Raymond V - Search Results

1

Co-variation of STI1 and WDR36/UTP21 alters cell proliferation in a glaucoma model.

Footz T, Dubois S, Sarfarazi M, Raymond V, Walter MA. Footz T, et al. Among authors: raymond v. Mol Vis. 2011;17:1957-69. Epub 2011 Jul 19. Mol Vis. 2011. PMID: 21850170 Free PMC article.

2

Glaucoma-associated WDR36 variants encode functional defects in a yeast model system.

Footz TK, Johnson JL, Dubois S, Boivin N, Raymond V, Walter MA. Footz TK, et al. Among authors: raymond v. Hum Mol Genet. 2009 Apr 1;18(7):1276-87. doi: 10.1093/hmg/ddp027. Epub 2009 Jan 15. Hum Mol Genet. 2009. PMID: 19150991

3

A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5q.

Pang CP, Fan BJ, Canlas O, Wang DY, Dubois S, Tam PO, Lam DS, Raymond V, Ritch R. Pang CP, et al. Among authors: raymond v. Mol Vis. 2006 Feb 14;12:85-92. Mol Vis. 2006. PMID: 16518310 Free article.

4

PITX2 is involved in stress response in cultured human trabecular meshwork cells through regulation of SLC13A3.

Strungaru MH, Footz T, Liu Y, Berry FB, Belleau P, Semina EV, Raymond V, Walter MA. Strungaru MH, et al. Among authors: raymond v. Invest Ophthalmol Vis Sci. 2011 Sep 29;52(10):7625-33. doi: 10.1167/iovs.10-6967. Invest Ophthalmol Vis Sci. 2011. PMID: 21873665 Free PMC article.

5

Protein localization in the human eye and genetic screen of opticin.

Friedman JS, Faucher M, Hiscott P, Biron VL, Malenfant M, Turcotte P, Raymond V, Walter MA. Friedman JS, et al. Among authors: raymond v. Hum Mol Genet. 2002 May 15;11(11):1333-42. doi: 10.1093/hmg/11.11.1333. Hum Mol Genet. 2002. PMID: 12019215

6

The novel Y371D myocilin mutation causes an aggressive form of juvenile open-angle glaucoma in a Caucasian family from the Middle-East.

Avisar I, Lusky M, Robinson A, Shohat M, Dubois S, Raymond V, Gaton DD. Avisar I, et al. Among authors: raymond v. Mol Vis. 2009 Sep 24;15:1945-50. Mol Vis. 2009. PMID: 19784393 Free PMC article.

7

FOXC1 modulates MYOC secretion through regulation of the exocytic proteins RAB3GAP1, RAB3GAP2 and SNAP25.

Rasnitsyn A, Doucette L, Seifi M, Footz T, Raymond V, Walter MA. Rasnitsyn A, et al. Among authors: raymond v. PLoS One. 2017 Jun 2;12(6):e0178518. doi: 10.1371/journal.pone.0178518. eCollection 2017. PLoS One. 2017. PMID: 28575017 Free PMC article.

8

FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A.

Berry FB, Skarie JM, Mirzayans F, Fortin Y, Hudson TJ, Raymond V, Link BA, Walter MA. Berry FB, et al. Among authors: raymond v. Hum Mol Genet. 2008 Feb 15;17(4):490-505. doi: 10.1093/hmg/ddm326. Epub 2007 Nov 9. Hum Mol Genet. 2008. PMID: 17993506

9

Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.

Mears AJ, Jordan T, Mirzayans F, Dubois S, Kume T, Parlee M, Ritch R, Koop B, Kuo WL, Collins C, Marshall J, Gould DB, Pearce W, Carlsson P, Enerbäck S, Morissette J, Bhattacharya S, Hogan B, Raymond V, Walter MA. Mears AJ, et al. Among authors: raymond v. Am J Hum Genet. 1998 Nov;63(5):1316-28. doi: 10.1086/302109. Am J Hum Genet. 1998. PMID: 9792859 Free PMC article.

10

Founder TIGR/myocilin mutations for glaucoma in the Québec population.

Faucher M, Anctil JL, Rodrigue MA, Duchesne A, Bergeron D, Blondeau P, Côté G, Dubois S, Bergeron J, Arseneault R, Morissette J, Raymond V; Québec Glaucoma Network. Faucher M, et al. Among authors: raymond v. Hum Mol Genet. 2002 Sep 1;11(18):2077-90. doi: 10.1093/hmg/11.18.2077. Hum Mol Genet. 2002. PMID: 12189160

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