Swaroop A - Search Results

1

Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations.

Aleman TS, Cideciyan AV, Sumaroka A, Schwartz SB, Roman AJ, Windsor EA, Steinberg JD, Branham K, Othman M, Swaroop A, Jacobson SG. Aleman TS, et al. Among authors: swaroop a. Invest Ophthalmol Vis Sci. 2007 Oct;48(10):4759-65. doi: 10.1167/iovs.07-0453. Invest Ophthalmol Vis Sci. 2007. PMID: 17898302 Free PMC article.

2

Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene.

Andréasson S, Ponjavic V, Abrahamson M, Ehinger B, Wu W, Fujita R, Buraczynska M, Swaroop A. Andréasson S, et al. Among authors: swaroop a. Am J Ophthalmol. 1997 Jul;124(1):95-102. doi: 10.1016/s0002-9394(14)71649-6. Am J Ophthalmol. 1997. PMID: 9222238

3

RPGR: part one of the X-linked retinitis pigmentosa story.

Fujita R, Swaroop A. Fujita R, et al. Among authors: swaroop a. Mol Vis. 1996 Jun 4;2:4. Mol Vis. 1996. PMID: 9233985 Free article. Review. No abstract available.

4

Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: paucity of mutations in the coding region but splice defects in two families.

Fujita R, Buraczynska M, Gieser L, Wu W, Forsythe P, Abrahamson M, Jacobson SG, Sieving PA, Andréasson S, Swaroop A. Fujita R, et al. Among authors: swaroop a. Am J Hum Genet. 1997 Sep;61(3):571-80. doi: 10.1086/515523. Am J Hum Genet. 1997. PMID: 9326322 Free PMC article.

5

Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.

Jacobson SG, Buraczynska M, Milam AH, Chen C, Järvaläinen M, Fujita R, Wu W, Huang Y, Cideciyan AV, Swaroop A. Jacobson SG, et al. Among authors: swaroop a. Invest Ophthalmol Vis Sci. 1997 Sep;38(10):1983-97. Invest Ophthalmol Vis Sci. 1997. PMID: 9331262

6

Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa.

Buraczynska M, Wu W, Fujita R, Buraczynska K, Phelps E, Andréasson S, Bennett J, Birch DG, Fishman GA, Hoffman DR, Inana G, Jacobson SG, Musarella MA, Sieving PA, Swaroop A. Buraczynska M, et al. Among authors: swaroop a. Am J Hum Genet. 1997 Dec;61(6):1287-92. doi: 10.1086/301646. Am J Hum Genet. 1997. PMID: 9399904 Free PMC article.

7

Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration.

Swain PK, Chen S, Wang QL, Affatigato LM, Coats CL, Brady KD, Fishman GA, Jacobson SG, Swaroop A, Stone E, Sieving PA, Zack DJ. Swain PK, et al. Among authors: swaroop a. Neuron. 1997 Dec;19(6):1329-36. doi: 10.1016/s0896-6273(00)80423-7. Neuron. 1997. PMID: 9427255 Free article.

8

A new 2-base pair deletion in the RPGR gene in a black family with X-linked retinitis pigmentosa.

Fishman GA, Grover S, Buraczynska M, Wu W, Swaroop A. Fishman GA, et al. Among authors: swaroop a. Arch Ophthalmol. 1998 Feb;116(2):213-8. doi: 10.1001/archopht.116.2.213. Arch Ophthalmol. 1998. PMID: 9488274

9

A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27.

Gieser L, Fujita R, Göring HH, Ott J, Hoffman DR, Cideciyan AV, Birch DG, Jacobson SG, Swaroop A. Gieser L, et al. Among authors: swaroop a. Am J Hum Genet. 1998 Nov;63(5):1439-47. doi: 10.1086/302121. Am J Hum Genet. 1998. PMID: 9792872 Free PMC article.

10

Phenotype of an X-linked retinitis pigmentosa family with a novel splice defect in the RPGR gene.

Bauer S, Fujita R, Buraczynska M, Abrahamson M, Ehinger B, Wu W, Falls TJ, Andréasson S, Swaroop A. Bauer S, et al. Among authors: swaroop a. Invest Ophthalmol Vis Sci. 1998 Nov;39(12):2470-4. Invest Ophthalmol Vis Sci. 1998. PMID: 9804156

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