Jessica Root

Proximity-based labeling reveals DNA damage–induced phosphorylation of fused in sarcoma (FUS) causes distinct changes in the FUS protein interactome

N. Seyfried, P. Bagchi, Michelle A Johnson, 2022, The Journal of biological chemistry.

Lysosome dysfunction as a cause of neurodegenerative diseases: Lessons from frontotemporal dementia and amyotrophic lateral sclerosis

T. Kukar, Michelle A Johnson, Paola Merino, 2021, Neurobiology of Disease.

Allele‐specific cis‐regulatory methylation of the gene for vasoactive intestinal peptide in white‐throated sparrows

K. Grogan, D. Maney, Kathleen E. Grogan, 2022, Genes, brain, and behavior.

Proximity-based labeling reveals DNA damage-induced N-terminal phosphorylation of fused in sarcoma (FUS) leads to distinct changes in the FUS protein interactome

N. Seyfried, P. Bagchi, Michelle A Johnson, 2021 .

Divergent FUS phosphorylation in primate and mouse cells following double-strand DNA damage

A. Chan, G. Bassell, Qiudong Deng, 2020, Neurobiology of Disease.

Association between Rare Variants in AP4E1, a Component of Intracellular Trafficking, and Persistent Stuttering.

J. Bonifacino, Shaheen N. Khan, S. Riazuddin, 2015, American journal of human genetics.

Granulins rescue inflammation, lysosome dysfunction, and neuropathology in a mouse model of progranulin deficiency

Bonne M. Thompson, G. Astarita, Minzheng Wang, 2023, bioRxiv.

Human GNPTAB stuttering mutations engineered into mice cause vocalization deficits and astrocyte pathology in the corpus callosum

Terra D. Barnes, D. Drayna, Wang-Sik Lee, 2019, Proceedings of the National Academy of Sciences.