Hasil Pencarian - Wan‐Jin Chen

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  1. 1
    The research progress of clinical diagnosis of spinal muscular atrophy

    The research progress of clinical diagnosis of spinal muscular atrophy oleh Ning WANG, Jin HE, Wan⁃jin CHEN

    Diterbitkan 2012-06-01
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  2. 2
    Ten⁃year advance in the genomics study on neuropathic hereditary diseases

    Ten⁃year advance in the genomics study on neuropathic hereditary diseases oleh Ning WANG, Yu LIN, Wan⁃jin CHEN

    Diterbitkan 2010-02-01
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  3. 3
    Research progress of spinal muscular atrophy treatment in children

    Research progress of spinal muscular atrophy treatment in children oleh Miao ZHAO, Ying-qian LU, Ning WANG, Wan-jin CHEN

    Diterbitkan 2018-04-01
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  4. 4
    Target region capture sequencing for detecting GDAP1 gene mutation of autosomal recessive Charcot-Marie-Tooth disease

    Target region capture sequencing for detecting GDAP1 gene mutation of autosomal recessive Charcot-Marie-Tooth disease oleh Jin HE, Guo-rong XU, Han LIN, Ning WANG, Wan-jin CHEN

    Diterbitkan 2017-08-01
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  5. 5
    Median Nerve-Neurophysiological Index Correlates With the Survival of Patients With Amyotrophic Lateral Sclerosis

    Median Nerve-Neurophysiological Index Correlates With the Survival of Patients With Amyotrophic Lateral Sclerosis oleh Liu-Qing Xu, Wei Hu, Qi-Fu Guo, Lu-Lu Lai, Guo-Rong Xu, Wan-Jin Chen, Wan-Jin Chen, Ning Wang, Ning Wang, Qi-Jie Zhang, Qi-Jie Zhang

    Diterbitkan 2020-10-01
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  6. 6
    Progress in research on molecular mechanism of facioscapulohumeral muscular dystrophy

    Progress in research on molecular mechanism of facioscapulohumeral muscular dystrophy oleh Xiao-dan LIN, Jun-jie HE, Wan-jin CHEN, Ning WANG, Zhi-qiang WANG

    Diterbitkan 2017-08-01
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  7. 7
    Studies on the prenatal diagnosis of spinal muscular atrophy by multiplex ligation⁃dependent probe amplification

    Studies on the prenatal diagnosis of spinal muscular atrophy by multiplex ligation⁃dependent probe amplification oleh Ya⁃fang CHEN, Jin HE, Qi⁃jie ZHANG, Xiang LIN, Ning WANG, Wan⁃jin CHEN

    Diterbitkan 2012-06-01
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  8. 8
    Novel Compound Missense and Intronic Splicing Mutation in ALDH18A1 Causes Autosomal Recessive Spastic Paraplegia

    Novel Compound Missense and Intronic Splicing Mutation in ALDH18A1 Causes Autosomal Recessive Spastic Paraplegia oleh Yi-Jun Chen, Zai-Qiang Zhang, Meng-Wen Wang, Yu-Sen Qiu, Ru-Ying Yuan, En-Lin Dong, Zhe Zhao, Hai-Tao Zhou, Ning Wang, Ning Wang, Wan-Jin Chen, Wan-Jin Chen, Xiang Lin, Xiang Lin

    Diterbitkan 2021-05-01
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  9. 9
    Identification of a Novel Homozygous Splice-Site Mutation in SCARB2 that Causes Progressive Myoclonus Epilepsy with or without Renal Failure

    Identification of a Novel Homozygous Splice-Site Mutation in SCARB2 that Causes Progressive Myoclonus Epilepsy with or without Renal Failure oleh Jin He, Han Lin, Jin-Jing Li, Hui-Zhen Su, Dan-Ni Wang, Yu Lin, Ning Wang, Wan-Jin Chen

    Diterbitkan 2018-01-01
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  10. 10
    Mitochondrial DNA Haplogroups and the Risk of Sporadic Parkinson′s Disease in Han Chinese

    Mitochondrial DNA Haplogroups and the Risk of Sporadic Parkinson′s Disease in Han Chinese oleh Ya-Fang Chen, Wan-Jin Chen, Xiao-Zhen Lin, Qi-Jie Zhang, Jiang-Ping Cai, Chia-Wei Liou, Ning Wang

    Diterbitkan 2015-01-01
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  11. 11
    Altered corticalfunctional networks in Wilson's disease: A resting-state electroencephalogram study

    Altered corticalfunctional networks in Wilson's disease: A resting-state electroencephalogram study oleh Ru-Kai Chen, Chan Zhang, Jian-Wei Lin, Wu-Xiang Shi, Yu-Rong Li, Wan-Jin Chen, Nai-Qing Cai

    Diterbitkan 2024-11-01
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  12. 12
    Potential markers for sample size estimations in hereditary spastic paraplegia type 5

    Potential markers for sample size estimations in hereditary spastic paraplegia type 5 oleh Qianqian Lin, Ying Liu, Zhixian Ye, Jianping Hu, Wenjie Cai, Qiang Weng, Wan-Jin Chen, Ning Wang, Dairong Cao, Yi Lin, Ying Fu

    Diterbitkan 2021-09-01
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  13. 13
    Correction to: Potential markers for sample size estimations in hereditary spastic paraplegia type 5

    Correction to: Potential markers for sample size estimations in hereditary spastic paraplegia type 5 oleh Qianqian Lin, Ying Liu, Zhixian Ye, Jianping Hu, Wenjie Cai, Qiang Weng, Wan-Jin Chen, Ning Wang, Dairong Cao, Yi Lin, Ying Fu

    Diterbitkan 2021-10-01
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  14. 14
    Genetic screening method for analyzing survival motor neuron copy number in spinal muscular atrophy by multiplex ligation-dependent probe amplification and droplet digital polymerase chain reaction

    Genetic screening method for analyzing survival motor neuron copy number in spinal muscular atrophy by multiplex ligation-dependent probe amplification and droplet digital polymera... oleh Jing-Mei Hong, Miao Zhao, Jin He, Xue-Jing Huang, Zhi-Yuan Zhao, Wan-Jin Chen, Ning Wang, Jin-Jing Li, Ning-Ning Wang

    Diterbitkan 2020-10-01
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  15. 15
    High frequency of the TARDBP p.M337 V mutation among south-eastern Chinese patients with familial amyotrophic lateral sclerosis

    High frequency of the TARDBP p.M337 V mutation among south-eastern Chinese patients with familial amyotrophic lateral sclerosis oleh Guo-rong Xu, Wei Hu, Ling-Ling Zhan, Chong Wang, Liu-Qing Xu, Min-Ting Lin, Wan-Jin Chen, Ning Wang, Qi-Jie Zhang

    Diterbitkan 2018-04-01
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  16. 16
    Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mutations in CAPN1 (SPG76)

    Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mu... oleh Ying-qian Lu, En-lin Dong, Wei-qi Yang, Lu-lu Lai, Xiao-hong Lin, Li-xiang Ma, Wan-jin Chen, Ning Wang, Xiang Lin

    Diterbitkan 2019-01-01
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  17. 17
    Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia

    Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia oleh Lu‐Lu Lai, Yi‐Jun Chen, Yun‐Lu Li, Xiao‐Hong Lin, Meng‐Wen Wang, En‐Lin Dong, Ning Wang, Wan‐Jin Chen, Xiang Lin

    Diterbitkan 2020-10-01
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  18. 18
    Mutation Analysis of MYORG in a Chinese Cohort With Primary Familial Brain Calcification

    Mutation Analysis of MYORG in a Chinese Cohort With Primary Familial Brain Calcification oleh Yi-Heng Zeng, Bi-Wei Lin, Hui-Zhen Su, Xin-Xin Guo, Yun-Lu Li, Lu-Lu Lai, Wan-Jin Chen, Miao Zhao, Xiang-Ping Yao

    Diterbitkan 2021-10-01
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  19. 19
    Knockdown of myorg leads to brain calcification in zebrafish

    Knockdown of myorg leads to brain calcification in zebrafish oleh Miao Zhao, Xiao-Hong Lin, Yi-Heng Zeng, Hui-Zhen Su, Chong Wang, Kang Yang, Yi-Kun Chen, Bi-Wei Lin, Xiang-Ping Yao, Wan-Jin Chen

    Diterbitkan 2022-07-01
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  20. 20
    The Quantum Well of One-Dimensional Photonic Crystals

    The Quantum Well of One-Dimensional Photonic Crystals oleh Xiao-Jing Liu, Ji Ma, Xiang-Dong Meng, Hai-Bo Li, Jing-Bin Lu, Hong Li, Wan-Jin Chen, Xiang-Yao Wu, Si-Qi Zhang, Yi-Heng Wu

    Diterbitkan 2015-01-01
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