Sebastián C, Mostoslavsky R. The Various Metabolic Sources of Histone Acetylation. Trends Endocrinol Metab. 2017;28(2):85-87. doi:10.1016/j.tem.2016.11.001
Publications
Ahfeldt T, Litterman NK, Rubin LL. Studying human disease using human neurons. Brain Res. 2017;1656:40-48. doi:10.1016/j.brainres.2016.03.051
Arlotta P, Vanderhaeghen P. Editorial overview: Developmental neuroscience 2017. Curr Opin Neurobiol. 2017;42:A1-A4. doi:10.1016/j.conb.2017.01.003
Francioli LC, Cretu-Stancu M, Garimella KV, et al. A framework for the detection of de novo mutations in family-based sequencing data. Eur J Hum Genet. 2017;25(2):227-233. doi:10.1038/ejhg.2016.147
Johnson MB, Walsh CA. Cerebral cortical neuron diversity and development at single-cell resolution. Curr Opin Neurobiol. 2017;42:9-16. doi:10.1016/j.conb.2016.11.001
da Cunha NB, Cobacho NB, Viana JFC, et al. The next generation of antimicrobial peptides (AMPs) as molecular therapeutic tools for the treatment of diseases with social and economic impacts. Drug Discov Today. 2017;22(2):234-248. doi:10.1016/j.drudis.2016.10.017
Najmi LA, Aukrust I, Flannick J, et al. Functional Investigations of HNF1A Identify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population. Diabetes. 2017;66(2):335-346. doi:10.2337/db16-0460
Wollenberg KR, Desjardins CA, Zalutskaya A, et al. Whole-Genome Sequencing of Mycobacterium tuberculosis Provides Insight into the Evolution and Genetic Composition of Drug-Resistant Tuberculosis in Belarus. J Clin Microbiol. 2017;55(2):457-469. doi:10.1128/JCM.02116-16
Vargas MV, Moawad GN, Sievers C, et al. Feasibility, Safety, and Prediction of Complications for Minimally Invasive Myomectomy in Women With Large and Numerous Myomata. J Minim Invasive Gynecol. 2017;24(2):315-322. doi:10.1016/j.jmig.2016.11.014
Stanton BZ, Hodges C, Calarco JP, et al. Smarca4 ATPase mutations disrupt direct eviction of PRC1 from chromatin. Nat Genet. 2017;49(2):282-288. doi:10.1038/ng.3735