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Showing results (1021-1030 of 1,060) with videos related to
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Medscience
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February 24, 2026
Differential genetic analysis of ectrodactyly in a Fanconi anemia pedigree with FANCA mutations
Jian-Hui Zhang, Zi-Yan Xu, Hong-Ping Yu, et al.
Nature Communications
|
August 16, 2020
A single dose of an adenovirus-vectored vaccine provides protection against SARS-CoV-2 challenge
Shipo Wu, Gongxun Zhong, Jun Zhang, et al.
Phytomedicine : International Journal of Phytotherapy and Phytopharmacology
|
October 6, 2023
Ethyl ferulate suppresses post-myocardial infarction myocardial fibrosis by inhibiting transforming growth factor receptor 1
Ke-Feng Zeng, Hui-Juan Wang, Bo Deng, et al.
NPJ Digital Medicine
|
June 14, 2025
A scoping review and evidence gap analysis of clinical AI fairness
Mingxuan Liu, Yilin Ning, Salinelat Teixayavong, et al.
Journal of Cellular and Molecular Medicine
|
July 7, 2022
Targeting cancer stemness mediated by BMI1 and MCL1 for non-small cell lung cancer treatment
Erh-Hsuan Lin, Jhen-Wei Hsu, Ting-Fang Lee, et al.
Cell Reports
|
March 12, 2014
A chemical probe that labels human pluripotent stem cells
Nao Hirata, Masato Nakagawa, Yuto Fujibayashi, et al.
International Journal of Cardiology
|
June 9, 2020
Automated extraction of left atrial volumes from two-dimensional computer tomography images using a deep learning technique
Hung-Hsun Chen, Chih-Min Liu, Shih-Lin Chang, et al.
Nature Communications
|
May 21, 2024
A potent Henipavirus cross-neutralizing antibody reveals a dynamic fusion-triggering pattern of the G-tetramer
Pengfei Fan, Mengmeng Sun, Xinghai Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 23, 2014
Genomic and transcriptomic analyses of the medicinal fungus Antrodia cinnamomea for its metabolite biosynthesis and sexual development
Mei-Yeh Jade Lu, Wen-Lang Fan, Woei-Fuh Wang, et al.
Gene
|
September 25, 2025
Genetic analysis of a family with skeletal muscle ion channelopathy and hereditary spastic paraplegia type 7 caused by SCN4A and SPG7 double mutations
Hong-Ping Yu, Zi-Yan Xu, Meng-Qian Wu, et al.
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Search research articles
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Showing results (1021-1030 of 1,060) with videos related to
Sort By:
Page
of 106
Medscience
|
February 24, 2026
Differential genetic analysis of ectrodactyly in a Fanconi anemia pedigree with FANCA mutations
Jian-Hui Zhang, Zi-Yan Xu, Hong-Ping Yu, et al.
Nature Communications
|
August 16, 2020
A single dose of an adenovirus-vectored vaccine provides protection against SARS-CoV-2 challenge
Shipo Wu, Gongxun Zhong, Jun Zhang, et al.
Phytomedicine : International Journal of Phytotherapy and Phytopharmacology
|
October 6, 2023
Ethyl ferulate suppresses post-myocardial infarction myocardial fibrosis by inhibiting transforming growth factor receptor 1
Ke-Feng Zeng, Hui-Juan Wang, Bo Deng, et al.
NPJ Digital Medicine
|
June 14, 2025
A scoping review and evidence gap analysis of clinical AI fairness
Mingxuan Liu, Yilin Ning, Salinelat Teixayavong, et al.
Journal of Cellular and Molecular Medicine
|
July 7, 2022
Targeting cancer stemness mediated by BMI1 and MCL1 for non-small cell lung cancer treatment
Erh-Hsuan Lin, Jhen-Wei Hsu, Ting-Fang Lee, et al.
Cell Reports
|
March 12, 2014
A chemical probe that labels human pluripotent stem cells
Nao Hirata, Masato Nakagawa, Yuto Fujibayashi, et al.
International Journal of Cardiology
|
June 9, 2020
Automated extraction of left atrial volumes from two-dimensional computer tomography images using a deep learning technique
Hung-Hsun Chen, Chih-Min Liu, Shih-Lin Chang, et al.
Nature Communications
|
May 21, 2024
A potent Henipavirus cross-neutralizing antibody reveals a dynamic fusion-triggering pattern of the G-tetramer
Pengfei Fan, Mengmeng Sun, Xinghai Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 23, 2014
Genomic and transcriptomic analyses of the medicinal fungus Antrodia cinnamomea for its metabolite biosynthesis and sexual development
Mei-Yeh Jade Lu, Wen-Lang Fan, Woei-Fuh Wang, et al.
Gene
|
September 25, 2025
Genetic analysis of a family with skeletal muscle ion channelopathy and hereditary spastic paraplegia type 7 caused by SCN4A and SPG7 double mutations
Hong-Ping Yu, Zi-Yan Xu, Meng-Qian Wu, et al.
Page
of 106