175 related articles for article (PubMed ID: 18805803)
21. Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration.
Hayward C; Shu X; Cideciyan AV; Lennon A; Barran P; Zareparsi S; Sawyer L; Hendry G; Dhillon B; Milam AH; Luthert PJ; Swaroop A; Hastie ND; Jacobson SG; Wright AF
Hum Mol Genet; 2003 Oct; 12(20):2657-67. PubMed ID: 12944416
[TBL] [Abstract][Full Text] [Related]
22. Efficiency of lentiviral transduction during development in normal and rd mice.
Pang J; Cheng M; Haire SE; Barker E; Planelles V; Blanks JC
Mol Vis; 2006 Jul; 12():756-67. PubMed ID: 16862069
[TBL] [Abstract][Full Text] [Related]
23. Suppression of developmental retinal cell death but not of photoreceptor degeneration in Bax-deficient mice.
Mosinger Ogilvie J; Deckwerth TL; Knudson CM; Korsmeyer SJ
Invest Ophthalmol Vis Sci; 1998 Aug; 39(9):1713-20. PubMed ID: 9699561
[TBL] [Abstract][Full Text] [Related]
24. Development and degeneration of retina in rds mutant mice: the electroretinogram.
Reuter JH; Sanyal S
Neurosci Lett; 1984 Jul; 48(2):231-7. PubMed ID: 6483282
[TBL] [Abstract][Full Text] [Related]
25. Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal Dystrophy.
Arno G; Hull S; Robson AG; Holder GE; Cheetham ME; Webster AR; Plagnol V; Moore AT
Invest Ophthalmol Vis Sci; 2015 Apr; 56(4):2358-65. PubMed ID: 25766589
[TBL] [Abstract][Full Text] [Related]
26. Assessment of retinal function and morphology in aging Ccl2 knockout mice.
Vessey KA; Waugh M; Jobling AI; Phipps JA; Ho T; Trogrlic L; Greferath U; Fletcher EL
Invest Ophthalmol Vis Sci; 2015 Jan; 56(2):1238-52. PubMed ID: 25626968
[TBL] [Abstract][Full Text] [Related]
27. Visual electrophysiological features of two naturally occurring mouse models with retinal dysfunction.
Miyamoto M; Imai R; Sugimoto S; Aoki M; Nagai H; Ando T
Curr Eye Res; 2006 Apr; 31(4):329-35. PubMed ID: 16603466
[TBL] [Abstract][Full Text] [Related]
28. The retina of c-fos-/- mice: electrophysiologic, morphologic and biochemical aspects.
Kueng-Hitz N; Grimm C; Lansel N; Hafezi F; He L; Fox DA; Remé CE; Niemeyer G; Wenzel A
Invest Ophthalmol Vis Sci; 2000 Mar; 41(3):909-16. PubMed ID: 10711713
[TBL] [Abstract][Full Text] [Related]
29. Lack of paraoxonase 1 alters phospholipid composition, but not morphology and function of the mouse retina.
Oczos J; Sutter I; Kloeckener-Gruissem B; Berger W; Riwanto M; Rentsch K; Hornemann T; von Eckardstein A; Grimm C
Invest Ophthalmol Vis Sci; 2014 Jul; 55(8):4714-27. PubMed ID: 25028362
[TBL] [Abstract][Full Text] [Related]
30. Retinoschisin gene therapy and natural history in the Rs1h-KO mouse: long-term rescue from retinal degeneration.
Kjellstrom S; Bush RA; Zeng Y; Takada Y; Sieving PA
Invest Ophthalmol Vis Sci; 2007 Aug; 48(8):3837-45. PubMed ID: 17652759
[TBL] [Abstract][Full Text] [Related]
31. Impaired channel targeting and retinal degeneration in mice lacking the cyclic nucleotide-gated channel subunit CNGB1.
Hüttl S; Michalakis S; Seeliger M; Luo DG; Acar N; Geiger H; Hudl K; Mader R; Haverkamp S; Moser M; Pfeifer A; Gerstner A; Yau KW; Biel M
J Neurosci; 2005 Jan; 25(1):130-8. PubMed ID: 15634774
[TBL] [Abstract][Full Text] [Related]
32. Sirtuin 1 participates in the process of age-related retinal degeneration.
Zeng Y; Yang K
Biochem Biophys Res Commun; 2015 Dec 4-11; 468(1-2):167-72. PubMed ID: 26522222
[TBL] [Abstract][Full Text] [Related]
33. Crb1 is a determinant of retinal apical Müller glia cell features.
van de Pavert SA; Sanz AS; Aartsen WM; Vos RM; Versteeg I; Beck SC; Klooster J; Seeliger MW; Wijnholds J
Glia; 2007 Nov; 55(14):1486-97. PubMed ID: 17705196
[TBL] [Abstract][Full Text] [Related]
34. Retinal Structure in Cobalamin C Disease: Mechanistic and Therapeutic Implications.
Aleman TS; Brodie F; Garvin C; Gewaily DY; Ficicioglu CH; Mills MD; Forbes BJ; Maguire AM; Davidson SL
Ophthalmic Genet; 2015; 36(4):339-48. PubMed ID: 24512365
[TBL] [Abstract][Full Text] [Related]
35. Retinal degeneration mutation in Sftpa1tm1Kor/J and Sftpd -/- targeted mice.
Bhatti F; Kung JW; Vieira F
PLoS One; 2018; 13(7):e0199824. PubMed ID: 29969487
[TBL] [Abstract][Full Text] [Related]
36. Retinal degeneration and RPE transplantation in Rpe65(-/-) mice.
Gouras P; Kong J; Tsang SH
Invest Ophthalmol Vis Sci; 2002 Oct; 43(10):3307-11. PubMed ID: 12356839
[TBL] [Abstract][Full Text] [Related]
37. Retinal Phenotype following Combined Deletion of the Chemokine Receptor CCR2 and the Chemokine CX3CL1 in Mice.
Hagbi-Levi S; Grunin M; Elbaz-Hayoun S; Tal D; Obolensky A; Hanhart J; Banin E; Burstyn-Cohen T; Chowers I
Ophthalmic Res; 2016; 55(3):126-34. PubMed ID: 26670885
[TBL] [Abstract][Full Text] [Related]
38. Increased sensitivity to light-induced damage in a mouse model of autosomal dominant retinal disease.
White DA; Fritz JJ; Hauswirth WW; Kaushal S; Lewin AS
Invest Ophthalmol Vis Sci; 2007 May; 48(5):1942-51. PubMed ID: 17460245
[TBL] [Abstract][Full Text] [Related]
39. Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases.
Nishiguchi KM; Sandberg MA; Gorji N; Berson EL; Dryja TP
Hum Mutat; 2005 Mar; 25(3):248-58. PubMed ID: 15712225
[TBL] [Abstract][Full Text] [Related]
40. Slow-progressing photoreceptor cell degeneration in night blindness c mutant zebrafish.
Maaswinkel H; Ren JQ; Li L
J Neurocytol; 2003 Nov; 32(9):1107-16. PubMed ID: 15044842
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
