336 related articles for article (PubMed ID: 20007830)
1. Cone versus rod disease in a mutant Rpgr mouse caused by different genetic backgrounds.
Brunner S; Skosyrski S; Kirschner-Schwabe R; Knobeloch KP; Neidhardt J; Feil S; Glaus E; Luhmann UF; Rüther K; Berger W
Invest Ophthalmol Vis Sci; 2010 Feb; 51(2):1106-15. PubMed ID: 20007830
[TBL] [Abstract][Full Text] [Related]
2. Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.
Jacobson SG; Buraczynska M; Milam AH; Chen C; Järvaläinen M; Fujita R; Wu W; Huang Y; Cideciyan AV; Swaroop A
Invest Ophthalmol Vis Sci; 1997 Sep; 38(10):1983-97. PubMed ID: 9331262
[TBL] [Abstract][Full Text] [Related]
3. A frameshift mutation in RPGR exon ORF15 causes photoreceptor degeneration and inner retina remodeling in a model of X-linked retinitis pigmentosa.
Beltran WA; Hammond P; Acland GM; Aguirre GD
Invest Ophthalmol Vis Sci; 2006 Apr; 47(4):1669-81. PubMed ID: 16565408
[TBL] [Abstract][Full Text] [Related]
4. Biphasic photoreceptor degeneration induced by light in a T17M rhodopsin mouse model of cone bystander damage.
Krebs MP; White DA; Kaushal S
Invest Ophthalmol Vis Sci; 2009 Jun; 50(6):2956-65. PubMed ID: 19136713
[TBL] [Abstract][Full Text] [Related]
5. Cone opsin mislocalization in Rpe65-/- mice: a defect that can be corrected by 11-cis retinal.
Rohrer B; Lohr HR; Humphries P; Redmond TM; Seeliger MW; Crouch RK
Invest Ophthalmol Vis Sci; 2005 Oct; 46(10):3876-82. PubMed ID: 16186377
[TBL] [Abstract][Full Text] [Related]
6. Connexin 36 in photoreceptor cells: studies on transgenic rod-less and cone-less mouse retinas.
Dang L; Pulukuri S; Mears AJ; Swaroop A; Reese BE; Sitaramayya A
Mol Vis; 2004 May; 10():323-7. PubMed ID: 15152186
[TBL] [Abstract][Full Text] [Related]
7. Retinal histopathology of an XLRP carrier with a mutation in the RPGR exon ORF15.
Aguirre GD; Yashar BM; John SK; Smith JE; Breuer DK; Hiriyanna S; Swaroop A; Milam AH
Exp Eye Res; 2002 Oct; 75(4):431-43. PubMed ID: 12387791
[TBL] [Abstract][Full Text] [Related]
8. Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).
Pang JJ; Chang B; Hawes NL; Hurd RE; Davisson MT; Li J; Noorwez SM; Malhotra R; McDowell JH; Kaushal S; Hauswirth WW; Nusinowitz S; Thompson DA; Heckenlively JR
Mol Vis; 2005 Feb; 11():152-62. PubMed ID: 15765048
[TBL] [Abstract][Full Text] [Related]
9. Residual photosensitivity in mice lacking both rod opsin and cone photoreceptor cyclic nucleotide gated channel 3 alpha subunit.
Barnard AR; Appleford JM; Sekaran S; Chinthapalli K; Jenkins A; Seeliger M; Biel M; Humphries P; Douglas RH; Wenzel A; Foster RG; Hankins MW; Lucas RJ
Vis Neurosci; 2004; 21(5):675-83. PubMed ID: 15683556
[TBL] [Abstract][Full Text] [Related]
10. In vivo analysis of cone survival in mice.
Beck SC; Schaeferhoff K; Michalakis S; Fischer MD; Huber G; Rieger N; Riess O; Wissinger B; Biel M; Bonin M; Seeliger MW; Tanimoto N
Invest Ophthalmol Vis Sci; 2010 Jan; 51(1):493-7. PubMed ID: 19737879
[TBL] [Abstract][Full Text] [Related]
11. Gene replacement therapy rescues photoreceptor degeneration in a murine model of Leber congenital amaurosis lacking RPGRIP.
Pawlyk BS; Smith AJ; Buch PK; Adamian M; Hong DH; Sandberg MA; Ali RR; Li T
Invest Ophthalmol Vis Sci; 2005 Sep; 46(9):3039-45. PubMed ID: 16123399
[TBL] [Abstract][Full Text] [Related]
12. Rod and cone opsin mislocalization in an autopsy eye from a carrier of X-linked retinitis pigmentosa with a Gly436Asp mutation in the RPGR gene.
Adamian M; Pawlyk BS; Hong DH; Berson EL
Am J Ophthalmol; 2006 Sep; 142(3):515-8. PubMed ID: 16935610
[TBL] [Abstract][Full Text] [Related]
13. Impaired opsin targeting and cone photoreceptor migration in the retina of mice lacking the cyclic nucleotide-gated channel CNGA3.
Michalakis S; Geiger H; Haverkamp S; Hofmann F; Gerstner A; Biel M
Invest Ophthalmol Vis Sci; 2005 Apr; 46(4):1516-24. PubMed ID: 15790924
[TBL] [Abstract][Full Text] [Related]
14. Retinoschisislike alterations in the mouse eye caused by gene targeting of the Norrie disease gene.
Ruether K; van de Pol D; Jaissle G; Berger W; Tornow RP; Zrenner E
Invest Ophthalmol Vis Sci; 1997 Mar; 38(3):710-8. PubMed ID: 9071226
[TBL] [Abstract][Full Text] [Related]
15. The status of cones in the rhodopsin mutant P23H-3 retina: light-regulated damage and repair in parallel with rods.
Chrysostomou V; Stone J; Stowe S; Barnett NL; Valter K
Invest Ophthalmol Vis Sci; 2008 Mar; 49(3):1116-25. PubMed ID: 18326739
[TBL] [Abstract][Full Text] [Related]
16. Development of the cone photoreceptor mosaic in the mouse retina revealed by fluorescent cones in transgenic mice.
Fei Y
Mol Vis; 2003 Feb; 9():31-42. PubMed ID: 12592228
[TBL] [Abstract][Full Text] [Related]
17. Ribozyme knockdown of the gamma-subunit of rod cGMP phosphodiesterase alters the ERG and retinal morphology in wild-type mice.
Liu J; Timmers AM; Lewin AS; Hauswirth WW
Invest Ophthalmol Vis Sci; 2005 Oct; 46(10):3836-44. PubMed ID: 16186371
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Does recombinant adeno-associated virus-vectored proximal region of mouse rhodopsin promoter support only rod-type specific expression in vivo?
Glushakova LG; Timmers AM; Issa TM; Cortez NG; Pang J; Teusner JT; Hauswirth WW
Mol Vis; 2006 Apr; 12():298-309. PubMed ID: 16617297
[TBL] [Abstract][Full Text] [Related]
20. The transcription factor Nr2e3 functions in retinal progenitors to suppress cone cell generation.
Haider NB; Demarco P; Nystuen AM; Huang X; Smith RS; McCall MA; Naggert JK; Nishina PM
Vis Neurosci; 2006; 23(6):917-29. PubMed ID: 17266784
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
