Coulombe B, Cloutier P, Gauthier MS, How do our cells build their protein interactome? - Nature Communications 2018 Jul 27

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, Bi-allelic Mutations in EPRS, Encoding the Glutamyl-Prolyl-Aminoacyl-tRNA Synthetase, Cause a Hypomyelinating Leukodystrophy. - American Journal Of Human Genetics 2018 Apr 5

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, Posttranslational modification of proprotein convertase subtilisin/kexin type 9 is differentially regulated in response to distinct cardiometabolic treatments as revealed by targeted proteomics. - Journal Of Clinical Lipidology 2018 Jul - Aug

Houry WA, Bertrand E, Coulombe B, The PAQosome, an R2TP-Based Chaperone for Quaternary Structure Formation. - Trends In Biochemical Sciences 2018 Jan

Lavallée-Adam M, Cloutier P, Coulombe B, Blanchette M, Functional 5' UTR motif discovery with LESMoN: Local Enrichment of Sequence Motifs in biological Networks. - Nucleic Acids Research 2017 Oct 13

Cloutier P, Poitras C, Durand M, Hekmat O, Fiola-Masson É, Bouchard A, Faubert D, Chabot B, Coulombe B, R2TP/Prefoldin-like component RUVBL1/RUVBL2 directly interacts with ZNHIT2 to regulate assembly of U5 small nuclear ribonucleoprotein. - Nature Communications 2017 May 31

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, Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutation. - Molecular Brain 2017 Apr 13

Coulombe BJ, Games KE, Neil ER, Eberman LE, Core Stability Exercise Versus General Exercise for Chronic Low Back Pain. - Journal Of Athletic Training 2017 Jan

Guglielmi V, Marini M, Masson ÉF, Malatesta M, Forget D, Tomelleri G, Coulombe B, Vattemi G, Abnormal expression of RNA polymerase II-associated proteins in muscle of patients with myofibrillar myopathies. - Histopathology 2015 Dec

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, Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III. - Nature Communications 2015 Jul 7