Hasil Pencarian - Chufeng He

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  1. 1
    A Model of Waardenburg Syndrome Using Patient-Derived iPSCs With a SOX10 Mutation Displays Compromised Maturation and Function of the Neural Crest That Involves Inner Ear Development

    A Model of Waardenburg Syndrome Using Patient-Derived iPSCs With a SOX10 Mutation Displays Compromised Maturation and Function of the Neural Crest That Involves Inner Ear Developme... oleh Jie Wen, Jie Wen, Jie Wen, Jian Song, Jian Song, Jian Song, Yijiang Bai, Yijiang Bai, Yijiang Bai, Yalan Liu, Yalan Liu, Yalan Liu, Xinzhang Cai, Xinzhang Cai, Xinzhang Cai, Lingyun Mei, Lingyun Mei, Lingyun Mei, Lu Ma, Chufeng He, Chufeng He, Chufeng He, Yong Feng, Yong Feng

    Diterbitkan 2021-08-01
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  2. 2
    Short-term effects of intravenous batroxobin in treatment of sudden sensorineural hearing loss: a propensity score-matched study

    Short-term effects of intravenous batroxobin in treatment of sudden sensorineural hearing loss: a propensity score-matched study oleh Mengzhu Jiang, Mengzhu Jiang, Huping Huang, Huping Huang, Lingyun Mei, Lingyun Mei, Lingyun Mei, Chufeng He, Chufeng He, Chufeng He, Xinzhang Cai, Xinzhang Cai, Xinzhang Cai, Lu Jiang, Lu Jiang, Lu Jiang, Hong Wu, Hong Wu, Hong Wu, Xin Wang, Xin Wang, Xuewen Wu, Xuewen Wu, Xuewen Wu

    Diterbitkan 2023-04-01
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  3. 3
    <i>Houttuynia cordata</i> Thunb. Extracts Alleviate Atherosclerosis and Modulate Gut Microbiota in Male Hypercholesterolemic Hamsters

    <i>Houttuynia cordata</i> Thunb. Extracts Alleviate Atherosclerosis and Modulate Gut Microbiota in Male Hypercholesterolemic Hamsters oleh Yuhong Lin, Chufeng He, Jianhui Liu, Hau-Yin Chung, Zhen-Yu Chen, Wing-Tak Wong

    Diterbitkan 2024-09-01
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  4. 4
    A comprehensive genotype–phenotype evaluation of eight Chinese probands with Waardenburg syndrome

    A comprehensive genotype–phenotype evaluation of eight Chinese probands with Waardenburg syndrome oleh Sijun Li, Mengyao Qin, Shuang Mao, Lingyun Mei, Xinzhang Cai, Yong Feng, Chufeng He, Jian Song

    Diterbitkan 2022-11-01
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  5. 5
    Nutritional Assessment of Plant-Based Meat Products Available on Hong Kong Market: A Cross-Sectional Survey

    Nutritional Assessment of Plant-Based Meat Products Available on Hong Kong Market: A Cross-Sectional Survey oleh Qile Zhang, Yilin Liu, Chufeng He, Ruiwen Zhu, Minghui Li, Hon-Ming Lam, Wing-Tak Wong

    Diterbitkan 2023-08-01
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  6. 6
    A Combined Fuzzy Optimization Model for the Location of an Intelligent Energy-Efficient Manufacturing Industrial Park

    A Combined Fuzzy Optimization Model for the Location of an Intelligent Energy-Efficient Manufacturing Industrial Park oleh Chufeng He, Aijun Liu, Lei Xu, Shuailei Yuan, Mingbao Cheng, Huan Wang, Fang Wang, Hui Lu, Xiaoxue Liu

    Diterbitkan 2022-12-01
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  7. 7
    Establishment of an iPSC line (CSUXHi003-A) from a patient with Waardenburg syndrome type Ⅱ caused by a MITF mutation

    Establishment of an iPSC line (CSUXHi003-A) from a patient with Waardenburg syndrome type Ⅱ caused by a MITF mutation oleh Jie Wen, Jian Song, Chufeng He, Jie Ling, Yalan Liu, Hongsheng Chen, Wei Gong, Lingyun Mei, Yong Feng

    Diterbitkan 2021-03-01
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  8. 8
    Licorice Extract Isoliquiritigenin Protects Endothelial Function in Type 2 Diabetic Mice

    Licorice Extract Isoliquiritigenin Protects Endothelial Function in Type 2 Diabetic Mice oleh Lin Wang, Ruiwen Zhu, Chufeng He, Huixian Li, Qile Zhang, Yiu Ming Cheung, Fung Ping Leung, Wing Tak Wong

    Diterbitkan 2024-09-01
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  9. 9
    Establishment of an iPSC line (CSUXHi004-A) from a patient with Waardenburg syndrome type I caused by a PAX3 splice mutation

    Establishment of an iPSC line (CSUXHi004-A) from a patient with Waardenburg syndrome type I caused by a PAX3 splice mutation oleh Jie Wen, Chufeng He, Yong Feng, Jian Song, Jing Liu, Xianlin Liu, Lingyun Mei, Jie Ling, Hongsheng Chen, Yalan Liu

    Diterbitkan 2021-05-01
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  10. 10
    A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing loss.

    A rapid improved multiplex ligation detection reaction method for the identification of gene mutations in hereditary hearing loss. oleh Yalan Liu, Chang Hu, Chang Liu, Deyuan Liu, Lingyun Mei, Chufeng He, Lu Jiang, Hong Wu, Hongsheng Chen, Yong Feng

    Diterbitkan 2019-01-01
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  11. 11
    LEF-1 Regulates Tyrosinase Gene Transcription In Vitro.

    LEF-1 Regulates Tyrosinase Gene Transcription In Vitro. oleh Xueping Wang, Yalan Liu, Hongsheng Chen, Lingyun Mei, Chufeng He, Lu Jiang, Zhijie Niu, Jie Sun, Hunjin Luo, Jiada Li, Yong Feng

    Diterbitkan 2015-01-01
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  12. 12
    A New Genetic Diagnostic for Enlarged Vestibular Aqueduct Based on Next-Generation Sequencing.

    A New Genetic Diagnostic for Enlarged Vestibular Aqueduct Based on Next-Generation Sequencing. oleh Yalan Liu, Lili Wang, Yong Feng, Chufeng He, Deyuan Liu, Xinzhang Cai, Lu Jiang, Hongsheng Chen, Chang Liu, Hong Wu, Lingyun Mei

    Diterbitkan 2016-01-01
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  13. 13
    Type 2 cytokines promote angiogenesis in ischemic muscle via endothelial IL-4Rα signaling

    Type 2 cytokines promote angiogenesis in ischemic muscle via endothelial IL-4Rα signaling oleh Huixian Li, Chufeng He, Ruiwen Zhu, Francis M. Chen, Lin Wang, Fung Ping Leung, Xiao Yu Tian, Gary Tse, Wing Tak Wong

    Diterbitkan 2023-08-01
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  14. 14
    Establishment of two iPSC lines from healthy donor with heterozygous mutation in the SLC26A4 gene

    Establishment of two iPSC lines from healthy donor with heterozygous mutation in the SLC26A4 gene oleh SiJun Li, Chufeng He, Qi Feng, YiJiang Bai, Xianlin Liu, Jie Ling, Lingyun Mei, XueWen Wu, Yong Feng, Jian Song

    Diterbitkan 2022-10-01
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  15. 15
    Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China.

    Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China. oleh Hong Wu, Yong Feng, Lu Jiang, Qian Pan, Yalan Liu, Chang Liu, Chufeng He, Hongsheng Chen, Xueming Liu, Chang Hu, Yiqiao Hu, Lingyun Mei

    Diterbitkan 2016-01-01
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  16. 16
    A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family.

    A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family. oleh Zhijie Niu, Yong Feng, Lingyun Mei, Jie Sun, Xueping Wang, Juncheng Wang, Zhengmao Hu, Yunpeng Dong, Hongsheng Chen, Chufeng He, Yalan Liu, Xinzhang Cai, Xuezhong Liu, Lu Jiang

    Diterbitkan 2017-01-01
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  17. 17
    Gene regulation analysis of patient-derived iPSCs and its CRISPR-corrected control provides a new tool for studying perturbations of ELMOD3 c.512A>G mutation during the development of inherited hearing loss.

    Gene regulation analysis of patient-derived iPSCs and its CRISPR-corrected control provides a new tool for studying perturbations of ELMOD3 c.512A>G mutation during the development... oleh Xianlin Liu, Jie Wen, Xuezhong Liu, Anhai Chen, Sijun Li, Jing Liu, Jie Sun, Wei Gong, Xiaoming Kang, Zhili Feng, Chufeng He, Lingyun Mei, Jie Ling, Yong Feng

    Diterbitkan 2023-01-01
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  18. 18
    Gene regulation analysis of patient-derived iPSCs and its CRISPR-corrected control provides a new tool for studying perturbations of ELMOD3 c.512A>G mutation during the development of inherited hearing loss

    Gene regulation analysis of patient-derived iPSCs and its CRISPR-corrected control provides a new tool for studying perturbations of ELMOD3 c.512A>G mutation during the development... oleh Xianlin Liu, Jie Wen, Xuezhong Liu, Anhai Chen, Sijun Li, Jing Liu, Jie Sun, Wei Gong, Xiaoming Kang, Zhili Feng, Chufeng He, Lingyun Mei, Jie Ling, Yong Feng

    Diterbitkan 2023-01-01
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  19. 19
    A Novel Mutation Causing Alternative RNA Splicing in a Chinese Family With Branchio-Oto Syndrome: Implications for Molecular Diagnosis and Clinical Application

    A Novel Mutation Causing Alternative RNA Splicing in a Chinese Family With Branchio-Oto Syndrome: Implications for Molecular Diagnosis and Clinical Application oleh Anhai Chen, Jie Ling, Xin Peng, Xianlin Liu, Shuang Mao, Yongjia Chen, Mengyao Qin, Shuai Zhang, Yijiang Bai, Jian Song, Zhili Feng, Lu Ma, Dinghua He, Lingyun Mei, Chufeng He, Yong Feng

    Diterbitkan 2023-11-01
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  20. 20
    Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families

    Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families oleh Shushan Sang, Shushan Sang, Jie Ling, Jie Ling, Jie Ling, Xuezhong Liu, Xuezhong Liu, Xuezhong Liu, Lingyun Mei, Lingyun Mei, Xinzhang Cai, Xinzhang Cai, Taoxi Li, Taoxi Li, Taoxi Li, Wu Li, Wu Li, Meng Li, Meng Li, Jie Wen, Jie Wen, Xianlin Liu, Xianlin Liu, Jing Liu, Jing Liu, Yalan Liu, Yalan Liu, Hongsheng Chen, Hongsheng Chen, Chufeng He, Chufeng He, Yong Feng, Yong Feng, Yong Feng, Yong Feng

    Diterbitkan 2019-07-01
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