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Yanmeng Li

Showing results (41-50 of 55) with videos related to

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American Journal of Physiology. Gastrointestinal and Liver Physiology|January 6, 2021
14-kDa phosphohistidine phosphatase is a potential therapeutic target for liver fibrosisAnjian Xu, Jichao Zhou, Yanmeng Li, et al.
Journal of Hepatocellular Carcinoma|April 8, 2026
CENPF Overexpression Induced by HBV Infection Facilitates the G1/S Cell Cycle Transition of Hepatocellular Carcinoma Cells via MYC PathwaySaiping Qi, Donghu Zhou, Sisi Chen, et al.
Frontiers in Oncology|August 15, 2020
Identification and Validation of Novel Serum Autoantibody Biomarkers for Early Detection of Colorectal Cancer and Advanced AdenomaHejing Wang, Bei Zhang, Xiaojin Li, et al.
Frontiers in Oncology|May 30, 2023
Identification of novel serum autoantibody biomarkers for early esophageal squamous cell carcinoma and high-grade intraepithelial neoplasia detectionZhibin Chen, Jie Xing, Cuiling Zheng, et al.
Orphanet Journal of Rare Diseases|June 6, 2022
Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosisWei Zhang, Yanmeng Li, Anjian Xu, et al.
Apoptosis : an International Journal on Programmed Cell Death|June 18, 2026
USP9X regulates copper-induced CASP9/CASP3/GSDME-dependent pyroptosis by deubiquitinating JAK1Huaduan Zi, Hengcheng Tang, Xiaoxi Yang, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|December 1, 2018
A novel SLC40A1 p.Y333H mutation with gain of function of ferroportin: A recurrent cause of haemochromatosis in ChinaWei Zhang, Anjian Xu, Yanmeng Li, et al.
The European Respiratory Journal|November 9, 2019
Genomic characterisation of pulmonary subsolid nodules: mutational landscape and radiological featuresYanmeng Li, Xiao Li, Hao Li, et al.
Orphanet Journal of Rare Diseases|September 29, 2021
Correlation of genotype and phenotype in 32 patients with hereditary hemochromatosis in ChinaLiyan Wu, Wei Zhang, Yanmeng Li, et al.
American Journal of Hematology|May 27, 2024
SUGP2 p.(Arg639Gln) variant is involved in the pathogenesis of hemochromatosis via the CIRBP/BMPER signaling pathwayYanmeng Li, Anjian Xu, Susu Liu, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
American Journal of Physiology. Gastrointestinal and Liver Physiology|January 6, 2021
14-kDa phosphohistidine phosphatase is a potential therapeutic target for liver fibrosisAnjian Xu, Jichao Zhou, Yanmeng Li, et al.
Journal of Hepatocellular Carcinoma|April 8, 2026
CENPF Overexpression Induced by HBV Infection Facilitates the G1/S Cell Cycle Transition of Hepatocellular Carcinoma Cells via MYC PathwaySaiping Qi, Donghu Zhou, Sisi Chen, et al.
Frontiers in Oncology|August 15, 2020
Identification and Validation of Novel Serum Autoantibody Biomarkers for Early Detection of Colorectal Cancer and Advanced AdenomaHejing Wang, Bei Zhang, Xiaojin Li, et al.
Frontiers in Oncology|May 30, 2023
Identification of novel serum autoantibody biomarkers for early esophageal squamous cell carcinoma and high-grade intraepithelial neoplasia detectionZhibin Chen, Jie Xing, Cuiling Zheng, et al.
Orphanet Journal of Rare Diseases|June 6, 2022
Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosisWei Zhang, Yanmeng Li, Anjian Xu, et al.
Apoptosis : an International Journal on Programmed Cell Death|June 18, 2026
USP9X regulates copper-induced CASP9/CASP3/GSDME-dependent pyroptosis by deubiquitinating JAK1Huaduan Zi, Hengcheng Tang, Xiaoxi Yang, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|December 1, 2018
A novel SLC40A1 p.Y333H mutation with gain of function of ferroportin: A recurrent cause of haemochromatosis in ChinaWei Zhang, Anjian Xu, Yanmeng Li, et al.
The European Respiratory Journal|November 9, 2019
Genomic characterisation of pulmonary subsolid nodules: mutational landscape and radiological featuresYanmeng Li, Xiao Li, Hao Li, et al.
Orphanet Journal of Rare Diseases|September 29, 2021
Correlation of genotype and phenotype in 32 patients with hereditary hemochromatosis in ChinaLiyan Wu, Wei Zhang, Yanmeng Li, et al.
American Journal of Hematology|May 27, 2024
SUGP2 p.(Arg639Gln) variant is involved in the pathogenesis of hemochromatosis via the CIRBP/BMPER signaling pathwayYanmeng Li, Anjian Xu, Susu Liu, et al.
Pageof 6