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Second-generation shRNA libraries covering the mouse and human genomes.
Silva JM, Li MZ, Chang K, Ge W, Golding MC, Rickles RJ, Siolas D, Hu G, Paddison PJ, Schlabach MR, Sheth N, Bradshaw J, Burchard J, Kulkarni A, Cavet G, Sachidanandam R, McCombie WR, Cleary MA, Elledge SJ, Hannon GJ. Silva JM, et al. Among authors: ge w. Nat Genet. 2005 Nov;37(11):1281-8. doi: 10.1038/ng1650. Epub 2005 Oct 2. Nat Genet. 2005. PMID: 16200065
Synthetic shRNAs as potent RNAi triggers.
Siolas D, Lerner C, Burchard J, Ge W, Linsley PS, Paddison PJ, Hannon GJ, Cleary MA. Siolas D, et al. Among authors: ge w. Nat Biotechnol. 2005 Feb;23(2):227-31. doi: 10.1038/nbt1052. Epub 2004 Dec 26. Nat Biotechnol. 2005. PMID: 15619616
A large-scale RNAi screen in human cells identifies new components of the p53 pathway.
Berns K, Hijmans EM, Mullenders J, Brummelkamp TR, Velds A, Heimerikx M, Kerkhoven RM, Madiredjo M, Nijkamp W, Weigelt B, Agami R, Ge W, Cavet G, Linsley PS, Beijersbergen RL, Bernards R. Berns K, et al. Among authors: ge w. Nature. 2004 Mar 25;428(6981):431-7. doi: 10.1038/nature02371. Nature. 2004. PMID: 15042092
Biallelic variants in SREBF2 cause autosomal recessive spastic paraplegia.
Wei Q, Fan W, Li HF, Wanga PS, Xu M, Dong HL, Yu H, Lyu J, Luo WJ, Chen DF, Ge W, Wu ZY. Wei Q, et al. Among authors: ge w. J Genet Genomics. 2025 Jan 14:S1673-8527(25)00019-0. doi: 10.1016/j.jgg.2025.01.004. Online ahead of print. J Genet Genomics. 2025. PMID: 39814172
2,548 results