Penney J, Ralvenius WT, Loon A, et al. iPSC-derived microglia carrying the TREM2 R47H/+ mutation are proinflammatory and promote synapse loss. Glia. 2024;72(2):452-469. doi:10.1002/glia.24485
Publications
Zhou Y, Mouw KW. DNA repair deficiency and the immune microenvironment: A pathways perspective. DNA repair. 2024;133:103594. doi:10.1016/j.dnarep.2023.103594
Tomasi J, Zai CC, Pouget JG, Tiwari AK, Kennedy JL. Heart rate variability: Evaluating a potential biomarker of anxiety disorders. Psychophysiology. 2024;61(2):e14481. doi:10.1111/psyp.14481
Duy PQ, Mehta NH, Kahle KT. The "microcephalic hydrocephalus" paradox as a paradigm of altered neural stem cell biology. Cerebral cortex (New York, N.Y. : 1991). 2024;34(1). doi:10.1093/cercor/bhad432
López-Erauskin J, Bravo-Hernández M, Presa M, et al. Stathmin-2 loss leads to neurofilament-dependent axonal collapse driving motor and sensory denervation. Nature neuroscience. 2024;27(1):34-47. doi:10.1038/s41593-023-01496-0
Oren O, Natarajan P, Bhatt DL. SGLT2 Inhibitors in Patients With Cancer Therapy-Related Cardiotoxicity: An Unexpected Benefit? JACC. Heart failure. 2024;12(1):79-82. doi:10.1016/j.jchf.2023.10.005
Dejanovic B, Sheng M, Hanson JE. Targeting synapse function and loss for treatment of neurodegenerative diseases. Nature reviews. Drug discovery. 2024;23(1):23-42. doi:10.1038/s41573-023-00823-1
McClellan JM, Zoghbi AW, Buxbaum JD, et al. An evolutionary perspective on complex neuropsychiatric disease. Neuron. 2024;112(1):7-24. doi:10.1016/j.neuron.2023.10.037
Syeda SB, Lone MA, Mohassel P, et al. Recurrent de novo variant causes childhood-onset amyotrophic lateral sclerosis (ALS) by excess sphingolipid synthesis. Journal of neurology, neurosurgery, and psychiatry. 2024;95(2):103-113. doi:10.1136/jnnp-2023-332132
Grob NM, Remarcik C, Rössler SL, et al. Electrophile Scanning Reveals Reactivity Hotspots for the Design of Covalent Peptide Binders. ACS chemical biology. 2024;19(1):101-109. doi:10.1021/acschembio.3c00538