| Year |
Citation |
Score |
| 2015 |
Jung CC, Atan D, Ng D, Ploder L, Ross SE, Klein M, Birch DG, Diez E, McInnes RR. Transcription factor PRDM8 is required for rod bipolar and type 2 OFF-cone bipolar cell survival and amacrine subtype identity. Proceedings of the National Academy of Sciences of the United States of America. 112: E3010-9. PMID 26023183 DOI: 10.1073/Pnas.1505870112 |
0.334 |
|
| 2014 |
Jiang K, Wright KL, Zhu P, Szego MJ, Bramall AN, Hauswirth WW, Li Q, Egan SE, McInnes RR. STAT3 promotes survival of mutant photoreceptors in inherited photoreceptor degeneration models. Proceedings of the National Academy of Sciences of the United States of America. 111: E5716-23. PMID 25512545 DOI: 10.1073/Pnas.1411248112 |
0.71 |
|
| 2013 |
Chang I, Bramall AN, Baynash AG, Rattner A, Rakheja D, Post M, Joza S, McKerlie C, Stewart DJ, McInnes RR, Yanagisawa M. Endothelin-2 deficiency causes growth retardation, hypothermia, and emphysema in mice. The Journal of Clinical Investigation. 123: 2643-53. PMID 23676500 DOI: 10.1172/Jci66735 |
0.674 |
|
| 2013 |
Bramall AN, Szego MJ, Pacione LR, Chang I, Diez E, D'Orleans-Juste P, Stewart DJ, Hauswirth WW, Yanagisawa M, McInnes RR. Endothelin-2-mediated protection of mutant photoreceptors in inherited photoreceptor degeneration. Plos One. 8: e58023. PMID 23469133 DOI: 10.1371/Journal.Pone.0058023 |
0.706 |
|
| 2012 |
Ross SE, McCord AE, Jung C, Atan D, Mok SI, Hemberg M, Kim TK, Salogiannis J, Hu L, Cohen S, Lin Y, Harrar D, McInnes RR, Greenberg ME. Bhlhb5 and Prdm8 form a repressor complex involved in neuronal circuit assembly. Neuron. 73: 292-303. PMID 22284184 DOI: 10.1016/J.Neuron.2011.09.035 |
0.319 |
|
| 2011 |
Vlachantoni D, Bramall AN, Murphy MP, Taylor RW, Shu X, Tulloch B, Van Veen T, Turnbull DM, McInnes RR, Wright AF. Evidence of severe mitochondrial oxidative stress and a protective effect of low oxygen in mouse models of inherited photoreceptor degeneration. Human Molecular Genetics. 20: 322-35. PMID 21051333 DOI: 10.1093/Hmg/Ddq467 |
0.682 |
|
| 2010 |
Bramall AN, Wright AF, Jacobson SG, McInnes RR. The genomic, biochemical, and cellular responses of the retina in inherited photoreceptor degenerations and prospects for the treatment of these disorders. Annual Review of Neuroscience. 33: 441-72. PMID 20572772 DOI: 10.1146/Annurev-Neuro-060909-153227 |
0.695 |
|
| 2010 |
Inoue T, Coles BL, Dorval K, Bremner R, Bessho Y, Kageyama R, Hino S, Matsuoka M, Craft CM, McInnes RR, Tremblay F, Prusky GT, van der Kooy D. Maximizing functional photoreceptor differentiation from adult human retinal stem cells. Stem Cells (Dayton, Ohio). 28: 489-500. PMID 20014120 DOI: 10.1002/Stem.279 |
0.414 |
|
| 2009 |
Erclik T, Hartenstein V, McInnes RR, Lipshitz HD. Eye evolution at high resolution: the neuron as a unit of homology. Developmental Biology. 332: 70-9. PMID 19467226 DOI: 10.1016/J.Ydbio.2009.05.565 |
0.331 |
|
| 2008 |
Erclik T, Hartenstein V, Lipshitz HD, McInnes RR. Conserved role of the Vsx genes supports a monophyletic origin for bilaterian visual systems. Current Biology : Cb. 18: 1278-87. PMID 18723351 DOI: 10.1016/J.Cub.2008.07.076 |
0.33 |
|
| 2007 |
Xu S, Sunderland ME, Coles BL, Kam A, Holowacz T, Ashery-Padan R, Marquardt T, McInnes RR, van der Kooy D. The proliferation and expansion of retinal stem cells require functional Pax6. Developmental Biology. 304: 713-21. PMID 17316600 DOI: 10.1016/J.Ydbio.2007.01.021 |
0.411 |
|
| 2007 |
de Velasco B, Erclik T, Shy D, Sclafani J, Lipshitz H, McInnes R, Hartenstein V. Specification and development of the pars intercerebralis and pars lateralis, neuroendocrine command centers in the Drosophila brain. Developmental Biology. 302: 309-23. PMID 17070515 DOI: 10.1016/J.Ydbio.2006.09.035 |
0.304 |
|
| 2006 |
Coles BL, Horsford DJ, McInnes RR, van der Kooy D. Loss of retinal progenitor cells leads to an increase in the retinal stem cell population in vivo. The European Journal of Neuroscience. 23: 75-82. PMID 16420417 DOI: 10.1111/J.1460-9568.2005.04537.X |
0.368 |
|
| 2005 |
Cheng CW, Chow RL, Lebel M, Sakuma R, Cheung HO, Thanabalasingham V, Zhang X, Bruneau BG, Birch DG, Hui CC, McInnes RR, Cheng SH. The Iroquois homeobox gene, Irx5, is required for retinal cone bipolar cell development. Developmental Biology. 287: 48-60. PMID 16182275 DOI: 10.1016/J.Ydbio.2005.08.029 |
0.421 |
|
| 2005 |
Horsford DJ, Nguyen MT, Sellar GC, Kothary R, Arnheiter H, McInnes RR. Chx10 repression of Mitf is required for the maintenance of mammalian neuroretinal identity. Development (Cambridge, England). 132: 177-87. PMID 15576400 DOI: 10.1242/Dev.01571 |
0.431 |
|
| 2004 |
Wright AF, Jacobson SG, Cideciyan AV, Roman AJ, Shu X, Vlachantoni D, McInnes RR, Riemersma RA. Lifespan and mitochondrial control of neurodegeneration. Nature Genetics. 36: 1153-8. PMID 15514669 DOI: 10.1038/Ng1448 |
0.322 |
|
| 2004 |
Coles BL, Angénieux B, Inoue T, Del Rio-Tsonis K, Spence JR, McInnes RR, Arsenijevic Y, van der Kooy D. Facile isolation and the characterization of human retinal stem cells. Proceedings of the National Academy of Sciences of the United States of America. 101: 15772-7. PMID 15505221 DOI: 10.1073/Pnas.0401596101 |
0.354 |
|
| 2004 |
Jacobson SG, Sumaroka A, Aleman TS, Cideciyan AV, Schwartz SB, Roman AJ, McInnes RR, Sheffield VC, Stone EM, Swaroop A, Wright AF. Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration. Human Molecular Genetics. 13: 1893-902. PMID 15229190 DOI: 10.1093/Hmg/Ddh198 |
0.32 |
|
| 2004 |
Chow RL, Volgyi B, Szilard RK, Ng D, McKerlie C, Bloomfield SA, Birch DG, McInnes RR. Control of late off-center cone bipolar cell differentiation and visual signaling by the homeobox gene Vsx1. Proceedings of the National Academy of Sciences of the United States of America. 101: 1754-9. PMID 14745032 DOI: 10.1073/Pnas.0306520101 |
0.431 |
|
| 2003 |
Pacione LR, Szego MJ, Ikeda S, Nishina PM, McInnes RR. Progress toward understanding the genetic and biochemical mechanisms of inherited photoreceptor degenerations. Annual Review of Neuroscience. 26: 657-700. PMID 14527271 DOI: 10.1146/annurev.neuro.26.041002.131416 |
0.334 |
|
| 2001 |
Chow RL, Snow B, Novak J, Looser J, Freund C, Vidgen D, Ploder L, McInnes RR. Vsx1, a rapidly evolving paired-like homeobox gene expressed in cone bipolar cells Mechanisms of Development. 109: 315-322. PMID 11731243 DOI: 10.1016/S0925-4773(01)00585-8 |
0.42 |
|
| 2001 |
Kedzierski W, Nusinowitz S, Birch D, Clarke G, McInnes RR, Bok D, Travis GH. Deficiency of rds/peripherin causes photoreceptor death in mouse models of digenic and dominant retinitis pigmentosa Proceedings of the National Academy of Sciences of the United States of America. 98: 7718-7723. PMID 11427722 DOI: 10.1073/Pnas.141124198 |
0.353 |
|
| 2000 |
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. Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. Nature Genetics. 25: 397-401. PMID 10932181 DOI: 10.1038/78071 |
0.428 |
|
| 2000 |
Clarke G, Collins RA, Leavitt BR, Andrews DF, Hayden MR, Lumsden CJ, McInnes RR. A one-hit model of cell death in inherited neuronal degenerations. Nature. 406: 195-9. PMID 10910361 DOI: 10.1038/35018098 |
0.304 |
|
| 2000 |
Clarke G, Héon E, McInnes RR. Recent advances in the molecular basis of inherited photoreceptor degeneration Clinical Genetics. 57: 313-329. PMID 10852366 DOI: 10.1034/J.1399-0004.2000.570501.X |
0.366 |
|
| 2000 |
Clarke G, Goldberg AF, Vidgen D, Collins L, Ploder L, Schwarz L, Molday LL, Rossant J, Szél A, Molday RS, Birch DG, McInnes RR. Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis. Nature Genetics. 25: 67-73. PMID 10802659 DOI: 10.1038/75621 |
0.321 |
|
| 2000 |
Tropepe V, Coles BL, Chiasson BJ, Horsford DJ, Elia AJ, McInnes RR, van der Kooy D. Retinal stem cells in the adult mammalian eye. Science (New York, N.Y.). 287: 2032-6. PMID 10720333 DOI: 10.1126/Science.287.5460.2032 |
0.364 |
|
| 1999 |
Xu S, Ladak R, Swanson DA, Soltyk A, Sun H, Ploder L, Vidgen D, Duncan AMV, Garami E, Valle D, McInnes RR. PHR1 encodes an abundant, pleckstrin homology domain-containing integral membrane protein in the photoreceptor outer segments Journal of Biological Chemistry. 274: 35676-35685. PMID 10585447 DOI: 10.1074/Jbc.274.50.35676 |
0.349 |
|
| 1998 |
Tang SJ, Suen TC, McInnes RR, Buchwald M. Association of the TLX-2 homeodomain and 14-3-3eta signaling proteins. The Journal of Biological Chemistry. 273: 25356-63. PMID 9738002 DOI: 10.1074/Jbc.273.39.25356 |
0.351 |
|
| 1998 |
Howell PL, Turner MA, Christodoulou J, Walker DC, Craig HJ, Simard LR, Ploder L, McInnes RR. Intragenic complementation at the argininosuccinate lyase locus: reconstruction of the active site. Journal of Inherited Metabolic Disease. 21: 72-85. PMID 9686346 DOI: 10.1023/A:1005361724967 |
0.332 |
|
| 1997 |
Turner MA, Simpson A, Mcinnes RR, Howell PL. Human argininosuccinate lyase: A structural basis for intragenic complementation Proceedings of the National Academy of Sciences of the United States of America. 94: 9063-9068. PMID 9256435 DOI: 10.1073/Pnas.94.17.9063 |
0.325 |
|
| 1997 |
Swanson DA, Freund CL, Steel JM, Xu S, Ploder L, McInnes RR, Valle D. A differential hybridization scheme to identify photoreceptor-specific genes Genome Research. 7: 513-521. PMID 9149946 DOI: 10.1101/Gr.7.5.513 |
0.37 |
|
| 1996 |
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. Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation. Nature Genetics. 12: 376-84. PMID 8630490 DOI: 10.1038/Ng0496-376 |
0.446 |
|
| 1996 |
Egan SE, McInnes RR. Retinitis pigmentosa: The Ran connection Nature. 381: 194. DOI: 10.1038/381194B0 |
0.348 |
|
| 1995 |
Bascom RA, Liu L, Heckenlively JR, Stone EM, Mcinnes RR. Mutation analysis of the ROM1 gene in retinitis pigmentosa Human Molecular Genetics. 4: 1895-1902. PMID 8595413 DOI: 10.1093/Hmg/4.10.1895 |
0.339 |
|
| 1993 |
Taylor RG, Grieco D, Clarke GA, McInnes RR, Taylor BA. Identification of the mutation in murine histidinemia (his) and genetic mapping of the murine histidase locus (Hal) on chromosome 10. Genomics. 16: 231-40. PMID 8486363 DOI: 10.1006/Geno.1993.1164 |
0.601 |
|
| 1992 |
McInnes RR, Bascom RA. Retinal genetics: A nullifying effect for rhodopsin Nature Genetics. 1: 155-157. PMID 1303226 DOI: 10.1038/Ng0692-155 |
0.331 |
|
| 1991 |
Connell G, Bascom R, Molday L, Reid D, McInnes RR, Molday RS. Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse Proceedings of the National Academy of Sciences of the United States of America. 88: 723-726. PMID 1992463 DOI: 10.1073/Pnas.88.3.723 |
0.439 |
|
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