Vincent Raymond
- Formation
- à venir
Aucune offre active
Autres opportunités de carrière
- Axe principal
- Endocrinologie et génomique
- Adresse
- 2705, boulevard Laurier, T-3-67
Québec (Québec)
CANADA G1V 4G2 - Téléphone
- +1 418-525-4444, poste 42296
- Télécopieur
- +1 418-654-2298
- Courriel
- Vincent.Raymond@crchul.ulaval.ca
Projet(s) de recherche reconnu(s) par l'Université Laval
Autre(s) projet(s) de recherche actif(s)
Aucun projet de recherche à afficher
Publications récentes (voir toutes les publications de ce chercheur)
Footz T, Dubois S, Sarfarazi M, Raymond V, Walter MA. Co-variation of STI1 and WDR36/UTP21 alters cell proliferation in a glaucoma model. Molecular vision,
2011. 17: 1957-69
Strungaru MH, Footz T, Liu Y, Berry FB, Belleau P, Semina EV, Raymond V, Walter MA. PITX2 is involved in stress response in cultured human trabecular meshwork cells through regulation of SLC13A3. Investigative ophthalmology & visual science,
2011. 52: 7625-33
Footz TK, Johnson JL, Dubois S, Boivin N, Raymond V, Walter MA. Glaucoma-associated WDR36 variants encode functional defects in a yeast model system. Human molecular genetics,
2009. 18: 1276-87
Avisar I, Lusky M, Robinson A, Shohat M, Dubois S, Raymond V, Gaton DD. The novel Y371D myocilin mutation causes an aggressive form of juvenile open-angle glaucoma in a Caucasian family from the Middle-East. Molecular vision,
2009. 15: 1945-50
Berry FB, Skarie JM, Mirzayans F, Fortin Y, Hudson TJ, Raymond V, Link BA, Walter MA. FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A. Human molecular genetics,
2008. 17: 490-505
Yoshioka M, Bolduc C, Raymond V, St-Amand J. High-fat meal-induced changes in the duodenum mucosa transcriptome. Obesity (Silver Spring, Md.),
2008. 16: 2302-7
Fan BJ, Leung DY, Wang DY, Gobeil S, Raymond V, Tam PO, Lam DS, Pang CP. Novel myocilin mutation in a Chinese family with juvenile-onset open-angle glaucoma.
Archives of ophthalmology,
2006. 124: 102-6
Pang CP, Fan BJ, Canlas O, Wang DY, Dubois S, Tam PO, Lam DS, Raymond V, Ritch R. A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5q.
Molecular vision,
2006. 12: 85-92
Gobeil S, Letartre L, Raymond V. Functional analysis of the glaucoma-causing TIGR/myocilin protein: integrity of amino-terminal coiled-coil regions and olfactomedin homology domain is essential for extracellular adhesion and secretion.
Experimental eye research,
2006. 82: 1017-29
Baird PN, Richardson AJ, Mackey DA, Craig JE, Faucher M, Raymond V. A common disease haplotype for the Q368STOP mutation of the myocilin gene in Australian and Canadian glaucoma families.
American journal of ophthalmology,
2005. 140: 760-2
