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Human Genomics|March 25, 2021
How to design a national genomic project-a systematic review of active projectsAnja Kovanda, Ana Nyasha Zimani, Borut PeterlinHuman Genomics|August 2, 2019
Identification of a novel long non-coding RNA within RUNX1 intron 5Nicolás Schnake, Marcela Hinojosa, Soraya GutiérrezHuman Genomics|April 22, 2016
Organization, evolution and functions of the human and mouse Ly6/uPAR family genesChelsea L Loughner, Elspeth A Bruford, Monica S McAndrews, et al.Human Genomics|November 13, 2015
Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligamentsYichuan Liu, Yun Li, Michael E March, et al.Human Genomics|September 17, 2015
Copy number alterations detected by whole-exome and whole-genome sequencing of esophageal adenocarcinomaXiaoyu Wang, Xiaohong Li, Yichen Cheng, et al.Human Genomics|May 20, 2016
Exploring the interaction among EPHX1, GSTP1, SERPINE2, and TGFB1 contributing to the quantitative traits of chronic obstructive pulmonary disease in Chinese Han populationLi An, Yingxiang Lin, Ting Yang, et al.Human Genomics|April 6, 2016
Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistryAdalgisa Pietropolli, Maria Vittoria Capogna, Raffaella Cascella, et al.Human Genomics|July 21, 2017
Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndromeBenjamin M Helm, Jason R Willer, Azita Sadeghpour, et al.Human Genomics|September 15, 2019
lncRNA TUG1 modulates proliferation, apoptosis, invasion, and angiogenesis via targeting miR-29b in trophoblast cellsQian Li, Jing Zhang, Dong-Mei Su, et al.Human Genomics|February 24, 2021
cfDNA deconvolution via NIPT of a pregnant woman after bone marrow transplant and donor egg IVFJianjiang Zhu, Feng Hui, Xuequn Mao, et al.Pageof 112