Vincent Picher-Martel

发表

Whole-exome sequencing identifies homozygous mutation in TTI2 in a child with primary microcephaly: a case report

Y. Labrie, S. Rivest, B. Lāce, 2020, BMC Neurology.

Key role of UBQLN2 in pathogenesis of amyotrophic lateral sclerosis and frontotemporal dementia

J. Julien, P. Codron, L. Renaud, 2019, Acta Neuropathologica Communications.

From animal models to human disease: a genetic approach for personalized medicine in ALS

J. Julien, N. Dupré, P. Valdmanis, 2016, Acta neuropathologica communications.

Inhibition of NF-κB with an Analog of Withaferin-A Restores TDP-43 Homeostasis and Proteome Profiles in a Model of Sporadic ALS

D. Phaneuf, H. Boutej, Nicolas Dupré, 2024, Biomedicines.

CAPTURE ALS: the comprehensive analysis platform to understand, remedy and eliminate ALS

Alan C. Evans, Y. Iturria-Medina, E. Rogaeva, 2022, Amyotrophic lateral sclerosis & frontotemporal degeneration.

The Occurrence of FUS Mutations in Pediatric Amyotrophic Lateral Sclerosis: A Case Report and Review of the Literature

N. Dupré, F. Brunet, V. Picher-Martel, 2020, Journal of child neurology.

Distinct Plasma Immune Profile in ALS Implicates sTNFR-II in pAMPK/Leptin Homeostasis

J. Julien, N. Dupré, J. Kriz, 2023, International journal of molecular sciences.

Chronically activated microglia in ALS gradually lose their immune functions and develop unconventional proteome

Romina Barreto-Núñez, Louis-Charles Béland, H. Boutej, 2024, Glia.

Ubiquilin-2 drives NF-κB activity and cytosolic TDP-43 aggregation in neuronal cells

G. Sobue, J. Julien, D. Phaneuf, 2015, Molecular Brain.

Clinical Characteristics of Charcot-Marie-Tooth Disease Type 4J.

Brett A. McCray, Mary M Reilly, Vincent Picher-Martel, 2024, Neurology.

Neuronal Expression of UBQLN2P497H Exacerbates TDP-43 Pathology in TDP-43G348C Mice through Interaction with Ubiquitin

J. Julien, L. Renaud, V. Picher-Martel, 2018, Molecular Neurobiology.