PRRT2 deficiency induces paroxysmal kinesigenic dyskinesia by regulating synaptic transmission in cerebellum
Tan, Guo-He, Liu, Yuan-Yuan, Wang, Lu, Li, Kui, Zhang, Ze-Qiang, Li, Hong-Fu, Yang, Zhong-Fei, Li, Yang, Li, Dan, Wu, Ming-Yue, Yu, Chun-Lei, Long, Juan-Juan, Chen, Ren-Chao, Li, Li-Xi, Yin, Lu-Ping, Liu, Ji-Wei, Cheng, Xue-Wen, Shen, Qi, Shu, You-Sheng, Sakimura, Kenji, Liao, Lu-Jian, Wu, Zhi-Ying, Xiong, Zhi-Qi
Published in Cell research (01.01.2018)
Published in Cell research (01.01.2018)
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Genetic spectrum of NOTCH3 and clinical phenotype of CADASIL patients in different populations
Ni, Wang, Zhang, Yi, Zhang, Liang, Xie, Juan‐Juan, Li, Hong‐Fu, Wu, Zhi‐Ying
Published in CNS neuroscience & therapeutics (01.11.2022)
Published in CNS neuroscience & therapeutics (01.11.2022)
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Purification and Structure Characterization of the Crude Polysaccharide from the Fruiting Bodies of Butyriboletus pseudospeciosus and Its Modulation Effects on Gut Microbiota
Tian, Run, Wu, Lu-Ling, Li, Hong-Fu, Liang, Zhi-Qun, Li, Pei-Hu, Wang, Yong, Zeng, Nian-Kai
Published in Molecules (Basel, Switzerland) (16.03.2023)
Published in Molecules (Basel, Switzerland) (16.03.2023)
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Evaluation of hemostatic, anti-inflammatory, wound healing, skin irritation and allergy, and antimicrobial properties of active fraction from the ethanol extract of Chromolaena odorata (L.) R.M. King & H. Rob
Li, Hong-Fu, Feng, Han, Wang, Yong, Pan, Zhang-Chao, Yin, Liang, Qiu, Hai-Long, Qiao, Hong, Zhao, Jin-Qiu, Xia, Xin-Yu, Hou, Jing-Chen, Wang, Rui-Xin
Published in Journal of ethnopharmacology (15.09.2024)
Published in Journal of ethnopharmacology (15.09.2024)
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Biallelic variants in the COQ4 gene caused hereditary spastic paraplegia predominant phenotype
Wei, Qiao, Yu, Hao, Wang, Pei‐Shan, Xie, Juan‐Juan, Dong, Hai‐Lin, Wu, Zhi‐Ying, Li, Hong‐Fu
Published in CNS neuroscience & therapeutics (01.04.2024)
Published in CNS neuroscience & therapeutics (01.04.2024)
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Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy
Dong, Hai-Lin, Ma, Yin, Yu, Hao, Wei, Qiao, Li, Jia-Qi, Liu, Gong-Lu, Li, Hong-Fu, Chen, Lei, Chen, Dian-Fu, Bai, Ge, Wu, Zhi-Ying
Published in Brain (London, England : 1878) (04.09.2021)
Published in Brain (London, England : 1878) (04.09.2021)
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Genetic spectrum and clinical profiles in a southeast Chinese cohort of Charcot‐Marie‐Tooth disease
Chen, Cong‐Xin, Dong, Hai‐Lin, Wei, Qiao, Li, Li‐Xi, Yu, Hao, Li, Jia‐Qi, Liu, Gong‐Lu, Li, Hong‐Fu, Bai, Ge, Ma, Huan, Wu, Zhi‐Ying
Published in Clinical genetics (01.11.2019)
Published in Clinical genetics (01.11.2019)
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SOD1 Mutation Spectrum and Natural History of ALS Patients in a 15-Year Cohort in Southeastern China
Chen, Lu-Xi, Xu, Hai-Feng, Wang, Pei-Shan, Yang, Xin-Xia, Wu, Zhi-Ying, Li, Hong-Fu
Published in Frontiers in genetics (14.10.2021)
Published in Frontiers in genetics (14.10.2021)
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20 potentially new compounds and 11 new bioactive constituents found in Smilacis Glabrae Rhizoma utilizing HPLC‐DAD‐ESI‐IT‐TOF‐MSn
Gegentana, Xu, Feng, Huang, Yan‐Fei, Li, Hong‐Fu, Yang, Ping, Shang, Ming‐Ying, Liu, Guang‐Xue, Li, Yao‐Li, Wang, Xuan, Cai, Shao‐Qing
Published in Phytochemical analysis (01.07.2024)
Published in Phytochemical analysis (01.07.2024)
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Common genetic variants in PRRC2A are associated with both neuromyelitis optica spectrum disorder and multiple sclerosis in Han Chinese population
Zhang, Juan, Chen, Mei-Jiao, Zhao, Gui-Xian, Li, Hong-Fu, Wu, Lei, Xu, Yong-Feng, Liao, Yajin, Yuan, Zengqiang, Wu, Zhi-Ying
Published in Journal of neurology (01.02.2021)
Published in Journal of neurology (01.02.2021)
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Genetic spectrum of MCM3AP and its relationship with phenotype of Charcot‐Marie‐Tooth disease
Dong, Hai‐Lin, Wei, Qiao, Li, Jia‐Qi, Li, Hong‐Fu, Bai, Ge, Ma, Huan, Wu, Zhi‐Ying
Published in Journal of the peripheral nervous system (01.06.2020)
Published in Journal of the peripheral nervous system (01.06.2020)
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Taste loss as the sole presenting symptom in Chinese patient with facial onset sensory and motor neuronopathy
Chen, Lu‐Xi, Liu, Gong‐Lu, Yu, Hao, Wu, Zhi‐Ying, Li, Hong‐Fu
Published in CNS neuroscience & therapeutics (01.12.2021)
Published in CNS neuroscience & therapeutics (01.12.2021)
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Identification of a large homozygous SPG21 deletion in a Chinese patient with Mast syndrome
Xue, Yan‐Yan, Huang, Xue‐Rong, Dong, Hai‐Lin, Wu, Zhi‐Ying, Li, Hong‐Fu
Published in CNS neuroscience & therapeutics (01.10.2021)
Published in CNS neuroscience & therapeutics (01.10.2021)
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CHIP control degradation of mutant ETF:QO through ubiquitylation in late‐onset multiple acyl‐CoA dehydrogenase deficiency
Liu, Xin‐Yi, Chen, Xue‐Jiao, Zhao, Miao, Wang, Zhi‐qiang, Chen, Hai‐zhu, Li, Hong‐Fu, Wang, Chen‐Ji, Wu, Shi‐Fei, Peng, Chao, Yin, Yue, Fu, Hong‐Xia, Lin, Min‐Ting, Yu, Long, Xiong, Zhi‐Qi, Wu, Zhi‐Ying, Wang, Ning
Published in Journal of inherited metabolic disease (01.03.2021)
Published in Journal of inherited metabolic disease (01.03.2021)
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Associations between neuroanatomical abnormality and motor symptoms in paroxysmal kinesigenic dyskinesia
Li, Hong-Fu, Yang, Liqin, Yin, Dazhi, Chen, Wan-Jin, Liu, Gong-Lu, Ni, Wang, Wang, Ning, Yu, Wenwen, Wu, Zhi-Ying, Wang, Zheng
Published in Parkinsonism & related disorders (01.05.2019)
Published in Parkinsonism & related disorders (01.05.2019)
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Clinical features and mutation spectrum in Chinese patients with CADASIL: A multicenter retrospective study
Chen, Sheng, Ni, Wang, Yin, Xin‐Zhen, Liu, Han‐Qiu, Lu, Cong, Zheng, Qiao‐Juan, Zhao, Gui‐Xian, Xu, Yong‐Feng, Wu, Lei, Zhang, Liang, Wang, Ning, Li, Hong‐Fu, Wu, Zhi‐Ying
Published in CNS neuroscience & therapeutics (01.09.2017)
Published in CNS neuroscience & therapeutics (01.09.2017)
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