Long Chen - Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, Fujian Medical University

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论文共 15 篇作者统计合作学者相似作者

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Detection of Ptdp-43 Via Routine Muscle Biopsy: A Promising Diagnostic Biomarker for Amyotrophic Lateral Sclerosis

Brain pathology (Zurich, Switzerland)no. 6 (2024): e13261-e13261

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Comprehensive Proteomic Analysis of Dysferlinopathy Unveiling Molecular Mechanisms and Biomarkers Linked to Pathological Progression

Di Wang,Xin-yi Liu,Qi-Fang He,Fu-ze Zheng,Long Chen, Ying Zheng, Ming-hui Zeng, Yu-hua Lin,Xin Lin,Hai-zhu Chen,Min-ting Lin,Ning Wang,Zhi-qiang Wang,Feng Lin

CNS NEUROSCIENCE & THERAPEUTICSno. 10 (2024)

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Correction of human non-sense mutation via adenine base editing for Duchenne muscular dystrophy treatment in mouse

Ming Jin,Jiajia Lin,Haisen Li, Zhifang Li, Dong Yang, Yin Wang,Yuyang Yu,Zhurui Shao,Long Chen,Zhiqiang Wang, Yu Zhang, Xiumei Zhang,Ning Wang,Chunlong Xu,Hui Yang,Wan-Jin Chen,Guoling Li

Molecular Therapy - Nucleic Acidsno. 2 (2024): 102165-102165

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Inhibition of CILP2 Improves Glucose Metabolism and Mitochondrial Dysfunction in Sarcopenia Via the Wnt Signalling Pathway

Zhibo Deng,Chao Song,Long Chen, Rongsheng Zhang, Linhai Yang, Peng Zhang, Yu Xiu, Yibin Su,Fenqi Luo, Jun Luo,Hanhao Dai,Jie Xu

Journal of cachexia, sarcopenia and muscle（2024）

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Music Therapy in Hemodialysis Patients: Systematic Review and Meta-Analysis

Feng Lin,Long Chen,Yin Gao

Complementary therapies in medicine (2024): 103090-103090

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CGG Repeat Expansion in LOC642361/NUTM2B-AS1 Typically Presents As Oculopharyngodistal Myopathy

Yan Shi,Chunyan Cao,Yiheng Zeng,Yuanliang Ding,Long Chen,Fuze Zheng,Xuejiao Chen, Fanggui Zhou,Xiefeng Yang,Jinjing Li,Liuqing Xu,Guorong Xu,Minting Lin,Hiroyuki Ishiura,Shoji Tsuji,Ning Wang,Zhiqiang Wang,Wan-Jin Chen,Kang Yang

JOURNAL OF GENETICS AND GENOMICSno. 2 (2024): 184-196

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Association of 4Qa-Specific Distal D4Z4 Hypomethylation with Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy

Fuze Zheng,Liangliang Qiu,Long Chen, Ying Zheng,Xiaodan Lin,Junjie He,Xin Lin,Qifang He, Yuhua Lin, Lin, Lili Wang,Feng Lin,Kang Yang,Minting Lin,Yi Lin,Ying Fu,Ning Wang,Zhiqiang Wang

NEUROLOGYno. 3 (2023): E225-E237

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Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients

Feng Lin,Kang Yang, Xin Lin,Ming Jin,Long Chen,Fu-ze Zheng,Liang-liang Qiu,Zhi-xian Ye,Hai-zhu Chen,Min-ting Lin,Ning Wang,Zhi-qiang Wang

Orphanet Journal of Rare Diseasesno. 1 (2023): 1-18

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The phenotypic and genotypic features of Chinese patients with oculopharyngeal muscular dystrophy

Feng Lin,Kang Yang,Min-ting Lin,Fu-ze Zheng,Long Chen,Yuan-liang Ding,Zhi-xian Ye, Xin Lin,Ning Wang,Zhi-qiang Wang

Ann Clin Transl Neurol（2023）

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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

Zhiqiang Wang,Liangliang Qiu,Minting Lin,Long Chen,Fuze Zheng,Lin Lin,Feng Lin,Zhixian Ye,Xiaodan Lin,Junjie He, Lili Wang,Xin Lin,Qifang He,Wanjin Chen,Yi Lin,Ying Fu,Ning Wang

The Lancet Regional Health - Western Pacific（2022）

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