Author

E. Schaeffer

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

Biology Disciplines

Click to filter author papers

Biophysics· 2 Cell Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Assay:fluorescence / live-cell microscopy· 1 Organism:human· 1 Assay:imaging· 1 Approach:microscopy & imaging analysis· 1

Frequent Co-Authors

A. Ciorita· 1 shared A. J. Garcia-Saez· 1 shared A. Jannasch· 1 shared A. Jenner· 1 shared A. Luchniak· 1 shared A. Scholz· 1 shared B. Macek· 1 shared C. Cavarischia-Rega· 1 shared

Activity by Year

2018-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperBiophysics

A. Ciorita

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Nanobodies as novel tools to monitor the mitochondrial fission factor Drp1

T. Froehlich, A. Jenner, C. Cavarischia-Rega, F. O. Fagbadebo, Y. Lurz, D. I. Frecot, P. D. Kaiser, S. Nueske, A. Scholz, E. Schaeffer, A. J. Garcia-Saez, B. Macek, U. Rothbauer

This study develops nanobodies to monitor Drp1, a mitochondrial fission factor, using proteomics, microscopy, and live-cell imaging techniques to study its dynamics in disease models.

bioRxiv · Dec 18, 2023 · PreprintCell Biology

Single depolymerizing and transport kinesins stabilize microtubule ends

A. Ciorita, M. Bugiel, S. Sudhakar, E. Schaeffer, A. Jannasch

The paper shows that single kinesin motors stabilize microtubule ends by reducing depolymerization rates, contrary to their collective depolymerizing activity.

bioRxiv · Oct 5, 2020Biophysics

Label-free high-speed wide-field imaging of single microtubules using interference reflection microscopy

M. Mahamdeh, S. Simmert, A. Luchniak, E. Schaeffer, J. Howard

This paper introduces interference reflection microscopy for high-speed, label-free imaging of single microtubules, showing it outperforms existing techniques in contrast and simplicity.

bioRxiv · Mar 6, 2018Biophysics