-
1
-
-
31644446394
-
Mouse models of age-related macular degeneration
-
Rakoczy EP, Yu MJ, Nusinowitz S, Chang B, Heckenlively JR. Mouse models of age-related macular degeneration. Exp Eye Res. 2006;82:741-752.
-
(2006)
Exp Eye Res.
, vol.82
, pp. 741-752
-
-
Rakoczy, E.P.1
Yu, M.J.2
Nusinowitz, S.3
Chang, B.4
Heckenlively, J.R.5
-
2
-
-
0018611506
-
Rods and cones in the mouse retina. I. Structural analysis using light and electron microscopy
-
Carter-Dawson LD, LaVail MM. Rods and cones in the mouse retina. I. Structural analysis using light and electron microscopy. J Comp Neurol. 1979;188:245-262.
-
(1979)
J Comp Neurol.
, vol.188
, pp. 245-262
-
-
Carter-Dawson, L.D.1
LaVail, M.M.2
-
3
-
-
77954879972
-
Transcriptional regulation of photoreceptor development and homeostasis in the mammalian retina
-
Swaroop A, Kim D, Forrest D. Transcriptional regulation of photoreceptor development and homeostasis in the mammalian retina. Nat Rev Neurosci. 2010;11:563-576.
-
(2010)
Nat Rev Neurosci.
, vol.11
, pp. 563-576
-
-
Swaroop, A.1
Kim, D.2
Forrest, D.3
-
4
-
-
0035734382
-
Nrl is required for rod photoreceptor development
-
Mears AJ, Kondo M, Swain PK, et al. Nrl is required for rod photoreceptor development. Nat Genet. 2001;29:447-452.
-
(2001)
Nat Genet.
, vol.29
, pp. 447-452
-
-
Mears, A.J.1
Kondo, M.2
Swain, P.K.3
-
5
-
-
33847727462
-
RPE65 is essential for the function of cone photoreceptors in NRL-deficient mice
-
Wenzel A, von Lintig J, Oberhauser V, Tanimoto N, Grimm C, Seeliger MW. RPE65 is essential for the function of cone photoreceptors in NRL-deficient mice. Invest Ophthalmol Vis Sci. 2007;48:534-542.
-
(2007)
Invest Ophthalmol Vis Sci.
, vol.48
, pp. 534-542
-
-
Wenzel, A.1
von Lintig, J.2
Oberhauser, V.3
Tanimoto, N.4
Grimm, C.5
Seeliger, M.W.6
-
6
-
-
70349572811
-
Cone outer segment morphology and cone function in the Rpe65-/-Nrl-/-mouse retina are amenable to retinoid replacement
-
Kunchithapautham K, Coughlin B, Crouch RK, Rohrer B. Cone outer segment morphology and cone function in the Rpe65-/-Nrl-/-mouse retina are amenable to retinoid replacement. Invest Ophthalmol Vis Sci. 2009;50:4858-4864.
-
(2009)
Invest Ophthalmol Vis Sci.
, vol.50
, pp. 4858-4864
-
-
Kunchithapautham, K.1
Coughlin, B.2
Crouch, R.K.3
Rohrer, B.4
-
7
-
-
41949094268
-
Nrl-knockout mice deficient in Rpe65 fail to synthesize 11-cis retinal and cone outer segments
-
Feathers KL, Lyubarsky AL, Khan NW, et al. Nrl-knockout mice deficient in Rpe65 fail to synthesize 11-cis retinal and cone outer segments. Invest Ophthalmol Vis Sci. 2008;49:1126-1135.
-
(2008)
Invest Ophthalmol Vis Sci.
, vol.49
, pp. 1126-1135
-
-
Feathers, K.L.1
Lyubarsky, A.L.2
Khan, N.W.3
-
8
-
-
63149106897
-
In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death
-
Samardzija M, Tanimoto N, Kostic C, et al. In conditions of limited chromophore supply rods entrap 11-cis-retinal leading to loss of cone function and cell death. Hum Mol Genet. 2009; 18:1266-1275.
-
(2009)
Hum Mol Genet.
, vol.18
, pp. 1266-1275
-
-
Samardzija, M.1
Tanimoto, N.2
Kostic, C.3
-
9
-
-
37849031514
-
R91W mutation in Rpe65 leads to milder early-onset retinal dystrophy due to the generation of low levels of 11-cis-retinal
-
Samardzija M, von Lintig J, Tanimoto N, et al. R91W mutation in Rpe65 leads to milder early-onset retinal dystrophy due to the generation of low levels of 11-cis-retinal. Hum Mol Genet. 2008;17:281-292.
-
(2008)
Hum Mol Genet.
, vol.17
, pp. 281-292
-
-
Samardzija, M.1
von Lintig, J.2
Tanimoto, N.3
-
10
-
-
0033862099
-
Early-onset severe rodcone dystrophy in young children with RPE65 mutations
-
Lorenz B, Gyurus P, Preising M, et al. Early-onset severe rodcone dystrophy in young children with RPE65 mutations. Invest Ophthalmol Vis Sci. 2000;41:2735-2742.
-
(2000)
Invest Ophthalmol Vis Sci.
, vol.41
, pp. 2735-2742
-
-
Lorenz, B.1
Gyurus, P.2
Preising, M.3
-
11
-
-
0036181472
-
Retinal degeneration mutants in the mouse
-
Chang B, Hawes NL, Hurd RE, Davisson MT, Nusinowitz S, Heckenlively JR. Retinal degeneration mutants in the mouse. Vision Res. 2002;42:517-525.
-
(2002)
Vision Res.
, vol.42
, pp. 517-525
-
-
Chang, B.1
Hawes, N.L.2
Hurd, R.E.3
Davisson, M.T.4
Nusinowitz, S.5
Heckenlively, J.R.6
-
12
-
-
1842570287
-
Phototransduction in transgenic mice after targeted deletion of the rod transducin alpha-subunit
-
Calvert PD, Krasnoperova NV, Lyubarsky AL, et al. Phototransduction in transgenic mice after targeted deletion of the rod transducin alpha-subunit. Proc Natl Acad Sci U S A. 2000; 97:13913-13918.
-
(2000)
Proc Natl Acad Sci U S A.
, vol.97
, pp. 13913-13918
-
-
Calvert, P.D.1
Krasnoperova, N.V.2
Lyubarsky, A.L.3
-
13
-
-
0034094703
-
Genetic analysis of RPE65: From human disease to mouse model
-
Redmond TM, Hamel CP. Genetic analysis of RPE65: from human disease to mouse model. Methods Enzymol. 2000;316: 705-724.
-
(2000)
Methods Enzymol.
, vol.316
, pp. 705-724
-
-
Redmond, T.M.1
Hamel, C.P.2
-
14
-
-
23844496400
-
The retinal G protein-coupled receptor (RGR) enhances isomerohydrolase activity independent of light
-
Wenzel A, Oberhauser V, Pugh EN Jr, et al. The retinal G protein-coupled receptor (RGR) enhances isomerohydrolase activity independent of light. J Biol Chem. 2005;280:29874-29884.
-
(2005)
J Biol Chem.
, vol.280
, pp. 29874-29884
-
-
Wenzel, A.1
Oberhauser, V.2
Pugh Jr., E.N.3
-
15
-
-
83055164488
-
Retinal degeneration modulates intracellular localization of CDC42 in photoreceptors
-
Heynen SR, Tanimoto N, Joly S, Seeliger MW, Samardzija M, Grimm C. Retinal degeneration modulates intracellular localization of CDC42 in photoreceptors. Mol Vis. 2011;17:2934-2946.
-
(2011)
Mol Vis.
, vol.17
, pp. 2934-2946
-
-
Heynen, S.R.1
Tanimoto, N.2
Joly, S.3
Seeliger, M.W.4
Samardzija, M.5
Grimm, C.6
-
16
-
-
79956011185
-
HIF1A is essential for the development of the intermediate plexus of the retinal vasculature
-
Caprara C, Thiersch M, Lange C, Joly S, Samardzija M, Grimm C. HIF1A is essential for the development of the intermediate plexus of the retinal vasculature. Invest Ophthalmol Vis Sci. 2011;52:2109-2117.
-
(2011)
Invest Ophthalmol Vis Sci.
, vol.52
, pp. 2109-2117
-
-
Caprara, C.1
Thiersch, M.2
Lange, C.3
Joly, S.4
Samardzija, M.5
Grimm, C.6
-
17
-
-
69449107546
-
Genetic address book for retinal cell types
-
Siegert S, Scherf BG, Del Punta K, Didkovsky N, Heintz N, Roska B. Genetic address book for retinal cell types. Nat Neurosci. 2009;12:1197-1204.
-
(2009)
Nat Neurosci.
, vol.12
, pp. 1197-1204
-
-
Siegert, S.1
Scherf, B.G.2
Del Punta, K.3
Didkovsky, N.4
Heintz, N.5
Roska, B.6
-
18
-
-
84872761888
-
CDC42 is required for tissue lamination and cell survival in the mouse retina
-
Heynen SR, Meneau I, Caprara C, et al. CDC42 is required for tissue lamination and cell survival in the mouse retina. PLoS One. 2013;8:e53806.
-
(2013)
PLoS One.
, vol.8
-
-
Heynen, S.R.1
Meneau, I.2
Caprara, C.3
-
19
-
-
9444222740
-
Rapid quantification of adult and developing mouse spatial vision using a virtual optomotor system
-
Prusky GT, Alam NM, Beekman S, Douglas RM. Rapid quantification of adult and developing mouse spatial vision using a virtual optomotor system. Invest Ophthalmol Vis Sci. 2004;45:4611-4616.
-
(2004)
Invest Ophthalmol Vis Sci.
, vol.45
, pp. 4611-4616
-
-
Prusky, G.T.1
Alam, N.M.2
Beekman, S.3
Douglas, R.M.4
-
20
-
-
32544436444
-
Independent visual threshold measurements in the two eyes of freely moving rats and mice using a virtual-reality optokinetic system
-
Douglas RM, Alam NM, Silver BD, McGill TJ, Tschetter WW, Prusky GT. Independent visual threshold measurements in the two eyes of freely moving rats and mice using a virtual-reality optokinetic system. Vis Neurosci. 2005;22:677-684.
-
(2005)
Vis Neurosci.
, vol.22
, pp. 677-684
-
-
Douglas, R.M.1
Alam, N.M.2
Silver, B.D.3
McGill, T.J.4
Tschetter, W.W.5
Prusky, G.T.6
-
21
-
-
84863723643
-
The Rd8 mutation of the Crb1 gene is present in vendor lines of C57BL/ 6N mice and embryonic stem cells, and confounds ocular induced mutant phenotypes
-
Mattapallil MJ, Wawrousek EF, Chan CC, et al. The Rd8 mutation of the Crb1 gene is present in vendor lines of C57BL/ 6N mice and embryonic stem cells, and confounds ocular induced mutant phenotypes. Invest Ophthalmol Vis Sci. 2012; 53:2921-2927.
-
(2012)
Invest Ophthalmol Vis Sci.
, vol.53
, pp. 2921-2927
-
-
Mattapallil, M.J.1
Wawrousek, E.F.2
Chan, C.C.3
-
22
-
-
10744224972
-
CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina
-
Mehalow AK, Kameya S, Smith RS, et al. CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina. Hum Mol Genet. 2003;12:2179-2189.
-
(2003)
Hum Mol Genet.
, vol.12
, pp. 2179-2189
-
-
Mehalow, A.K.1
Kameya, S.2
Smith, R.S.3
-
23
-
-
84863393686
-
Preservation of cone photoreceptors after a rapid yet transient degeneration and remodeling in cone-only Nrl-/-mouse retina
-
Roger JE, Ranganath K, Zhao L, et al. Preservation of cone photoreceptors after a rapid yet transient degeneration and remodeling in cone-only Nrl-/-mouse retina. J Neurosci. 2012;32:528-541.
-
(2012)
J Neurosci.
, vol.32
, pp. 528-541
-
-
Roger, J.E.1
Ranganath, K.2
Zhao, L.3
-
24
-
-
3543082672
-
Expression profiling of the developing and mature Nrl-/-mouse retina: Identification of retinal disease candidates and transcriptional regulatory targets of Nrl
-
Yoshida S, Mears AJ, Friedman JS, et al. Expression profiling of the developing and mature Nrl-/-mouse retina: identification of retinal disease candidates and transcriptional regulatory targets of Nrl. Hum Mol Genet. 2004;13:1487-1503.
-
(2004)
Hum Mol Genet.
, vol.13
, pp. 1487-1503
-
-
Yoshida, S.1
Mears, A.J.2
Friedman, J.S.3
-
25
-
-
80052661270
-
Defective photoreceptor phagocytosis in a mouse model of enhanced S-cone syndrome causes progressive retinal degeneration
-
Mustafi D, Kevany BM, Genoud C, et al. Defective photoreceptor phagocytosis in a mouse model of enhanced S-cone syndrome causes progressive retinal degeneration. FASEB J. 2011;25:3157-3176.
-
(2011)
FASEB J.
, vol.25
, pp. 3157-3176
-
-
Mustafi, D.1
Kevany, B.M.2
Genoud, C.3
-
26
-
-
34047161845
-
Afferent control of horizontal cell morphology revealed by genetic respecification of rods and cones
-
Raven MA, Oh EC, Swaroop A, Reese BE. Afferent control of horizontal cell morphology revealed by genetic respecification of rods and cones. J Neurosci. 2007;27:3540-3547.
-
(2007)
J Neurosci.
, vol.27
, pp. 3540-3547
-
-
Raven, M.A.1
Oh, E.C.2
Swaroop, A.3
Reese, B.E.4
-
27
-
-
15244346017
-
Cone-like morphological, molecular, and electrophysiological features of the photoreceptors of the Nrl knockout mouse
-
Daniele LL, Lillo C, Lyubarsky AL, et al. Cone-like morphological, molecular, and electrophysiological features of the photoreceptors of the Nrl knockout mouse. Invest Ophthalmol Vis Sci. 2005;46:2156-2167.
-
(2005)
Invest Ophthalmol Vis Sci.
, vol.46
, pp. 2156-2167
-
-
Daniele, L.L.1
Lillo, C.2
Lyubarsky, A.L.3
-
28
-
-
33845627240
-
Differential role of Jak-STAT signaling in retinal degenerations
-
Samardzija M, Wenzel A, Aufenberg S, Thiersch M, Reme C, Grimm C. Differential role of Jak-STAT signaling in retinal degenerations. FASEB J. 2006;20:2411-2413.
-
(2006)
FASEB J.
, vol.20
, pp. 2411-2413
-
-
Samardzija, M.1
Wenzel, A.2
Aufenberg, S.3
Thiersch, M.4
Reme, C.5
Grimm, C.6
-
29
-
-
73349130033
-
A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene
-
Chang B, Grau T, Dangel S, et al. A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene. Proc Natl Acad Sci U S A. 2009;106:19581-19586.
-
(2009)
Proc Natl Acad Sci U S A.
, vol.106
, pp. 19581-19586
-
-
Chang, B.1
Grau, T.2
Dangel, S.3
-
30
-
-
77954582476
-
cGMP-dependent cone photoreceptor degeneration in the cpfl1 mouse retina
-
Trifunovic D, Dengler K, Michalakis S, Zrenner E, Wissinger B, Paquet-Durand F. cGMP-dependent cone photoreceptor degeneration in the cpfl1 mouse retina. J Comp Neurol. 2010; 518:3604-3617.
-
(2010)
J Comp Neurol.
, vol.518
, pp. 3604-3617
-
-
Trifunovic, D.1
Dengler, K.2
Michalakis, S.3
Zrenner, E.4
Wissinger, B.5
Paquet-Durand, F.6
-
31
-
-
80053037818
-
Rod phosphodiesterase-6 (PDE6) catalytic subunits restore cone function in a mouse model lacking cone PDE6 catalytic subunit
-
Kolandaivelu S, Chang B, Ramamurthy V. Rod phosphodiesterase-6 (PDE6) catalytic subunits restore cone function in a mouse model lacking cone PDE6 catalytic subunit. J Biol Chem. 2011;286:33252-33259.
-
(2011)
J Biol Chem.
, vol.286
, pp. 33252-33259
-
-
Kolandaivelu, S.1
Chang, B.2
Ramamurthy, V.3
-
32
-
-
77951254301
-
Retinal ultrastructure of murine models of dry age-related macular degeneration (AMD)
-
Ramkumar HL, Zhang J, Chan CC. Retinal ultrastructure of murine models of dry age-related macular degeneration (AMD). Prog Retin Eye Res. 2010;29:169-190.
-
(2010)
Prog Retin Eye Res.
, vol.29
, pp. 169-190
-
-
Ramkumar, H.L.1
Zhang, J.2
Chan, C.C.3
-
34
-
-
18244385003
-
The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration
-
Milam AH, Rose L, Cideciyan AV, et al. The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration. Proc Natl Acad Sci U S A. 2002;99: 473-478.
-
(2002)
Proc Natl Acad Sci U S A.
, vol.99
, pp. 473-478
-
-
Milam, A.H.1
Rose, L.2
Cideciyan, A.V.3
-
35
-
-
4544267698
-
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration
-
Jacobson SG, Sumaroka A, Aleman TS, et al. Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration. Hum Mol Genet. 2004;13:1893-1902.
-
(2004)
Hum Mol Genet.
, vol.13
, pp. 1893-1902
-
-
Jacobson, S.G.1
Sumaroka, A.2
Aleman, T.S.3
-
36
-
-
84858052916
-
Defects in the outer limiting membrane are associated with rosette development in the Nrl-/-retina
-
Stuck MW, Conley SM, Naash MI. Defects in the outer limiting membrane are associated with rosette development in the Nrl-/-retina. PLoS One. 2012;7:e32484.
-
(2012)
PLoS One.
, vol.7
-
-
Stuck, M.W.1
Conley, S.M.2
Naash, M.I.3
-
37
-
-
3042850903
-
Identification and characterization of rod-derived cone viability factor
-
Leveillard T, Mohand-Said S, Lorentz O, et al. Identification and characterization of rod-derived cone viability factor. Nat Genet. 2004;36:755-759.
-
(2004)
Nat Genet.
, vol.36
, pp. 755-759
-
-
Leveillard, T.1
Mohand-Said, S.2
Lorentz, O.3
-
38
-
-
67349127313
-
Functional cone rescue by RdCVF protein in a dominant model of retinitis pigmentosa
-
Yang Y, Mohand-Said S, Danan A, et al. Functional cone rescue by RdCVF protein in a dominant model of retinitis pigmentosa. Mol Ther. 2009;17:787-795.
-
(2009)
Mol Ther.
, vol.17
, pp. 787-795
-
-
Yang, Y.1
Mohand-Said, S.2
Danan, A.3
-
39
-
-
58149141478
-
Stimulation of the insulin/ mTOR pathway delays cone death in a mouse model of retinitis pigmentosa
-
Punzo C, Kornacker K, Cepko CL. Stimulation of the insulin/ mTOR pathway delays cone death in a mouse model of retinitis pigmentosa. Nat Neurosci. 2009;12:44-52.
-
(2009)
Nat Neurosci.
, vol.12
, pp. 44-52
-
-
Punzo, C.1
Kornacker, K.2
Cepko, C.L.3
-
40
-
-
0036181472
-
Retinal degeneration mutants in the mouse
-
Chang B, Hawes NL, Hurd RE, Davisson MT, Nusinowitz S, Heckenlively JR. Retinal degeneration mutants in the mouse. Vision Res. 2002;42:517-525.
-
(2002)
Vision Res.
, vol.42
, pp. 517-525
-
-
Chang, B.1
Hawes, N.L.2
Hurd, R.E.3
Davisson, M.T.4
Nusinowitz, S.5
Heckenlively, J.R.6
|