Marie-Soleil Gauthier
Overview
Explore the profile of Marie-Soleil Gauthier including associated specialties, affiliations and a list of published articles.
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Articles
41
Citations
969
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Recent Articles
1.
Hashimoto-Roth E, Forget D, Gaspar V, Gaspar V, Bennett S, Gauthier M, et al.
J Proteome Res
. 2025 Jan;
24(2):383-396.
PMID: 39772751
Immunoprecipitation coupled to tandem mass spectrometry (IP-MS/MS) methods are often used to identify protein-protein interactions (PPIs). While these approaches are prone to false positive identifications through contamination and antibody nonspecific...
2.
Luo H, Lao L, Au K, Northrup H, He X, Forget D, et al.
Genome Biol
. 2024 Jan;
25(1):19.
PMID: 38225631
Background: Neural tube defects (NTDs) are caused by genetic and environmental factors. ARMC5 is part of a novel ubiquitin ligase specific for POLR2A, the largest subunit of RNA polymerase II...
3.
Pinard M, Dastpeyman S, Poitras C, Bernard G, Gauthier M, Coulombe B
Mol Brain
. 2022 Nov;
15(1):98.
PMID: 36451185
The mechanism of assembly of RNA polymerase III (Pol III), the 17-subunit enzyme that synthesizes tRNAs, 5 S rRNA, and other small-nuclear (sn) RNAs in eukaryotes, is not clearly understood....
4.
Djordjevic D, Pinard M, Gauthier M, Smith-Hicks C, Hoffman T, Wolf N, et al.
Am J Hum Genet
. 2022 Apr;
109(4):759-763.
PMID: 35395209
No abstract available.
5.
Ghaleb Y, Elbitar S, Philippi A, Khoury P, Azar Y, Andrianirina M, et al.
Metabolites
. 2022 Mar;
12(3).
PMID: 35323704
Autosomal Dominant Hypercholesterolemia (ADH) is a genetic disorder caused by pathogenic variants in , , and genes. We sought to identify new candidate genes responsible for the ADH phenotype in...
6.
Pinard M, Cloutier P, Poitras C, Gauthier M, Coulombe B
J Proteome Res
. 2022 Feb;
21(4):1073-1082.
PMID: 35129352
The PAQosome (particle for arrangement of quaternary structure) is a 12-subunit HSP90 co-chaperone involved in the biogenesis of several human protein complexes. Two mechanisms of client selection have previously been...
7.
Derksen A, Shih H, Forget D, Darbelli L, Tran L, Poitras C, et al.
HGG Adv
. 2022 Jan;
2(3):100034.
PMID: 35047835
Leukodystrophies, genetic neurodevelopmental and/or neurodegenerative disorders of cerebral white matter, result from impaired myelin homeostasis and metabolism. Numerous genes have been implicated in these heterogeneous disorders; however, many individuals remain...
8.
Sokullu E, Gauthier M, Coulombe B
Viruses
. 2021 Jul;
13(6).
PMID: 34200959
The latest coronavirus disease outbreak, COVID-19, has brought attention to viral infections which have posed serious health threats to humankind throughout history. The rapid global spread of COVID-19 is attributed...
9.
Sokullu E, Pinard M, Gauthier M, Coulombe B
Expert Opin Drug Discov
. 2021 Mar;
16(8):881-895.
PMID: 33769912
: The COVID-19 pandemic originated from the emergence of anovel coronavirus, SARS-CoV-2, which has been intensively studied since its discovery in order to generate the knowledge necessary to accelerate the...
10.
Coulombe B, Derksen A, La Piana R, Brais B, Gauthier M, Bernard G
Fac Rev
. 2021 Mar;
10:12.
PMID: 33659930
Hypomyelinating leukodystrophies are a group of genetic disorders characterized by insufficient myelin deposition during development. A subset of hypomyelinating leukodystrophies, named RNA polymerase III (Pol III or POLR3)-related leukodystrophy or...