Ayyagari R - Search Results

1

Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment gene.

Ayyagari R, Kakuk LE, Coats CL, Bingham EL, Toda Y, Felius J, Sieving PA. Ayyagari R, et al. Mol Vis. 1999 Jul 28;5:13. Mol Vis. 1999. PMID: 10427103 Free article.

2

Autosomal dominant macular atrophy at 6q14 excludes CORD7 and MCDR1/PBCRA loci.

Griesinger IB, Sieving PA, Ayyagari R. Griesinger IB, et al. Among authors: ayyagari r. Invest Ophthalmol Vis Sci. 2000 Jan;41(1):248-55. Invest Ophthalmol Vis Sci. 2000. PMID: 10634627

3

Autosomal dominant hemorrhagic macular dystrophy not associated with the TIMP3 gene.

Ayyagari R, Griesinger IB, Bingham E, Lark KK, Moroi SE, Sieving PA. Ayyagari R, et al. Arch Ophthalmol. 2000 Jan;118(1):85-92. doi: 10.1001/archopht.118.1.85. Arch Ophthalmol. 2000. PMID: 10636420

4

Spectrum of color gene deletions and phenotype in patients with blue cone monochromacy.

Ayyagari R, Kakuk LE, Bingham EL, Szczesny JJ, Kemp J, Toda Y, Felius J, Sieving PA. Ayyagari R, et al. Hum Genet. 2000 Jul;107(1):75-82. doi: 10.1007/s004390000338. Hum Genet. 2000. PMID: 10982039 Free article.

5

X-linked recessive atrophic macular degeneration from RPGR mutation.

Ayyagari R, Demirci FY, Liu J, Bingham EL, Stringham H, Kakuk LE, Boehnke M, Gorin MB, Richards JE, Sieving PA. Ayyagari R, et al. Genomics. 2002 Aug;80(2):166-71. doi: 10.1006/geno.2002.6815. Genomics. 2002. PMID: 12160730

6

Stargardt-like macular dystrophy protein ELOVL4 exerts a dominant negative effect by recruiting wild-type protein into aggresomes.

Vasireddy V, Vijayasarathy C, Huang J, Wang XF, Jablonski MM, Petty HR, Sieving PA, Ayyagari R. Vasireddy V, et al. Among authors: ayyagari r. Mol Vis. 2005 Aug 30;11:665-76. Mol Vis. 2005. PMID: 16163264 Free article.

7

Evaluation of the ELOVL4 gene in patients with age-related macular degeneration.

Ayyagari R, Zhang K, Hutchinson A, Yu Z, Swaroop A, Kakuk LE, Seddon JM, Bernstein PS, Lewis RA, Tammur J, Yang Z, Li Y, Zhang H, Yashar BM, Liu J, Petrukhin K, Sieving PA, Allikmets R. Ayyagari R, et al. Ophthalmic Genet. 2001 Dec;22(4):233-9. doi: 10.1076/opge.22.4.233.2219. Ophthalmic Genet. 2001. PMID: 11803489

8

Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change.

Hiriyanna KT, Bingham EL, Yashar BM, Ayyagari R, Fishman G, Small KW, Weinberg DV, Weleber RG, Lewis RA, Andreasson S, Richards JE, Sieving PA. Hiriyanna KT, et al. Among authors: ayyagari r. Hum Mutat. 1999;14(5):423-7. doi: 10.1002/(SICI)1098-1004(199911)14:5<423::AID-HUMU8>3.0.CO;2-D. Hum Mutat. 1999. PMID: 10533068 Free article.

9

Juvenile retinoschisis: a model for molecular diagnostic testing of X-linked ophthalmic disease.

Sieving PA, Yashar BM, Ayyagari R. Sieving PA, et al. Among authors: ayyagari r. Trans Am Ophthalmol Soc. 1999;97:451-64; discussion 464-9. Trans Am Ophthalmol Soc. 1999. PMID: 10703138 Free PMC article.

10

Evaluation of the ELOVL4 gene in patients with autosomal recessive retinitis pigmentosa and Leber congenital amaurosis.

Rivolta C, Ayyagari R, Sieving PA, Berson EL, Dryja TP. Rivolta C, et al. Among authors: ayyagari r. Mol Vis. 2003 Feb 18;9:49-51. Mol Vis. 2003. PMID: 12592226 Free article.

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