241 related articles for article (PubMed ID: 8516292)
1. 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
Proc Natl Acad Sci U S A; 1993 Jun; 90(12):5499-503. PubMed ID: 8516292
[TBL] [Abstract][Full Text] [Related]
2. Polygenic disease and retinitis pigmentosa: albinism exacerbates photoreceptor degeneration induced by the expression of a mutant opsin in transgenic mice.
Naash MI; Ripps H; Li S; Goto Y; Peachey NS
J Neurosci; 1996 Dec; 16(24):7853-8. PubMed ID: 8987813
[TBL] [Abstract][Full Text] [Related]
3. Functional abnormalities in transgenic mice expressing a mutant rhodopsin gene.
Goto Y; Peachey NS; Ripps H; Naash MI
Invest Ophthalmol Vis Sci; 1995 Jan; 36(1):62-71. PubMed ID: 7822160
[TBL] [Abstract][Full Text] [Related]
4. A 221-bp fragment of the mouse opsin promoter directs expression specifically to the rod photoreceptors of transgenic mice.
Quiambao AB; Peachey NS; Mangini NJ; Röhlich P; Hollyfield JG; al-Ubaidi MR
Vis Neurosci; 1997; 14(4):617-25. PubMed ID: 9278991
[TBL] [Abstract][Full Text] [Related]
5. Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa.
Olsson JE; Gordon JW; Pawlyk BS; Roof D; Hayes A; Molday RS; Mukai S; Cowley GS; Berson EL; Dryja TP
Neuron; 1992 Nov; 9(5):815-30. PubMed ID: 1418997
[TBL] [Abstract][Full Text] [Related]
6. P23H opsin knock-in mice reveal a novel step in retinal rod disc morphogenesis.
Sakami S; Kolesnikov AV; Kefalov VJ; Palczewski K
Hum Mol Genet; 2014 Apr; 23(7):1723-41. PubMed ID: 24214395
[TBL] [Abstract][Full Text] [Related]
7. AAV delivery of wild-type rhodopsin preserves retinal function in a mouse model of autosomal dominant retinitis pigmentosa.
Mao H; James T; Schwein A; Shabashvili AE; Hauswirth WW; Gorbatyuk MS; Lewin AS
Hum Gene Ther; 2011 May; 22(5):567-75. PubMed ID: 21126223
[TBL] [Abstract][Full Text] [Related]
8. Opsin localization and rhodopsin photochemistry in a transgenic mouse model of retinitis pigmentosa.
Wu TH; Ting TD; Okajima TI; Pepperberg DR; Ho YK; Ripps H; Naash MI
Neuroscience; 1998 Dec; 87(3):709-17. PubMed ID: 9758235
[TBL] [Abstract][Full Text] [Related]
9. Retinal degeneration in humanized mice expressing mutant rhodopsin under the control of the endogenous murine promoter.
Liu X; Jia R; Meng X; Li Y; Yang L
Exp Eye Res; 2022 Feb; 215():108893. PubMed ID: 34919893
[TBL] [Abstract][Full Text] [Related]
10. Hammerhead ribozymes designed to cleave all human rod opsin mRNAs which cause autosomal dominant retinitis pigmentosa.
Sullivan JM; Pietras KM; Shin BJ; Misasi JN
Mol Vis; 2002 Apr; 8():102-13. PubMed ID: 11961505
[TBL] [Abstract][Full Text] [Related]
11. Expression of a mutant opsin gene increases the susceptibility of the retina to light damage.
Wang M; Lam TT; Tso MO; Naash MI
Vis Neurosci; 1997; 14(1):55-62. PubMed ID: 9057268
[TBL] [Abstract][Full Text] [Related]
12. Retinal morphological and functional changes in an animal model of retinitis pigmentosa.
Lu B; Morgans CW; Girman S; Lund R; Wang S
Vis Neurosci; 2013 May; 30(3):77-89. PubMed ID: 23510618
[TBL] [Abstract][Full Text] [Related]
13. 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; Okano K; Golczak M; Sumaroka A; Roman AJ; Cideciyan AV; Jacobson SG; Palczewski K
J Biol Chem; 2011 Mar; 286(12):10551-67. PubMed ID: 21224384
[TBL] [Abstract][Full Text] [Related]
14. Light-induced acceleration of photoreceptor degeneration in transgenic mice expressing mutant rhodopsin.
Naash ML; Peachey NS; Li ZY; Gryczan CC; Goto Y; Blanks J; Milam AH; Ripps H
Invest Ophthalmol Vis Sci; 1996 Apr; 37(5):775-82. PubMed ID: 8603862
[TBL] [Abstract][Full Text] [Related]
15. Inherent instability of the retinitis pigmentosa P23H mutant opsin.
Chen Y; Jastrzebska B; Cao P; Zhang J; Wang B; Sun W; Yuan Y; Feng Z; Palczewski K
J Biol Chem; 2014 Mar; 289(13):9288-303. PubMed ID: 24515108
[TBL] [Abstract][Full Text] [Related]
16. Restoration of visual function in P23H rhodopsin transgenic rats by gene delivery of BiP/Grp78.
Gorbatyuk MS; Knox T; LaVail MM; Gorbatyuk OS; Noorwez SM; Hauswirth WW; Lin JH; Muzyczka N; Lewin AS
Proc Natl Acad Sci U S A; 2010 Mar; 107(13):5961-6. PubMed ID: 20231467
[TBL] [Abstract][Full Text] [Related]
17. The heat-shock response co-inducer arimoclomol protects against retinal degeneration in rhodopsin retinitis pigmentosa.
Parfitt DA; Aguila M; McCulley CH; Bevilacqua D; Mendes HF; Athanasiou D; Novoselov SS; Kanuga N; Munro PM; Coffey PJ; Kalmar B; Greensmith L; Cheetham ME
Cell Death Dis; 2014 May; 5(5):e1236. PubMed ID: 24853414
[TBL] [Abstract][Full Text] [Related]
18. Ablation of the X-linked retinitis pigmentosa 2 (Rp2) gene in mice results in opsin mislocalization and photoreceptor degeneration.
Li L; Khan N; Hurd T; Ghosh AK; Cheng C; Molday R; Heckenlively JR; Swaroop A; Khanna H
Invest Ophthalmol Vis Sci; 2013 Jul; 54(7):4503-11. PubMed ID: 23745007
[TBL] [Abstract][Full Text] [Related]
19. Rd9 is a naturally occurring mouse model of a common form of retinitis pigmentosa caused by mutations in RPGR-ORF15.
Thompson DA; Khan NW; Othman MI; Chang B; Jia L; Grahek G; Wu Z; Hiriyanna S; Nellissery J; Li T; Khanna H; Colosi P; Swaroop A; Heckenlively JR
PLoS One; 2012; 7(5):e35865. PubMed ID: 22563472
[TBL] [Abstract][Full Text] [Related]
20. Preservation of photoreceptor morphology and function in P23H rats using an allele independent ribozyme.
Gorbatyuk M; Justilien V; Liu J; Hauswirth WW; Lewin AS
Exp Eye Res; 2007 Jan; 84(1):44-52. PubMed ID: 17083931
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
