
Open for Rare
PUBLICATIONS
De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathy.
Djurdja Djordjevic, Maxime Pinard, Marie-Soleil Gauthier, Constance Smith-Hicks, Trevor L. Hoffman, Nicole I. Wolf, Renske Oegema, Ellen van Binsbergen, Berivan Baskin, Geneviève Bernard, Sébastien Fribourg, Benoit Coulombe, Grace Yoon.
The American Journal of Human Genetics. 2021.
Upstream ORF-encoded ASDURF is a novel prefoldin-like subunit of the PAQosome.
Philippe Cloutier, Christian Poitras, Denis Faubert, Annie Bouchard, Mathieu Blanchette, Marie-Soleil Gauthier, Benoit Coulombe.
J. Proteome Res. 2019.
Ben Djoudi Ouadda A, Gauthier MS, Susan-Resiga D, Girard E, Essalmani R, Black M, Marcinkiewicz J, Forget D, Hamelin J, Evagelidis A, Ly K, Day R, Galarneau L, Corbin F, Coulombe B, Çaku A, Tagliabracci VS, Seidah NG.
Arterioscler Thromb Vasc Biol. 2019 Oct;39(10):1996-2013.
Choquet K, Pinard M, Yang S, Moir RD, Poitras C, Dicaire MJ, Sgarioto N, Larivière R, Kleinman C, Willis IM, Gauthier MS, Coulombe B, Brais B.
Mol Brain. 2019 Jun 20;12(1):59.
Choquet K, Forget D, Meloche E, Dicaire MJ, Bernard G, Vanderver A, Schiffmann R, Fabian MR, Teichmann M, Coulombe B, Brais B, Kleinman CL.
J Biol Chem. 2019 Mar 21. pii: jbc.RA118.006271.
Gauthier MS, Cloutier P, Coulombe B.
Adv Exp Med Biol. 2018;1106:25-36.
How do our cells build their protein interactome?
Coulombe B, Cloutier P, Gauthier MS.
Nat Commun. 2018 Jul 27;9(1):2955.
Posttranslational modification of proprotein convertase subtilisin/kexin type 9 is differentially regulated in response to distinct cardiometabolic treatments as revealed by targeted proteomics.
Gauthier MS, Awan Z, Bouchard A, Champagne J, Tessier S, Faubert D, Chabot K, Garneau PY, Rabasa-Lhoret R, Seidah NG, Ridker PM, Genest J, Coulombe B.
J Clin Lipidol. 2018 Jul - Aug;12(4):1027-1038.
Mendes MI, Gutierrez Salazar M, Guerrero K, Thiffault I, Salomons GS, Gauquelin L, Tran LT, Forget D, Gauthier MS, Waisfisz Q, Smith DEC, Simons C, van der Knaap MS, Marquardt I, Lemes A, Mierzewska H, Weschke B, Koehler W, Coulombe B, Wolf NI, Bernard G.
Am J Hum Genet. 2018 Apr 5;102(4):676-684.
The PAQosome, an R2TP-Based Chaperone for Quaternary Structure Formation.
Houry WA, Bertrand E, Coulombe B.
Trends Biochem Sci. 2018 Jan;43(1):4-9.
Lavallée-Adam M, Cloutier P, Coulombe B, Blanchette M.Nucleic Acids Res. 2017 Oct 13;45(18):10415-10427.
Cloutier P, Poitras C, Durand M, Hekmat O, Fiola-Masson É, Bouchard A, Faubert D, Chabot B, Coulombe B.
Nat Commun. 2017 May 31;8:15615.
Choquet K, Yang S, Moir RD, Forget D, Larivière R, Bouchard A, Poitras C, Sgarioto N, Dicaire MJ, Noohi F, Kennedy TE, Rochford J, Bernard G, Teichmann M, Coulombe B, Willis IM, Kleinman CL, Brais B.
Mol Brain. 2017 Apr 13;10(1):13.
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III.
Thiffault I, Wolf NI, Forget D, Guerrero K, Tran LT, Choquet K, Lavallée-Adam M, Poitras C, Brais B, Yoon G, Sztriha L, Webster RI, Timmann D, van de Warrenburg BP, Seeger J, Zimmermann A, Máté A, Goizet C, Fung E, van der Knaap MS, Fribourg S, Vanderver A, Simons C, Taft RJ, Yates JR 3rd, Coulombe B, Bernard G.
Nat Commun. 2015 Jul 7;6:7623.
Coulombe B, Gauthier MS.
Methods. 2015 Jun 15;81:1-2.
Guglielmi V, Marini M, Masson ÉF, Malatesta M, Forget D, Tomelleri G, Coulombe B, Vattemi G.
Histopathology. 2015 Dec;67(6):859-65.
Gauthier MS, Pérusse JR, Awan Z, Bouchard A, Tessier S, Champagne J, Krastins B, Byram G, Chabot K, Garneau P, Rabasa-Lhoret R, Faubert D, Lopez MF, Seidah NG, Coulombe B.
Methods. 2015 Jun 15;81:66-73.