Tsvetkov P, Adler J, Myers N, Biran A, Reuven N, Shaul Y. Oncogenic addiction to high 26S proteasome level. Cell Death Dis. 2018;9(7):773. doi:10.1038/s41419-018-0806-4
Publications
Miyamoto K, Nguyen KT, Allen GE, et al. Chromatin Accessibility Impacts Transcriptional Reprogramming in Oocytes. Cell Rep. 2018;24(2):304-311. doi:10.1016/j.celrep.2018.06.030
Zhang Y, Yang L, Kucherlapati M, et al. A Pan-Cancer Compendium of Genes Deregulated by Somatic Genomic Rearrangement across More Than 1,400 Cases. Cell Rep. 2018;24(2):515-527. doi:10.1016/j.celrep.2018.06.025
Amal H, Barak B, Bhat V, et al. Shank3 mutation in a mouse model of autism leads to changes in the S-nitroso-proteome and affects key proteins involved in vesicle release and synaptic function. Mol Psychiatry. 2018. doi:10.1038/s41380-018-0113-6
Holm IA, Agrawal PB, Ceyhan-Birsoy O, et al. The BabySeq project: implementing genomic sequencing in newborns. BMC Pediatr. 2018;18(1):225. doi:10.1186/s12887-018-1200-1
Rikhye RV, Wimmer RD, Halassa MM. Toward an Integrative Theory of Thalamic Function. Annu Rev Neurosci. 2018;41:163-183. doi:10.1146/annurev-neuro-080317-062144
Bedbrook CN, Deverman BE, Gradinaru V. Viral Strategies for Targeting the Central and Peripheral Nervous Systems. Annu Rev Neurosci. 2018;41:323-348. doi:10.1146/annurev-neuro-080317-062048
Lipson M, Cheronet O, Mallick S, et al. Ancient genomes document multiple waves of migration in Southeast Asian prehistory. Science. 2018;361(6397):92-95. doi:10.1126/science.aat3188
Goodman L, Karlsson EK. America’s lost dogs. Science. 2018;361(6397):27-28. doi:10.1126/science.aau1306
Di Gioia SA, Shaaban S, Tuysuz B, et al. Recessive MYF5 Mutations Cause External Ophthalmoplegia, Rib, and Vertebral Anomalies. Am J Hum Genet. 2018;103(1):115-124. doi:10.1016/j.ajhg.2018.05.003