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Faquan Lin

Showing results (71-80 of 82) with videos related to

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FEBS Open Bio|December 19, 2020
Nicotinamide mononucleotide (NMN) protects bEnd.3 cells against H<sub>2</sub> O<sub>2</sub> -induced damage via NAMPT and the NF-κB p65 signalling pathwayXiujun Deng, Xinghuan Liang, Haiyan Yang, et al.
Aging|April 20, 2020
Long intergenic non-protein coding RNA 324 prevents breast cancer progression by modulating miR-10b-5pBo Wang, Yangyang Zhang, Haitian Zhang, et al.
Laboratory Medicine|November 14, 2025
Congenital hypofibrinogenemia with bleeding risk: mutations in the FGA, FGB, and FGG genesYangyang Wu, Kaili Qin, Liqun Xiang, et al.
Annals of Translational Medicine|September 17, 2021
A novel fibrinogen γ-chain frameshift mutation, p. Cys365Phefs*41, causing hypofibrinogenemia with bleeding phenotype in a Chinese familyWeijie Zhou, Yan Huang, Jie Wei, et al.
Frontiers in Immunology|February 17, 2025
Case report: Novel multi-exon homozygous deletion of <i>ZBTB24</i> causes immunodeficiency, centromeric instability, and facial anomalies syndrome 2Yan Long, Chenghan Wang, Jie Xiao, et al.
Neoplasma|January 22, 2026
LINC00324 suppresses abnormal proliferation and promotes apoptosis of leukemia cells through the miR-10b-5p/PTEN pathwayYiyu Li, Bo Wang, Faquan Lin, et al.
Journal of Clinical Laboratory Analysis|April 5, 2019
Blood cell parameters for screening and diagnosis of hereditary spherocytosisLin Liao, Yuchan Xu, Hongying Wei, et al.
Gene|August 30, 2024
Corrigendum to "A novel duplication mutation of SLC2A1 gene causing glucose transporter 1 deficiency syndrome" [Gene 928 (2024) 148762]Chaoyu Huang, Yunhua Huang, Liqiu Pan, et al.
Gene|July 15, 2024
A novel duplication mutation of SLC2A1 gene causing glucose transporter 1 deficiency syndromeChaoyu Huang, Yunhua Huang, Liqiu Pan, et al.
Journal of Diabetes Research|November 17, 2022
GLP-1 RA Improves Diabetic Retinopathy by Protecting the Blood-Retinal Barrier through GLP-1R-ROCK-p-MLC Signaling PathwayLiufeng Wei, Weiwei Mo, Shanshan Lan, et al.
Pageof 9

Showing results (71-80 of 82) with videos related to

Sort By:
Pageof 9
FEBS Open Bio|December 19, 2020
Nicotinamide mononucleotide (NMN) protects bEnd.3 cells against H<sub>2</sub> O<sub>2</sub> -induced damage via NAMPT and the NF-κB p65 signalling pathwayXiujun Deng, Xinghuan Liang, Haiyan Yang, et al.
Aging|April 20, 2020
Long intergenic non-protein coding RNA 324 prevents breast cancer progression by modulating miR-10b-5pBo Wang, Yangyang Zhang, Haitian Zhang, et al.
Laboratory Medicine|November 14, 2025
Congenital hypofibrinogenemia with bleeding risk: mutations in the FGA, FGB, and FGG genesYangyang Wu, Kaili Qin, Liqun Xiang, et al.
Annals of Translational Medicine|September 17, 2021
A novel fibrinogen γ-chain frameshift mutation, p. Cys365Phefs*41, causing hypofibrinogenemia with bleeding phenotype in a Chinese familyWeijie Zhou, Yan Huang, Jie Wei, et al.
Frontiers in Immunology|February 17, 2025
Case report: Novel multi-exon homozygous deletion of <i>ZBTB24</i> causes immunodeficiency, centromeric instability, and facial anomalies syndrome 2Yan Long, Chenghan Wang, Jie Xiao, et al.
Neoplasma|January 22, 2026
LINC00324 suppresses abnormal proliferation and promotes apoptosis of leukemia cells through the miR-10b-5p/PTEN pathwayYiyu Li, Bo Wang, Faquan Lin, et al.
Journal of Clinical Laboratory Analysis|April 5, 2019
Blood cell parameters for screening and diagnosis of hereditary spherocytosisLin Liao, Yuchan Xu, Hongying Wei, et al.
Gene|August 30, 2024
Corrigendum to "A novel duplication mutation of SLC2A1 gene causing glucose transporter 1 deficiency syndrome" [Gene 928 (2024) 148762]Chaoyu Huang, Yunhua Huang, Liqiu Pan, et al.
Gene|July 15, 2024
A novel duplication mutation of SLC2A1 gene causing glucose transporter 1 deficiency syndromeChaoyu Huang, Yunhua Huang, Liqiu Pan, et al.
Journal of Diabetes Research|November 17, 2022
GLP-1 RA Improves Diabetic Retinopathy by Protecting the Blood-Retinal Barrier through GLP-1R-ROCK-p-MLC Signaling PathwayLiufeng Wei, Weiwei Mo, Shanshan Lan, et al.
Pageof 9