McInnes RR - Search Results

1

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

2

Control of late off-center cone bipolar cell differentiation and visual signaling by the homeobox gene Vsx1.

Chow RL, Volgyi B, Szilard RK, Ng D, McKerlie C, Bloomfield SA, Birch DG, McInnes RR. Chow RL, et al. Among authors: mcinnes rr. Proc Natl Acad Sci U S A. 2004 Feb 10;101(6):1754-9. doi: 10.1073/pnas.0306520101. Epub 2004 Jan 26. Proc Natl Acad Sci U S A. 2004. PMID: 14745032 Free PMC article.

3

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

4

Vsx1, a rapidly evolving paired-like homeobox gene expressed in cone bipolar cells.

Chow RL, Snow B, Novak J, Looser J, Freund C, Vidgen D, Ploder L, McInnes RR. Chow RL, et al. Among authors: mcinnes rr. Mech Dev. 2001 Dec;109(2):315-22. doi: 10.1016/s0925-4773(01)00585-8. Mech Dev. 2001. PMID: 11731243 Free article.

5

Recent advances in the molecular basis of inherited photoreceptor degeneration.

Clarke G, Héon E, McInnes RR. Clarke G, et al. Among authors: mcinnes rr. Clin Genet. 2000 May;57(5):313-29. doi: 10.1034/j.1399-0004.2000.570501.x. Clin Genet. 2000. PMID: 10852366 Review.

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 Iroquois homeobox gene, Irx5, is required for retinal cone bipolar cell development.

Cheng CW, Chow RL, Lebel M, Sakuma R, Cheung HO, Thanabalasingham V, Zhang X, Bruneau BG, Birch DG, Hui CC, McInnes RR, Cheng SH. Cheng CW, et al. Among authors: mcinnes rr. Dev Biol. 2005 Nov 1;287(1):48-60. doi: 10.1016/j.ydbio.2005.08.029. Epub 2005 Sep 22. Dev Biol. 2005. PMID: 16182275 Free article.

8

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

9

Polymorphisms and rare sequence variants at the ROM1 locus.

Bascom RA, Liu L, Humphries P, Fishman GA, Murray JC, McInnes RR. Bascom RA, et al. Among authors: mcinnes rr. Hum Mol Genet. 1993 Nov;2(11):1975-7. doi: 10.1093/hmg/2.11.1975. Hum Mol Genet. 1993. PMID: 7904211

10

Cloning of the human and murine ROM1 genes: genomic organization and sequence conservation.

Bascom RA, Schappert K, McInnes RR. Bascom RA, et al. Among authors: mcinnes rr. Hum Mol Genet. 1993 Apr;2(4):385-91. doi: 10.1093/hmg/2.4.385. Hum Mol Genet. 1993. PMID: 8504299

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