Bercier V - Search Results

1

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.

2

Existing and Emerging Metabolomic Tools for ALS Research.

Germeys C, Vandoorne T, Bercier V, Van Den Bosch L. Germeys C, et al. Among authors: bercier v. Genes (Basel). 2019 Dec 5;10(12):1011. doi: 10.3390/genes10121011. Genes (Basel). 2019. PMID: 31817338 Free PMC article. Review.

3

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.

4

ALS-associated KIF5A mutations abolish autoinhibition resulting in a toxic gain of function.

Baron DM, Fenton AR, Saez-Atienzar S, Giampetruzzi A, Sreeram A, Shankaracharya, Keagle PJ, Doocy VR, Smith NJ, Danielson EW, Andresano M, McCormack MC, Garcia J, Bercier V, Van Den Bosch L, Brent JR, Fallini C, Traynor BJ, Holzbaur ELF, Landers JE. Baron DM, et al. Among authors: bercier v. Cell Rep. 2022 Apr 5;39(1):110598. doi: 10.1016/j.celrep.2022.110598. Cell Rep. 2022. PMID: 35385738 Free PMC article.

5

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.

6

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.

7

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

8

Zebrafish as a Model for the Study of Live in vivo Processive Transport in Neurons.

Bercier V, Rosello M, Del Bene F, Revenu C. Bercier V, et al. Front Cell Dev Biol. 2019 Feb 19;7:17. doi: 10.3389/fcell.2019.00017. eCollection 2019. Front Cell Dev Biol. 2019. PMID: 30838208 Free PMC article.

9

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.

10

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

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