The redox activity of protein disulfide isomerase inhibits ALS phenotypes in cellular and zebrafish models

Sonam Parakh, Sina Shadfar, Emma R. Perri, Audrey M. G. Ragagnin, Claudia V. Piattoni, Mariela B. Fogolín, Kristy C. Yuan, Hamideh Shahheydari, Emily K. Don, Collen J. Thomas, Yuning Hong, Marcelo A. Comini, Angela S. Laird, Damian M. Spencer, Julie D. Atkin

Research output: Contribution to journal › Article › peer-review

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Developing insight into the molecular origins of familial and sporadic frontotemporal dementia and amyotrophic lateral sclerosis
Blair, I., Atkin, J., Chung, R., Guillemin, G., Ooi, L., Denis, B., Molloy, M., Yerbury, J., Cole, N., Karl, T. & Wilson, W.
1/01/16 → …
Project: Research
Disruption to intracellular trafficking as a central pathogenic mechanism in amyotrophic lateral sclerosis
Atkin, J., Cole, N., Chung, R., Rizos, H. & Bell, T.
1/01/15 → …
Project: Research