Eveline S. Arnold

Wild type human TDP-43 potentiates ALS-linked mutant TDP-43 driven progressive motor and cortical neuron degeneration with pathological features of ALS

T. Hortobágyi, C. Shaw, C. Vance, 2015, Acta neuropathologica communications.

ALS-linked TDP-43 mutations produce aberrant RNA splicing and adult-onset motor neuron disease without aggregation or loss of nuclear TDP-43

Gene W. Yeo, C. Shaw, L. Tessarollo, 2013, Proceedings of the National Academy of Sciences.

CNS uptake of bortezomib is enhanced by P-glycoprotein inhibition: implications for spinal muscular atrophy

K. Fischbeck, M. Hall, Barrington G. Burnett, 2016, Neurobiology of Disease.

A high-throughput genome-wide RNAi screen identifies modifiers of survival motor neuron protein

Eugen C. Buehler, K. Fischbeck, Barrington G. Burnett, 2021, Cell reports.

Mutant TDP-43 within motor neurons drives disease onset but not progression in amyotrophic lateral sclerosis

D. Pizzo, Kevin Drenner, D. Cleveland, 2017, Acta Neuropathologica.

Spinal muscular atrophy.

K. Fischbeck, Eveline S. Arnold, 2018, Handbook of clinical neurology.