{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,16]],"date-time":"2026-10-16T05:42:37Z","timestamp":1792129357489,"version":"4.4.0"},"reference-count":127,"publisher":"Springer Science and Business Media LLC","issue":"4","license":[{"start":{"date-parts":[[2012,5,30]],"date-time":"2012-05-30T00:00:00Z","timestamp":1338336000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Jpn J Ophthalmol"],"published-print":{"date-parts":[[2012,7]]},"DOI":"10.1007\/s10384-012-0147-2","type":"journal-article","created":{"date-parts":[[2012,5,29]],"date-time":"2012-05-29T08:30:19Z","timestamp":1338280219000},"page":"289-306","source":"Crossref","is-referenced-by-count":158,"title":["Retinal remodeling"],"prefix":"10.1007","volume":"56","author":[{"given":"B. W.","family":"Jones","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M.","family":"Kondo","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H.","family":"Terasaki","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Y.","family":"Lin","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M.","family":"McCall","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R. E.","family":"Marc","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2012,5,30]]},"reference":[{"key":"147_CR1","doi-asserted-by":"crossref","first-page":"4759","DOI":"10.1167\/iovs.07-0453","volume":"48","author":"TS Aleman","year":"2007","unstructured":"Aleman TS, Cideciyan AV, Sumaroka A, Schwartz SB, Roman AJ, Windsor EAM, et al. Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations. Invest Ophthalmol Vis Sci. 2007;48:4759\u201365.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR2","doi-asserted-by":"crossref","first-page":"301","DOI":"10.1016\/j.neuroscience.2004.04.042","volume":"127","author":"N Cuenca","year":"2004","unstructured":"Cuenca N, Pinilla I, Sauv\u00e9 Y, Lu B, Wang S, Lund RD. Regressive and reactive changes in the connectivity patterns of rod and cone pathways of P23H transgenic rat retina. Neuroscience. 2004;127:301\u201317.","journal-title":"Neuroscience"},{"key":"147_CR3","doi-asserted-by":"crossref","first-page":"1057","DOI":"10.1111\/j.1460-9568.2005.04300.x","volume":"22","author":"N Cuenca","year":"2005","unstructured":"Cuenca N, Pinilla I, Sauv\u00e9 Y, Lund RD. Early changes in synaptic connectivity following progressive photoreceptor degeneration in RCS rats. Eur J Neurosci. 2005;22:1057\u201372.","journal-title":"Eur J Neurosci"},{"key":"147_CR4","doi-asserted-by":"crossref","first-page":"99","DOI":"10.1159\/000267881","volume":"28","author":"S Raad de","year":"1996","unstructured":"de Raad S, Szczesny PJ, Munz K, Rem\u00e9 CE. Light damage in the rat retina: glial fibrillary acidic protein accumulates in M\u00fcller cells in correlation with photoreceptor damage. Ophthalmic Res. 1996;28:99\u2013107.","journal-title":"Ophthalmic Res"},{"key":"147_CR5","doi-asserted-by":"crossref","first-page":"215","DOI":"10.1016\/S0002-9394(99)00401-8","volume":"129","author":"RN Fariss","year":"2000","unstructured":"Fariss RN, Li ZY, Milam AH. Abnormalities in rod photoreceptors, amacrine cells, and horizontal cells in human retinas with retinitis pigmentosa. Am J Ophthalmol. 2000;129:215\u201323.","journal-title":"Am J Ophthalmol"},{"key":"147_CR6","doi-asserted-by":"crossref","first-page":"343","DOI":"10.1002\/(SICI)1096-9861(19961216)376:3<343::AID-CNE1>3.0.CO;2-2","volume":"376","author":"EL Fletcher","year":"1996","unstructured":"Fletcher EL, Kalloniatis M. Neurochemical architecture of the normal and degenerating rat retina. J Comp Neurol. 1996;376:343\u201360.","journal-title":"J Comp Neurol"},{"key":"147_CR7","doi-asserted-by":"crossref","first-page":"123","DOI":"10.1016\/j.exer.2005.03.006","volume":"81","author":"BW Jones","year":"2005","unstructured":"Jones BW, Marc RE. Retinal remodeling during retinal degeneration. Exp Eye Res. 2005;81:123\u201337.","journal-title":"Exp Eye Res"},{"key":"147_CR8","doi-asserted-by":"crossref","first-page":"405","DOI":"10.1007\/0-387-32442-9_57","volume":"572","author":"BW Jones","year":"2006","unstructured":"Jones BW, Marc RE, Watt CB, Vaughan DK, Organisciak DT. Neural plasticity revealed by light-induced photoreceptor lesions. Adv Exp Med Biol. 2006;572:405\u201310.","journal-title":"Adv Exp Med Biol"},{"key":"147_CR9","doi-asserted-by":"crossref","first-page":"282","DOI":"10.1111\/j.1444-0938.2005.tb06712.x","volume":"88","author":"BW Jones","year":"2005","unstructured":"Jones BW, Watt CB, Marc RE. Retinal remodelling. Clin Exp Optom. 2005;88:282\u201391.","journal-title":"Clin Exp Optom"},{"key":"147_CR10","doi-asserted-by":"crossref","first-page":"413","DOI":"10.1523\/JNEUROSCI.22-02-00413.2002","volume":"22","author":"RE Marc","year":"2002","unstructured":"Marc RE, Jones BW. Molecular phenotyping of retinal ganglion cells. J Neurosci. 2002;22:413\u201327.","journal-title":"J Neurosci"},{"key":"147_CR11","doi-asserted-by":"crossref","first-page":"139","DOI":"10.1385\/MN:28:2:139","volume":"28","author":"RE Marc","year":"2003","unstructured":"Marc RE, Jones BW. Retinal remodeling in inherited photoreceptor degenerations. Mol Neurobiol. 2003;28:139\u201347.","journal-title":"Mol Neurobiol"},{"key":"147_CR12","doi-asserted-by":"crossref","first-page":"607","DOI":"10.1016\/S1350-9462(03)00039-9","volume":"22","author":"RE Marc","year":"2003","unstructured":"Marc RE, Jones BW, Watt CB, Strettoi E. Neural remodeling in retinal degeneration. Prog Retin Eye Res. 2003;22:607\u201355.","journal-title":"Prog Retin Eye Res"},{"key":"147_CR13","first-page":"782","volume":"14","author":"RE Marc","year":"2008","unstructured":"Marc RE, Jones BW, Vazquez-Chona F, Vaughan DK, Organisciak DT. Extreme retinal remodeling triggered by light damage: implications for age related macular degeneration. Mol Vis. 2008;14:782\u2013805.","journal-title":"Mol Vis"},{"key":"147_CR14","first-page":"487","volume":"13","author":"H Kolb","year":"1974","unstructured":"Kolb H, Gouras P. Electron microscopic observations of human retinitis pigmentosa, dominantly inherited. Invest Ophthalmol. 1974;13:487\u201398.","journal-title":"Invest Ophthalmol"},{"key":"147_CR15","doi-asserted-by":"crossref","first-page":"5429","DOI":"10.1523\/JNEUROSCI.15-08-05429.1995","volume":"15","author":"ZY Li","year":"1995","unstructured":"Li ZY, Kljavin IJ, Milam AH. Rod photoreceptor neurite sprouting in retinitis pigmentosa. J Neurosci. 1995;15:5429\u201338.","journal-title":"J Neurosci"},{"key":"147_CR16","first-page":"3200","volume":"41","author":"S Machida","year":"2000","unstructured":"Machida S, Kondo M, Jamison JA, Khan NW, Kononen LT, Sugawara T, et al. P23H rhodopsin transgenic rat: correlation of retinal function with histopathology. Invest Ophthalmol Vis Sci. 2000;41:3200\u20139.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR17","doi-asserted-by":"crossref","unstructured":"Pu M, Xu L, Zhang H. Visual response properties of retinal ganglion cells in the Royal College of Surgeons dystrophic rat. Invest Ophthalmol Vis Sci. 2006;47:3579\u201385.","DOI":"10.1167\/iovs.05-1450"},{"key":"147_CR18","doi-asserted-by":"crossref","first-page":"2506","DOI":"10.1111\/j.1460-9568.2007.05886.x","volume":"26","author":"D Specht","year":"2007","unstructured":"Specht D, Tom Dieck S, Ammerm\u00fcller J, Regus-Leidig H, Gundelfinger ED, Brandst\u00e4tter JH. Structural and functional remodeling in the retina of a mouse with a photoreceptor synaptopathy: plasticity in the rod and degeneration in the cone system. Eur J Neurosci. 2007;26:2506\u201315.","journal-title":"Eur J Neurosci"},{"key":"147_CR19","doi-asserted-by":"crossref","first-page":"1408","DOI":"10.1152\/jn.00144.2007","volume":"99","author":"SF Stasheff","year":"2008","unstructured":"Stasheff SF. Emergence of sustained spontaneous hyperactivity and temporary preservation of OFF responses in ganglion cells of the retinal degeneration (rd1) mouse. J Neurophysiol. 2008;99:1408\u201321.","journal-title":"J Neurophysiol"},{"key":"147_CR20","doi-asserted-by":"crossref","first-page":"11020","DOI":"10.1073\/pnas.190291097","volume":"97","author":"E Strettoi","year":"2000","unstructured":"Strettoi E, Pignatelli V. Modifications of retinal neurons in a mouse model of retinitis pigmentosa. Proc Natl Acad Sci USA. 2000;97:11020\u20135.","journal-title":"Proc Natl Acad Sci USA"},{"key":"147_CR21","doi-asserted-by":"crossref","first-page":"867","DOI":"10.1016\/S0042-6989(02)00594-1","volume":"43","author":"E Strettoi","year":"2003","unstructured":"Strettoi E, Pignatelli V, Rossi C, Porciatti V, Falsini B. Remodeling of second-order neurons in the retina of rd\/rd mutant mice. Vision Res. 2003;43:867\u201377.","journal-title":"Vision Res"},{"key":"147_CR22","doi-asserted-by":"crossref","first-page":"5492","DOI":"10.1523\/JNEUROSCI.22-13-05492.2002","volume":"22","author":"E Strettoi","year":"2002","unstructured":"Strettoi E, Porciatti V, Falsini B, Pignatelli V, Rossi C. Morphological and functional abnormalities in the inner retina of the rd\/rd mouse. J Neurosci. 2002;22:5492\u2013504.","journal-title":"J Neurosci"},{"key":"147_CR23","doi-asserted-by":"crossref","first-page":"2782","DOI":"10.1167\/iovs.06-1283","volume":"48","author":"RK Sullivan","year":"2007","unstructured":"Sullivan RK, Woldemussie E, Pow DV. Dendritic and synaptic plasticity of neurons in the human age-related macular degeneration retina. Invest Ophthalmol Vis Sci. 2007;48:2782\u20139.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR24","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1002\/cne.10703","volume":"464","author":"BW Jones","year":"2003","unstructured":"Jones BW, Watt CB, Frederick JM, Baehr W, Chen CK, Levine EM, et al. Retinal remodeling triggered by photoreceptor degenerations. J Comp Neurol. 2003;464:1\u201316.","journal-title":"J Comp Neurol"},{"key":"147_CR25","doi-asserted-by":"crossref","first-page":"856","DOI":"10.1167\/iovs.02-0416","volume":"44","author":"R Sullivan","year":"2003","unstructured":"Sullivan R, Penfold P, Pow DV. Neuronal migration and glial remodeling in degenerating retinas of aged rats and in nonneovascular AMD. Invest Ophthalmol Vis Sci. 2003;44:856\u201365.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR26","doi-asserted-by":"crossref","first-page":"3364","DOI":"10.1167\/iovs.07-0032","volume":"48","author":"RE Marc","year":"2007","unstructured":"Marc RE, Jones BW, Anderson JR, Kinard K, Marshak DW, Wilson JH, et al. Neural reprogramming in retinal degeneration. Invest Ophthalmol Vis Sci. 2007;48:3364\u201371.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR27","doi-asserted-by":"crossref","first-page":"2636","DOI":"10.1016\/j.visres.2009.04.008","volume":"49","author":"W Baehr","year":"2009","unstructured":"Baehr W, Frederick JM. Naturally occurring animal models with outer retina phenotypes. Vision Res. 2009;49:2636\u201352.","journal-title":"Vision Res"},{"key":"147_CR28","doi-asserted-by":"crossref","first-page":"880","DOI":"10.1001\/archopht.1995.01100070054025","volume":"113","author":"CJ Chang","year":"1995","unstructured":"Chang CJ, Lai WW, Edward DP, Tso MOM. Apoptotic photoreceptor cell death after traumatic retinal detachment in humans. Arch Ophthalmol. 1995;113:880\u20136.","journal-title":"Arch Ophthalmol"},{"key":"147_CR29","first-page":"826","volume":"42","author":"JM Frederick","year":"2001","unstructured":"Frederick JM, Krasnoperova NV, Hoffmann K, Church-Kopish J, R\u00fcther K, Howes K, et al. Mutant rhodopsin transgene expression on a null background. Invest Ophthalmol Vis Sci. 2001;42:826\u201333.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR30","doi-asserted-by":"crossref","first-page":"216","DOI":"10.1038\/ng0297-216","volume":"15","author":"MM Humphries","year":"1997","unstructured":"Humphries MM, Rancourt D, Farrar GJ, Kenna P, Hazel M, Bush RA, et al. Retinopathy induced in mice by targeted disruption of the rhodopsin gene. Nat Genet. 1997;15:216\u20139.","journal-title":"Nat Genet"},{"key":"147_CR31","first-page":"23","volume":"4","author":"GD Aguirre","year":"1998","unstructured":"Aguirre GD, Baldwin V, Pearce-Kelling S, Narfstr\u00f6m K, Ray K, Acland GM. Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect. Mol Vis. 1998;4:23.","journal-title":"Mol Vis"},{"key":"147_CR32","doi-asserted-by":"crossref","first-page":"194","DOI":"10.1038\/ng1097-194","volume":"17","author":"SM Gu","year":"1997","unstructured":"Gu SM, Thompson DA, Srikumari CR, Lorenz B, Finckh U, Nicoletti A, et al. Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy. Nat Genet. 1997;17:194\u20137.","journal-title":"Nat Genet"},{"key":"147_CR33","doi-asserted-by":"crossref","first-page":"3088","DOI":"10.1073\/pnas.95.6.3088","volume":"95","author":"H Morimura","year":"1998","unstructured":"Morimura H, Fishman GA, Grover SA, Fulton AB, Berson EL, Dryja TP. Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis. Proc Natl Acad Sci USA. 1998;95:3088\u201393.","journal-title":"Proc Natl Acad Sci USA"},{"key":"147_CR34","doi-asserted-by":"crossref","first-page":"236","DOI":"10.1038\/ng0397-236","volume":"15","author":"R Allikmets","year":"1997","unstructured":"Allikmets R, Singh N, Sun H, Shroyer NF, Hutchinson A, Chidambaram A, et al. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. Nat Genet. 1997;15:236\u201346.","journal-title":"Nat Genet"},{"key":"147_CR35","doi-asserted-by":"crossref","first-page":"793","DOI":"10.1086\/303100","volume":"67","author":"R Allikmets","year":"2000","unstructured":"Allikmets R. Simple and complex ABCR: genetic predisposition to retinal disease. Am J Hum Genet. 2000;67:793\u20139.","journal-title":"Am J Hum Genet"},{"key":"147_CR36","doi-asserted-by":"crossref","first-page":"1805","DOI":"10.1126\/science.277.5333.1805","volume":"277","author":"R Allikmets","year":"1997","unstructured":"Allikmets R, Shroyer NF, Singh N, Seddon JM, Lewis RA, Bernstein PS, et al. Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration. Science. 1997;277:1805\u20137.","journal-title":"Science"},{"key":"147_CR37","doi-asserted-by":"crossref","first-page":"355","DOI":"10.1093\/hmg\/7.3.355","volume":"7","author":"FP Cremers","year":"1998","unstructured":"Cremers FP, van de Pol DJ, van Driel M, den Hollander AI, van Haren FJ, Knoers NV, et al. Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt\u2019s disease gene ABCR. Hum Mol Genet. 1998;7:355\u201362.","journal-title":"Hum Mol Genet"},{"key":"147_CR38","doi-asserted-by":"crossref","first-page":"257","DOI":"10.1038\/77004","volume":"25","author":"LL Molday","year":"2000","unstructured":"Molday LL, Rabin AR, Molday RS. ABCR expression in foveal cone photoreceptors and its role in Stargardt macular dystrophy. Nat Genet. 2000;25:257\u20138.","journal-title":"Nat Genet"},{"key":"147_CR39","doi-asserted-by":"crossref","first-page":"645","DOI":"10.1093\/hmg\/9.4.645","volume":"9","author":"PM D\u2019Cruz","year":"2000","unstructured":"D\u2019Cruz PM, Yasumura D, Weir J, Matthes MT, Abderrahim H, LaVail MM, et al. Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat. Hum Mol Genet. 2000;9:645\u201351.","journal-title":"Hum Mol Genet"},{"key":"147_CR40","doi-asserted-by":"crossref","first-page":"165","DOI":"10.1007\/978-1-4615-0067-4_21","volume":"533","author":"JL Duncan","year":"2003","unstructured":"Duncan JL, Yang H, Vollrath D, Yasumura D, Matthes MT, Trautmann N, et al. Inherited retinal dystrophy in Mer knockout mice. Adv Exp Med Biol. 2003;533:165\u201372.","journal-title":"Adv Exp Med Biol"},{"key":"147_CR41","doi-asserted-by":"crossref","first-page":"541","DOI":"10.1016\/S0092-8674(04)00450-7","volume":"117","author":"JB Li","year":"2004","unstructured":"Li JB, Gerdes JM, Haycraft CJ, Fan Y, Teslovich TM, May-Simera H, et al. Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene. Cell. 2004;117:541\u201352.","journal-title":"Cell"},{"key":"147_CR42","doi-asserted-by":"crossref","first-page":"667","DOI":"10.1093\/hmg\/ddi468","volume":"15","author":"HJ Yen","year":"2006","unstructured":"Yen HJ, Tayeh MK, Mullins RF, Stone EM, Sheffield VC, Slusarski DC. Bardet\u2013Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer\u2019s vesicle cilia function. Hum Mol Genet. 2006;15:667\u201377.","journal-title":"Hum Mol Genet"},{"key":"147_CR43","doi-asserted-by":"crossref","first-page":"280","DOI":"10.1038\/ng0793-280","volume":"4","author":"TP Dryja","year":"1993","unstructured":"Dryja TP, Berson EL, Rao VR, Oprian DD. Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness. Nat Genet. 1993;4:280\u20133.","journal-title":"Nat Genet"},{"key":"147_CR44","doi-asserted-by":"crossref","first-page":"4105","DOI":"10.1167\/iovs.08-1717","volume":"49","author":"C Zeitz","year":"2008","unstructured":"Zeitz C, Gross AK, Leifert D, Kloeckener-Gruissem B, McAlear SD, Lemke J, et al. Identification and functional characterization of a novel rhodopsin mutation associated with autosomal dominant CSNB. Invest Ophthalmol Vis Sci. 2008;49:4105\u201314.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR45","doi-asserted-by":"crossref","first-page":"4532","DOI":"10.1016\/j.visres.2006.08.031","volume":"46","author":"ME Sommer","year":"2006","unstructured":"Sommer ME, Farrens DL. Arrestin can act as a regulator of rhodopsin photochemistry. Vision Res. 2006;46:4532\u201346.","journal-title":"Vision Res"},{"key":"147_CR46","doi-asserted-by":"crossref","first-page":"9407","DOI":"10.1074\/jbc.M510037200","volume":"281","author":"ME Sommer","year":"2006","unstructured":"Sommer ME, Smith WC, Farrens DL. Dynamics of arrestin\u2013rhodopsin interactions: acidic phospholipids enable binding of arrestin to purified rhodopsin in detergent. J Biol Chem. 2006;281:9407\u201317.","journal-title":"J Biol Chem"},{"key":"147_CR47","doi-asserted-by":"crossref","first-page":"468","DOI":"10.1038\/ng1295-468","volume":"11","author":"SH Huang","year":"1995","unstructured":"Huang SH, Pittler SJ, Huang X, Oliveira L, Berson EL, Dryja TP. Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase. Nat Genet. 1995;11:468\u201371.","journal-title":"Nat Genet"},{"key":"147_CR48","doi-asserted-by":"crossref","first-page":"3249","DOI":"10.1073\/pnas.92.8.3249","volume":"92","author":"ME McLaughlin","year":"1995","unstructured":"McLaughlin ME, Ehrhart TL, Berson EL, Dryja TP. Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa. Proc Natl Acad Sci USA. 1995;92:3249\u201353.","journal-title":"Proc Natl Acad Sci USA"},{"key":"147_CR49","doi-asserted-by":"crossref","first-page":"130","DOI":"10.1038\/ng0693-130","volume":"4","author":"ME McLaughlin","year":"1993","unstructured":"McLaughlin ME, Sandberg MA, Berson EL, Dryja TP. Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa. Nat Genet. 1993;4:130\u20134.","journal-title":"Nat Genet"},{"key":"147_CR50","doi-asserted-by":"crossref","first-page":"67","DOI":"10.1038\/75621","volume":"25","author":"G Clarke","year":"2000","unstructured":"Clarke G, Goldberg AF, Vidgen D, Collins L, Ploder L, Schwarz L, et al. Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis. Nat Genet. 2000;25:67\u201373.","journal-title":"Nat Genet"},{"key":"147_CR51","doi-asserted-by":"crossref","first-page":"4884","DOI":"10.1073\/pnas.0501233102","volume":"102","author":"TP Dryja","year":"2005","unstructured":"Dryja TP, McGee TL, Berson EL, Fishman GA, Sandberg MA, Alexander KR, et al. Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6. Proc Natl Acad Sci USA. 2005;102:4884\u20139.","journal-title":"Proc Natl Acad Sci USA"},{"key":"147_CR52","doi-asserted-by":"crossref","first-page":"4328","DOI":"10.1167\/iovs.05-0526","volume":"46","author":"C Zeitz","year":"2005","unstructured":"Zeitz C, van Genderen M, Neidhardt J, Luhmann UF, Hoeben F, Forster U, et al. Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram. Invest Ophthalmol Vis Sci. 2005;46:4328\u201335.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR53","doi-asserted-by":"crossref","first-page":"471","DOI":"10.1093\/hmg\/ddl480","volume":"16","author":"V Vasireddy","year":"2007","unstructured":"Vasireddy V, Uchida Y, Salem N Jr, Kim SY, Mandal MNA, Reddy GB, et al. Loss of functional ELOVL4 depletes very long-chain fatty acids (\u2265C28) and the unique \u03c9-O-acylceramides in skin leading to neonatal death. Hum Mol Genet. 2007;16:471\u201382.","journal-title":"Hum Mol Genet"},{"key":"147_CR54","doi-asserted-by":"crossref","first-page":"89","DOI":"10.1038\/83817","volume":"27","author":"K Zhang","year":"2001","unstructured":"Zhang K, Kniazeva M, Han M, Li W, Yu Z, Yang Z, et al. A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy. Nat Genet. 2001;27:89\u201393.","journal-title":"Nat Genet"},{"key":"147_CR55","doi-asserted-by":"crossref","first-page":"557","DOI":"10.1038\/35000601","volume":"403","author":"CK Chen","year":"2000","unstructured":"Chen CK, Burns ME, He W, Wensel TG, Baylor DA, Simon MI. Slowed recovery of rod photoresponse in mice lacking the GTPase accelerating protein RGS9-1. Nature. 2000;403:557\u201360.","journal-title":"Nature"},{"key":"147_CR56","doi-asserted-by":"crossref","first-page":"9755","DOI":"10.1073\/pnas.152094799","volume":"99","author":"G Hu","year":"2002","unstructured":"Hu G, Wensel TG. R9AP, a membrane anchor for the photoreceptor GTPase accelerating protein, RGS9-1. Proc Natl Acad Sci USA. 2002;99:9755\u201360.","journal-title":"Proc Natl Acad Sci USA"},{"key":"147_CR57","doi-asserted-by":"crossref","first-page":"14550","DOI":"10.1074\/jbc.M212046200","volume":"278","author":"G Hu","year":"2003","unstructured":"Hu G, Zhang Z, Wensel TG. Activation of RGS9-1GTPase acceleration by its membrane anchor, R9AP. J Biol Chem. 2003;278:14550\u20134.","journal-title":"J Biol Chem"},{"key":"147_CR58","doi-asserted-by":"crossref","first-page":"2052","DOI":"10.1016\/j.visres.2008.03.010","volume":"48","author":"TG Wensel","year":"2008","unstructured":"Wensel TG. Signal transducing membrane complexes of photoreceptor outer segments. Vision Res. 2008;48:2052\u201361.","journal-title":"Vision Res"},{"key":"147_CR59","doi-asserted-by":"crossref","first-page":"516","DOI":"10.1016\/j.ajhg.2007.11.007","volume":"82","author":"CJF Boon","year":"2008","unstructured":"Boon CJF, Klevering BJ, Hoyng CB, Zonneveld-Vrieling MN, Nabuurs SB, Blokland E, et al. Basal laminar drusen caused by compound heterozygous variants in the CFH gene. Am J Hum Genet. 2008;82:516\u201323.","journal-title":"Am J Hum Genet"},{"key":"147_CR60","doi-asserted-by":"crossref","first-page":"1122","DOI":"10.4161\/cc.6.9.4157","volume":"6","author":"DJ Cameron","year":"2007","unstructured":"Cameron DJ, Yang Z, Gibbs D, Chen H, Kaminoh Y, Jorgensen A, et al. HTRA1 variant confers similar risks to geographic atrophy and neovascular age-related macular degeneration. Cell Cycle. 2007;6:1122\u20135.","journal-title":"Cell Cycle"},{"key":"147_CR61","doi-asserted-by":"crossref","first-page":"690","DOI":"10.1016\/j.visres.2007.10.014","volume":"48","author":"H Chen","year":"2008","unstructured":"Chen H, Yang Z, Gibbs D, Yang X, Hau V, Zhao P, et al. Association of HTRA1 polymorphism and bilaterality in advanced age-related macular degeneration. Vision Res. 2008;48:690\u20134.","journal-title":"Vision Res"},{"key":"147_CR62","doi-asserted-by":"crossref","first-page":"989","DOI":"10.1126\/science.1133807","volume":"314","author":"A Dewan","year":"2006","unstructured":"Dewan A, Liu M, Hartman S, Zhang SS, Liu DT, Zhao C, et al. HTRA1 promoter polymorphism in wet age-related macular degeneration. Science. 2006;314:989\u201392.","journal-title":"Science"},{"key":"147_CR63","doi-asserted-by":"crossref","first-page":"421","DOI":"10.1126\/science.1110189","volume":"308","author":"AO Edwards","year":"2005","unstructured":"Edwards AO, Ritter R III, Abel KJ, Manning A, Panhuysen C, Farrer LA. Complement factor H polymorphism and age-related macular degeneration. Science. 2005;308:421\u20134.","journal-title":"Science"},{"key":"147_CR64","doi-asserted-by":"crossref","first-page":"458","DOI":"10.1038\/ng1750","volume":"38","author":"B Gold","year":"2006","unstructured":"Gold B, Merriam JE, Zernant J, Hancox LS, Taiber AJ, Gehrs K, et al. Variation in factor B (BF) and complement component 2 (C2) genes is associated with age-related macular degeneration. Nat Genet. 2006;38:458\u201362.","journal-title":"Nat Genet"},{"key":"147_CR65","doi-asserted-by":"crossref","first-page":"7227","DOI":"10.1073\/pnas.0501536102","volume":"102","author":"GS Hageman","year":"2005","unstructured":"Hageman GS, Anderson DH, Johnson LV, Hancox LS, Taiber AJ, Hardisty LI, et al. A common haplotype in the complement regulatory gene factor H (HF1\/CFH) predisposes individuals to age-related macular degeneration. Proc Natl Acad Sci USA. 2005;102:7227\u201332.","journal-title":"Proc Natl Acad Sci USA"},{"key":"147_CR66","doi-asserted-by":"crossref","first-page":"389","DOI":"10.1086\/444437","volume":"77","author":"J Jakobsdottir","year":"2005","unstructured":"Jakobsdottir J, Conley YP, Weeks DE, Mah TS, Ferrell RE, Gorin MB. Susceptibility genes for age-related maculopathy on chromosome 10q26. Am J Hum Genet. 2005;77:389\u2013407.","journal-title":"Am J Hum Genet"},{"key":"147_CR67","doi-asserted-by":"crossref","first-page":"308","DOI":"10.1038\/ng1193-308","volume":"5","author":"J Kaplan","year":"1993","unstructured":"Kaplan J, Gerber S, Larget-Piet D, Rozet JM, Dollfus H, Dufier JL, et al. A gene for Stargardt\u2019s disease (fundus flavimaculatus) maps to the short arm of chromosome 1. Nat Genet. 1993;5:308\u201311.","journal-title":"Nat Genet"},{"key":"147_CR68","doi-asserted-by":"crossref","first-page":"1200","DOI":"10.1038\/ng2131","volume":"39","author":"JB Maller","year":"2007","unstructured":"Maller JB, Fagerness JA, Reynolds RC, Neale BM, Daly MJ, Seddon JM. Variation in complement factor 3 is associated with risk of age-related macular degeneration. Nat Genet. 2007;39:1200\u20131.","journal-title":"Nat Genet"},{"key":"147_CR69","doi-asserted-by":"crossref","first-page":"346","DOI":"10.1056\/NEJMoa040833","volume":"351","author":"EM Stone","year":"2004","unstructured":"Stone EM, Braun TA, Russell SR, Kuehn MH, Lotery AJ, Moore PA, et al. Missense variations in the fibulin 5 gene and age-related macular degeneration. N Engl J Med. 2004;351:346\u201353.","journal-title":"N Engl J Med"},{"key":"147_CR70","doi-asserted-by":"crossref","first-page":"553","DOI":"10.1056\/NEJMoa072618","volume":"357","author":"JRW Yates","year":"2007","unstructured":"Yates JRW, Sepp T, Matharu BK, Khan JC, Thurlby DA, Shahid H, et al. Complement C3 variant and the risk of age-related macular degeneration. N Engl J Med. 2007;357:553\u201361.","journal-title":"N Engl J Med"},{"key":"147_CR71","doi-asserted-by":"crossref","first-page":"3187","DOI":"10.1167\/iovs.05-1493","volume":"47","author":"JA Phipps","year":"2006","unstructured":"Phipps JA, Yee P, Fletcher EL, Vingrys AJ. Rod photoreceptor dysfunction in diabetes: activation, deactivation, and dark adaptation. Invest Ophthalmol Vis Sci. 2006;47:3187\u201394.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR72","doi-asserted-by":"crossref","first-page":"131","DOI":"10.1136\/bjo.2010.183756","volume":"95","author":"SS Choi","year":"2011","unstructured":"Choi SS, Zawadzki RJ, Lim MC, Brandt JD, Keltner JL, Doble N, et al. Evidence of outer retinal changes in glaucoma patients as revealed by ultrahigh-resolution in vivo retinal imaging. Br J Ophthalmol. 2011;95:131\u201341.","journal-title":"Br J Ophthalmol"},{"key":"147_CR73","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1016\/S1350-9462(97)00012-8","volume":"17","author":"AH Milam","year":"1998","unstructured":"Milam AH, Li ZY, Fariss RN. Histopathology of the human retina in retinitis pigmentosa. Prog Retin Eye Res. 1998;17:175\u2013205.","journal-title":"Prog Retin Eye Res"},{"key":"147_CR74","doi-asserted-by":"crossref","first-page":"2713","DOI":"10.1002\/cne.22703","volume":"519","author":"BW Jones","year":"2011","unstructured":"Jones BW, Kondo M, Terasaki H, Watt CB, Rapp K, Anderson J, et al. Retinal remodeling in the Tg p347l rabbit, a large-eye model of retinal degeneration. J Comp Neurol. 2011;519:2713\u201333.","journal-title":"J Comp Neurol"},{"key":"147_CR75","doi-asserted-by":"crossref","first-page":"879","DOI":"10.1016\/S0042-6989(02)00493-5","volume":"43","author":"C Varela","year":"2003","unstructured":"Varela C, Igartua I, De la Rosa EJ, De la Villa P. Functional modifications in rod bipolar cells in a mouse model of retinitis pigmentosa. Vision Res. 2003;43:879\u201385.","journal-title":"Vision Res"},{"key":"147_CR76","doi-asserted-by":"crossref","first-page":"473","DOI":"10.1002\/cne.22029","volume":"514","author":"J Chua","year":"2009","unstructured":"Chua J, Fletcher EL, Kalloniatis M. Functional remodeling of glutamate receptors by inner retinal neurons occurs from an early stage of retinal degeneration. J Comp Neurol. 2009;514:473\u201391.","journal-title":"J Comp Neurol"},{"key":"147_CR77","doi-asserted-by":"crossref","first-page":"1121","DOI":"10.1038\/80639","volume":"3","author":"YW Peng","year":"2000","unstructured":"Peng YW, Hao Y, Petters RM, Wong F. Ectopic synaptogenesis in the mammalian retina caused by rod photoreceptor-specific mutations. Nat Neurosci. 2000;3:1121\u20137.","journal-title":"Nat Neurosci"},{"key":"147_CR78","doi-asserted-by":"crossref","first-page":"341","DOI":"10.1007\/s004410100453","volume":"306","author":"SJ Park","year":"2001","unstructured":"Park SJ, Kim IB, Choi KR, Moon JI, Oh SJ, Chung JW, et al. Reorganization of horizontal cell processes in the developing FVB\/N mouse retina. Cell Tissue Res. 2001;306:341\u20136.","journal-title":"Cell Tissue Res"},{"key":"147_CR79","doi-asserted-by":"crossref","unstructured":"Marc RE, Jones BW, Watt CB. Retinal remodeling: circuitry revisions triggered by photoreceptor degeneration. In: Pinaud R, Tremere L, De Weerd P, editors. Plasticity in the visual system: from genes to circuits. New York: Springer; 2006. p. 33\u201354.","DOI":"10.1007\/0-387-28190-8_3"},{"key":"147_CR80","doi-asserted-by":"crossref","first-page":"805","DOI":"10.1016\/S0161-6420(95)30953-0","volume":"102","author":"ZY Li","year":"1995","unstructured":"Li ZY, Possin DE, Milam AH. Histopathology of bone spicule pigmentation in retinitis pigmentosa. Ophthalmology. 1995;102:805\u201316.","journal-title":"Ophthalmology"},{"issue":"Suppl 1","key":"147_CR81","doi-asserted-by":"crossref","first-page":"S10","DOI":"10.1016\/S0039-6257(99)00086-7","volume":"44","author":"CW Spraul","year":"1999","unstructured":"Spraul CW, Lang GE, Grossniklaus HE, Lang GK. Histologic and morphometric analysis of the choroid, Bruch\u2019s membrane, and retinal pigment epithelium in postmortem eyes with age-related macular degeneration and histologic examination of surgically excised choroidal neovascular membranes. Surv Ophthalmol. 1999;44(Suppl 1):S10\u201332.","journal-title":"Surv Ophthalmol"},{"key":"147_CR82","first-page":"489","volume":"17","author":"LD Carter-Dawson","year":"1978","unstructured":"Carter-Dawson LD, LaVail MM, Sidman RL. Differential effect of the rd mutation on rods and cones in the mouse retina. Invest Ophthalmol Vis Sci. 1978;17:489\u201398.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR83","author":"DJ Margolis","year":"2011","unstructured":"Margolis DJ, Detwiler PB. Cellular origin of spontaneous ganglion cell spike activity in animal models of retinitis pigmentosa. J Ophthalmol. 2011. doi: 10.1155\/2011\/507037 .","journal-title":"J Ophthalmol"},{"key":"147_CR84","doi-asserted-by":"crossref","first-page":"3260","DOI":"10.1152\/jn.00663.2009","volume":"102","author":"C Sekirnjak","year":"2009","unstructured":"Sekirnjak C, Hulse C, Jepson LH, Hottowy P, Sher A, Dabrowski W, et al. Loss of responses to visual but not electrical stimulation in ganglion cells of rats with severe photoreceptor degeneration. J Neurophysiol. 2009;102:3260\u20139.","journal-title":"J Neurophysiol"},{"key":"147_CR85","first-page":"424","volume":"39","author":"GP Lewis","year":"1998","unstructured":"Lewis GP, Linberg KA, Fisher SK. Neurite outgrowth from bipolar and horizontal cells after experimental retinal detachment. Invest Ophthalmol Vis Sci. 1998;39:424\u201334.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR86","first-page":"1674","volume":"12","author":"KA Linberg","year":"2006","unstructured":"Linberg KA, Lewis GP, Matsumoto B, Fisher SK. Immunocytochemical evidence that rod-connected horizontal cell axon terminals remodel in response to experimental retinal detachment in the cat. Mol Vis. 2006;12:1674\u201386.","journal-title":"Mol Vis"},{"key":"147_CR87","doi-asserted-by":"crossref","first-page":"685","DOI":"10.1002\/neu.480220704","volume":"22","author":"RO Wong","year":"1991","unstructured":"Wong RO, Herrmann K, Shatz CJ. Remodeling of retinal ganglion cell dendrites in the absence of action potential activity. J Neurobiol. 1991;22:685\u201397.","journal-title":"J Neurobiol"},{"key":"147_CR88","doi-asserted-by":"crossref","first-page":"1669","DOI":"10.1167\/iovs.05-0845","volume":"47","author":"WA Beltran","year":"2006","unstructured":"Beltran WA, Hammond P, Acland GM, Aguirre GD. A frameshift mutation in RPGR exon ORF15 causes photoreceptor degeneration and inner retina remodeling in a model of X-linked retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2006;47:1669\u201381.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR89","doi-asserted-by":"crossref","first-page":"481","DOI":"10.1007\/s00441-009-0916-5","volume":"339","author":"A Ray","year":"2010","unstructured":"Ray A, Sun GJ, Chan L, Grzywacz NM, Weiland J, Lee EJ. Morphological alterations in retinal neurons in the S334ter-line3 transgenic rat. Cell Tissue Res. 2010;339:481\u201391.","journal-title":"Cell Tissue Res"},{"key":"147_CR90","doi-asserted-by":"crossref","first-page":"2161","DOI":"10.1167\/iovs.05-0595","volume":"47","author":"I Iandiev","year":"2006","unstructured":"Iandiev I, Uckermann O, Pannicke T, Wurm A, Tenckhoff S, Pietsch UC, et al. Glial cell reactivity in a porcine model of retinal detachment. Invest Ophthalmol Vis Sci. 2006;47:2161\u201371.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR91","doi-asserted-by":"crossref","first-page":"501","DOI":"10.1167\/iovs.11-8784","volume":"53","author":"JW Ross","year":"2012","unstructured":"Ross JW, Fernandez de Castro JP, Zhao J, Samuel M, Walters E, Rios C, et al. Generation of an inbred miniature pig model of retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2012;53:501\u20137.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR92","doi-asserted-by":"crossref","first-page":"355","DOI":"10.3390\/molecules17010355","volume":"17","author":"JR Anderson","year":"2011","unstructured":"Anderson JR, Bones JW, Watt CB, Shaw MV, Yang JH, Demill D, et al. Exploring the retinal connectome. Mol Vis. 2011;17:355\u201379.","journal-title":"Mol Vis"},{"key":"147_CR93","doi-asserted-by":"crossref","first-page":"273","DOI":"10.1016\/j.exer.2010.05.020","volume":"91","author":"N Cuenca","year":"2010","unstructured":"Cuenca N, Pinilla I, Fern\u00e1ndez-S\u00e1nchez L, Salinas-Navarro M, Alarc\u00f3n-Mart\u00ednez L, Avil\u00e9s-Trigueros M, et al. Changes in the inner and outer retinal layers after acute increase of the intraocular pressure in adult albino Swiss mice. Exp Eye Res. 2010;91:273\u201385.","journal-title":"Exp Eye Res"},{"key":"147_CR94","doi-asserted-by":"crossref","first-page":"311","DOI":"10.1016\/j.nbd.2010.06.005","volume":"40","author":"MG Yefimova","year":"2010","unstructured":"Yefimova MG, Messaddeq N, Karam A, Jacquard C, Weber C, Jonet L, et al. Polyglutamine toxicity induces rod photoreceptor division, morphological transformation or death in spinocerebellar ataxia 7 mouse retina. Neurobiol Dis. 2010;40:311\u201324.","journal-title":"Neurobiol Dis"},{"key":"147_CR95","doi-asserted-by":"crossref","first-page":"807","DOI":"10.1017\/S095252380623013X","volume":"23","author":"SI Firth","year":"2006","unstructured":"Firth SI, Feller MB. Dissociated GABAergic retinal interneurons exhibit spontaneous increases in intracellular calcium. Vis Neurosci. 2006;23:807\u201314.","journal-title":"Vis Neurosci"},{"key":"147_CR96","doi-asserted-by":"crossref","first-page":"4115","DOI":"10.1523\/JNEUROSCI.07-12-04115.1987","volume":"7","author":"T Voigt","year":"1987","unstructured":"Voigt T, Wassle H. Dopaminergic innervation of A II amacrine cells in mammalian retina. J Neurosci. 1987;7:4115\u201328.","journal-title":"J Neurosci"},{"key":"147_CR97","doi-asserted-by":"crossref","first-page":"267","DOI":"10.1002\/cne.903100210","volume":"310","author":"H Kolb","year":"1991","unstructured":"Kolb H, Cuenca N, Dekorver L. Postembedding immunocytochemistry for GABA and glycine reveals the synaptic relationships of the dopaminergic amacrine cell of the cat retina. J Comp Neurol. 1991;310:267\u201384.","journal-title":"J Comp Neurol"},{"key":"147_CR98","doi-asserted-by":"crossref","first-page":"6776","DOI":"10.1523\/JNEUROSCI.18-17-06776.1998","volume":"18","author":"A Feigenspan","year":"1998","unstructured":"Feigenspan A, Gustincich S, Bean BP, Raviola E. Spontaneous activity of solitary dopaminergic cells of the retina. J Neurosci. 1998;18:6776\u201389.","journal-title":"J Neurosci"},{"key":"147_CR99","unstructured":"Jones BW, Marc RE, Watt CB. Dopaminergic amacrine and interplexiform cells exhibit glutamatergic signatures. Invest Ophthalmol Vis Sci. 2004;45:E (abstract 5435)."},{"key":"147_CR100","doi-asserted-by":"crossref","first-page":"650","DOI":"10.1002\/jnr.22216","volume":"88","author":"JE VanLeeuwen","year":"2010","unstructured":"VanLeeuwen JE, Petzinger GM, Walsh JP, Akopian GK, Vuckovic M, Jakowec MW. Altered AMPA receptor expression with treadmill exercise in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-lesioned mouse model of basal ganglia injury. J Neurosci Res. 2010;88:650\u201368.","journal-title":"J Neurosci Res"},{"key":"147_CR101","doi-asserted-by":"crossref","first-page":"1720","DOI":"10.1126\/science.1084174","volume":"301","author":"M Kim","year":"2003","unstructured":"Kim M, Carman CV, Springer TA. Bidirectional transmembrane signaling by cytoplasmic domain separation in integrins. Science. 2003;301:1720\u20135.","journal-title":"Science"},{"key":"147_CR102","doi-asserted-by":"crossref","first-page":"485","DOI":"10.1146\/annurev.biophys.31.101101.140922","volume":"31","author":"M Shimaoka","year":"2002","unstructured":"Shimaoka M, Takagi J, Springer TA. Conformational regulation of integrin structure and function. Annu Rev Biophys Biomol Struct. 2002;31:485\u2013516.","journal-title":"Annu Rev Biophys Biomol Struct"},{"key":"147_CR103","doi-asserted-by":"crossref","first-page":"1708","DOI":"10.1126\/science.1064829","volume":"294","author":"E Cukierman","year":"2001","unstructured":"Cukierman E, Pankov R, Stevens DR, Yamada KM. Taking cell-matrix adhesions to the third dimension. Science. 2001;294:1708\u201312.","journal-title":"Science"},{"key":"147_CR104","doi-asserted-by":"crossref","unstructured":"Kremer H, van Wijk E, M\u00e4rker T, Wolfrum U, Roepman R. Usher syndrome: molecular links of pathogenesis, proteins and pathways. Hum Mol Genet. 2006;15(Spec No 2):R262\u201370.","DOI":"10.1093\/hmg\/ddl205"},{"key":"147_CR105","first-page":"81","volume":"36","author":"Y Lin","year":"2011","unstructured":"Lin Y, Jones BW, Liu A, Tucker JF, Rapp K, Luo L, et al. Retinoid receptors trigger neuritogenesis in retinal degenerations. FASEB J. 2011;36:81\u201392.","journal-title":"FASEB J"},{"key":"147_CR106","first-page":"5592","volume":"51","author":"Y Lin","year":"2010","unstructured":"Lin Y, Jones BW, Rapp K, Shaw MV, Yang J-H, Watt CB, et al. Roles of retinoic acid signaling in neuritogenesis during light-induced retinal degeneration. ARVO Meeting Abstracts. 2010;51:5592.","journal-title":"ARVO Meeting Abstracts"},{"key":"147_CR107","first-page":"1846","volume":"52","author":"Y Lin","year":"2011","unstructured":"Lin Y, Jones BW, Rapp K, Shaw MV, Yang J-H, Watt CB, et al. CaMKII signaling is contributive to neuritogenesis in light-induced retinal degeneration. ARVO Meeting Abstracts. 2011;52:1846.","journal-title":"ARVO Meeting Abstracts"},{"key":"147_CR108","doi-asserted-by":"crossref","first-page":"560","DOI":"10.1002\/1096-9861(20001002)425:4<560::AID-CNE7>3.0.CO;2-D","volume":"425","author":"RE Marc","year":"2000","unstructured":"Marc RE, Liu W. Fundamental GABAergic amacrine cell circuitries in the retina: nested feedback, concatenated inhibition, and axosomatic synapses. J Comp Neurol. 2000;425:560\u201382.","journal-title":"J Comp Neurol"},{"key":"147_CR109","doi-asserted-by":"crossref","first-page":"e1000074","DOI":"10.1371\/journal.pbio.1000074","volume":"7","author":"JR Anderson","year":"2009","unstructured":"Anderson JR, Jones BW, Yang J-H, Shaw MV, Watt CB, Koshevoy P, et al. A computational framework for ultrastructural mapping of neural circuitry. PLoS Biol. 2009;7:e1000074.","journal-title":"PLoS Biol"},{"key":"147_CR110","doi-asserted-by":"crossref","first-page":"1371","DOI":"10.1167\/iovs.08-2863","volume":"50","author":"M Kondo","year":"2009","unstructured":"Kondo M, Sakai T, Komeima K, Kurimoto Y, Ueno S, Nishizawa Y, et al. Generation of a transgenic rabbit model of retinal degeneration. Invest Ophthalmol Vis Sci. 2009;50:1371\u20137.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR111","doi-asserted-by":"crossref","first-page":"270","DOI":"10.1038\/81555","volume":"26","author":"A Gal","year":"2000","unstructured":"Gal A, Li Y, Thompson DA, Weir J, Orth U, Jacobson SG, et al. Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa. Nat Genet. 2000;26:270\u20131.","journal-title":"Nat Genet"},{"key":"147_CR112","doi-asserted-by":"crossref","first-page":"508","DOI":"10.1111\/j.1460-9568.2010.07085.x","volume":"31","author":"MJ Seiler","year":"2010","unstructured":"Seiler MJ, Aramant RB, Thomas BB, Peng Q, Sadda SR, Keirstead HS. Visual restoration and transplant connectivity in degenerate rats implanted with retinal progenitor sheets. Eur J Neurosci. 2010;31:508\u201320.","journal-title":"Eur J Neurosci"},{"key":"147_CR113","doi-asserted-by":"crossref","first-page":"153","DOI":"10.1016\/j.jns.2009.02.370","volume":"283","author":"SJ Baloyannis","year":"2009","unstructured":"Baloyannis SJ. Dendritic pathology in Alzheimer\u2019s disease. J Neurol Sci. 2009;283:153\u20137.","journal-title":"J Neurol Sci"},{"key":"147_CR114","doi-asserted-by":"crossref","first-page":"306","DOI":"10.1006\/exnr.1999.7259","volume":"161","author":"PT Bywood","year":"2000","unstructured":"Bywood PT, Johnson SM. Dendrite loss is a characteristic early indicator of toxin-induced neurodegeneration in rat midbrain slices. Exp Neurol. 2000;161:306\u201316.","journal-title":"Exp Neurol"},{"issue":"Suppl 2","key":"147_CR115","doi-asserted-by":"crossref","first-page":"30","DOI":"10.1111\/j.1528-1167.2008.02008.x","volume":"50","author":"DA Prince","year":"2009","unstructured":"Prince DA, Parada I, Scalise K, Graber K, Shen F. Epilepsy following cortical injury: cellular and molecular mechanisms as targets for potential prophylaxis. Epilepsia. 2009;50(Suppl 2):30\u201340.","journal-title":"Epilepsia"},{"key":"147_CR116","doi-asserted-by":"crossref","first-page":"741","DOI":"10.1562\/2005-10-05-RA-712","volume":"82","author":"T Duncan","year":"2006","unstructured":"Duncan T, Wiggert B, Whittaker N, Darrow R, Organisciak DT. Effect of visible light on normal and p23h-3 transgenic rat retinas: characterization of a novel retinoic acid derivative present in the p23h-3 retina. Photochem Photobiol. 2006;82:741\u20135.","journal-title":"Photochem Photobiol"},{"key":"147_CR117","doi-asserted-by":"crossref","first-page":"739","DOI":"10.1002\/neu.20241","volume":"66","author":"M Clagett-Dame","year":"2006","unstructured":"Clagett-Dame M, McNeill E, Muley P. Role of all-trans retinoic acid in neurite outgrowth and axonal elongation. J Neurobiol. 2006;66:739\u201356.","journal-title":"J Neurobiol"},{"key":"147_CR118","doi-asserted-by":"crossref","first-page":"1103","DOI":"10.1016\/S0896-6273(02)01049-8","volume":"36","author":"TC Thiagarajan","year":"2002","unstructured":"Thiagarajan TC, Piedras-Renteria ES, Tsien RW. Alpha and beta CAMKII: inverse regulation by neuronal activity and opposing effects on synaptic strength. Neuron. 2002;36:1103\u201314.","journal-title":"Neuron"},{"key":"147_CR119","first-page":"4488","volume":"51","author":"L Jiang","year":"2011","unstructured":"Jiang L, Boye SL, Dizhoor A, Hauswirth WW, Baehr W. Knock-down of GCAP1 by RNA interference delays photoreceptor degeneration in GCAP1-Y99C transgenic mice. Invest Ophthalmol Vis Sci. 2011;51:4488.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR120","doi-asserted-by":"crossref","first-page":"542","DOI":"10.1038\/nature730","volume":"416","author":"N Terada","year":"2002","unstructured":"Terada N, Hamazaki T, Oka M, Hoki M, Mastalerz DM, Nakano Y, et al. Bone marrow cells adopt the phenotype of other cells by spontaneous cell fusion. Nature. 2002;416:542\u20135.","journal-title":"Nature"},{"key":"147_CR121","doi-asserted-by":"crossref","first-page":"446","DOI":"10.1167\/iovs.06-0190","volume":"48","author":"K Canola","year":"2007","unstructured":"Canola K, Ang\u00e9nieux B, Tekaya M, Quiambao A, Naash MI, Munier FL, et al. Retinal stem cells transplanted into models of late stages of retinitis pigmentosa preferentially adopt a glial or a retinal ganglion cell fate. Invest Ophthalmol Vis Sci. 2007;48:446\u201354.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR122","doi-asserted-by":"crossref","first-page":"3449","DOI":"10.1167\/iovs.08-1770","volume":"49","author":"ND Bull","year":"2008","unstructured":"Bull ND, Limb GA, Martin KR. Human Muller stem cell (MIO-M1) transplantation in a rat model of glaucoma: survival, differentiation, and integration. Invest Ophthalmol Vis Sci. 2008;49:3449\u201356.","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"147_CR123","doi-asserted-by":"crossref","first-page":"413","DOI":"10.1126\/science.1190897","volume":"329","author":"V Busskamp","year":"2010","unstructured":"Busskamp V, Duebel J, Balya D, Fradot M, Viney TJ, Siegert S, et al. Genetic reactivation of cone photoreceptors restores visual responses in retinitis pigmentosa. Science. 2010;329:413\u20137.","journal-title":"Science"},{"key":"147_CR124","doi-asserted-by":"crossref","first-page":"667","DOI":"10.1038\/nn.2117","volume":"11","author":"P Lagali","year":"2008","unstructured":"Lagali P, Balya D, Awatramani GB, M\u00fcnch TA, Kim DS, Busskamp V, et al. Light-activated channels targeted to ON bipolar cells restore visual function in retinal degeneration. Nat Neurosci. 2008;11:667\u201375.","journal-title":"Nat Neurosci"},{"key":"147_CR125","doi-asserted-by":"crossref","first-page":"1220","DOI":"10.1038\/mt.2011.69","volume":"19","author":"MM Doroudchi","year":"2011","unstructured":"Doroudchi MM, Greenberg KP, Liu J, Silka KA, Boyden ES, Lockridge JA, et al. Virally delivered channelrhodopsin-2 safely and effectively restores visual function in multiple mouse models of blindness. Mol Ther. 2011;19:1220\u20139.","journal-title":"Mol Ther"},{"key":"147_CR126","doi-asserted-by":"crossref","unstructured":"Marc R. Injury and repair: retinal remodeling. In: Dana R, editor. Encyclopedia of the eye. Amsterdam: Elsevier; 2009.","DOI":"10.1016\/B978-0-12-374203-2.00220-7"},{"key":"147_CR127","first-page":"1680","volume":"15","author":"E Ivanova","year":"2009","unstructured":"Ivanova E, Pan Z-H. Evaluation of the adeno-associated virus mediated long-term expression of channelrhodopsin-2 in the mouse retina. Mol Vis. 2009;15:1680\u20139.","journal-title":"Mol Vis"}],"container-title":["Japanese Journal of Ophthalmology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10384-012-0147-2.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s10384-012-0147-2\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10384-012-0147-2","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,3,29]],"date-time":"2025-03-29T00:22:35Z","timestamp":1743207755000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s10384-012-0147-2"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,5,30]]},"references-count":127,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2012,7]]}},"alternative-id":["147"],"URL":"https:\/\/doi.org\/10.1007\/s10384-012-0147-2","relation":{},"ISSN":["0021-5155","1613-2246"],"issn-type":[{"value":"0021-5155","type":"print"},{"value":"1613-2246","type":"electronic"}],"subject":[],"published":{"date-parts":[[2012,5,30]]}}}