ӳ��ý

Publications

Evidence of persistent hunger following dietary weight loss in mice.

Heyward FD, Rosen ED. Evidence of persistent hunger following dietary weight loss in mice. iScience. 2026;29(4):115248. doi:10.1016/j.isci.2026.115248

PMCID

PMC13053754

SMARCB1 missense mutants disrupt SWI/SNF complex stability and remodeling activity.

Cooper GW, Lee BP, Kim WJ, et al. SMARCB1 missense mutants disrupt SWI/SNF complex stability and remodeling activity. Nature communications. 2026. doi:10.1038/s41467-026-71531-8

Daratumumab in high-risk MGUS and low-risk smoldering myeloma: results of the Phase II D-PRISM study.

Nadeem O, Aranha MP, Redd RA, et al. Daratumumab in high-risk MGUS and low-risk smoldering myeloma: results of the Phase II D-PRISM study. Nature communications. 2026. doi:10.1038/s41467-026-71483-z

RB loss modulates chromatin organization by regulating cohesin-dependent loops and enhancer-promoter interactions.

Lee H, Gkotinakou IM, McGrath CG, et al. RB loss modulates chromatin organization by regulating cohesin-dependent loops and enhancer-promoter interactions. Nature communications. 2026. doi:10.1038/s41467-026-71655-x

Saturation editing of RNU4-2 reveals distinct dominant and recessive disorders.

De Jonghe J, Kim HC, Adedeji A, et al. Saturation editing of RNU4-2 reveals distinct dominant and recessive disorders. Nature. 2026. doi:10.1038/s41586-026-10334-9

An affinity reagent-conjugated biotin ligase for amplified cell surface labelling in vitro and in vivo.

Holden B, Mutaher M, Raychowdhury R, et al. An affinity reagent-conjugated biotin ligase for amplified cell surface labelling in vitro and in vivo. Scientific reports. 2026. doi:10.1038/s41598-026-46452-7

Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

Rius R, Blakes AJM, Chen Y, et al. Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes. Nature genetics. 2026. doi:10.1038/s41588-026-02554-6

Personalized artificial intelligence based left ventricular ejection fraction and systolic dysfunction assessment.

Thambiraj G, Bollepalli SC, Johnson A, et al. Personalized artificial intelligence based left ventricular ejection fraction and systolic dysfunction assessment. NPJ digital medicine. 2026. doi:10.1038/s41746-026-02462-3

Reconstruction of human metabolic models with large language models.

Luo J, Wang H, Moyer D, et al. Reconstruction of human metabolic models with large language models. Proceedings of the National Academy of Sciences of the United States of America. 2026;123(15):e2516511123. doi:10.1073/pnas.2516511123

Multi-trait polygenic scores for COPD and COPD exacerbations implicate druggable proteins.

Zhang C, Konigsberg IR, He Y, et al. Multi-trait polygenic scores for COPD and COPD exacerbations implicate druggable proteins. JCI insight. 2026;11(7). doi:10.1172/jci.insight.199951