Marutani E, Miranda M, Durham TJ, et al. Hypoxia ameliorates neurodegeneration and movement disorder in a mouse model of Parkinson’s disease. Nature neuroscience. 2025. doi:10.1038/s41593-025-02010-4
Metabolism Program
Zhou Y, Ahsan FM, Emans SW, Soukas AA. The nuclear pore complex connects energy sensing to transcriptional plasticity in longevity. Molecular cell. 2025. doi:10.1016/j.molcel.2025.08.035
Deutsch AJ, Bell AS, Michalek DA, et al. Development and Validation of a Type 1 Diabetes Multi-Ancestry Polygenic Score. Diabetes. 2025. doi:10.2337/db25-0772
Meisel JD, Joshi PR, Spelbring AN, et al. Mutations in mitochondrial ferredoxin FDX2 suppress frataxin deficiency. Nature. 2025. doi:10.1038/s41586-025-09821-2
Reiner AP, Raffield LM, Franceschini N, et al. Effect of Sickle Cell Trait and Genotype on the Association of Soluble uPAR with Kidney Function Measures in Black Americans. Clinical journal of the American Society of Nephrology : CJASN. 2021;16(2):287-289. doi:10.2215/CJN.12100720
Sherva R, Gross A, Mukherjee S, et al. Genome-wide association study of rate of cognitive decline in Alzheimer’s disease patients identifies novel genes and pathways. Alzheimer’s & dementia : the journal of the Alzheimer’s Association. 2020;16(8):1134-1145. doi:10.1002/alz.12106
PMCID
PMC7924136
Bao XR, Ong SE, Goldberger O, et al. Mitochondrial dysfunction remodels one-carbon metabolism in human cells. Elife. 2016;5. doi:10.7554/eLife.10575
Rees MG, Seashore-Ludlow B, Cheah JH, et al. Correlating chemical sensitivity and basal gene expression reveals mechanism of action. Nat Chem Biol. 2016;12(2):109-16. doi:10.1038/nchembio.1986