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International Journal of Molecular Sciences|March 27, 2025
Analysis of the Expression Patterns of piRNAs in Response to Microsporidian Invasion in Midgut of Workers (<i>Apis cerana cerana</i>)Yiqiong Zhang, Mengyi Wang, Wenhua Xu, et al.Frontiers in Genetics|August 16, 2021
Tandem Mass Spectrometry Screening for Inborn Errors of Metabolism in Newborns and High-Risk Infants in Southern China: Disease Spectrum and Genetic Characteristics in a Chinese PopulationJianqiang Tan, Dayu Chen, Rongni Chang, et al.Journal of Clinical Laboratory Analysis|September 18, 2018
Copy number variations in the GATA4, NKX2-5, TBX5, BMP4 CRELD1, and 22q11.2 gene regions in Chinese children with sporadic congenital heart diseaseZhetao Li, Jiwei Huang, Biao Liang, et al.Frontiers in Genetics|December 30, 2021
Identification and Functional Characterization of a Novel Nonsense Variant in <i>ARR3</i> in a Southern Chinese Family With High MyopiaDejian Yuan, Tizhen Yan, Shiqiang Luo, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|November 3, 2023
Molecular spectrum and prevalence of thalassemia investigated by third-generation sequencing in the Dongguan region of Guangdong Province, Southern ChinaJiwu Lou, Manna Sun, Aiping Mao, et al.Theranostics|April 11, 2025
Free glutaraldehyde gelatin microsphere loaded mesenchymal stem cells alleviate osteoarthritis by promoting <i>Ext1</i> expressionYe Yuan, Longsheng Xu, Yu Zhao, et al.Frontiers in Genetics|September 26, 2022
Detection of four rare thalassemia variants using Single-molecule realtime sequencingShiqiang Luo, Xingyuan Chen, Dingyuan Zeng, et al.Genes|September 28, 2024
Full-Length Transcriptome Construction and Systematic Characterization of Virulence Factor-Associated Isoforms in <i>Vairimorpha</i> (<i>Nosema</i>) <i>Ceranae</i>Sijia Guo, He Zang, Xiaoyu Liu, et al.Frontiers in Physiology|October 14, 2024
ame-miR-5119-<i>Eth</i> axis modulates larval-pupal transition of western honeybee workerShunan Dong, Kunze Li, He Zang, et al.Blood|November 23, 2020
A natural DNMT1 mutation elevates the fetal hemoglobin level via epigenetic derepression of the γ-globin gene in β-thalassemiaYi Gong, Xinhua Zhang, Qianqian Zhang, et al.Pageof 6