Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Mathieu Larivière"'
Autor:
Jean-Charles Hogue, Benoît Lamarche, Daniel Gaudet, Mathieu Larivière, André J. Tremblay, Jean Bergeron, Isabelle Lemieux, Jean-Pierre Després, Claude Gagné, Patrick Couture
Publikováno v:
Journal of Lipid Research, Vol 45, Iss 6, Pp 1077-1083 (2004)
Small, dense LDL particles have been associated with an increased risk of coronary artery disease, and cholesteryl ester transfer protein (CETP) has been suggested to play a role in LDL particle remodeling. We examined the relationship between LDL he
Externí odkaz:
https://doaj.org/article/a58a572867f24bbfabf2d2386126dfd9
Autor:
Ferran Casals, Alan Hodgkinson, Julie Hussin, Youssef Idaghdour, Vanessa Bruat, Thibault de Maillard, Jean-Christophe Grenier, Elias Gbeha, Fadi F Hamdan, Simon Girard, Jean-François Spinella, Mathieu Larivière, Virginie Saillour, Jasmine Healy, Isabel Fernández, Daniel Sinnett, Jacques L Michaud, Guy A Rouleau, Elie Haddad, Françoise Le Deist, Philip Awadalla
Publikováno v:
PLoS Genetics, Vol 9, Iss 9, p e1003815 (2013)
Whole-exome or gene targeted resequencing in hundreds to thousands of individuals has shown that the majority of genetic variants are at low frequency in human populations. Rare variants are enriched for functional mutations and are expected to expla
Externí odkaz:
https://doaj.org/article/9cc47deb1ace4078a7e93a220fcc9d66
Autor:
Jing Ma, Julie Hussin, Linda Holmfeldt, Lei Wei, Philip Awadalla, Greg Gibson, Jean-Christophe Grenier, Daniel Sinnett, Virginie Saillour, Jasmine Healy, Gregor Andelfinger, Jean-François Spinella, James R. Downing, Charles G. Mullighan, Thibault De Malliard, Ferran Casals, Vanessa Bruat, Jinghui Zhang, Youssef Idaghdour, Stephan Busche, Anna Andersson, Mathieu Larivière
Publikováno v:
Genome Research. 23:419-430
One of the most rapidly evolving genes in humans, PRDM9, is a key determinant of the distribution of meiotic recombination events. Mutations in this meiotic-specific gene have previously been associated with male infertility in humans and recent stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a028119f6baee05b7a620f94a62b69f0
https://doi.org/10.1101/gr.144188.112
https://doi.org/10.1101/gr.144188.112
Autor:
Mathieu Larivière, Anna K. Naumova, Tony Kwan, Gary M. Hunninghake, Kevin C. L. Lam, Daniel Sinnett, Joana Dias, Manon Ouimet, Sanny Moussette, Anne-Marie Madore, Eef Harmsen, Manuel E. Soto-Quiros, Scott T. Weiss, Ken Dewar, Juan C. Celedón, Vonda Koka, Bing Ge, Tomi Pastinen, Soizik Berlivet, Elin Grundberg, Marcin Swiatek, Lydiana Avila, Dominique J. Verlaan, Rose Hoberman, Benjamin A. Raby, Catherine Laprise
Publikováno v:
The American Journal of Human Genetics. 85(3):377-393
Common SNPs in the chromosome 17q12-q21 region alter the risk for asthma, type 1 diabetes, primary biliary cirrhosis, and Crohn disease. Previous reports by us and others have linked the disease-associated genetic variants with changes in expression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7d2452415bb29562dc20ae2c3b454c1
Autor:
Daniel Sinnett, Régen Drouin, Mathieu Larivière, Stéphane Ouellet, Gino Boily, Sylvie Langlois
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1769:182-193
Glypican 3 (GPC3) is an X-linked gene that has its peak expression during development and is down-regulated in all studied tissues after birth. We have shown that GPC3 was expressed in neuroblastoma and Wilms' tumor. To understand the mechanisms regu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b25d279281b6a3966456979e2fc3efb
https://doi.org/10.1016/j.bbaexp.2007.01.014
https://doi.org/10.1016/j.bbaexp.2007.01.014
Autor:
Benoît Lamarche, Mathieu Larivière, Claude Gagné, Jean Bergeron, Jean-Charles Hogue, Patrick Couture, Matteo Pirro
Publikováno v:
Atherosclerosis. 167:97-104
The effects of the HMG CoA reductase inhibitor atorvastatin on electrophoretic characteristics of LDL particles were evaluated in 46 patients (28 males and 18 females) with heterozygous familial hypercholesterolemia (FH) aged 20-61 carrying either a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::181bf499cebd4a28e37d11c8692e8cbf
https://doi.org/10.1016/s0021-9150(02)00385-4
https://doi.org/10.1016/s0021-9150(02)00385-4
Autor:
Thibault de Maillard, Virginie Saillour, Guy A. Rouleau, Jacques L. Michaud, Alan Hodgkinson, Simon Girard, Jean Cristophe Grenier, Philip Awadalla, Mathieu Larivière, Fadi F. Hamdan, Julie Hussin, Daniel Sinnett, Jean-François Spinella, Vanessa Bruat, Ferran Casals, Elias Gbeha, Youssef Idaghdour, Elie Haddad, Françoise Le Deist, Jasmine Healy, Isabel Fernandez
Publikováno v:
PLoS Genetics, Vol 9, Iss 9, p e1003815 (2013)
PLoS Genetics
PLoS Genetics
Whole-exome or gene targeted resequencing in hundreds to thousands of individuals has shown that the majority of genetic variants are at low frequency in human populations. Rare variants are enriched for functional mutations and are expected to expla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0aab4aa798f808ed7e4ab0aaeb833a51
http://europepmc.org/articles/PMC3784517?pdf=render
http://europepmc.org/articles/PMC3784517?pdf=render
Autor:
Jacques Simard, Pauline Cassart, Ekaterini A. Kritikou, Daniel Sinnett, Mathieu Larivière, Manon Ouimet
Publikováno v:
Genes, chromosomescancer. 51(11)
KU70 is involved in the DNA double-strand break repair pathway, which plays a critical role in maintaining genomic stability and preventing cancer. Genetic variation within the KU70 gene has been shown to be associated with increased risk of several
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::935412bffe8c3f8684f0e522e9906be5
https://pubmed.ncbi.nlm.nih.gov/22833453
https://pubmed.ncbi.nlm.nih.gov/22833453
Autor:
Tomi Pastinen, Joana Dias, Dave Sirois-Gagnon, Daniel Sinnett, Kevin C. L. Lam, Véronique Adoue, Patrick Beaulieu, Dominique J. Verlaan, Manon Ouimet, Catherine Laprise, Bing Ge, Mathieu Larivière, Vonda Koka
Publikováno v:
The Journal of allergy and clinical immunology. 130(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17c5dbba8fcceef531a3361a67ae9686
https://pubmed.ncbi.nlm.nih.gov/22534532
https://pubmed.ncbi.nlm.nih.gov/22534532
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e19368 (2011)
PLoS ONE
PLoS ONE
Single nucleotide polymorphisms (SNPs) are the most commonly used polymorphic markers in genetics studies. Among the different platforms for SNP genotyping, Luminex is one of the less exploited mainly due to the lack of a robust (semi-automated and r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e8f10841dfd72f7b5fa6999ea4326aa
http://europepmc.org/articles/PMC3089621?pdf=render
http://europepmc.org/articles/PMC3089621?pdf=render