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Haibo Li

Showing results (931-940 of 960) with videos related to

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Frontiers in Pharmacology|November 15, 2018
Association Between Folic Acid Supplementation and Retinal Atherosclerosis in Chinese Adults With Hypertension Complicated by Diabetes MellitusYing Meng, Jun Li, Xuling Chen, et al.
Signal Transduction and Targeted Therapy|October 7, 2020
The efficacy assessment of convalescent plasma therapy for COVID-19 patients: a multi-center case seriesHao Zeng, Dongfang Wang, Jingmin Nie, et al.
Hepatology (Baltimore, Md.)|September 11, 2023
Single-cell immune profiling of mouse liver aging reveals Cxcl2+ macrophages recruit neutrophils to aggravate liver injuryYasong Liu, Jiaqi Xiao, Jianye Cai, et al.
Science Advances|September 19, 2018
Mechanically active materials in three-dimensional mesostructuresXin Ning, Xinge Yu, Heling Wang, et al.
Emerging Microbes & Infections|March 18, 2021
Cross-reactive antibody against human coronavirus OC43 spike protein correlates with disease severity in COVID-19 patients: a retrospective studyLi Guo, Yeming Wang, Liang Kang, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 4, 2021
Compliant 3D frameworks instrumented with strain sensors for characterization of millimeter-scale engineered muscle tissuesHangbo Zhao, Yongdeok Kim, Heling Wang, et al.
Emerging Microbes & Infections|November 30, 2024
High-throughput single-cell analysis reveals Omp38-specific monoclonal antibodies that protect against <i>Acinetobacter baumannii</i> infectionYiwei Zhang, Hao Cheng, Peng Yu, et al.
Prenatal Diagnosis|October 18, 2025
Prenatal Exome Sequencing Analysis in Fetuses With Structural Anomalies: A Multicenter Prospective Cohort Study With Practical ImplicationsYulin Jiang, Haibo Li, Xiangyu Zhu, et al.
Human Genetics|May 2, 2018
ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing lossWu Li, Jie Sun, Jie Ling, et al.
Journal of Human Genetics|January 16, 2015
Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese familyHonghan Wang, Xinwei Wang, Chufeng He, et al.
Pageof 96

Showing results (931-940 of 960) with videos related to

Sort By:
Pageof 96
Frontiers in Pharmacology|November 15, 2018
Association Between Folic Acid Supplementation and Retinal Atherosclerosis in Chinese Adults With Hypertension Complicated by Diabetes MellitusYing Meng, Jun Li, Xuling Chen, et al.
Signal Transduction and Targeted Therapy|October 7, 2020
The efficacy assessment of convalescent plasma therapy for COVID-19 patients: a multi-center case seriesHao Zeng, Dongfang Wang, Jingmin Nie, et al.
Hepatology (Baltimore, Md.)|September 11, 2023
Single-cell immune profiling of mouse liver aging reveals Cxcl2+ macrophages recruit neutrophils to aggravate liver injuryYasong Liu, Jiaqi Xiao, Jianye Cai, et al.
Science Advances|September 19, 2018
Mechanically active materials in three-dimensional mesostructuresXin Ning, Xinge Yu, Heling Wang, et al.
Emerging Microbes & Infections|March 18, 2021
Cross-reactive antibody against human coronavirus OC43 spike protein correlates with disease severity in COVID-19 patients: a retrospective studyLi Guo, Yeming Wang, Liang Kang, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 4, 2021
Compliant 3D frameworks instrumented with strain sensors for characterization of millimeter-scale engineered muscle tissuesHangbo Zhao, Yongdeok Kim, Heling Wang, et al.
Emerging Microbes & Infections|November 30, 2024
High-throughput single-cell analysis reveals Omp38-specific monoclonal antibodies that protect against <i>Acinetobacter baumannii</i> infectionYiwei Zhang, Hao Cheng, Peng Yu, et al.
Prenatal Diagnosis|October 18, 2025
Prenatal Exome Sequencing Analysis in Fetuses With Structural Anomalies: A Multicenter Prospective Cohort Study With Practical ImplicationsYulin Jiang, Haibo Li, Xiangyu Zhu, et al.
Human Genetics|May 2, 2018
ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing lossWu Li, Jie Sun, Jie Ling, et al.
Journal of Human Genetics|January 16, 2015
Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese familyHonghan Wang, Xinwei Wang, Chufeng He, et al.
Pageof 96