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Human Genomics|November 27, 2022
The integration of large-scale public data and network analysis uncovers molecular characteristics of psoriasisAntonio Federico, Alisa Pavel, Lena Möbus, et al.Human Genomics|January 5, 2023
Mutations of TP53 and genes related to homologous recombination repair in breast cancer with germline BRCA1/2 mutationsJinyong Kim, Kyeonghun Jeong, Hyeji Jun, et al.Human Genomics|June 24, 2021
Regulatory VCAN polymorphism is associated with shoulder pain and disability in breast cancer survivorsTrevor S Mafu, Alison V September, Delva ShamleyHuman Genomics|June 30, 2021
Identification of hub genes associated with prognosis, diagnosis, immune infiltration and therapeutic drug in liver cancer by integrated analysisXinyi Lei, Miao Zhang, Bingsheng Guan, et al.Human Genomics|July 3, 2021
Performances of NIPT for copy number variations at different sequencing depths using the semiconductor sequencing platformJiexia Yang, Jing Wu, Haishan Peng, et al.Human Genomics|July 10, 2021
High-throughput screening of circRNAs reveals novel mechanisms of tuberous sclerosis complex-related renal angiomyolipomaYang Zhao, Hao Guo, Wenda Wang, et al.Human Genomics|September 16, 2018
Secondary findings in 421 whole exome-sequenced Chinese childrenWen Chen, Wenke Li, Yi Ma, et al.Human Genomics|June 30, 2018
Abundance of clinical variants in exons included in multiple transcriptsSankar SubramanianHuman Genomics|September 25, 2016
Variation of global DNA methylation levels with age and in autistic childrenShui-Ying Tsang, Tanveer Ahmad, Flora W K Mat, et al.Human Genomics|June 24, 2018
The tale of histone modifications and its role in multiple sclerosisHui He, Zhiping Hu, Han Xiao, et al.Pageof 112