Author

C. A. Saunders

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biophysics· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 2 Approach:experimental assay· 2 Organism:human· 2 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Assay:fluorescence / live-cell microscopy· 1 Assay:imaging· 1 Research Focus:metabolism & bioenergetics· 1

Frequent Co-Authors

A. C. Rowat· 1 shared A. Schoenhoefen· 1 shared C. Ly· 1 shared C. M. Morris· 1 shared G. G. Luxton· 1 shared G. W. G. Luxton· 1 shared J. D. Mueller· 1 shared J. W. Hennen· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperBiophysics

A. C. Rowat

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2 papers

Recent·Most cited

The luminal AAA+ ATPase torsinA mediates distinct mechanisms of nuclear-cytoplasmic communication by adopting different functional assembly states.

K.-H. Hur, J. W. Hennen, C. A. Saunders, A. Schoenhoefen, P. T. Willey, C. M. Morris, R. H. Ibrahim, R. S. Maisuria, J. D. Mueller, G. W. G. Luxton

This study investigates how torsinA, a luminal AAA+ ATPase, mediates nuclear-cytoplasmic communication by adopting distinct functional assembly states during LINC complex and NPC biogenesis.

bioRxiv · Dec 9, 2021 · PreprintCell Biology

DYT1 dystonia patient-derived fibroblasts have increased deformability and susceptibility to damage by mechanical forces.

N. K. Gill, C. Ly, P. H. Kim, C. A. Saunders, L. G. Fong, S. G. Young, G. G. Luxton, A. C. Rowat

This study examines the mechanotype of fibroblasts from DYT1 dystonia patients and mice lacking torsinA, finding increased deformability and susceptibility to mechanical damage.

bioRxiv · Nov 28, 2018Biophysics