cao Xu, Kun Yang, Ming-Yu Han, Xin Zhang, Su-Yan Yang, Yong-Yi Yuan, Pu Dai

    Diterbitkan 2022-05-01
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  10. 10
    Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family.

    Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family. oleh 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

    Diterbitkan 2015-01-01
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  11. 11
    Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A

    Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site v... oleh Jin-Yuan Yang, Wei-Qian Wang, Ming-Yu Han, Sha-Sha Huang, Guo-Jian Wang, Yu Su, Jin-Cao Xu, Ying Fu, Dong-Yang Kang, Kun Yang, Xin Zhang, Xing Liu, Xue Gao, Yong-Yi Yuan, Pu Dai

    Diterbitkan 2022-11-01
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  12. 12
    A novel mutation in the TECTA gene in a Chinese family with autosomal dominant nonsyndromic hearing loss.

    A novel mutation in the TECTA gene in a Chinese family with autosomal dominant nonsyndromic hearing loss. oleh 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

    Diterbitkan 2014-01-01
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