McInnes RR - Search Results

1

Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration.

Jacobson SG, Sumaroka A, Aleman TS, Cideciyan AV, Schwartz SB, Roman AJ, McInnes RR, Sheffield VC, Stone EM, Swaroop A, Wright AF. Jacobson SG, et al. Among authors: mcinnes rr. Hum Mol Genet. 2004 Sep 1;13(17):1893-902. doi: 10.1093/hmg/ddh198. Epub 2004 Jun 30. Hum Mol Genet. 2004. PMID: 15229190

2

Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) gene.

Jacobson SG, Cideciyan AV, Huang Y, Hanna DB, Freund CL, Affatigato LM, Carr RE, Zack DJ, Stone EM, McInnes RR. Jacobson SG, et al. Among authors: mcinnes rr. Invest Ophthalmol Vis Sci. 1998 Nov;39(12):2417-26. Invest Ophthalmol Vis Sci. 1998. PMID: 9804150

3

Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM1.

Nichols BE, Bascom R, Litt M, McInnes R, Sheffield VC, Stone EM. Nichols BE, et al. Am J Hum Genet. 1994 Jan;54(1):95-103. Am J Hum Genet. 1994. PMID: 8279475 Free PMC article.

4

Lifespan and mitochondrial control of neurodegeneration.

Wright AF, Jacobson SG, Cideciyan AV, Roman AJ, Shu X, Vlachantoni D, McInnes RR, Riemersma RA. Wright AF, et al. Among authors: mcinnes rr. Nat Genet. 2004 Nov;36(11):1153-8. doi: 10.1038/ng1448. Nat Genet. 2004. PMID: 15514669 Review.

5

Mutation analysis of the ROM1 gene in retinitis pigmentosa.

Bascom RA, Liu L, Heckenlively JR, Stone EM, McInnes RR. Bascom RA, et al. Among authors: mcinnes rr. Hum Mol Genet. 1995 Oct;4(10):1895-902. doi: 10.1093/hmg/4.10.1895. Hum Mol Genet. 1995. PMID: 8595413

6

The genomic, biochemical, and cellular responses of the retina in inherited photoreceptor degenerations and prospects for the treatment of these disorders.

Bramall AN, Wright AF, Jacobson SG, McInnes RR. Bramall AN, et al. Among authors: mcinnes rr. Annu Rev Neurosci. 2010;33:441-72. doi: 10.1146/annurev-neuro-060909-153227. Annu Rev Neurosci. 2010. PMID: 20572772 Review.

7

Evidence of severe mitochondrial oxidative stress and a protective effect of low oxygen in mouse models of inherited photoreceptor degeneration.

Vlachantoni D, Bramall AN, Murphy MP, Taylor RW, Shu X, Tulloch B, Van Veen T, Turnbull DM, McInnes RR, Wright AF. Vlachantoni D, et al. Among authors: mcinnes rr. Hum Mol Genet. 2011 Jan 15;20(2):322-35. doi: 10.1093/hmg/ddq467. Epub 2010 Nov 3. Hum Mol Genet. 2011. PMID: 21051333

8

Blinded by the light.

Jacobson SG, McInnes RR. Jacobson SG, et al. Among authors: mcinnes rr. Nat Genet. 2002 Oct;32(2):215-6. doi: 10.1038/ng1002-215. Nat Genet. 2002. PMID: 12355075 No abstract available.

9

De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis.

Freund CL, Wang QL, Chen S, Muskat BL, Wiles CD, Sheffield VC, Jacobson SG, McInnes RR, Zack DJ, Stone EM. Freund CL, et al. Among authors: mcinnes rr. Nat Genet. 1998 Apr;18(4):311-2. doi: 10.1038/ng0498-311. Nat Genet. 1998. PMID: 9537410 No abstract available.

10

VSX1: a gene for posterior polymorphous dystrophy and keratoconus.

Héon E, Greenberg A, Kopp KK, Rootman D, Vincent AL, Billingsley G, Priston M, Dorval KM, Chow RL, McInnes RR, Heathcote G, Westall C, Sutphin JE, Semina E, Bremner R, Stone EM. Héon E, et al. Among authors: mcinnes rr. Hum Mol Genet. 2002 May 1;11(9):1029-36. doi: 10.1093/hmg/11.9.1029. Hum Mol Genet. 2002. PMID: 11978762

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