-
1
-
-
0027537949
-
Retinitis pigmentosa: The Friedenwald lecture
-
Berson EL, Retinitis pigmentosa: The Friedenwald lecture. Invest Ophthalmol Vis Sci. 1993;34:1659-1676.
-
(1993)
Invest Ophthalmol Vis Sci
, vol.34
, pp. 1659-1676
-
-
Berson, E.L.1
-
2
-
-
0027458668
-
Autosomal dominant retinitis pigmentosa: Molecular, genetic and clinical aspects
-
Osborne NN, Chader GJ, eds. Oxford: Pergamon Press
-
Humphries P, Farrar GJ, Kenna P. Autosomal dominant retinitis pigmentosa: Molecular, genetic and clinical aspects. In: Osborne NN, Chader GJ, eds. Progress in Retinal Research. Oxford: Pergamon Press; 1993:231-245.
-
(1993)
Progress in Retinal Research
, pp. 231-245
-
-
Humphries, P.1
Farrar, G.J.2
Kenna, P.3
-
3
-
-
0027103787
-
Doyne lecture: Rhodopsin and autosomal dominant retinitis pigmentosa
-
Dryja TP. Doyne lecture: Rhodopsin and autosomal dominant retinitis pigmentosa. Eye. 1992;6:1-10.
-
(1992)
Eye
, vol.6
, pp. 1-10
-
-
Dryja, T.P.1
-
4
-
-
0029035306
-
Retinal photoreceptor dystrophies: LI. Edward Jackson memorial lecture
-
Bird AC. Retinal photoreceptor dystrophies: LI. Edward Jackson memorial lecture. Am J Ophthalmol. 1995;119:543-562.
-
(1995)
Am J Ophthalmol
, vol.119
, pp. 543-562
-
-
Bird, A.C.1
-
5
-
-
0028018939
-
In the eye of the beholder: Visual pigments and inherited variation in human vision
-
Nathans J. In the eye of the beholder: Visual pigments and inherited variation in human vision. Cell. 1994;78:357-360.
-
(1994)
Cell
, vol.78
, pp. 357-360
-
-
Nathans, J.1
-
6
-
-
0026643593
-
Rhodopsin: Structure, function and genetics
-
Nathans J. Rhodopsin: Structure, function and genetics. Biochemistry. 1992;31:4923-4931.
-
(1992)
Biochemistry
, vol.31
, pp. 4923-4931
-
-
Nathans, J.1
-
8
-
-
0026058548
-
Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa
-
Sung C-H, Schneider BG, Agarwal N, Papermaster DS, Nathans J. Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa. Proc Natl Acad Sci USA. 1991;88:8840-8844.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 8840-8844
-
-
Sung, C.-H.1
Schneider, B.G.2
Agarwal, N.3
Papermaster, D.S.4
Nathans, J.5
-
9
-
-
0025768030
-
Retinal function and rhodopsin levels in autosomal dominant retinitis pigmentosa with rhodopsin mutations
-
Jacobson SG, Kemp CM, Sung C-H, Nathans J. Retinal function and rhodopsin levels in autosomal dominant retinitis pigmentosa with rhodopsin mutations. Am J Ophthalmol. 1991;112:256-271.
-
(1991)
Am J Ophthalmol
, vol.112
, pp. 256-271
-
-
Jacobson, S.G.1
Kemp, C.M.2
Sung, C.-H.3
Nathans, J.4
-
10
-
-
0027488507
-
Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: Implications for the structure and function of rhodopsin
-
Macke JP, Davenport CM, Jacobson SG, et al. Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: Implications for the structure and function of rhodopsin. Am. J Human Genet. 1993;53:80-89.
-
(1993)
Am. J Human Genet
, vol.53
, pp. 80-89
-
-
Macke, J.P.1
Davenport, C.M.2
Jacobson, S.G.3
-
11
-
-
0028215806
-
Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosa
-
Jacobson SG, Kemp CM, Cideciyan AV, Macke JP, Sung C-H, Nathans J. Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosa. Invest Ophthalmol Vis Sci. 1994;35:2521-2534.
-
(1994)
Invest Ophthalmol Vis Sci
, vol.35
, pp. 2521-2534
-
-
Jacobson, S.G.1
Kemp, C.M.2
Cideciyan, A.V.3
Macke, J.P.4
Sung, C.-H.5
Nathans, J.6
-
12
-
-
0027260657
-
Cellular interactions implicated in the mechanism of photoreceptor degeneration in transgenic mice expressing a mutant rhodopsin gene
-
Huang PC, Gaitan AE, Hao Y, Peters RM, Wong F. Cellular interactions implicated in the mechanism of photoreceptor degeneration in transgenic mice expressing a mutant rhodopsin gene. Proc Natl Acad Sci USA. 1993;90:8484-8488.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 8484-8488
-
-
Huang, P.C.1
Gaitan, A.E.2
Hao, Y.3
Peters, R.M.4
Wong, F.5
-
13
-
-
0028858741
-
Functional abnormalities in transgenic mice expressing a mutant rhodopsin gene
-
Goto Y, Peachey NS, Ripps H, Naash MI. Functional abnormalities in transgenic mice expressing a mutant rhodopsin gene. Invest Ophthalmol Vis Sci. 1995;36:62-71.
-
(1995)
Invest Ophthalmol Vis Sci
, vol.36
, pp. 62-71
-
-
Goto, Y.1
Peachey, N.S.2
Ripps, H.3
Naash, M.I.4
-
14
-
-
0026463972
-
Transgenic mice with a rhodopsin mutation (Pro-23-His) : A mouse model of autosomal dominant retinitis pigmentosa
-
Olsson JE, Gorden JW, Pawlyk BS, et al. Transgenic mice with a rhodopsin mutation (Pro-23-His) : A mouse model of autosomal dominant retinitis pigmentosa. Neuron. 1992;9:815-830.
-
(1992)
Neuron
, vol.9
, pp. 815-830
-
-
Olsson, J.E.1
Gorden, J.W.2
Pawlyk, B.S.3
-
15
-
-
0028110523
-
Rhodopsin accumulation at abnormal sites in retinas of mice with a human P23H rhodopsin transgene
-
Roof DJ, Adamian M, Hayes A. Rhodopsin accumulation at abnormal sites in retinas of mice with a human P23H rhodopsin transgene. Invest Ophthalmol Vis Sci. 1994;35:4049-4062.
-
(1994)
Invest Ophthalmol Vis Sci
, vol.35
, pp. 4049-4062
-
-
Roof, D.J.1
Adamian, M.2
Hayes, A.3
-
16
-
-
0027935666
-
A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment
-
Sung C-H, Makino C, Baylor D, Nathans J. A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment. J Neurosci. 1994;14:5818-5833.
-
(1994)
J Neurosci
, vol.14
, pp. 5818-5833
-
-
Sung, C.-H.1
Makino, C.2
Baylor, D.3
Nathans, J.4
-
17
-
-
0028955343
-
Mechanisms of rhodopsin inactivation in vivo as revealed by a COOH-terminal truncation mutant
-
Chen J, Makino CL, Peachey NS, Baylor DA, Simon MI. Mechanisms of rhodopsin inactivation in vivo as revealed by a COOH-terminal truncation mutant. Science. 1995;267:374-377.
-
(1995)
Science
, vol.267
, pp. 374-377
-
-
Chen, J.1
Makino, C.L.2
Peachey, N.S.3
Baylor, D.A.4
Simon, M.I.5
-
18
-
-
0023002215
-
Automated light- And dark-adapted perimetry for evaluating retinitis pigmentosa
-
Jacobson SG, Voigt WJ, Parel J-M, et al. Automated light- and dark-adapted perimetry for evaluating retinitis pigmentosa. Ophthalmology. 1986;93:1604-1611.
-
(1986)
Ophthalmology
, vol.93
, pp. 1604-1611
-
-
Jacobson, S.G.1
Voigt, W.J.2
Parel, J.-M.3
-
19
-
-
0027437911
-
Negative electroretino- Grams in retinitis pigmentosa
-
Cideciyan AV, Jacobson SG. Negative electroretino- grams in retinitis pigmentosa. Invest Ophthalmol Vis Sci. 1993;34:3253-3263.
-
(1993)
Invest Ophthalmol Vis Sci
, vol.34
, pp. 3253-3263
-
-
Cideciyan, A.V.1
Jacobson, S.G.2
-
20
-
-
0030220591
-
An alternative phototransduction model for human rod and cone ERG a-waves: Normal parameters and variation with age
-
in press
-
Cideciyan AV, Jacobson SG. An alternative phototransduction model for human rod and cone ERG a-waves: Normal parameters and variation with age. Vision Res. 1996; in press.
-
(1996)
Vision Res
-
-
Cideciyan, A.V.1
Jacobson, S.G.2
-
21
-
-
0026505707
-
A quantitative account of the activation steps involved in phototransduction in amphibian photoreceptors
-
Lamb TD, Pugh EN Jr. A quantitative account of the activation steps involved in phototransduction in amphibian photoreceptors. J Physiol (Lond). 1992;449:719-758.
-
(1992)
J Physiol (Lond)
, vol.449
, pp. 719-758
-
-
Lamb, T.D.1
Pugh Jr., E.N.2
-
22
-
-
0027407602
-
Amplification and kinetics of the activation steps in phototransduction
-
Pugh EN Jr, Lamb TD. Amplification and kinetics of the activation steps in phototransduction. Biochim Biophys Acta. 1993;1141:111-149.
-
(1993)
Biochim Biophys Acta
, vol.1141
, pp. 111-149
-
-
Pugh Jr., E.N.1
Lamb, T.D.2
-
23
-
-
0027199939
-
Light adaptation of human rod receptors: The leading edge of the human a-wave and models of rod receptor activity
-
Hood DC, Birch DG. Light adaptation of human rod receptors: The leading edge of the human a-wave and models of rod receptor activity. Vision Res. 1993;33:1605-1618.
-
(1993)
Vision Res
, vol.33
, pp. 1605-1618
-
-
Hood, D.C.1
Birch, D.G.2
-
24
-
-
0028158701
-
Analysis of ERG a-wave amplification and kinetics in terms of the G-protein cascade of phototransduction
-
Breton ME, Schueller AW, Lamb TD, Pugh EN Jr. Analysis of ERG a-wave amplification and kinetics in terms of the G-protein cascade of phototransduction. Invest Ophthalmol Vis Sci. 1994;35:295-309.
-
(1994)
Invest Ophthalmol Vis Sci
, vol.35
, pp. 295-309
-
-
Breton, M.E.1
Schueller, A.W.2
Lamb, T.D.3
Pugh Jr., E.N.4
-
25
-
-
0027664945
-
Human cone receptor activity: The leading edge of the a-wave and models of receptor activity
-
Hood DC, Birch DG. Human cone receptor activity: The leading edge of the a-wave and models of receptor activity. Vis Neurosci. 1993;10:857-871.
-
(1993)
Vis Neurosci
, vol.10
, pp. 857-871
-
-
Hood, D.C.1
Birch, D.G.2
-
26
-
-
0029125152
-
Rod photoreceptor neurite sprouting in retinitis pigmentosa
-
Li Z-Y, Kljavin IJ, Milam AH. Rod photoreceptor neurite sprouting in retinitis pigmentosa. J Neurosci. 1995;15:5429-5438.
-
(1995)
J Neurosci
, vol.15
, pp. 5429-5438
-
-
Li, Z.-Y.1
Kljavin, I.J.2
Milam, A.H.3
-
27
-
-
0025598147
-
Photoreceptor rosettes with blue cone opsin immunoreactivity in retinitis pigmentosa
-
Milam AH, Jacobson SG. Photoreceptor rosettes with blue cone opsin immunoreactivity in retinitis pigmentosa. Ophthalmology. 1990;97:1620-1631.
-
(1990)
Ophthalmology
, vol.97
, pp. 1620-1631
-
-
Milam, A.H.1
Jacobson, S.G.2
-
29
-
-
0029022426
-
Histopathology of bone spicule pigmentation in retinitis pigmentosa
-
Li Z-Y, Possin DE, Milam AH. Histopathology of bone spicule pigmentation in retinitis pigmentosa. Ophthalmology. 1995;102:805-816.
-
(1995)
Ophthalmology
, vol.102
, pp. 805-816
-
-
Li, Z.-Y.1
Possin, D.E.2
Milam, A.H.3
-
30
-
-
0028298405
-
Autosomal dominant retinitis pigmentosa caused by the threonine-17-methionine rhodopsin mutation: Retinal histopathology and immunocytochemistry
-
Li Z-Y, Jacobson SG, Milam AH. Autosomal dominant retinitis pigmentosa caused by the threonine-17-methionine rhodopsin mutation: Retinal histopathology and immunocytochemistry. Exp Eye Res. 1994;58:397-408.
-
(1994)
Exp Eye Res
, vol.58
, pp. 397-408
-
-
Li, Z.-Y.1
Jacobson, S.G.2
Milam, A.H.3
-
31
-
-
0020551985
-
Immunocytochemical localization of two retinoid-binding proteins in vertebrate retinas
-
Bunt-Milam AH, Saari JC. Immunocytochemical localization of two retinoid-binding proteins in vertebrate retinas. J Cell Biol. 1983;97:703-712.
-
(1983)
J Cell Biol
, vol.97
, pp. 703-712
-
-
Bunt-Milam, A.H.1
Saari, J.C.2
-
32
-
-
0016169602
-
Electron microscopic observations of human retinitis pigmentosa, dominantly inherited
-
Kolb H, Gouras P. Electron microscopic observations of human retinitis pigmentosa, dominantly inherited. Invest Ophthalmol. 1974;13:487-98.
-
(1974)
Invest Ophthalmol
, vol.13
, pp. 487-498
-
-
Kolb, H.1
Gouras, P.2
-
33
-
-
0026089384
-
Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His)
-
Berson EL, Rosner B, Sandberg MA, Dryja TP. Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His). Arch Ophthalmol. 1991;109:92-101.
-
(1991)
Arch Ophthalmol
, vol.109
, pp. 92-101
-
-
Berson, E.L.1
Rosner, B.2
Sandberg, M.A.3
Dryja, T.P.4
-
34
-
-
0023944679
-
Morphological findings in retinitis pigmentosa with early diffuse rod dysfunction
-
Tucker GS, Jacobson SG. Morphological findings in retinitis pigmentosa with early diffuse rod dysfunction. Retina. 1988;8:30-41.
-
(1988)
Retina
, vol.8
, pp. 30-41
-
-
Tucker, G.S.1
Jacobson, S.G.2
-
35
-
-
0003150498
-
Abnormal cone receptor activity in patients with hereditary degeneration
-
Anderson RE, Hollyfield JG, LaVail MM, eds. New York: Plenum
-
Hood DC, Birch DG. Abnormal cone receptor activity in patients with hereditary degeneration. In: Anderson RE, Hollyfield JG, LaVail MM, eds. Degenerative Diseases of the Retina. New York: Plenum; 1995:349-358.
-
(1995)
Degenerative Diseases of the Retina
, pp. 349-358
-
-
Hood, D.C.1
Birch, D.G.2
-
36
-
-
0028926182
-
Rod phototransduction in retinitis pigmentosa: Distinguishing alternative mechanisms of degeneration
-
Shady S, Hood DS, Birch DG. Rod phototransduction in retinitis pigmentosa: Distinguishing alternative mechanisms of degeneration. Invest Ophthalmol Vis Sci. 1995;36:1027-1057.
-
(1995)
Invest Ophthalmol Vis Sci.
, vol.36
, pp. 1027-1057
-
-
Shady, S.1
Hood, D.S.2
Birch, D.G.3
-
37
-
-
0028229520
-
Rod phototransduction in retinitis pigmentosa: Estimation and interpretation of parameters derived from the rod a-wave
-
Hood DC, Birch DG. Rod phototransduction in retinitis pigmentosa: Estimation and interpretation of parameters derived from the rod a-wave. Invest Ophthalmol Vis Sci. 1994;35:2948-2961.
-
(1994)
Invest Ophthalmol Vis Sci
, vol.35
, pp. 2948-2961
-
-
Hood, D.C.1
Birch, D.G.2
-
38
-
-
0027190742
-
Assessment of foveal cone photoreceptors in Stargardt's macular dystrophy using a small dot detection task
-
Geller AM, Sieving PA. Assessment of foveal cone photoreceptors in Stargardt's macular dystrophy using a small dot detection task. Vision Res. 1993;33:1509-1524.
-
(1993)
Vision Res
, vol.33
, pp. 1509-1524
-
-
Geller, A.M.1
Sieving, P.A.2
-
39
-
-
0028062942
-
Postreceptoral contribution to macular dysfunction in retinitis pigmentosa
-
Falsini B, Iarossi G, Porciatti V, et al. Postreceptoral contribution to macular dysfunction in retinitis pigmentosa. Invest Ophthalmol Vis Sci. 1994;35:4282-4299.
-
(1994)
Invest Ophthalmol Vis Sci
, vol.35
, pp. 4282-4299
-
-
Falsini, B.1
Iarossi, G.2
Porciatti, V.3
-
40
-
-
0024538020
-
Degenerative changes in a retina affected with autosomal dominant retinitis pigmentosa
-
Flannery JG, Farber DB, Bird AC, Bok D. Degenerative changes in a retina affected with autosomal dominant retinitis pigmentosa. Invest Ophthalmol Vis Sci. 1989;30:191-211.
-
(1989)
Invest Ophthalmol Vis Sci
, vol.30
, pp. 191-211
-
-
Flannery, J.G.1
Farber, D.B.2
Bird, A.C.3
Bok, D.4
-
41
-
-
0018411075
-
Sex-linked retinitis pigmentosa: Ultrastructure of photoreceptors and pigment epithelium
-
Szamier RB, Berson EL, Klein R, Meyers S. Sex-linked retinitis pigmentosa: Ultrastructure of photoreceptors and pigment epithelium. Invest Ophthalmol Vis Sci. 1979;18:145-160.
-
(1979)
Invest Ophthalmol Vis Sci
, vol.18
, pp. 145-160
-
-
Szamier, R.B.1
Berson, E.L.2
Klein, R.3
Meyers, S.4
-
42
-
-
0029937553
-
Abnormalities of the retinal cone system in retinitis pigmentosa
-
in press
-
Hood DC, Birch DG. Abnormalities of the retinal cone system in retinitis pigmentosa. Vision Res. 1996; in press.
-
(1996)
Vision Res
-
-
Hood, D.C.1
Birch, D.G.2
-
43
-
-
84907115546
-
Investigation of disease mechanisms in retinitis pigmentosa
-
Bird AC. Investigation of disease mechanisms in retinitis pigmentosa. Ophthalmic Paediatr Genet. 1992;13:57-66.
-
(1992)
Ophthalmic Paediatr Genet
, vol.13
, pp. 57-66
-
-
Bird, A.C.1
-
44
-
-
0027422752
-
Strategies for rescue of retinal photoreceptor cells
-
Milam AH. Strategies for rescue of retinal photoreceptor cells. Curr Opin Neurobiol. 1993;3:797-804.
-
(1993)
Curr Opin Neurobiol
, vol.3
, pp. 797-804
-
-
Milam, A.H.1
-
45
-
-
0021991546
-
Synthesis and secretion of interstitial retinol-binding protein by the human retina
-
Hollyfield JG, Fliesler SJ, Rayborn ME, Fong S-L, Landers RA, Bridges CD. Synthesis and secretion of interstitial retinol-binding protein by the human retina. Invest Ophthalmol Vis Sci. 1985;26:58-67.
-
(1985)
Invest Ophthalmol Vis Sci
, vol.26
, pp. 58-67
-
-
Hollyfield, J.G.1
Fliesler, S.J.2
Rayborn, M.E.3
Fong, S.-L.4
Landers, R.A.5
Bridges, C.D.6
-
46
-
-
0022541901
-
Interphotoreceptor retinoid-binding protein in retinal rod cells and pineal gland
-
Rodrigues MM, Hackett J, Gaskins R, et al. Interphotoreceptor retinoid-binding protein in retinal rod cells and pineal gland. Invest Ophthalmol Vis Sci. 1986;27:844-850.
-
(1986)
Invest Ophthalmol Vis Sci
, vol.27
, pp. 844-850
-
-
Rodrigues, M.M.1
Hackett, J.2
Gaskins, R.3
-
47
-
-
0026067421
-
Detection of interphotoreceptor retinoid binding protein (IRBP) mRNA in human and cone-dominant squirrel retinas by in situ hybridization. J
-
Porello K, Bhat JP, Bok D. Detection of interphotoreceptor retinoid binding protein (IRBP) mRNA in human and cone-dominant squirrel retinas by in situ hybridization. J Histochem. Cytochem. 1991;39:171-176.
-
(1991)
Histochem. Cytochem.
, vol.39
, pp. 171-176
-
-
Porello, K.1
Bhat, J.P.2
Bok, D.3
-
48
-
-
0021964847
-
Dominantly inherited retinitis pigmentosa: Ultrastructure and biochemical analysis
-
Rodrigues MM, Wiggert B, Hackett J, Lee L, Fletcher RT, Chader GJ. Dominantly inherited retinitis pigmentosa: Ultrastructure and biochemical analysis. Ophthalmology. 1985;92:1165-1172.
-
(1985)
Ophthalmology
, vol.92
, pp. 1165-1172
-
-
Rodrigues, M.M.1
Wiggert, B.2
Hackett, J.3
Lee, L.4
Fletcher, R.T.5
Chader, G.J.6
-
49
-
-
0021798064
-
Vitamin A and interstitial retinol-binding protein in an eye with recessive retinitis pigmentosa
-
Bridges CD, O'Gorman S, Fong S-L, Alvarez RA, Berson E. Vitamin A and interstitial retinol-binding protein in an eye with recessive retinitis pigmentosa. Invest Ophthalmol Vis Sci. 1985;26:684-691.
-
(1985)
Invest Ophthalmol Vis Sci
, vol.26
, pp. 684-691
-
-
Bridges, C.D.1
O'Gorman, S.2
Fong, S.-L.3
Alvarez, R.A.4
Berson, E.5
-
50
-
-
0002774642
-
The effect of vitamin A deficiency on the fine structure of the retina
-
Smelser G, eds. New York: Academic Press
-
Dowling JE, Gibbons IR. The effect of vitamin A deficiency on the fine structure of the retina. In: Smelser G, eds. The Structure of the Eye. New York: Academic Press; 1961:85-99.
-
(1961)
The Structure of the Eye
, pp. 85-99
-
-
Dowling, J.E.1
Gibbons, I.R.2
-
52
-
-
0026592409
-
Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation
-
Kemp CM, Jacobson SG, Roman AJ, Sung C-H, Nathans J. Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation. Am J Ophthalmol. 1992;113:165-174.
-
(1992)
Am J Ophthalmol
, vol.113
, pp. 165-174
-
-
Kemp, C.M.1
Jacobson, S.G.2
Roman, A.J.3
Sung, C.-H.4
Nathans, J.5
-
53
-
-
0029042741
-
Abnormal activation and inactivation mechanisms of rod transduction in patients with autosomal dominant retinitis pigmentosa and the pro-23-his mutation
-
Birch DG, Hood DC, Nusinowitz S, Pepperberg DR. Abnormal activation and inactivation mechanisms of rod transduction in patients with autosomal dominant retinitis pigmentosa and the pro-23-his mutation. Invest Ophthalmol Vis Sci. 1995;36:1603-1614.
-
(1995)
Invest Ophthalmol Vis Sci
, vol.36
, pp. 1603-1614
-
-
Birch, D.G.1
Hood, D.C.2
Nusinowitz, S.3
Pepperberg, D.R.4
-
54
-
-
0027157881
-
An immunohistochemical study of opsin in photoreceptor cells following light-induced retinal degeneration in the rat
-
Deepak PE, Lim K, Sawaguchi S, Tso MOM. An immunohistochemical study of opsin in photoreceptor cells following light-induced retinal degeneration in the rat. Graefe's Arch Clin Exp Ophthalmol 1993;231:289-294.
-
(1993)
Graefe's Arch Clin Exp Ophthalmol
, vol.231
, pp. 289-294
-
-
Deepak, P.E.1
Lim, K.2
Sawaguchi, S.3
Tso, M.O.M.4
-
55
-
-
0028914025
-
Defective intracellular transport is the molecular basis of rhodopsin-dependent dominant retinal degeneration
-
Colley NJ, Cassill JA, Baker EK, Zuker CS. Defective intracellular transport is the molecular basis of rhodopsin-dependent dominant retinal degeneration. Proc Natl Acad Sci USA. 1995;92:3070-3074.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 3070-3074
-
-
Colley, N.J.1
Cassill, J.A.2
Baker, E.K.3
Zuker, C.S.4
-
56
-
-
0020359828
-
Retinal degeneration in the pcd cerebellar mutant mouse: II: Electron microscopic analysis
-
Blanks JC, Mullen RJ, LaVail MM. Retinal degeneration in the pcd cerebellar mutant mouse: II: Electron microscopic analysis. J Comp Neural. 1982;212:231-246.
-
(1982)
J Comp Neural
, vol.212
, pp. 231-246
-
-
Blanks, J.C.1
Mullen, R.J.2
LaVail, M.M.3
-
57
-
-
0023241706
-
Development and degeneration of retina in rds mutant mice: Ultraimmunohistochemical localization of opsin
-
Jansen HG, Sanyal S, DeGrip WJ, Schalken JJ. Development and degeneration of retina in rds mutant mice: Ultraimmunohistochemical localization of opsin. Exp Eye Res. 1987;44:347-361.
-
(1987)
Exp Eye Res
, vol.44
, pp. 347-361
-
-
Jansen, H.G.1
Sanyal, S.2
DeGrip, W.J.3
Schalken, J.J.4
-
58
-
-
0023519505
-
Changes in the localization and content of opsin during retinal development in the rds mutant mouse: Immunocytochemistry and immunoassay
-
Usukura J, Bok D. Changes in the localization and content of opsin during retinal development in the rds mutant mouse: Immunocytochemistry and immunoassay. Exp Eye Res. 1987;45:501-515.
-
(1987)
Exp Eye Res
, vol.45
, pp. 501-515
-
-
Usukura, J.1
Bok, D.2
-
60
-
-
0003098244
-
Apoptosis in retinitis pigmentosa
-
Anderson RE, Hollyfield JG, LaVail MM, eds. New York: Plenum
-
Li Z-Y, Milam AH. Apoptosis in retinitis pigmentosa. In: Anderson RE, Hollyfield JG, LaVail MM, eds. De generative Diseases of the Retina. New York: Plenum; 1995:1-8.
-
(1995)
De Generative Diseases of the Retina
, pp. 1-8
-
-
Li, Z.-Y.1
Milam, A.H.2
-
61
-
-
84970296852
-
Glial influences on neuronal signaling
-
Sontheimer H. Glial influences on neuronal signaling. The Neuroscientist. 1995;1:123-126.
-
(1995)
The Neuroscientist
, vol.1
, pp. 123-126
-
-
Sontheimer, H.1
-
63
-
-
0019403651
-
The relationship between visual sensitivity and rhodopsin density in retinitis pigmentosa
-
Perlman I, Auerbach E. The relationship between visual sensitivity and rhodopsin density in retinitis pigmentosa. Invest Ophthalmol Vis Sci. 1981;20:758-765.
-
(1981)
Invest Ophthalmol Vis Sci
, vol.20
, pp. 758-765
-
-
Perlman, I.1
Auerbach, E.2
-
64
-
-
0023750581
-
Two types of visual dysfunction in autosomal dominant retinitis pigmentosa
-
Kemp CM, Jacobson SG, Faulkner DJ. Two types of visual dysfunction in autosomal dominant retinitis pigmentosa. Invest Ophthalmol Vis Sci. 1988;29:1235-1241.
-
(1988)
Invest Ophthalmol Vis Sci
, vol.29
, pp. 1235-1241
-
-
Kemp, C.M.1
Jacobson, S.G.2
Faulkner, D.J.3
|