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Fuyong Zhang

Showing results (11-20 of 35) with videos related to

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Clinical Laboratory|June 12, 2023
Baseline Data and HLA Alleles and Haplotypes Diversity and Panel Reactive Antibody in Kidney Transplant Candidates in Southwest ChinaYanqiong Liu, Linlin Li, Yanling Liu, et al.
Clinical Biochemistry|August 4, 2020
Novel SERPINC1 missense mutation (Cys462Tyr) causes disruption of the 279Cys-462Cys disulfide bond and leads to type Ⅰ hereditary antithrombin deficiencyFuyong Zhang, Ying Gui, Yu Lu, et al.
Annals of Hematology|February 13, 2026
Machine learning and AI-Assisted red blood cell morphology analysis for effective thalassemia screeningYing Gui, Weiwei Chen, Yuangang Su, et al.
Journal of Pediatric Orthopedics. Part B|February 16, 2022
Potential influence of factors for genu valgus with hereditary multiple exostosesYa Liu, Jianfeng Fang, Yao Liu, et al.
International Journal of Molecular Medicine|June 8, 2019
Protective effects of salvianolic acid B against hydrogen peroxide‑induced apoptosis of human umbilical vein endothelial cells and underlying mechanismsShan Gao, Shiqin Li, Qin Li, et al.
Frontiers in Pediatrics|January 31, 2024
The use of the ratio of C-reactive protein to albumin for the diagnosis of pediatric septic arthritisChong Ren, Quanwen Yuan, Chunhua Yin, et al.
Clinical Biochemistry|January 12, 2025
KNG1 mutations (c.618 T > G and c.1165C > T) cause disruption of the Cys206-Cys218 disulfide bond and truncation of the D5 domain leading to hereditary high molecular weight kininogen deficiencyXiaoying Lv, Pingping Li, Ying Gui, et al.
JACS Au|October 27, 2023
Relay Catalysis for Highly Selective Conversion of Methanol to Ethylene in SyngasKuo Chen, Fenfang Wang, Yu Wang, et al.
Journal of Pediatric Orthopedics. Part B|October 9, 2023
Preliminary fracture reduction in children with type III supracondylar humerus fractures during the COVID-19 pandemicChengda Zou, Wendong Liu, Yunfang Zhen, et al.
Cancer Cell International|July 31, 2021
Association between WNT-1-inducible signaling pathway protein-1 (WISP1) genetic polymorphisms and the risk of gastric cancer in Guangxi ChineseYanqiong Liu, Weijuan Qin, Fuyong Zhang, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Clinical Laboratory|June 12, 2023
Baseline Data and HLA Alleles and Haplotypes Diversity and Panel Reactive Antibody in Kidney Transplant Candidates in Southwest ChinaYanqiong Liu, Linlin Li, Yanling Liu, et al.
Clinical Biochemistry|August 4, 2020
Novel SERPINC1 missense mutation (Cys462Tyr) causes disruption of the 279Cys-462Cys disulfide bond and leads to type Ⅰ hereditary antithrombin deficiencyFuyong Zhang, Ying Gui, Yu Lu, et al.
Annals of Hematology|February 13, 2026
Machine learning and AI-Assisted red blood cell morphology analysis for effective thalassemia screeningYing Gui, Weiwei Chen, Yuangang Su, et al.
Journal of Pediatric Orthopedics. Part B|February 16, 2022
Potential influence of factors for genu valgus with hereditary multiple exostosesYa Liu, Jianfeng Fang, Yao Liu, et al.
International Journal of Molecular Medicine|June 8, 2019
Protective effects of salvianolic acid B against hydrogen peroxide‑induced apoptosis of human umbilical vein endothelial cells and underlying mechanismsShan Gao, Shiqin Li, Qin Li, et al.
Frontiers in Pediatrics|January 31, 2024
The use of the ratio of C-reactive protein to albumin for the diagnosis of pediatric septic arthritisChong Ren, Quanwen Yuan, Chunhua Yin, et al.
Clinical Biochemistry|January 12, 2025
KNG1 mutations (c.618 T > G and c.1165C > T) cause disruption of the Cys206-Cys218 disulfide bond and truncation of the D5 domain leading to hereditary high molecular weight kininogen deficiencyXiaoying Lv, Pingping Li, Ying Gui, et al.
JACS Au|October 27, 2023
Relay Catalysis for Highly Selective Conversion of Methanol to Ethylene in SyngasKuo Chen, Fenfang Wang, Yu Wang, et al.
Journal of Pediatric Orthopedics. Part B|October 9, 2023
Preliminary fracture reduction in children with type III supracondylar humerus fractures during the COVID-19 pandemicChengda Zou, Wendong Liu, Yunfang Zhen, et al.
Cancer Cell International|July 31, 2021
Association between WNT-1-inducible signaling pathway protein-1 (WISP1) genetic polymorphisms and the risk of gastric cancer in Guangxi ChineseYanqiong Liu, Weijuan Qin, Fuyong Zhang, et al.
Pageof 4