Hasil Pencarian - Hong‐Fu Li

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  1. 1
    A multi-locus linear mixed model methodology for detecting small-effect QTLs for quantitative traits in MAGIC, NAM, and ROAM populations

    A multi-locus linear mixed model methodology for detecting small-effect QTLs for quantitative traits in MAGIC, NAM, and ROAM populations oleh Guo Li, Ya-Hui Zhou, Hong-Fu Li, Yuan-Ming Zhang

    Diterbitkan 2023-01-01
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  2. 2
    Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia Patients

    Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia Patients oleh Hong-Xia Wang, Hong-Fu Li, Gong-Lu Liu, Xiao-Dan Wen, Zhi-Ying Wu

    Diterbitkan 2016-01-01
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  3. 3
    (E)-2-{4-[1-(Hydroxyimino)ethyl]phenyliminomethyl}-6-methoxyphenol monohydrate

    (E)-2-{4-[1-(Hydroxyimino)ethyl]phenyliminomethyl}-6-methoxyphenol monohydrate oleh Jun-Feng Tong, Su-Xia Gao, Wen-Kui Dong, Hong-Fu Li, Jian-Chao Wu

    Diterbitkan 2009-11-01
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  4. 4
    Clinical characterization and founder effect analysis in Chinese amyotrophic lateral sclerosis patients with SOD1 common variants

    Clinical characterization and founder effect analysis in Chinese amyotrophic lateral sclerosis patients with SOD1 common variants oleh Pei-Shan Wang, Xin-Xia Yang, Qiao Wei, Yong-Ting Lv, Zhi-Ying Wu, Hong-Fu Li

    Diterbitkan 2024-12-01
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  5. 5
    A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia

    A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia oleh Qiao Wei, Pei‐Shan Wang, Hai‐Lin Dong, Wen‐Jiao Luo, Zhi‐Ying Wu, Hong‐Fu Li

    Diterbitkan 2022-05-01
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  6. 6
    Clinical Characterization and Founder Effect Analysis in Chinese Patients with Phospholipase A2-Associated Neurodegeneration

    Clinical Characterization and Founder Effect Analysis in Chinese Patients with Phospholipase A2-Associated Neurodegeneration oleh Hao-Ling Cheng, Yi-Jun Chen, Yan-Yan Xue, Zhi-Ying Wu, Hong-Fu Li, Ning Wang

    Diterbitkan 2022-04-01
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  7. 7
    Spastic paraplegia as the predominant phenotype in a cohort of Chinese patients with adrenoleukodystrophy

    Spastic paraplegia as the predominant phenotype in a cohort of Chinese patients with adrenoleukodystrophy oleh Wen‐Jiao Luo, Qiao Wei, Hai‐Lin Dong, Yang‐Tian Yan, Mei‐Jiao Chen, Hong‐Fu Li

    Diterbitkan 2020-01-01
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  8. 8
    SOD1 Mutation Spectrum and Natural History of ALS Patients in a 15-Year Cohort in Southeastern China

    SOD1 Mutation Spectrum and Natural History of ALS Patients in a 15-Year Cohort in Southeastern China oleh Lu-Xi Chen, Hai-Feng Xu, Pei-Shan Wang, Xin-Xia Yang, Zhi-Ying Wu, Hong-Fu Li

    Diterbitkan 2021-10-01
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  9. 9
    Urine-derived induced pluripotent stem cells as a modeling tool for paroxysmal kinesigenic dyskinesia

    Urine-derived induced pluripotent stem cells as a modeling tool for paroxysmal kinesigenic dyskinesia oleh Shu-Zhen Zhang, Hong-Fu Li, Li-Xiang Ma, Wen-Jing Qian, Zhong-Feng Wang, Zhi-Ying Wu

    Diterbitkan 2015-12-01
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  10. 10
    Purification and Structure Characterization of the Crude Polysaccharide from the Fruiting Bodies of <i>Butyriboletus pseudospeciosus</i> and Its Modulation Effects on Gut Microbiota

    Purification and Structure Characterization of the Crude Polysaccharide from the Fruiting Bodies of <i>Butyriboletus pseudospeciosus</i> and Its Modulation Effects on Gut Microbiot... oleh Run Tian, Lu-Ling Wu, Hong-Fu Li, Zhi-Qun Liang, Pei-Hu Li, Yong Wang, Nian-Kai Zeng

    Diterbitkan 2023-03-01
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  11. 11
    Modeling Neurological Disease by Rapid Conversion of Human Urine Cells into Functional Neurons

    Modeling Neurological Disease by Rapid Conversion of Human Urine Cells into Functional Neurons oleh Shu-Zhen Zhang, Li-Xiang Ma, Wen-Jing Qian, Hong-Fu Li, Zhong-Feng Wang, Hong-Xia Wang, Zhi-Ying Wu

    Diterbitkan 2016-01-01
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  12. 12
    Detection of 191 Taxifolin Metabolites and Their Distribution in Rats Using HPLC-ESI-IT-TOF-MSn

    Detection of 191 Taxifolin Metabolites and Their Distribution in Rats Using HPLC-ESI-IT-TOF-MSn oleh Ping Yang, Feng Xu, Hong-Fu Li, Yi Wang, Feng-Chun Li, Ming-Ying Shang, Guang-Xue Liu, Xuan Wang, Shao-Qing Cai

    Diterbitkan 2016-09-01
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  13. 13
    Variant of EOMES Associated with Increasing Risk in Chinese Patients with Relapsing-remitting Multiple Sclerosis

    Variant of EOMES Associated with Increasing Risk in Chinese Patients with Relapsing-remitting Multiple Sclerosis oleh Sheng Chen, Juan Zhang, Qi-Bing Liu, Jing-Cong Zhuang, Lei Wu, Yong-Feng Xu, Hong-Fu Li, Zhi-Ying Wu, Bao-Gou Xiao

    Diterbitkan 2018-01-01
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  14. 14
    Exploring the In Vivo Existence Forms (23 Original Constituents and 147 Metabolites) of Astragali Radix Total Flavonoids and Their Distributions in Rats Using HPLC-DAD-ESI-IT-TOF-MS<sup>n</sup>

    Exploring the In Vivo Existence Forms (23 Original Constituents and 147 Metabolites) of Astragali Radix Total Flavonoids and Their Distributions in Rats Using HPLC-DAD-ESI-IT-TOF-M... oleh Li-Jia Liu, Hong-Fu Li, Feng Xu, Hong-Yan Wang, Yi-Fan Zhang, Guang-Xue Liu, Ming-Ying Shang, Xuan Wang, Shao-Qing Cai

    Diterbitkan 2020-11-01
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  15. 15
    Identified novel heterozygous HTRA1 pathogenic variants in Chinese patients with HTRA1-associated dominant cerebral small vessel disease

    Identified novel heterozygous HTRA1 pathogenic variants in Chinese patients with HTRA1-associated dominant cerebral small vessel disease oleh Mei-Jiao Chen, Mei-Jiao Chen, Yi Zhang, Wen-Jiao Luo, Hai-Lin Dong, Qiao Wei, Juan Zhang, Juan Zhang, Qi-Qi Ruan, Wang Ni, Hong-Fu Li

    Diterbitkan 2022-08-01
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  16. 16
    Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia

    Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia oleh Qiao Wei, Hai-Lin Dong, Li-Ying Pan, Cong-Xin Chen, Yang-Tian Yan, Rou-Min Wang, Hong-Fu Li, Zhi-Jun Liu, Qing-Qing Tao, Zhi-Ying Wu

    Diterbitkan 2019-06-01
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  17. 17
    TMEM151A variants cause paroxysmal kinesigenic dyskinesia

    TMEM151A variants cause paroxysmal kinesigenic dyskinesia oleh Hong-Fu Li, Yu-Lan Chen, Ling Zhuang, Dian-Fu Chen, Hua-Zhen Ke, Wen-Jiao Luo, Gong-Lu Liu, Sheng-Nan Wu, Wen-Hao Zhou, Zhi-Qi Xiong, Zhi-Ying Wu

    Diterbitkan 2021-09-01
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  18. 18
    Author Correction: TMEM151A variants cause paroxysmal kinesigenic dyskinesia

    Author Correction: TMEM151A variants cause paroxysmal kinesigenic dyskinesia oleh Hong-Fu Li, Yu-Lan Chen, Ling Zhuang, Dian-Fu Chen, Hua-Zhen Ke, Wen-Jiao Luo, Gong-Lu Liu, Sheng-Nan Wu, Wen-Hao Zhou, Zhi-Qi Xiong, Zhi-Ying Wu

    Diterbitkan 2021-10-01
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