Recent Faculty Publications

We share our research studies with physicians and scientists worldwide through publications in leading academic journals. View a listing of our faculty’s most recent publications.

Jacob Favret, Mohammed Haseeb Nawaz, Mayuri Patel, Hamid Khaledi, Michael Gelb, and Daesung Shin. (2024) Perinatal loss of galactosylceramidase in both oligodendrocytes and microglia is crucial for the pathogenesis of Krabbe disease in mice. Molecular Therapy (Jul), 32(7): 2207-2222. doi:10.1016/j.ymthe.2024.05.019
Alessandrini F, Wright M, Kurosaki T, Maquat LE, Kiskinis E. (2024) ALS-Associated TDP-43 Dysfunction Compromises UPF1-Dependent mRNA Metabolism Pathways Including Alternative Polyadenylation and 3'UTR Length. bioRxiv : the preprint server for biology (Feb). doi:10.1101/2024.01.31.578311
Kurosaki T, Rambout X, Maquat LE. (2024) FMRP-mediated spatial regulation of physiologic NMD targets in neuronal cells. Genome biology (Jan), 25(1): 31. doi:10.1186/s13059-023-03146-x
Pauly RC, Bhimani RV, Li JX, Blough BE, Landavazo A, Park J. (2023) Distinct Effects of Methamphetamine Isomers on Limbic Norepinephrine and Dopamine Transmission in the Rat Brain. ACS chemical neuroscience (Mar), 14(8): 1399-1411.
Kurosaki T, Mitsutomi S, Hewko A, Akimitsu N, Maquat LE. (2022) Integrative omics indicate FMRP sequesters mRNA from translation and deadenylation in human neuronal cells. Molecular cell (Dec), 82(23): 4564-4581.e11. doi:10.1016/j.molcel.2022.10.018
Conlan Kreher, Jacob Favret , Nadav I. Weinstock, Malabika Maulik, Xinying Hong, Michael H. Gelb, Lawrence Wrabetz, M. Laura Feltri, and Daesung Shin. (2022) Neuron-specific ablation of the Krabbe disease gene galactosylceramidase in mice results in neurodegeneration. PLoS Biology (Jul), 20(7): e3001661. doi:https://doi.org/10.1371/journal.pbio.3001661
Bhimani RV, Yates R, Bass CE, Park J. (2022) Distinct limbic dopamine regulation across olfactory-tubercle subregions through integration of in vivo fast-scan cyclic voltammetry and optogenetics. Journal of neurochemistry (Jan), 161(1): 53-68.
Kurosaki T, Ashizawa T. (2022) The genetic and molecular features of the intronic pentanucleotide repeat expansion in spinocerebellar ataxia type 10. Frontiers in genetics (Jan), 13: 936869. doi:10.3389/fgene.2022.936869
Kurosaki T, Sakano H, Pröschel C, Wheeler J, Hewko A, Maquat LE. (2021) NMD abnormalities during brain development in the Fmr1-knockout mouse model of fragile X syndrome. Genome biology (Nov), 22(1): 317. doi:10.1186/s13059-021-02530-9

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