McInnes RR - Search Results

1

The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase.

Attree O, Olivos IM, Okabe I, Bailey LC, Nelson DL, Lewis RA, McInnes RR, Nussbaum RL. Attree O, et al. Among authors: mcinnes rr. Nature. 1992 Jul 16;358(6383):239-42. doi: 10.1038/358239a0. Nature. 1992. PMID: 1321346

2

A ubiquitin C-terminal hydrolase gene on the proximal short arm of the X chromosome: implications for X-linked retinal disorders.

Swanson DA, Freund CL, Ploder L, McInnes RR, Valle D. Swanson DA, et al. Among authors: mcinnes rr. Hum Mol Genet. 1996 Apr;5(4):533-8. doi: 10.1093/hmg/5.4.533. Hum Mol Genet. 1996. PMID: 8845848

3

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.

Ferda Percin E, Ploder LA, Yu JJ, Arici K, Horsford DJ, Rutherford A, Bapat B, Cox DW, Duncan AM, Kalnins VI, Kocak-Altintas A, Sowden JC, Traboulsi E, Sarfarazi M, McInnes RR. Ferda Percin E, et al. Among authors: mcinnes rr. Nat Genet. 2000 Aug;25(4):397-401. doi: 10.1038/78071. Nat Genet. 2000. PMID: 10932181

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

PHR1 encodes an abundant, pleckstrin homology domain-containing integral membrane protein in the photoreceptor outer segments.

Xu S, Ladak R, Swanson DA, Soltyk A, Sun H, Ploder L, Vidgen D, Duncan AM, Garami E, Valle D, McInnes RR. Xu S, et al. Among authors: mcinnes rr. J Biol Chem. 1999 Dec 10;274(50):35676-85. doi: 10.1074/jbc.274.50.35676. J Biol Chem. 1999. PMID: 10585447 Free article.

6

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

7

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.

8

Human genetics. Blindness and the X.

Egan SE, McInnes RR. Egan SE, et al. Among authors: mcinnes rr. Nature. 1996 May 16;381(6579):194-5. doi: 10.1038/381194a0. Nature. 1996. PMID: 8622755 No abstract available.

9

Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation.

Burmeister M, Novak J, Liang MY, Basu S, Ploder L, Hawes NL, Vidgen D, Hoover F, Goldman D, Kalnins VI, Roderick TH, Taylor BA, Hankin MH, McInnes RR. Burmeister M, et al. Among authors: mcinnes rr. Nat Genet. 1996 Apr;12(4):376-84. doi: 10.1038/ng0496-376. Nat Genet. 1996. PMID: 8630490

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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