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Linlin Wan

Showing results (11-20 of 61) with videos related to

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Biomedical Engineering Online|July 31, 2024
Attention-enhanced dilated convolution for Parkinson's disease detection using transcranial sonographyShuang Chen, Yuting Shi, Linlin Wan, et al.
Lipids in Health and Disease|September 21, 2018
Hypolipidemic effect of Fragarianilgerrensis Schlecht. medicine compound on hyperlipidemic ratsLiangcai Gao, Zejie Lin, Yilian Liu, et al.
Quantitative Imaging in Medicine and Surgery|August 15, 2023
Characterizing stenosis severity of coronary heart disease by myocardial work measurement in patients with preserved ejection fractionHong Ran, Yujuan Yao, Linlin Wan, et al.
Arthritis and Rheumatism|May 1, 2009
Th17 and natural Treg cell population dynamics in systemic lupus erythematosusJi Yang, Yiwei Chu, Xue Yang, et al.
Molecular and Cellular Biochemistry|May 13, 2026
Dose- and time-dependent cardioprotection of liproxstatin-1 via sequential modulation of ferroptosis pathways after myocardial ischemia-reperfusionZiwei Huang, Xixi Chen, Junyi Ren, et al.
Expert Reviews in Molecular Medicine|February 3, 2025
Lactylation and human diseaseLinlin Wan, HuiJuan Zhang, Jialing Liu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 19, 2024
Genetic Analysis of GCA Repeats in the GLS Gene: Implications for Undiagnosed Ataxia and Spinocerebellar Ataxia 3 in Mainland ChinaLijing Lei, Linliu Peng, Linlin Wan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 4, 2026
Genomic Landscape and Phenotypic Spectrum of Autosomal Recessive Cerebellar Ataxia in ChinaXiaokai Shen, Zhao Chen, Huirong Peng, et al.
Gene|April 12, 2025
Pathogenicity analysis of three SCA14-associated missense mutations in PRKCG gene of Chinese patients with ataxiaHongyu Yuan, Zhao Chen, Linlin Wan, et al.
Neurobiology of Aging|August 10, 2020
No genetic evidence for the involvement of GGC repeat expansions of the NOTCH2NLC gene in Chinese patients with multiple system atrophyKeqin Xu, Linlin Wan, Zhao Chen, et al.
Pageof 7

Showing results (11-20 of 61) with videos related to

Sort By:
Pageof 7
Biomedical Engineering Online|July 31, 2024
Attention-enhanced dilated convolution for Parkinson's disease detection using transcranial sonographyShuang Chen, Yuting Shi, Linlin Wan, et al.
Lipids in Health and Disease|September 21, 2018
Hypolipidemic effect of Fragarianilgerrensis Schlecht. medicine compound on hyperlipidemic ratsLiangcai Gao, Zejie Lin, Yilian Liu, et al.
Quantitative Imaging in Medicine and Surgery|August 15, 2023
Characterizing stenosis severity of coronary heart disease by myocardial work measurement in patients with preserved ejection fractionHong Ran, Yujuan Yao, Linlin Wan, et al.
Arthritis and Rheumatism|May 1, 2009
Th17 and natural Treg cell population dynamics in systemic lupus erythematosusJi Yang, Yiwei Chu, Xue Yang, et al.
Molecular and Cellular Biochemistry|May 13, 2026
Dose- and time-dependent cardioprotection of liproxstatin-1 via sequential modulation of ferroptosis pathways after myocardial ischemia-reperfusionZiwei Huang, Xixi Chen, Junyi Ren, et al.
Expert Reviews in Molecular Medicine|February 3, 2025
Lactylation and human diseaseLinlin Wan, HuiJuan Zhang, Jialing Liu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 19, 2024
Genetic Analysis of GCA Repeats in the GLS Gene: Implications for Undiagnosed Ataxia and Spinocerebellar Ataxia 3 in Mainland ChinaLijing Lei, Linliu Peng, Linlin Wan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 4, 2026
Genomic Landscape and Phenotypic Spectrum of Autosomal Recessive Cerebellar Ataxia in ChinaXiaokai Shen, Zhao Chen, Huirong Peng, et al.
Gene|April 12, 2025
Pathogenicity analysis of three SCA14-associated missense mutations in PRKCG gene of Chinese patients with ataxiaHongyu Yuan, Zhao Chen, Linlin Wan, et al.
Neurobiology of Aging|August 10, 2020
No genetic evidence for the involvement of GGC repeat expansions of the NOTCH2NLC gene in Chinese patients with multiple system atrophyKeqin Xu, Linlin Wan, Zhao Chen, et al.
Pageof 7