-
1
-
-
0012702641
-
Présentation du rapport sur la biomicroscopie du du corps vitré et du fond d'oeil
-
Goldmann H. Présentation du rapport sur la biomicroscopie du du corps vitré et du fond d'oeil. Bull Mem Soc Fr Ophtalmol. 1957;70:265-272.
-
(1957)
Bull Mem Soc Fr Ophtalmol
, vol.70
, pp. 265-272
-
-
Goldmann, H.1
-
2
-
-
84924636477
-
Two cases of hyaloid-retinal degeneration
-
Favre M. Two cases of hyaloid-retinal degeneration. Ophthalmologica. 1958;135:604-609.
-
(1958)
Ophthalmologica
, vol.135
, pp. 604-609
-
-
Favre, M.1
-
4
-
-
0017012697
-
Atypical retinopathia pigmentosa with central retinoschisis (Goldmann-Favre)
-
Schmidt B., Weinberg M. Atypical retinopathia pigmentosa with central retinoschisis (Goldmann-Favre). Klin Monatsbl Augenheilkd. 1976;169:508-512.
-
(1976)
Klin Monatsbl Augenheilkd
, vol.169
, pp. 508-512
-
-
Schmidt, B.1
Weinberg, M.2
-
5
-
-
0017327546
-
Histopathology of Goldmann-Favre syndrome obtained by full-thickness eye-wall biopsy
-
Peyman GA, Fishman GA, Sanders DR, Vlchek J. Histopathology of Goldmann-Favre syndrome obtained by full-thickness eye-wall biopsy. Ann Ophthalmol. 1977;9:479-484.
-
(1977)
Ann Ophthalmol
, vol.9
, pp. 479-484
-
-
Peyman, G.A.1
Fishman, G.A.2
Sanders, D.R.3
Vlchek, J.4
-
6
-
-
0023618176
-
Goldmann-Favre syndrome in a four-year-old-girl
-
Izumi K, Matsuhashi M. Goldmann-Favre syndrome in a four-year-old-girl. Doc Ophthalmol. 1977;66:219-226.
-
(1977)
Doc Ophthalmol
, vol.66
, pp. 219-226
-
-
Izumi, K.1
Matsuhashi, M.2
-
8
-
-
0025875936
-
Treatment of Goldmann- Favre syndrome with cyclosporin A and bromocriptine
-
Garweg J, Bohnke M, Mangold I. Treatment of Goldmann- Favre syndrome with cyclosporin A and bromocriptine. Klin Monatsbl Augenheilkd. 1991;199:199-205.
-
(1991)
Klin Monatsbl Augenheilkd
, vol.199
, pp. 199-205
-
-
Garweg, J.1
Bohnke, M.2
Mangold, I.3
-
10
-
-
0025817471
-
Relatively enhanced S cone function in the Goldmann- Favre syndrome
-
Jacobson SG, Roman AJ, Roman MI, Gass JDM, Parker JA. Relatively enhanced S cone function in the Goldmann- Favre syndrome. Am J Ophthalmol. 1991;111:446-453.
-
(1991)
Am J Ophthalmol
, vol.111
, pp. 446-453
-
-
Jacobson, S.G.1
Roman, A.J.2
Roman, M.I.3
Gass, J.D.M.4
Parker, J.A.5
-
11
-
-
0033608979
-
Identification of a photoreceptor cell-specific nuclear receptor
-
Kobayashi M, Takezawa S, Hara K, Yu RT, Umesono Y, Agata K, Taniwaki M, Yasuda K, Umesono K. Identification of a photoreceptor cell-specific nuclear receptor. Proc Natl Acad Sci USA. 1999;96:4814-4819.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 4814-4819
-
-
Kobayashi, M.1
Takezawa, S.2
Hara, K.3
Yu, R.T.4
Umesono, Y.5
Agata, K.6
Taniwaki, M.7
Yasuda, K.8
Umesono, K.9
-
12
-
-
0033975061
-
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate
-
Haider NB, Jacobson SG, Cideciyan AV, Swiderski R, Streb LM, Searby C, Beck G, Hockey R, Hanna DB, Gorman S, Duhl D, Carmi R, Bennett J, Weleber RG, Fishman GA, Wright AF, Stone EM, Sheffield VC. Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate. Nat Genet. 2000;24:127-131.
-
(2000)
Nat Genet
, vol.24
, pp. 127-131
-
-
Haider, N.B.1
Jacobson, S.G.2
Cideciyan, A.V.3
Swiderski, R.4
Streb, L.M.5
Searby, C.6
Beck, G.7
Hockey, R.8
Hanna, D.B.9
Gorman, S.10
Duhl, D.11
Carmi, R.12
Bennett, J.13
Weleber, R.G.14
Fishman, G.A.15
Wright, A.F.16
Stone, E.M.17
Sheffield, V.C.18
-
13
-
-
33747884762
-
In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development
-
Cheng H, Aleman TS, Cideciyan AV, Khanna R, Jacobisn SG, Swaroop A. In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development. Hum Mol Genet. 2006;15:2588-2602.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 2588-2602
-
-
Cheng, H.1
Aleman, T.S.2
Cideciyan, A.V.3
Khanna, R.4
Jacobisn, S.G.5
Swaroop, A.6
-
14
-
-
24644484408
-
Abnormal distribution of red/green cone opsins in a patient with an autosomal dominant cone dystrophy
-
Bonilha VL, Hollyfield JG, Grover S, Hollyfield JG. Abnormal distribution of red/green cone opsins in a patient with an autosomal dominant cone dystrophy. Ophthalmic Genet. 2005;26:69-76.
-
(2005)
Ophthalmic Genet
, vol.26
, pp. 69-76
-
-
Bonilha, V.L.1
Hollyfield, J.G.2
Grover, S.3
Hollyfield, J.G.4
-
15
-
-
0037562853
-
Identification and light-dependent translocation of a cone-specific antigen, cone arrestin, recognized by monoclonal antibody 7G6
-
Zhang H, Cuenca N, Ivanova T, Church-Kopish J, Frederick JM, MacLeish PR, Baebr W. Identification and light-dependent translocation of a cone-specific antigen, cone arrestin, recognized by monoclonal antibody 7G6. Invest Ophthalmol Vis Sci. 2003:44:2858-2867.
-
(2003)
Invest Ophthalmol Vis Sci
, vol.44
, pp. 2858-2867
-
-
Zhang, H.1
Cuenca, N.2
Ivanova, T.3
Church-Kopish, J.4
Frederick, J.M.5
MacLeish, P.R.6
Baebr, W.7
-
16
-
-
50949166611
-
Choroideremia: Analysis of the retina from a female symptomatic carrier
-
Bonilha VL, Trzupek KM, Li Y, et al. Choroideremia: Analysis of the retina from a female symptomatic carrier. Ophthalmic Genet. 2008;29:99-110.
-
(2008)
Ophthalmic Genet
, vol.29
, pp. 99-110
-
-
Bonilha, V.L.1
Trzupek, K.M.2
Li, Y.3
-
17
-
-
0030584081
-
Two critical periods of Sonic Hedgehog signaling required for the specification of motor neuron identity
-
Ericson J, Morton S, Kawakami A, Roelink H, Jessell TM. Two critical periods of Sonic Hedgehog signaling required for the specification of motor neuron identity. Cell. 1996;87:661-673.
-
(1996)
Cell
, vol.87
, pp. 661-673
-
-
Ericson, J.1
Morton, S.2
Kawakami, A.3
Roelink, H.4
Jessell, T.M.5
-
18
-
-
0033932628
-
Progressive restriction in fate potential by neural progenitors during cerebral cortical development
-
Desai AR, McConnell SK. Progressive restriction in fate potential by neural progenitors during cerebral cortical development. Development. 2000;127:2863-2872.
-
(2000)
Development
, vol.127
, pp. 2863-2872
-
-
Desai, A.R.1
McConnell, S.K.2
-
19
-
-
0034098819
-
Soluble factors and the development of rod photoreceptors
-
Levine EM, Fuhrmann S, Reh TA. Soluble factors and the development of rod photoreceptors. Cell Mol Life Sci. 2000;57:224-234.
-
(2000)
Cell Mol Life Sci
, vol.57
, pp. 224-234
-
-
Levine, E.M.1
Fuhrmann, S.2
Reh, T.A.3
-
20
-
-
0035344212
-
Regulating proliferation during retinal development
-
Dyer MA, Cepko CL. Regulating proliferation during retinal development. Nat Rev Neurosci. 2001;2:333-342.
-
(2001)
Nat Rev Neurosci
, vol.2
, pp. 333-342
-
-
Dyer, M.A.1
Cepko, C.L.2
-
21
-
-
0141918786
-
Neurogenesis and the cell cycle
-
Ohnuma S, Harris WA. Neurogenesis and the cell cycle. Neuron. 2003;40:199-208.
-
(2003)
Neuron
, vol.40
, pp. 199-208
-
-
Ohnuma, S.1
Harris, W.A.2
-
22
-
-
0036469065
-
Signal transduction and the control of gene expression
-
Brivanlou AH, Darnell JE Jr. Signal transduction and the control of gene expression. Science. 2002;295:813-818.
-
(2002)
Science
, vol.295
, pp. 813-818
-
-
Brivanlou, A.H.1
Darnell Jr., J.E.2
-
23
-
-
0036155692
-
Generating neuronal diversity in the retina: One for nearly all
-
Marquardt T, Gruss P. Generating neuronal diversity in the retina: One for nearly all. Trends Neurosci. 2002;25:32-38.
-
(2002)
Trends Neurosci
, vol.25
, pp. 32-38
-
-
Marquardt, T.1
Gruss, P.2
-
24
-
-
17044368752
-
Gene regulatory networks for development
-
Levine M, Davidson EH. Gene regulatory networks for development. Proc Natl Acad Sci U S A. 2005;102: 4936-4942.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 4936-4942
-
-
Levine, M.1
Davidson, E.H.2
-
25
-
-
0026543201
-
A conserved retina-specific gene encodes a basic motif/leucine zipper domain
-
Swaroop A, Xu JZ, Pawar H, Jackson A, Skolnick C, Agarwal N. A conserved retina-specific gene encodes a basic motif/leucine zipper domain. Proc Natl Acad Sci U S A. 1992;89:266-270.
-
(1992)
Proc Natl Acad Sci U S A
, vol.89
, pp. 266-270
-
-
Swaroop, A.1
Xu, J.Z.2
Pawar, H.3
Jackson, A.4
Skolnick, C.5
Agarwal, N.6
-
26
-
-
0030781996
-
Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes
-
Chen S, Wang QL, Nie Z, Sun H, Lennon G, Copeland NG, Gilbert DJ, Jenkins NA, Zack DJ. Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes. Neuron. 1997;19: 1017-1030.
-
(1997)
Neuron
, vol.19
, pp. 1017-1030
-
-
Chen, S.1
Wang, Q.L.2
Nie, Z.3
Sun, H.4
Lennon, G.5
Copeland, N.G.6
Gilbert, D.J.7
Jenkins, N.A.8
Zack, D.J.9
-
27
-
-
0030725687
-
Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation
-
Furukawa T, Morrow EM, Cepko CL. Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation. Cell. 1997;91:531-541. (Pubitemid 27508242)
-
(1997)
Cell
, vol.91
, Issue.4
, pp. 531-541
-
-
Furukawa, T.1
Morrow, E.M.2
Cepko, C.L.3
-
28
-
-
18244385003
-
The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration
-
Epub 2002 Jan 2
-
Milam AH, Rose L, Cideciyan AV, Barakat MR, Tang WX, Gupta N, Aleman TS, Wright AF, Stone EM, Sheffield VC, Jacobson SG. 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. Epub 2002 Jan 2.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 473-478
-
-
Milam, A.H.1
Rose, L.2
Cideciyan, A.V.3
Barakat, M.R.4
Tang, W.X.5
Gupta, N.6
Aleman, T.S.7
Wright, A.F.8
Stone, E.M.9
Sheffield, V.C.10
Jacobson, S.G.11
-
29
-
-
0141722455
-
Shared mutations in NR2E3 in enhanced S-cone syndrome Goldmann-Favre syndrome and many cases of clumped pigmentary retinal degeneration
-
Sharon D, Sandberg MA, Caruso RC, Berson EL, Dryja TP. Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration. Arch Ophthalmol. 2003;121:1316-1323.
-
(2003)
Arch Ophthalmol
, vol.121
, pp. 1316-1323
-
-
Sharon, D.1
Sandberg, M.A.2
Caruso, R.C.3
Berson, E.L.4
Dryja, T.P.5
-
30
-
-
4544264183
-
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome
-
Wright AF, Reddick AC, Schwartz SB, Ferguson JS, Aleman TS, Kellner U, Jurklies B, Schuster A, Zrenner E, Wissinger B, Lennon A, Shu X, Cideciyan AV, Stone EM, Jacobson SG, Swaroop A. Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome. Hum Mutat. 2004;24:439.
-
(2004)
Hum Mutat
, vol.24
, pp. 439
-
-
Wright, A.F.1
Reddick, A.C.2
Schwartz, S.B.3
Ferguson, J.S.4
Aleman, T.S.5
Kellner, U.6
Jurklies, B.7
Schuster, A.8
Zrenner, E.9
Wissinger, B.10
Lennon, A.11
Shu, X.12
Cideciyan, A.V.13
Stone, E.M.14
Jacobson, S.G.15
Swaroop, A.16
-
31
-
-
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
-
32
-
-
12944293118
-
A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse
-
Akhmedov NB, Piriev NI, Chang B, Rapoport AL, Hawes NL, Nishina PM, Nusinowitz S, Heckenlively JR, Roderick TH, Kozak CA, Dacinger M, Davisson MT, Farber DB. A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse. Proc Natl Acad Sci U S A. 2000;97:5551-5556.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 5551-5556
-
-
Akhmedov, N.B.1
Piriev, N.I.2
Chang, B.3
Rapoport, A.L.4
Hawes, N.L.5
Nishina, P.M.6
Nusinowitz, S.7
Heckenlively, J.R.8
Roderick, T.H.9
Kozak, C.A.10
Dacinger, M.11
Davisson, M.T.12
Farber, D.B.13
-
33
-
-
0035421442
-
Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice
-
Haider NB, Naggert JK, Nishina PM. Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice. Hum Mol Genet. 2001;10:1619-1626.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1619-1626
-
-
Haider, N.B.1
Naggert, J.K.2
Nishina, P.M.3
-
34
-
-
0025939629
-
Distribution and morphology of human cone photoreceptors stained with anti-blue opsin
-
Curcio CA, Allen KA, Sloan KR, Lerea CL, Hurley JB, Klock IB, Milam AH. Distribution and morphology of human cone photoreceptors stained with anti-blue opsin. J Comp Neurol. 1991;312:610-624.
-
(1991)
J Comp Neurol
, vol.312
, pp. 610-624
-
-
Curcio, C.A.1
Allen, K.A.2
Sloan, K.R.3
Lerea, C.L.4
Hurley, J.B.5
Klock, I.B.6
Milam, A.H.7
-
35
-
-
33745276315
-
Effects of L1 retrotransposon insertion on transcript processing, localization and accumulation: Lessons from the retinal degeneration 7 mouse and implications for the genomic ecology of L1 elements
-
Chen J, Rattner A, Nathans J. Effects of L1 retrotransposon insertion on transcript processing, localization and accumulation: lessons from the retinal degeneration 7 mouse and implications for the genomic ecology of L1 elements. Hum Mol Genet. 2006;15:2146-2156.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 2146-2156
-
-
Chen, J.1
Rattner, A.2
Nathans, J.3
-
36
-
-
0035056214
-
Packing arrangement of the three cone classes in primate retina
-
Roorda A, Metha AB, Lennie P, Williams DR. Packing arrangement of the three cone classes in primate retina. Vision Res. 2001;41:1291-1306.
-
(2001)
Vision Res
, vol.41
, pp. 1291-1306
-
-
Roorda, A.1
Metha, A.B.2
Lennie, P.3
Williams, D.R.4
-
37
-
-
0033545288
-
The arrangement of the three cone classes in the living human eye
-
Roorda A, Williams DR. The arrangement of the three cone classes in the living human eye. Nature. 1999;397:520-522.
-
(1999)
Nature
, vol.397
, pp. 520-522
-
-
Roorda, A.1
Williams, D.R.2
-
38
-
-
0034724168
-
A retinitis pigmentosa GTPase regulator (RPGR)- deficient mouse model for X-linked retinitis pigmentosa (RP3)
-
Hong DH, Pawlyk BS, Shang J, Sandberg MA, Berson EL, Li T. A retinitis pigmentosa GTPase regulator (RPGR)- deficient mouse model for X-linked retinitis pigmentosa (RP3). Proc Natl Acad Sci U S A. 2000;97:3649-3654.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 3649-3654
-
-
Hong, D.H.1
Pawlyk, B.S.2
Shang, J.3
Sandberg, M.A.4
Berson, E.L.5
Li, T.6
-
39
-
-
70350479962
-
Life history of cones in the rhodopsin-mutant P23H-3 rat: Evidence of long term survival
-
Epub 2008 Dec 30
-
Chrysostomou V, Stone J, Valter K. Life history of cones in the rhodopsin-mutant P23H-3 rat: Evidence of long term survival. Invest Ophthalmol Vis Sci. 2008; Epub 2008 Dec 30.
-
(2008)
Invest Ophthalmol Vis Sci
-
-
Chrysostomou, V.1
Stone, J.2
Valter, K.3
|