McInnes RR - Search Results

1

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

2

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

3

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor.

Freund CL, Gregory-Evans CY, Furukawa T, Papaioannou M, Looser J, Ploder L, Bellingham J, Ng D, Herbrick JA, Duncan A, Scherer SW, Tsui LC, Loutradis-Anagnostou A, Jacobson SG, Cepko CL, Bhattacharya SS, McInnes RR. Freund CL, et al. Among authors: mcinnes rr. Cell. 1997 Nov 14;91(4):543-53. doi: 10.1016/s0092-8674(00)80440-7. Cell. 1997. PMID: 9390563 Free article.

4

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.

5

A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene.

Sohocki MM, Sullivan LS, Mintz-Hittner HA, Birch D, Heckenlively JR, Freund CL, McInnes RR, Daiger SP. Sohocki MM, et al. Among authors: mcinnes rr. Am J Hum Genet. 1998 Nov;63(5):1307-15. doi: 10.1086/302101. Am J Hum Genet. 1998. PMID: 9792858 Free PMC article.

6

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.

7

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.

8

A differential hybridization scheme to identify photoreceptor-specific genes.

Swanson DA, Freund CL, Steel JM, Xu S, Ploder L, McInnes RR, Valle D. Swanson DA, et al. Among authors: mcinnes rr. Genome Res. 1997 May;7(5):513-21. doi: 10.1101/gr.7.5.513. Genome Res. 1997. PMID: 9149946 Free article.

9

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

10

Transcription factor genes and the developing eye: a genetic perspective.

Freund C, Horsford DJ, McInnes RR. Freund C, et al. Among authors: mcinnes rr. Hum Mol Genet. 1996;5 Spec No:1471-88. doi: 10.1093/hmg/5.supplement_1.1471. Hum Mol Genet. 1996. PMID: 8875254 Review.

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