Ibrahim KE, Mears KS, Allen PM, et al. In vivo CAR T cell generation using retargeted and functionalized lentiviral vectors with reduced immunogenicity. Nature communications. 2026. doi:10.1038/s41467-026-71395-y
Publications
Zhuang Z, Byun WS, Chrustowicz J, et al. Charged molecular glue discovery enabled by targeted degron display. Nature chemical biology. 2026. doi:10.1038/s41589-026-02182-5
Sadagopan A, Carson M, Zamurs EJ, et al. An epigenetic bifunctional that toggles between transactivation and repression. bioRxiv : the preprint server for biology. 2026. doi:10.64898/2026.03.17.712509
PMCID
PMC13015318
Lazarev D, Sappington A, Chau G, Zhang R, Berger B. Constrained Diffusion as a Paradigm for Evolution. bioRxiv : the preprint server for biology. 2026. doi:10.64898/2026.03.10.710948
PMCID
PMC13015563
Patikas N, Yao H, Madhu R, Raychaudhuri S, Hemberg M, Korsunsky I. Integration of large, complex single-cell datasets with Harmony2. bioRxiv : the preprint server for biology. 2026. doi:10.64898/2026.03.16.711825
PMCID
PMC13015565
Yates J, Shavakhi M, Choueiri TK, Van Allen EM, Uhler C. SpatialFusion: A lightweight multimodal foundation model for pathway-informed spatial niche mapping. bioRxiv : the preprint server for biology. 2026. doi:10.64898/2026.03.16.712056
PMCID
PMC13015419
Kim B, Shin JG, Hong IS, et al. Transcriptomic profiling of chlorogenic acid and taurine treatment in human skin cells provides insights into cellular senescence mechanisms. Frontiers in molecular biosciences. 2026;13:1748185. doi:10.3389/fmolb.2026.1748185
PMCID
PMC13047320
Munro CE, Beltran J, Palmer P, et al. Baseline cortical amyloid-β levels are associated with subsequent study-partner-rated apathy in community-dwelling older adults. Journal of Alzheimer’s disease : JAD. 2026:13872877261436755. doi:10.1177/13872877261436755
Global burden of cancer in children and adolescents aged 0-19 years, 1990-2023: a systematic analysis for the Global Burden of Disease Study 2023. Lancet (London, England). 2026;407(10536):1360-1373. doi:10.1016/S0140-6736(26)00200-X
Ng BG, Zhang W, Neil JE, et al. A Homozygous Nonsense Variant in the Oligosaccharyltransferase Complex Gene, RPN1, Causes a Congenital Disorder of Glycosylation. HGG advances. 2026:100604. doi:10.1016/j.xhgg.2026.100604