Valérie Bercier
发表
E. Brustein,
G. Rouleau,
P. Drapeau,
2011,
PLoS genetics.
F. Del Bene,
T. Gacoin,
C. Langevin,
2022,
bioRxiv.
P. van Damme,
Matthieu Moisse,
S. Chandran,
2022,
Acta Neuropathologica.
V. Meininger,
G. Rouleau,
P. Drapeau,
2013,
Human molecular genetics.
F. Del Bene,
T. Gacoin,
F. Treussart,
2022,
bioRxiv.
Valérie Bercier,
2013,
Rare diseases.
L. Van Den Bosch,
G. Orlando,
Donya Pakravan,
2020,
Journal of molecular cell biology.
G. Rouleau,
P. Drapeau,
D. Rochefort,
2010,
Human molecular genetics.
F. Del Bene,
Marion Rosello,
Céline Revenu,
2019,
Front. Cell Dev. Biol..
F. Del Bene,
Claire Wyart,
Thomas O. Auer,
2019,
Molecular Neurodegeneration.
Massimo Pasqualetti,
Rajesh Khanna,
Raffaella Tonini,
2018,
Nature Methods.
Shankaracharya,
J. Landers,
B. Traynor,
2022,
Cell reports.
H. Baier,
K. Kawakami,
F. Del Bene,
2022
.
L. Van Den Bosch,
Valérie Bercier,
T. Vandoorne,
2019,
Genes.
FIGNL1 associates with KIF1Bβ and BICD1 to restrict dynein transport velocity during axon navigation
F. Del Bene,
L. Gasmi,
J. Hazan,
2019,
The Journal of cell biology.
E. Brustein,
G. Rouleau,
P. Drapeau,
2013,
PLoS genetics.
C. van Broeckhoven,
R. Vandenberghe,
P. van Damme,
2022,
Biomolecules.
F. Del Bene,
Claire Wyart,
Thomas O. Auer,
2019,
Molecular Neurodegeneration.