Sarkizova S, Hacohen N. How T cells spot tumour cells. Nature. 2017;551(7681):444-446. doi:10.1038/d41586-017-07267-9
Publications
Zhang P, He D, Xu Y, et al. Genome-wide identification and differential analysis of translational initiation. Nat Commun. 2017;8(1):1749. doi:10.1038/s41467-017-01981-8
Karp JM. A Slick and Stretchable Surgical Adhesive. N Engl J Med. 2017;377(21):2092-2094. doi:10.1056/NEJMcibr1709967
Gaudelli NM, Komor AC, Rees HA, et al. Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage. Nature. 2017;551(7681):464-471. doi:10.1038/nature24644
Thompson LR, Sanders JG, McDonald D, et al. A communal catalogue reveals Earth’s multiscale microbial diversity. Nature. 2017;551(7681):457-463. doi:10.1038/nature24621
Gönen M, Weir BA, Cowley GS, et al. A Community Challenge for Inferring Genetic Predictors of Gene Essentialities through Analysis of a Functional Screen of Cancer Cell Lines. Cell Syst. 2017;5(5):485-497.e3. doi:10.1016/j.cels.2017.09.004
Emdin CA, Khera AV, Kathiresan S. Mendelian Randomization. JAMA. 2017;318(19):1925-1926. doi:10.1001/jama.2017.17219
Kim WK, Yun S, Kwon Y, et al. mRNAs containing NMD-competent premature termination codons are stabilized and translated under UPF1 depletion. Sci Rep. 2017;7(1):15833. doi:10.1038/s41598-017-16177-9
Huang H, Duggal P, Thio CL, et al. Fine-mapping of genetic loci driving spontaneous clearance of hepatitis C virus infection. Sci Rep. 2017;7(1):15843. doi:10.1038/s41598-017-16011-2
Johnson K, Topf A, Bertoli M, et al. Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness. Orphanet J Rare Dis. 2017;12(1):173. doi:10.1186/s13023-017-0722-1