GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal Myopathy
Zeng, Yi‐Heng, Yang, Kang, Du, Gan‐Qin, Chen, Yi‐Kun, Cao, Chun‐Yan, Qiu, Yu‐Sen, He, Jin, Lv, Hai‐Dong, Qu, Qian‐Qian, Chen, Jian‐Nan, Xu, Guo‐Rong, Chen, Long, Zheng, Fu‐Ze, Zhao, Miao, Lin, Min‐Ting, Chen, Wan‐Jin, Hu, Jing, Wang, Zhi‐Qiang, Wang, Ning
Published in Annals of neurology (01.09.2022)
Published in Annals of neurology (01.09.2022)
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Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients
Lin, Feng, Yang, Kang, Lin, Xin, Jin, Ming, Chen, Long, Zheng, Fu-ze, Qiu, Liang-liang, Ye, Zhi-xian, Chen, Hai-zhu, Lin, Min-ting, Wang, Ning, Wang, Zhi-qiang
Published in Orphanet journal of rare diseases (16.11.2023)
Published in Orphanet journal of rare diseases (16.11.2023)
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Combinational Treatment of Curcumin and Quercetin against Gastric Cancer MGC-803 Cells in Vitro
Zhang, Jian-Ye, Lin, Min-Ting, Zhou, Meng-Jia, Yi, Tao, Tang, Yi-Na, Tang, Si-Li, Yang, Zhi-Jun, Zhao, Zhong-Zhen, Chen, Hu-Biao
Published in Molecules (Basel, Switzerland) (22.06.2015)
Published in Molecules (Basel, Switzerland) (22.06.2015)
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Detection of pTDP‐43 via routine muscle biopsy: A promising diagnostic biomarker for amyotrophic lateral sclerosis
Zhang, Qi‐Jie, Lin, Jie, Wang, You‐Liang, Chen, Long, Ding, Ying, Zheng, Fu‐Ze, Song, Huan‐Huan, Lv, Ao‐Wei, Li, Yu‐Ying, Guo, Qi‐Fu, Lin, Min‐Ting, Hu, Wei, Xu, Liu‐Qing, Zhao, Wen‐Long, Fang, Ling, Cui, Meng‐Chao, Fu, Zhi‐Fei, Chen, Wan‐Jin, Zhang, Jing, Wang, Zhi‐Qiang, Wang, Ning, Fu, Ying
Published in Brain pathology (Zurich, Switzerland) (01.11.2024)
Published in Brain pathology (Zurich, Switzerland) (01.11.2024)
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Expanding the phenotype and genotype spectra of PLIN4-associated myopathy with rimmed ubiquitin-positive autophagic vacuolation
Yang, Kang, Zeng, Yi-Heng, Qiu, Yu-Sen, Lin, Feng, Chen, Hai-Zhu, Jin, Ming, Chen, Long, Zheng, Fu-Ze, Ding, Yuan-Liang, Cao, Chun-Yan, Lin, Min-Ting, Chen, Wan-Jin, Wang, Zhi-Qiang, Wang, Ning
Published in Acta neuropathologica (01.06.2022)
Published in Acta neuropathologica (01.06.2022)
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Anticancer activity and mechanism investigation of beauvericin isolated from secondary metabolites of the mangrove endophytic fungi
Tao, Yi-wen, Lin, Yong-cheng, She, Zhi-gang, Lin, Min-ting, Chen, Pin-xian, Zhang, Jian-ye
Published in Anti-cancer agents in medicinal chemistry (01.01.2015)
Published in Anti-cancer agents in medicinal chemistry (01.01.2015)
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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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The phenotypic and genotypic features of Chinese patients with oculopharyngeal muscular dystrophy
Lin, Feng, Yang, Kang, Lin, Min‐ting, Zheng, Fu‐ze, Chen, Long, Ding, Yuan‐liang, Ye, Zhi‐xian, Lin, Xin, Wang, Ning, Wang, Zhi‐qiang
Published in Annals of clinical and translational neurology (01.03.2023)
Published in Annals of clinical and translational neurology (01.03.2023)
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Tuberous Sclerosis Complex in Chinese patients: Phenotypic analysis and mutational screening of TSC1/TSC2 genes
Lin, Shan, Zeng, Jia-Bin, Zhao, Gui-Xian, Yang, Zhen-Zhen, Huang, Hui-Ping, Lin, Min-Ting, Wu, Zhi-Ying, Wang, Ning, Chen, Wan-Jin, Fang, Ling
Published in Seizure (London, England) (01.10.2019)
Published in Seizure (London, England) (01.10.2019)
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A novel start codon variant in SMCHD1 from a Chinese family causes facioscapulohumeral muscular dystrophy type 2
Qiu, Liang-Liang, Lin, Xiao-Dan, Xu, Guo-Rong, Wang, Li-Li, Ye, Zhi-Xian, Lin, Feng, Chen, Hai-Zhu, Lin, Min-Ting, Cai, Nai-Qing, Jin, Ming, Xu, Liu-Qing, Hu, Wei, Wang, Ning, Wang, Zhi-Qiang
Published in Chinese medical journal (20.11.2021)
Published in Chinese medical journal (20.11.2021)
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Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency
Chen, Hai-Zhu, Jin, Ming, Cai, Nai-Qing, Lin, Xiao-Dan, Liu, Xin-Yi, Xu, Liu-Qing, Lin, Min-Ting, Lin, Feng, Wang, Ning, Wang, Zhi-Qiang, Xu, Guo-Rong
Published in Chinese medical journal (05.07.2019)
Published in Chinese medical journal (05.07.2019)
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Dysferlinopathy in a cohort of Chinese patients: clinical features, mutation spectrum, and imaging findings
Guo, Qi-Fu, Ye, Zhi-Xian, Qiu, Liang-Liang, Lin, Xin, Lai, Jia-He, Lin, Min-Ting, Wang, Zhi-Qiang, Wang, Ning, Lin, Feng
Published in Chinese medical journal (05.03.2021)
Published in Chinese medical journal (05.03.2021)
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Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations
Liu, Xin-Yi, Jin, Ming, Wang, Zhi-Qiang, Wang, Dan-Ni, He, Jun-Jie, Lin, Min-Ting, Fu, Hong-Xia, Wang, Ning
Published in Chinese medical journal (20.06.2016)
Published in Chinese medical journal (20.06.2016)
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Journal Article
Association Between Body Mass Index and Disease Severity in Chinese Spinocerebellar Ataxia Type 3 Patients
Yang, Jin-Shan, Chen, Ping-Ping, Lin, Min-Ting, Qian, Mei-Zhen, Lin, Hui-Xia, Chen, Xiao-Ping, Shang, Xian-Jin, Wang, Dan-Ni, Chen, Yu-Chao, Jiang, Bin, Chen, Yi-Jun, Wang, Ning, Chen, Wan-Jin, Gan, Shi-Rui
Published in Cerebellum (London, England) (01.08.2018)
Published in Cerebellum (London, England) (01.08.2018)
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Ataxic Severity Is Positively Correlated With Fatigue in Spinocerebellar Ataxia Type 3 Patients
Yang, Jin-Shan, Xu, Hao-Ling, Chen, Ping-Ping, Sikandar, Arif, Qian, Mei-Zhen, Lin, Hui-Xia, Lin, Min-Ting, Chen, Wan-Jin, Wang, Ning, Wu, Hua, Gan, Shi-Rui
Published in Frontiers in neurology (22.04.2020)
Published in Frontiers in neurology (22.04.2020)
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The influence of initial symptoms on phenotypes in spinocerebellar ataxia type 3
Xu, Hao‐Ling, Su, Qiu‐Ni, Shang, Xian‐Jin, Sikandar, Arif, Lin, Min‐Ting, Wang, Ning, Lin, Hong, Gan, Shi‐Rui
Published in Molecular genetics & genomic medicine (01.07.2019)
Published in Molecular genetics & genomic medicine (01.07.2019)
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