-
1
-
-
0033823792
-
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa
-
Dryja TP, McEvoy JA, McGee TL, Berson EL. Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2000;41:3124-3127.
-
(2000)
Invest Ophthalmol Vis Sci
, vol.41
, pp. 3124-33127
-
-
Dryja, T.P.1
McEvoy, J.A.2
McGee, T.L.3
Berson, E.L.4
-
3
-
-
0025105161
-
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
-
Dryja TP, McGee TL, Reichel E, et al. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa. Nature. 1990; 343:364-366.
-
(1990)
Nature
, vol.343
, pp. 364-366
-
-
Dryja, T.P.1
McGee, T.L.2
Reichel, E.3
-
4
-
-
0026058548
-
Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa
-
Sung CH, Schneider BG, Agarwal N, Papermaster DS, Nathans J. Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa. Proc Natl Acad Sci U S A. 1991;88:8840-8844.
-
(1991)
Proc Natl Acad Sci U S A
, vol.88
, pp. 8840-8844
-
-
Sung, C.H.1
Schneider, B.G.2
Agarwal, N.3
Papermaster, D.S.4
Nathans, J.5
-
5
-
-
0028287273
-
Structure and function in rhodopsin. 7. Point mutations associated with autosomal dominant retinitis pigmentosa
-
Kaushal S, Khorana HG. Structure and function in rhodopsin. 7. Point mutations associated with autosomal dominant retinitis pigmentosa. Biochemistry. 1994;33:6121-6128.
-
(1994)
Biochemistry
, vol.33
, pp. 6121-6128
-
-
Kaushal, S.1
Khorana, H.G.2
-
6
-
-
1942469395
-
Retinoids assist the cellular folding of the autosomal dominant retinitis pigmentosa opsin mutant P23H
-
Noorwez SM, Malhotra R, McDowell JH, Smith KA, Krebs MP, Kaushal S. Retinoids assist the cellular folding of the autosomal dominant retinitis pigmentosa opsin mutant P23H. J Biol Chem. 2004;279:16278-16284.
-
(2004)
J Biol Chem
, vol.279
, pp. 16278-16284
-
-
Noorwez, S.M.1
Malhotra, R.2
McDowell, J.H.3
Smith, K.A.4
Krebs, M.P.5
Kaushal, S.6
-
7
-
-
0037072934
-
A rhodopsin mutant linked to autosomal dominant retinitis pigmentosa is prone to aggregate and interacts with the ubiquitin proteasome system
-
Illing ME, Rajan RS, Bence NF, Kopito RR. A rhodopsin mutant linked to autosomal dominant retinitis pigmentosa is prone to aggregate and interacts with the ubiquitin proteasome system. J Biol Chem. 2002;277:34150-34160.
-
(2002)
J Biol Chem
, vol.277
, pp. 34150-34160
-
-
Illing, M.E.1
Rajan, R.S.2
Bence, N.F.3
Kopito, R.R.4
-
8
-
-
0037099080
-
The cellular fate of mutant rhodopsin: Quality control, degradation and aggresome formation
-
Saliba RS, Munro PM, Luthert PJ, Cheetham ME. The cellular fate of mutant rhodopsin: quality control, degradation and aggresome formation. J Cell Sci. 2002;115:2907-2918.
-
(2002)
J Cell Sci
, vol.115
, pp. 2907-2918
-
-
Saliba, R.S.1
Munro, P.M.2
Luthert, P.J.3
Cheetham, M.E.4
-
9
-
-
33748100274
-
Characterization of rhodopsin P23Hinduced retinal degeneration in a Xenopus laevis model of retinitis pigmentosa
-
Tam BM, Moritz OL. Characterization of rhodopsin P23Hinduced retinal degeneration in a Xenopus laevis model of retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2006;47:3234-3241.
-
(2006)
Invest Ophthalmol Vis Sci
, vol.47
, pp. 3234-33241
-
-
Tam, B.M.1
Moritz, O.L.2
-
10
-
-
36049049392
-
IRE1 signaling affects cell fate during the unfolded protein response
-
Lin JH, Li H, Yasumura D, et al. IRE1 signaling affects cell fate during the unfolded protein response. Science. 2007;318:944-949.
-
(2007)
Science
, vol.318
, pp. 944-949
-
-
Lin, J.H.1
Li, H.2
Yasumura, D.3
-
11
-
-
0026463972
-
Transgenic mice with a rhodopsin mutation (Pro23His): A mouse model of autosomal dominant retinitis pigmentosa
-
Olsson JE, Gordon JW, Pawlyk BS, et al. Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa. Neuron. 1992;9:815-830.
-
(1992)
Neuron
, vol.9
, pp. 815-830
-
-
Olsson, J.E.1
Gordon, J.W.2
Pawlyk, B.S.3
-
12
-
-
0027251934
-
Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene
-
Naash MI, Hollyfield JG, al-Ubaidi MR, Baehr W. Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene. Proc Natl Acad Sci U S A. 1993;90:5499-5503.
-
(1993)
Proc Natl Acad Sci U S A
, vol.90
, pp. 5499-5503
-
-
Naash, M.I.1
Hollyfield, J.G.2
al-Ubaidi, M.R.3
Baehr, W.4
-
13
-
-
79953181251
-
Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations
-
Sakami S, Maeda T, Bereta G, et al. Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations. J Biol Chem. 2011;286:10551-10567.
-
(2011)
J Biol Chem
, vol.286
, pp. 10551-10567
-
-
Sakami, S.1
Maeda, T.2
Bereta, G.3
-
14
-
-
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. 4049-44062
-
-
Roof, D.J.1
Adamian, M.2
Hayes, A.3
-
15
-
-
0032777192
-
Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgene
-
McNally N, Kenna P, Humphries MM, et al. Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgene. Hum Mol Genet. 1999;8:1309-1312.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1309-1312
-
-
McNally, N.1
Kenna, P.2
Humphries, M.M.3
-
16
-
-
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
-
17
-
-
0029972409
-
Light-induced acceleration of photoreceptor degeneration in transgenic mice expressing mutant rhodopsin
-
Naash ML, Peachey NS, Li ZY, et al. Light-induced acceleration of photoreceptor degeneration in transgenic mice expressing mutant rhodopsin. Invest Ophthalmol Vis Sci. 1996;37:775-782.
-
(1996)
Invest Ophthalmol Vis Sci
, vol.37
, pp. 775-782
-
-
Naash, M.L.1
Peachey, N.S.2
Li, Z.Y.3
-
18
-
-
0030729168
-
Defective phototransductive disk membrane morphogenesis in transgenic mice expressing opsin with a mutated N-terminal domain
-
Liu X, Wu TH, Stowe S, et al. Defective phototransductive disk membrane morphogenesis in transgenic mice expressing opsin with a mutated N-terminal domain. J Cell Sci. 1997;110:2589-2597.
-
(1997)
J Cell Sci
, vol.110
, pp. 2589-2597
-
-
Liu, X.1
Wu, T.H.2
Stowe, S.3
-
19
-
-
0032483063
-
Opsin localization and rhodopsin photochemistry in a transgenic mouse model of retinitis pigmentosa
-
Wu TH, Ting TD, Okajima TI, et al. Opsin localization and rhodopsin photochemistry in a transgenic mouse model of retinitis pigmentosa. Neuroscience. 1998;87:709-717.
-
(1998)
Neuroscience
, vol.87
, pp. 709-717
-
-
Wu, T.H.1
Ting, T.D.2
Okajima, T.I.3
-
21
-
-
79955372235
-
AAV delivery of wild-type rhodopsin preserves retinal function in a mouse model of autosomal dominant retinitis pigmentosa
-
Mao H, James T Jr, Schwein A, et al. AAV delivery of wild-type rhodopsin preserves retinal function in a mouse model of autosomal dominant retinitis pigmentosa. Hum Gene Ther. 2011;22: 567-575.
-
(2011)
Hum Gene Ther
, vol.22
, pp. 567-575
-
-
Mao, H.1
James Jr., T.2
Schwein, A.3
-
22
-
-
2942678703
-
Knock-in human rhodopsin-GFP fusions as mouse models for human disease and targets for gene therapy
-
Chan F, Bradley A, Wensel TG, Wilson JH. Knock-in human rhodopsin-GFP fusions as mouse models for human disease and targets for gene therapy. Proc Natl Acad Sci U S A. 2004;101: 9109-9114.
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, pp. 9109-99114
-
-
Chan, F.1
Bradley, A.2
Wensel, T.G.3
Wilson, J.H.4
-
23
-
-
80051741721
-
Efficient mutagenesis of the rhodopsin gene in rod photoreceptor neurons in mice
-
Chan F, Hauswirth WW, Wensel TG, Wilson JH. Efficient mutagenesis of the rhodopsin gene in rod photoreceptor neurons in mice. Nucleic Acids Res. 2011;39:5955-5966.
-
(2011)
Nucleic Acids Res
, vol.39
, pp. 5955-5966
-
-
Chan, F.1
Hauswirth, W.W.2
Wensel, T.G.3
Wilson, J.H.4
-
24
-
-
0033985437
-
Engineering mouse chromosomes with Cre-loxP: Range, efficiency, and somatic applications
-
Zheng B, Sage M, Sheppeard EA, Jurecic V, Bradley A. Engineering mouse chromosomes with Cre-loxP: range, efficiency, and somatic applications. Mol Cell Biol. 2000;20:648-655.
-
(2000)
Mol Cell Biol
, vol.20
, pp. 648-655
-
-
Zheng, B.1
Sage, M.2
Sheppeard, E.A.3
Jurecic, V.4
Bradley, A.5
-
25
-
-
6344249127
-
Differential oocyte-specific expression of Cre recombinase activity in GDF-9-iCre, Zp3cre, and Msx2Cre transgenic mice
-
Lan ZJ, Xu X, Cooney AJ. Differential oocyte-specific expression of Cre recombinase activity in GDF-9-iCre, Zp3cre, and Msx2Cre transgenic mice. Biol Reprod. 2004;71:1469-1474.
-
(2004)
Biol Reprod
, vol.71
, pp. 1469-1474
-
-
Lan, Z.J.1
Xu, X.2
Cooney, A.J.3
-
26
-
-
0015396799
-
Preparation and properties of phospholipid bilayers containing rhodopsin
-
Hong K, Hubbell WL. Preparation and properties of phospholipid bilayers containing rhodopsin. Proc Natl Acad Sci U S A. 1972;69: 2617-2621.
-
(1972)
Proc Natl Acad Sci U S A
, vol.69
, pp. 2617-2621
-
-
Hong, K.1
Hubbell, W.L.2
-
27
-
-
0025202278
-
Mouse opsin. Gene structure and molecular basis of multiple transcripts
-
al-Ubaidi MR, Pittler SJ, Champagne MS, Triantafyllos JT, McGinnis JF, Baehr W. Mouse opsin. Gene structure and molecular basis of multiple transcripts. J Biol Chem. 1990;265:20563-20569.
-
(1990)
J Biol Chem
, vol.265
, pp. 20563-20569
-
-
al-Ubaidi, M.R.1
Pittler, S.J.2
Champagne, M.S.3
Triantafyllos, J.T.4
McGinnis, J.F.5
Baehr, W.6
-
28
-
-
0031045876
-
Retinopathy induced in mice by targeted disruption of the rhodopsin gene
-
Humphries MM, Rancourt D, Farrar GJ, et al. Retinopathy induced in mice by targeted disruption of the rhodopsin gene. Nat Genet. 1997;15:216-219.
-
(1997)
Nat Genet
, vol.15
, pp. 216-219
-
-
Humphries, M.M.1
Rancourt, D.2
Farrar, G.J.3
-
29
-
-
0033582173
-
Morphological, physiological, and biochemical changes in rhodopsin knockout mice
-
Lem J, Krasnoperova NV, Calvert PD, et al. Morphological, physiological, and biochemical changes in rhodopsin knockout mice. Proc Natl Acad Sci U S A. 1999;96:736-741.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 736-741
-
-
Lem, J.1
Krasnoperova, N.V.2
Calvert, P.D.3
-
30
-
-
33750633662
-
Defective development of photoreceptor membranes in a mouse model of recessive retinal degeneration
-
Gross AK, Decker G, Chan F, Sandoval IM, Wilson JH, Wensel TG. Defective development of photoreceptor membranes in a mouse model of recessive retinal degeneration. Vision Res. 2006;46: 4510-4518.
-
(2006)
Vision Res
, vol.46
, pp. 4510-4518
-
-
Gross, A.K.1
Decker, G.2
Chan, F.3
Sandoval, I.M.4
Wilson, J.H.5
Wensel, T.G.6
-
31
-
-
0032168064
-
Regulation of sorting and post-Golgi trafficking of rhodopsin by its C-terminal sequence QVS(A)PA
-
Deretic D, Schmerl S, Hargrave PA, Arendt A, McDowell JH. Regulation of sorting and post-Golgi trafficking of rhodopsin by its C-terminal sequence QVS(A)PA. Proc Natl Acad Sci U S A. 1998; 95:10620-10625.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 10620-10625
-
-
Deretic, D.1
Schmerl, S.2
Hargrave, P.A.3
Arendt, A.4
McDowell, J.H.5
-
32
-
-
0742321905
-
The nature of dominant mutations of rhodopsin and implications for gene therapy
-
Wilson JH, Wensel TG. The nature of dominant mutations of rhodopsin and implications for gene therapy. Mol Neurobiol. 2003;28:149-158.
-
(2003)
Mol Neurobiol
, vol.28
, pp. 149-158
-
-
Wilson, J.H.1
Wensel, T.G.2
|