Bercier V - Search Results

1

FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis.

Kabashi E, Bercier V, Lissouba A, Liao M, Brustein E, Rouleau GA, Drapeau P. Kabashi E, et al. Among authors: bercier v. PLoS Genet. 2011 Aug;7(8):e1002214. doi: 10.1371/journal.pgen.1002214. Epub 2011 Aug 4. PLoS Genet. 2011. PMID: 21829392 Free PMC article.

2

WNK1/HSN2 mutation in human peripheral neuropathy deregulates KCC2 expression and posterior lateral line development in zebrafish (Danio rerio).

Bercier V, Brustein E, Liao M, Dion PA, Lafrenière RG, Rouleau GA, Drapeau P. Bercier V, et al. PLoS Genet. 2013;9(1):e1003124. doi: 10.1371/journal.pgen.1003124. Epub 2013 Jan 3. PLoS Genet. 2013. PMID: 23300475 Free PMC article.

3

Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo.

Kabashi E, Lin L, Tradewell ML, Dion PA, Bercier V, Bourgouin P, Rochefort D, Bel Hadj S, Durham HD, Vande Velde C, Rouleau GA, Drapeau P. Kabashi E, et al. Among authors: bercier v. Hum Mol Genet. 2010 Feb 15;19(4):671-83. doi: 10.1093/hmg/ddp534. Epub 2009 Dec 3. Hum Mol Genet. 2010. PMID: 19959528

4

Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis.

Kabashi E, El Oussini H, Bercier V, Gros-Louis F, Valdmanis PN, McDearmid J, Mejier IA, Dion PA, Dupre N, Hollinger D, Sinniger J, Dirrig-Grosch S, Camu W, Meininger V, Loeffler JP, René F, Drapeau P, Rouleau GA, Dupuis L. Kabashi E, et al. Among authors: bercier v. Hum Mol Genet. 2013 Jun 15;22(12):2350-60. doi: 10.1093/hmg/ddt080. Epub 2013 Feb 26. Hum Mol Genet. 2013. PMID: 23446633

5

Role and therapeutic potential of liquid-liquid phase separation in amyotrophic lateral sclerosis.

Pakravan D, Orlando G, Bercier V, Van Den Bosch L. Pakravan D, et al. Among authors: bercier v. J Mol Cell Biol. 2021 Apr 10;13(1):15-28. doi: 10.1093/jmcb/mjaa049. J Mol Cell Biol. 2021. PMID: 32976566 Free PMC article. Review.

6

Dynactin1 depletion leads to neuromuscular synapse instability and functional abnormalities.

Bercier V, Hubbard JM, Fidelin K, Duroure K, Auer TO, Revenu C, Wyart C, Del Bene F. Bercier V, et al. Mol Neurodegener. 2019 Jul 10;14(1):27. doi: 10.1186/s13024-019-0327-3. Mol Neurodegener. 2019. PMID: 31291987 Free PMC article.

7

Frontotemporal Lobar Degeneration Case with an N-Terminal TUBA4A Mutation Exhibits Reduced TUBA4A Levels in the Brain and TDP-43 Pathology.

Van Schoor E, Vandenbulcke M, Bercier V, Vandenberghe R, van der Zee J, Van Broeckhoven C, Otto M, Hanseeuw B, Van Damme P, Van Den Bosch L, Thal DR. Van Schoor E, et al. Among authors: bercier v. Biomolecules. 2022 Mar 12;12(3):440. doi: 10.3390/biom12030440. Biomolecules. 2022. PMID: 35327632 Free PMC article.

8

HNRNPK alleviates RNA toxicity by counteracting DNA damage in C9orf72 ALS.

Braems E, Bercier V, Van Schoor E, Heeren K, Beckers J, Fumagalli L, Dedeene L, Moisse M, Geudens I, Hersmus N, Mehta AR, Selvaraj BT, Chandran S, Ho R, Thal DR, Van Damme P, Swinnen B, Van Den Bosch L. Braems E, et al. Among authors: bercier v. Acta Neuropathol. 2022 Sep;144(3):465-488. doi: 10.1007/s00401-022-02471-y. Epub 2022 Jul 27. Acta Neuropathol. 2022. PMID: 35895140 Free PMC article.

9

Deletion of a kinesin I motor unmasks a mechanism of homeostatic branching control by neurotrophin-3.

Auer TO, Xiao T, Bercier V, Gebhardt C, Duroure K, Concordet JP, Wyart C, Suster M, Kawakami K, Wittbrodt J, Baier H, Del Bene F. Auer TO, et al. Among authors: bercier v. Elife. 2015 Jun 15;4:e05061. doi: 10.7554/eLife.05061. Elife. 2015. PMID: 26076409 Free PMC article.

10

FIGNL1 associates with KIF1Bβ and BICD1 to restrict dynein transport velocity during axon navigation.

Atkins M, Gasmi L, Bercier V, Revenu C, Del Bene F, Hazan J, Fassier C. Atkins M, et al. Among authors: bercier v. J Cell Biol. 2019 Oct 7;218(10):3290-3306. doi: 10.1083/jcb.201805128. Epub 2019 Sep 19. J Cell Biol. 2019. PMID: 31541015 Free PMC article.

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