Numerical Simulation of the Diffusion of Fissure Slurry at High Temperature
Niu, Jiandong, Sun, Yong, Liu, Jianxin, Li, Huimei, Tan, Xiaojun, Han, Ning, Wang, Bin, Qiu, Liangliang
Published in Geofluids (02.03.2022)
Published in Geofluids (02.03.2022)
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Reprogramming of adult human peripheral blood mononuclear cells into hiPSCs from two patients with facioscapulohumeral muscular dystrophy type 1
Zheng, Fuze, Chen, Long, Qiu, Liangliang, Lin, Lin, Lin, Xin, He, Qifang, Wang, Lili, Ye, Zhixian, Lin, Minting, Wang, Zhiqiang
Published in Stem cell research (01.04.2022)
Published in Stem cell research (01.04.2022)
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Grouting Treatment of Water and Mud Inrush in Fully Weathered Granite Tunnel: A Case Study
Qiu, Liangliang, Huang, Shiwu, Huang, Youhan, Zhang, Keneng, Wang, Bin, Sun, Yong, Niu, Jiandong, Yu, Jiaqin
Published in Geofluids (2020)
Published in Geofluids (2020)
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Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study
Wang, Zhiqiang, Qiu, Liangliang, Lin, Minting, Chen, Long, Zheng, Fuze, Lin, Lin, Lin, Feng, Ye, Zhixian, Lin, Xiaodan, He, Junjie, Wang, Lili, Lin, Xin, He, Qifang, Chen, Wanjin, Lin, Yi, Fu, Ying, Wang, Ning
Published in The Lancet regional health. Western Pacific (01.01.2022)
Published in The Lancet regional health. Western Pacific (01.01.2022)
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Wheelchair use in genetically-confirmed FSHD1 from a large cohort study in Chinese population
Qiu, Liangliang, Chen, Long, Zheng, Fuze, Lin, Minting, Lin, Yi, Fu, Ying, Wang, Ning, Wang, Zhiqiang
Published in Brain (London, England : 1878) (30.06.2022)
Published in Brain (London, England : 1878) (30.06.2022)
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An epigenetic basis for genetic anticipation in facioscapulohumeral muscular dystrophy type 1
Zheng, Fuze, Qiu, Liangliang, Chen, Long, Zheng, Ying, He, Qifang, Lin, Xiaodan, Lin, Minting, Lin, Yi, Fu, Ying, Wang, Ning, Wang, Zhiqiang
Published in Brain (London, England : 1878) (01.12.2023)
Published in Brain (London, England : 1878) (01.12.2023)
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Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy
Zheng, Fuze, Qiu, Liangliang, Chen, Long, Zheng, Ying, Lin, Xiaodan, He, Junjie, Lin, Xin, He, Qifang, Lin, Yuhua, Lin, Lin, Wang, Lili, Lin, Feng, Yang, Kang, Lin, Minting, Lin, Yi, Fu, Ying, Wang, Ning, Wang, Zhiqiang
Published in Neurology (18.07.2023)
Published in Neurology (18.07.2023)
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Clinical and genetic characterization of limb girdle muscular dystrophy R7 telethonin-related patients from three unrelated Chinese families
Chen, Haizhu, Xu, Guorong, Lin, Feng, Jin, Ming, Cai, Naiqing, Qiu, Liangliang, Ye, Zhixian, Wang, Lili, Lin, Minting, Wang, Ning
Published in Neuromuscular disorders : NMD (01.02.2020)
Published in Neuromuscular disorders : NMD (01.02.2020)
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Clinical and genetic features of somatic mosaicism in facioscapulohumeral dystrophy
Qiu, Liangliang, Ye, Zhixian, Lin, Lin, Wang, Lili, Lin, Xiaodan, He, Junjie, Lin, Feng, Xu, Guorong, Cai, Naiqing, Jin, Ming, Chen, Haizhu, Lin, Minting, Wang, Ning, Wang, Zhiqiang
Published in Journal of medical genetics (01.11.2020)
Published in Journal of medical genetics (01.11.2020)
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ATP1A1 mutations cause intermediate Charcot‐Marie‐Tooth disease
He, Jin, Guo, Lingling, Lin, Shan, Chen, Wenfeng, Xu, Guorong, Cai, Bin, Xu, Liuqing, Hong, Jingmei, Qiu, Liangliang, Wang, Ning, Chen, Wanjin
Published in Human mutation (01.12.2019)
Published in Human mutation (01.12.2019)
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Disease Progression and Multiparametric Imaging Characteristics of Spinocerebellar Ataxia Type 3 With Spastic Paraplegia
Ye, Zhi-Xian, Xu, Hao-Ling, Chen, Na-Ping, Chen, Xin-Yuan, Li, Meng-Cheng, Yuan, Ru-Ying, Lin, Wei, Qiu, Liangliang, Lin, Minting, Chen, Wan-Jin, Wang, Ning, Hu, Jian-Ping, Fu, Ying, Gan, Shi-Rui
Published in Neurology. Genetics (01.06.2024)
Published in Neurology. Genetics (01.06.2024)
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