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Carcinogenesis|January 5, 2002
Increased frequency of DNA deletions in pink-eyed unstable mice carrying a mutation in the Werner syndrome gene homologueMichel LebelAntioxidants & Redox Signaling|November 17, 2020
The Impact of Vitamin C on Different System Models of Werner SyndromeLucie Aumailley, Michel LebelPlos One|October 10, 2024
Sex and organ specific proteomic responses to vitamin C deficiency in the brain, heart, liver, and spleen of Gulo-/- miceLucie Aumailley, Michel LebelAgeing Research Reviews|November 18, 2017
Werner syndrome (WRN) gene variants and their association with altered function and age-associated diseasesMichel Lebel, Raymond J MonnatNucleic Acids Research|January 14, 2004
YB-1 promotes strand separation in vitro of duplex DNA containing either mispaired bases or cisplatin modifications, exhibits endonucleolytic activities and binds several DNA repair proteinsIsabelle Gaudreault, David Guay, Michel LebelAging|April 6, 2011
The Werner syndrome helicase protein is required for cell proliferation, immortalization, and tumorigenesis in Scaffold attachment factor B1 deficient miceSophie Lachapelle, Steffi Oesterreich, Michel LebelThe British Journal of Nutrition|July 14, 2026
Association of vitamin D Status with immune-associated serum protein pathways in overweight French-Canadian adults with hyperinsulinemia in the Quebec City metropolitan area, CanadaAtena Mahdavi, Michel Lebel, Iwona RudkowskaInternational Urogynecology Journal|December 17, 2009
Pudendal nerve neuromodulation with neurophysiology guidance: a potential treatment option for refractory chronic pelvi-perineal painMaude Carmel, Michel Lebel, Le Mai TuThe Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|March 12, 2011
Drugs, nutrients, and phytoactive principles improving the health span of rodent models of human age-related diseasesMichel Lebel, Frédéric Picard, Guylaine Ferland, et al.Cancer Genetics and Cytogenetics|January 12, 2005
Increased frequency of multiradial chromosome structures in mouse embryonic fibroblasts lacking functional Werner syndrome protein and poly(ADP-ribose) polymerase-1Josée Lavoie, Ronald Carter, Régen Drouin, et al.Pageof 6