Valerie Bercier
Affiliations: | Institut Curie, Bures-sur-Yvette, Île-de-France, France |
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| Grimaud B, Frétaud M, Terras F, et al. (2022) Fast Nonlinear Microscopy Reveals Impairment of Fast Axonal Transport Induced by Molecular Motor Imbalances in the Brain of Zebrafish Larvae. Acs Nano |
| Baron DM, Fenton AR, Saez-Atienzar S, et al. (2022) ALS-associated KIF5A mutations abolish autoinhibition resulting in a toxic gain of function. Cell Reports. 39: 110598 |
| Atkins M, Gasmi L, Bercier V, et al. (2019) FIGNL1 associates with KIF1Bβ and BICD1 to restrict dynein transport velocity during axon navigation. The Journal of Cell Biology. 218: 3290-3306 |
| Bercier V, Hubbard JM, Fidelin K, et al. (2019) Dynactin1 depletion leads to neuromuscular synapse instability and functional abnormalities. Molecular Neurodegeneration. 14: 27 |
| Bercier V, Rosello M, Del Bene F, et al. (2019) Zebrafish as a Model for the Study of Live Processive Transport in Neurons. Frontiers in Cell and Developmental Biology. 7: 17 |
| Alberio L, Locarno A, Saponaro A, et al. (2018) A light-gated potassium channel for sustained neuronal inhibition. Nature Methods |
| Auer TO, Xiao T, Bercier V, et al. (2015) Deletion of a kinesin I motor unmasks a mechanism of homeostatic branching control by neurotrophin-3. Elife. 4 |
| Auer TO, Xiao T, Bercier V, et al. (2015) Author response: Deletion of a kinesin I motor unmasks a mechanism of homeostatic branching control by neurotrophin-3 Elife |
| Kabashi E, El Oussini H, Bercier V, et al. (2013) Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis. Human Molecular Genetics. 22: 2350-60 |
| Kabashi E, Lin L, Tradewell ML, et al. (2010) Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo. Human Molecular Genetics. 19: 671-83 |