TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTD von Chou, Ching-Chieh, Zhang, Yi, Umoh, Mfon E., Vaughan, Spencer W., Lorenzini, Ileana, Liu, Feilin, Sayegh, Melissa, Donlin-Asp, Paul G., Chen, Yu Han, Duong, Duc M., Seyfried, Nicholas T., Powers, Maureen A., Kukar, Thomas, Hales, Chadwick M., Gearing, Marla, Cairns, Nigel J., Boylan, Kevin B., Dickson, Dennis W., Rademakers, Rosa, Zhang, Yong-Jie, Petrucelli, Leonard, Sattler, Rita, Zarnescu, Daniela C., Glass, Jonathan D., Rossoll, Wilfried

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Intraspinal neural stem cell transplantation in amyotrophic lateral sclerosis: Phase 1 trial outcomes von Feldman, Eva L., Boulis, Nicholas M., Hur, Junguk, Johe, Karl, Rutkove, Seward B., Federici, Thais, Polak, Meraida, Bordeau, Jane, Sakowski, Stacey A., Glass, Jonathan D.

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A proteomic network approach across the ALS‐FTD disease spectrum resolves clinical phenotypes and genetic vulnerability in human brain von Umoh, Mfon E, Dammer, Eric B, Dai, Jingting, Duong, Duc M, Lah, James J, Levey, Allan I, Gearing, Marla, Glass, Jonathan D, Seyfried, Nicholas T

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ATXN2 intermediate expansions in amyotrophic lateral sclerosis von Glass, Jonathan D, Dewan, Ramita, Ding, Jinhui, Gibbs, J Raphael, Dalgard, Clifton, Keagle, Pamela J, Shankaracharya, García-Redondo, Alberto, Traynor, Bryan J, Chia, Ruth, Landers, John E

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Stem cell transplantation for amyotrophic lateral sclerosis von Baloh, Robert H, Glass, Jonathan D, Svendsen, Clive N

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Protecting the nerve terminals von Glass, Jonathan D

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The gut microbiome and neuroinflammation in amyotrophic lateral sclerosis? Emerging clinical evidence von Fournier, Christina N., Houser, Madelyn, Tansey, Malú G., Glass, Jonathan D., Hertzberg, Vicki Stover

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Localization of a toxic form of superoxide dismutase 1 protein to pathologically affected tissues in familial ALS von Brotherton, Terrell E, Li, Yingjie, Cooper, Deborah, Gearing, Marla, Julien, Jean-Pierre, Rothstein, Jeffrey D, Boylan, Kevin, Glass, Jonathan D

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Distinct conformers of transmissible misfolded SOD1 distinguish human SOD1-FALS from other forms of familial and sporadic ALS von Ayers, Jacob I., Diamond, Jeffrey, Sari, Adriana, Fromholt, Susan, Galaleldeen, Ahmad, Ostrow, Lyle W., Glass, Jonathan D., Hart, P. John, Borchelt, David R.

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Absence of SOD1 leads to oxidative stress in peripheral nerve and causes a progressive distal motor axonopathy von Fischer, Lindsey R., Li, Yingjie, Asress, Seneshaw A., Jones, Dean P., Glass, Jonathan D.

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Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man von Fischer, Lindsey R., Culver, Deborah G., Tennant, Philip, Davis, Albert A., Wang, Minsheng, Castellano-Sanchez, Amilcar, Khan, Jaffar, Polak, Meraida A., Glass, Jonathan D.

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Longitudinal biomarkers in amyotrophic lateral sclerosis von Huang, Fen, Zhu, Yuda, Hsiao‐Nakamoto, Jennifer, Tang, Xinyan, Dugas, Jason C., Moscovitch‐Lopatin, Miriam, Glass, Jonathan D., Brown, Robert H., Ladha, Shafeeq S., Lacomis, David, Harris, Jeffrey M., Scearce‐Levie, Kimberly, Ho, Carole, Bowser, Robert, Berry, James D.

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Fibroblast bioenergetics to classify amyotrophic lateral sclerosis patients von Konrad, Csaba, Kawamata, Hibiki, Bredvik, Kirsten G, Arreguin, Andrea J, Cajamarca, Steven A, Hupf, Jonathan C, Ravits, John M, Miller, Timothy M, Maragakis, Nicholas J, Hales, Chadwick M, Glass, Jonathan D, Gross, Steven, Mitsumoto, Hiroshi, Manfredi, Giovanni

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Aggregates of Small Nuclear Ribonucleic Acids (snRNAs) in Alzheimer's Disease von Hales, Chadwick M., Dammer, Eric B., Diner, Ian, Yi, Hong, Seyfried, Nicholas T., Gearing, Marla, Glass, Jonathan D., Montine, Thomas J., Levey, Allan I., Lah, James J.

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SOD1 targeted to the mitochondrial intermembrane space prevents motor neuropathy in the Sod1 knockout mouse von FISCHER, Lindsey R, IGOUDJIL, Anissa, MAGRANE, Jordi, YINGJIE LI, HANSEN, Jason M, MANFREDI, Giovanni, GLASS, Jonathan D

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Stathmin-2: adding another piece to the puzzle of TDP-43 proteinopathies and neurodegeneration von Glass, Jonathan D.

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Cellular toxicity of mutant SOD1 protein is linked to an easily soluble, non-aggregated form in vitro von Brotherton, Terrell E, Li, Yingjie, Glass, Jonathan D

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Validation of machine learning models to detect amyloid pathologies across institutions von Vizcarra, Juan C., Gearing, Marla, Keiser, Michael J., Glass, Jonathan D., Dugger, Brittany N., Gutman, David A.

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The heritability of amyotrophic lateral sclerosis in a clinically ascertained United States research registry von Wingo, Thomas S, Cutler, David J, Yarab, Nicole, Kelly, Crystal M, Glass, Jonathan D

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Inactivation of sodium channels underlies reversible neuropathy during critical illness in rats von Novak, Kevin R, Nardelli, Paul, Cope, Tim C, Filatov, Gregory, Glass, Jonathan D, Khan, Jaffar, Rich, Mark M

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