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Fetal and Pediatric Pathology|December 7, 2019
A Case of a Derivative Chromosome: der(Y)t(Y;18)Pat with Congenital AbnormalitiesShufang Huang, Yu Xia, Hong Ding, et al.
Frontiers in Molecular Biosciences|December 26, 2024
Integrated multi-omics analysis describes immune profiles in ischemic heart failure and identifies PTN as a novel biomarkerTing Xiong, Quhuan Li, Yifan Wang, et al.
Molecular Genetics & Genomic Medicine|June 18, 2025
Whole Exome Sequencing Identifies a Novel Frameshift Mutation of the WRN Gene in a Werner Syndrome Family and Functional AnalysisHao Xiong, Haiqing Gao, Jianji Wan, et al.
Journal of Tissue Engineering and Regenerative Medicine|April 14, 2025
Transcriptome Analysis of Human Vascular Smooth Muscle Cells Cultured on a Polyglycolic Acid Mesh ScaffoldJiang Liu, Zibei Feng, Peng Liu, et al.
Theranostics|September 6, 2024
Transcriptome analysis reveals EBF1 ablation-induced injuries in cardiac systemYueheng Wu, Shaoxian Chen, Guiping Huang, et al.
The Journal of Gene Medicine|January 20, 2019
Ankyrin repeat domain 1: A novel gene for cardiac septal defectsYongchao Yang, Yu Xia, Yueheng Wu, et al.
European Journal of Medical Genetics|September 4, 2021
Novel insertion mutation (Arg1822_Glu1823dup) in MYH6 coiled-coil domain causing familial atrial septal defectShufang Huang, Yueheng Wu, Shaoxian Chen, et al.
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