Mirzayans F - Search Results

1

Genomic mismatch scanning for the mapping of genetic traits.

Mirzayans F, Walter MA. Mirzayans F, et al. Methods Mol Biol. 2001;175:37-46. doi: 10.1385/1-59259-235-X:037. Methods Mol Biol. 2001. PMID: 11462847 Review. No abstract available.

2

Identification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanning.

Mirzayans F, Mears AJ, Guo SW, Pearce WG, Walter MA. Mirzayans F, et al. Am J Hum Genet. 1997 Jul;61(1):111-9. doi: 10.1086/513894. Am J Hum Genet. 1997. PMID: 9245991 Free PMC article.

3

Yeast two-hybrid analysis of a human trabecular meshwork cDNA library identified EFEMP2 as a novel PITX2 interacting protein.

Acharya M, Sharp MW, Mirzayans F, Footz T, Huang L, Birdi C, Walter MA. Acharya M, et al. Among authors: mirzayans f. Mol Vis. 2012;18:2182-9. Epub 2012 Aug 7. Mol Vis. 2012. PMID: 22919265 Free PMC article.

4

Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25.

Mears AJ, Mirzayans F, Gould DB, Pearce WG, Walter MA. Mears AJ, et al. Among authors: mirzayans f. Am J Hum Genet. 1996 Dec;59(6):1321-7. Am J Hum Genet. 1996. PMID: 8940278 Free PMC article.

5

Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct.

Walter MA, Mirzayans F, Mears AJ, Hickey K, Pearce WG. Walter MA, et al. Among authors: mirzayans f. Ophthalmology. 1996 Nov;103(11):1907-15. doi: 10.1016/s0161-6420(96)30408-9. Ophthalmology. 1996. PMID: 8942889

6

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: mirzayans f. Am J Hum Genet. 1998 Nov;63(5):1316-28. doi: 10.1086/302109. Am J Hum Genet. 1998. PMID: 9792859 Free PMC article.

7

Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25.

Mirzayans F, Gould DB, Héon E, Billingsley GD, Cheung JC, Mears AJ, Walter MA. Mirzayans F, et al. Eur J Hum Genet. 2000 Jan;8(1):71-4. doi: 10.1038/sj.ejhg.5200354. Eur J Hum Genet. 2000. PMID: 10713890

8

Mutation of the PAX6 gene in patients with autosomal dominant keratitis.

Mirzayans F, Pearce WG, MacDonald IM, Walter MA. Mirzayans F, et al. Am J Hum Genet. 1995 Sep;57(3):539-48. Am J Hum Genet. 1995. PMID: 7668281 Free PMC article.

9

Regulation of FOXC1 stability and transcriptional activity by an epidermal growth factor-activated mitogen-activated protein kinase signaling cascade.

Berry FB, Mirzayans F, Walter MA. Berry FB, et al. Among authors: mirzayans f. J Biol Chem. 2006 Apr 14;281(15):10098-104. doi: 10.1074/jbc.M513629200. Epub 2006 Feb 21. J Biol Chem. 2006. PMID: 16492674 Free article.

10

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: mirzayans f. 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

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