Author

R. Giet

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

Cell Biology· 5

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cell signaling & trafficking· 5 Approach:experimental assay· 5 Organism:Drosophila· 4 Research Focus:development & morphogenesis· 2 Approach:biophysical modeling· 1 Research Focus:cancer & tumor microenvironment· 1 Assay:proteomics· 1

Frequent Co-Authors

E. Gallaud· 5 shared A. Pascal· 4 shared L. Richard-Parpaillon· 4 shared M. Metivier· 3 shared A. Guichet· 1 shared A. Hensley· 1 shared A. P. Carter· 1 shared A. Thomas· 1 shared

Activity by Year

2018-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 23 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

5 shared papersCell Biology

E. Gallaud

Mutual co-authors in cluster

Author profile →

5 papers

Recent·Most cited

A force-sensitive mutation reveals a spindle assembly checkpoint-independent role for dynein in anaphase progression

D. Salvador-Garcia, L. Jin, A. Hensley, M. Golcuk, E. Gallaud, S. Chaaban, F. Port, A. Vagnoni, V. J. Planelles-Herrero, M. A. McClintock, E. Derivery, A. P. Carter, R. Giet, M. Gur, A. Yildiz, S. L. Bullock

This study identifies a mutation in dynein that causes mitotic spindle arrest independent of the spindle assembly checkpoint, revealing a load-dependent role in anaphase progression.

bioRxiv · Aug 3, 2023 · PreprintCell Biology

The spindle assembly checkpoint and the spatial activation of Polo kinase determine the duration of cell division and prevent neural stem cells tumor formation

E. Gallaud, L. Richard-Parpaillon, A. Pascal, M. Metivier, V. Archambault, R. Giet

This study shows that Polo kinase activity, regulated by Aurora A and B, controls cell division duration and prevents tumor formation in Drosophila neural stem cells by coupling mitotic progression with polarization.

bioRxiv · Jan 4, 2021 · PreprintCell Biology

Peripheral microtubules ensure asymmetric furrow positioning in neural stem cells

A. Thomas, E. Gallaud, A. Pascal, L. Serre, I. Arnal, L. Richard-Parpaillon, M. S. Savoian, R. GIET

The paper shows that peripheral microtubules and the Chromosome Passenger Complex are required for cortical centralspindlin recruitment, which ensures asymmetric furrow positioning in neural stem cells.

bioRxiv · Sep 10, 2020 · PreprintCell Biology

Drosophila dTBCE recruits tubulin around chromatin to promote mitotic spindle assembly

M. Metivier, E. Gallaud, A. Pascal, J.-P. Gagne, G. Poirier, D. Chretien, R. Gibeaux, L. Richard-Parpaillon, C. Benaud, R. Giet

The paper identifies dTBCE's role in promoting mitotic spindle assembly by recruiting tubulin around chromatin in Drosophila.

bioRxiv · Jan 21, 2020Cell Biology

Mechanisms of Kinesin-1 activation by Ensconsin/MAP7 in vivo

M. Metivier, B. Monroy, E. Gallaud, R. Caous, A. Pascal, L. Richard-Parpaillon, A. Guichet, K. Ori-McKenney, R. Giet

This study identifies the Kinesin-1 activation mechanism by Ensconsin/MAP7, showing that the KBD domain binds and stimulates Kinesin-1 binding to Mts, with full-length Ensconsin enabling direct activation on microtubules.

bioRxiv · Jul 27, 2018Cell Biology