Research progress of circular RNA FOXO3 in diseases (review)

Authors: Zhao, Min ^{a, c}, Lin, Minting ^{a, c}, Zhang, Zhibo ^b, Ye, Linhu ^{c, ⁎}

Source: In Global Medical Genetics March 2025 12(1)

CGG repeat expansion in LOC642361/NUTM2B-AS1 typically presents as oculopharyngodistal myopathy

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

Source: In Journal of Genetics and Genomics February 2024 51(2):184-196

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

Authors: 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

Source: Neurology. 101(3):e225-e237

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Age at onset mediates genetic impact on disease severity in facioscapulohumeral muscular dystrophy.

Authors: Zheng, Fuze¹, Lin, Yawen², Qiu, Liangliang^1,3, Zheng, Ying¹, Zeng, Minghui¹, Lin, Xiaodan¹, He, Qifang¹, Lin, Yuhua¹, Chen, Long¹, Lin, Xin^1,3, Chen, Xinyue¹, Lin, Lin¹, Wang, Lili¹, He, Junjie¹, Lin, Feng^1,3, Yang, Kang^1,3, Wang, Ning^1,3, Lin, Minting^1,3, Lian, Sheng², Wang, Zhiqiang^1,3

Source: Brain: A Journal of Neurology; Feb2025, Vol. 148 Issue 2, p613-625, 13p

Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study

Authors: 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

Source: In The Lancet Regional Health - Western Pacific January 2022 18

Clinical and genetic characterization of limb girdle muscular dystrophy R7 telethonin-related patients from three unrelated Chinese families

Authors: Chen, Haizhu, Xu, Guorong, Lin, Feng, Jin, Ming, Cai, Naiqing, Qiu, Liangliang, Ye, Zhixian, Wang, Lili, Lin, Minting, Wang, Ning

Source: In Neuromuscular Disorders February 2020 30(2):137-143

Reprogramming of adult human peripheral blood mononuclear cells into hiPSCs from two patients with facioscapulohumeral muscular dystrophy type 1

Authors: Zheng, Fuze, Chen, Long, Qiu, Liangliang, Lin, Lin, Lin, Xin, He, Qifang, Wang, Lili, Ye, Zhixian, Lin, Minting, Wang, Zhiqiang

Source: Stem cell research. 60

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100188069502.0x000001&indx=1&recIds=ETOCvdc_100188069502.0x000001

Euphorbia factor L2 induces apoptosis in A549 cells through the mitochondrial pathway

Authors: Lin, Minting, Tang, Sili, Zhang, Chao, Chen, Hubiao, Huang, Wenjing, Liu, Yun, Zhang, Jianye

Source: In Acta Pharmaceutica Sinica B January 2017 7(1):59-64

Apicidin Inhibited Proliferation and Invasion and Induced Apoptosis via Mitochondrial Pathway in Non-small Cell Lung Cancer GLC-82 Cells

Authors: Zhang, Jianye, Lai, Zhenzhu, Huang, Wenjing, Ling, Huiping, Lin, Minting, Tang, Sili, Liu, Yun, Tao, Yiwen

Source: Anti-cancer agents in medicinal chemistry. 17(10):1374-1382

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100077940572.0x000001&indx=1&recIds=ETOCvdc_100077940572.0x000001

An epigenetic basis for genetic anticipation in facioscapulohumeral muscular dystrophy type 1.

Authors: Zheng, Fuze¹, Qiu, Liangliang^1,2, Chen, Long^1,2, Zheng, Ying¹, He, Qifang¹, Lin, Xiaodan¹, Lin, Minting^1,2, Lin, Yi^1,2, Fu, Ying^1,2, Wang, Ning^1,2, Wang, Zhiqiang^1,2, fmuwzq@fjmu.edu.cn

Source: Brain: A Journal of Neurology; Dec2023, Vol. 146 Issue 12, pe107-e110, 4p

Exosomes with low miR-34c-3p expression promote invasion and migration of non-small cell lung cancer by upregulating integrin α2β1

Authors: Huang, Wenjing, Yan, Yanyan, Liu, Yun, Lin, Minting, Ma, Jinxiang, Zhang, Wei, Dai, Jianwei, Li, Jiajun, Guo, Qiaoru, Chen, Hubiao, Makabel, Bolat, Liu, Hong, Su, Chaoyue, Bi, Hong, Zhang, Jianye

Source: Signal transduction and targeted therapy. 5(1)

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100172024249.0x000001&indx=1&recIds=ETOCvdc_100172024249.0x000001

TU-199. A comparative analysis of clinical and tremor features of essential tremor and Parkinson's disease from essential tremor

Authors: Zhang, Lei, Yang, Xuan, Lin, MinTing, Hu, JianYi, Li, Ming

Source: Clinical neurophysiology. 141(S):S39-S39

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100187711978.0x000001&indx=1&recIds=ETOCvdc_100187711978.0x000001

Wheelchair use in genetically confirmed FSHD1 from a large cohort study in Chinese population.

Authors: Qiu, Liangliang¹, Chen, Long¹, Zheng, Fuze¹, Lin, Minting¹, Lin, Yi¹, Fu, Ying¹, Wang, Ning¹, ningwang@fjmu.edu.cn, Wang, Zhiqiang¹, fmuwzq@fjmu.edu.cn

Source: Brain: A Journal of Neurology; Jun2022, Vol. 145 Issue 6, pe51-e54, 4p

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Clinical and genetic features of somatic mosaicism in facioscapulohumeral dystrophy

Authors: 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

Source: Journal of Medical Genetics (JMG); 2020, Vol. 57 Issue: 11 p777-785, 9p

CGG repeat expansion in LOC642361/NUTM2B-AS1typically presents as oculopharyngodistal myopathy

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

Source: Journal of Genetics and Genomics; 20240101, Issue: Preprints

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