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XBP1 signalling is essential for alleviating mutant protein aggregation in ER-stress related skeletal disease
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Katarzyna A. Piróg ,
Roles Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Validation, Visualization, Writing – original draft, Writing – review & editing
* E-mail: katarzyna.pirog@ncl.ac.uk
Affiliation Institute of Genetic Medicine, Newcastle University, Newcastle, United Kingdom
⨯ - Ella P. Dennis,
- Claire L. Hartley,
- Robert M. Jackson,
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Jamie Soul,
Roles Data curation, Formal analysis, Methodology
Affiliation Wellcome Trust Centre for Cell Matrix Research, University of Manchester, Manchester, United Kingdom
⨯ -
Jean-Marc Schwartz,
Roles Funding acquisition, Supervision
Affiliation Wellcome Trust Centre for Cell Matrix Research, University of Manchester, Manchester, United Kingdom
⨯ -
John F. Bateman,
Roles Funding acquisition, Resources, Supervision, Writing – review & editing
Affiliation Murdoch Children's Research Institute, Parkville, Victoria, Australia
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Raymond P. Boot-Handford,
Roles Conceptualization, Funding acquisition, Supervision, Writing – review & editing
Affiliation Wellcome Trust Centre for Cell Matrix Research, University of Manchester, Manchester, United Kingdom
⨯ - Michael D. Briggs
http://orcid.org/0000-0003-0736-3296
XBP1 signalling is essential for alleviating mutant protein aggregation in ER-stress related skeletal disease
- Katarzyna A. Piróg,
- Ella P. Dennis,
- Claire L. Hartley,
- Robert M. Jackson,
- Jamie Soul,
- Jean-Marc Schwartz,
- John F. Bateman,
- Raymond P. Boot-Handford,
- Michael D. Briggs
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- Published: July 1, 2019
- https://doi.org/10.1371/journal.pgen.1008215