199 related articles for article (PubMed ID: 9801367)
21. A common microRNA signature in mouse models of retinal degeneration.
Loscher CJ; Hokamp K; Wilson JH; Li T; Humphries P; Farrar GJ; Palfi A
Exp Eye Res; 2008 Dec; 87(6):529-34. PubMed ID: 18834879
[TBL] [Abstract][Full Text] [Related]
22. CNTF induces regeneration of cone outer segments in a rat model of retinal degeneration.
Li Y; Tao W; Luo L; Huang D; Kauper K; Stabila P; Lavail MM; Laties AM; Wen R
PLoS One; 2010 Mar; 5(3):e9495. PubMed ID: 20209167
[TBL] [Abstract][Full Text] [Related]
23. Systemic but not intraocular Epo gene transfer protects the retina from light-and genetic-induced degeneration.
Rex TS; Allocca M; Domenici L; Surace EM; Maguire AM; Lyubarsky A; Cellerino A; Bennett J; Auricchio A
Mol Ther; 2004 Nov; 10(5):855-61. PubMed ID: 15509503
[TBL] [Abstract][Full Text] [Related]
24. Gene therapy restores vision and delays degeneration in the CNGB1(-/-) mouse model of retinitis pigmentosa.
Michalakis S; Koch S; Sothilingam V; Garcia Garrido M; Tanimoto N; Schulze E; Becirovic E; Koch F; Seide C; Beck SC; Seeliger MW; Mühlfriedel R; Biel M
Adv Exp Med Biol; 2014; 801():733-9. PubMed ID: 24664765
[TBL] [Abstract][Full Text] [Related]
25. Glial cell line-derived neurotrophic factor induces histologic and functional protection of rod photoreceptors in the rd/rd mouse.
Frasson M; Picaud S; Léveillard T; Simonutti M; Mohand-Said S; Dreyfus H; Hicks D; Sabel J
Invest Ophthalmol Vis Sci; 1999 Oct; 40(11):2724-34. PubMed ID: 10509671
[TBL] [Abstract][Full Text] [Related]
26. Genetic supplementation of RDS alleviates a loss-of-function phenotype in C214S model of retinitis pigmentosa.
Nour M; Fliesler SJ; Naash MI
Adv Exp Med Biol; 2008; 613():129-38. PubMed ID: 18188937
[No Abstract] [Full Text] [Related]
27. Systemic administration of nilvadipine delays photoreceptor degeneration of heterozygous retinal degeneration slow (rds) mouse.
Takeuchi K; Nakazawa M; Mizukoshi S
Exp Eye Res; 2008 Jan; 86(1):60-9. PubMed ID: 17976582
[TBL] [Abstract][Full Text] [Related]
28. Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse.
Connell G; Bascom R; Molday L; Reid D; McInnes RR; Molday RS
Proc Natl Acad Sci U S A; 1991 Feb; 88(3):723-6. PubMed ID: 1992463
[TBL] [Abstract][Full Text] [Related]
29. Antioxidant or neurotrophic factor treatment preserves function in a mouse model of neovascularization-associated oxidative stress.
Dorrell MI; Aguilar E; Jacobson R; Yanes O; Gariano R; Heckenlively J; Banin E; Ramirez GA; Gasmi M; Bird A; Siuzdak G; Friedlander M
J Clin Invest; 2009 Mar; 119(3):611-23. PubMed ID: 19188685
[TBL] [Abstract][Full Text] [Related]
30. Glial cell line derived neurotrophic factor delays photoreceptor degeneration in a transgenic rat model of retinitis pigmentosa.
McGee Sanftner LH; Abel H; Hauswirth WW; Flannery JG
Mol Ther; 2001 Dec; 4(6):622-9. PubMed ID: 11735347
[TBL] [Abstract][Full Text] [Related]
31. A combination of CNTF and BDNF rescues rd photoreceptors but changes rod differentiation in the presence of RPE in retinal explants.
Caffé AR; Söderpalm AK; Holmqvist I; van Veen T
Invest Ophthalmol Vis Sci; 2001 Jan; 42(1):275-82. PubMed ID: 11133879
[TBL] [Abstract][Full Text] [Related]
32. Melatonin delays photoreceptor degeneration in the rds/rds mouse.
Liang FQ; Aleman TS; ZaixinYang ; Cideciyan AV; Jacobson SG; Bennett J
Neuroreport; 2001 Apr; 12(5):1011-4. PubMed ID: 11303736
[TBL] [Abstract][Full Text] [Related]
33. Optimal control with MANF treatment of photoreceptor degeneration.
Camacho ET; Lenhart S; Melara LA; Villalobos MC; Wirkus S
Math Med Biol; 2020 Feb; 37(1):1-21. PubMed ID: 30810166
[TBL] [Abstract][Full Text] [Related]
34. Pigment epithelium-derived factor delays the death of photoreceptors in mouse models of inherited retinal degenerations.
Cayouette M; Smith SB; Becerra SP; Gravel C
Neurobiol Dis; 1999 Dec; 6(6):523-32. PubMed ID: 10600408
[TBL] [Abstract][Full Text] [Related]
35. Evaluation of the rhodopsin knockout mouse as a model of pure cone function.
Jaissle GB; May CA; Reinhard J; Kohler K; Fauser S; Lütjen-Drecoll E; Zrenner E; Seeliger MW
Invest Ophthalmol Vis Sci; 2001 Feb; 42(2):506-13. PubMed ID: 11157890
[TBL] [Abstract][Full Text] [Related]
36. Peripherin-2 couples rhodopsin to the CNG channel in outer segments of rod photoreceptors.
Becirovic E; Nguyen ON; Paparizos C; Butz ES; Stern-Schneider G; Wolfrum U; Hauck SM; Ueffing M; Wahl-Schott C; Michalakis S; Biel M
Hum Mol Genet; 2014 Nov; 23(22):5989-97. PubMed ID: 24963162
[TBL] [Abstract][Full Text] [Related]
37. Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.
Lines MA; Hébert M; McTaggart KE; Flynn SJ; Tennant MT; MacDonald IM
Ophthalmology; 2002 Oct; 109(10):1862-70. PubMed ID: 12359607
[TBL] [Abstract][Full Text] [Related]
38. Increased expression of brain-derived neurotrophic factor preserves retinal function and slows cell death from rhodopsin mutation or oxidative damage.
Okoye G; Zimmer J; Sung J; Gehlbach P; Deering T; Nambu H; Hackett S; Melia M; Esumi N; Zack DJ; Campochiaro PA
J Neurosci; 2003 May; 23(10):4164-72. PubMed ID: 12764104
[TBL] [Abstract][Full Text] [Related]
39. Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.
Kajiwara K; Hahn LB; Mukai S; Travis GH; Berson EL; Dryja TP
Nature; 1991 Dec; 354(6353):480-3. PubMed ID: 1684223
[TBL] [Abstract][Full Text] [Related]
40. 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
Invest Ophthalmol Vis Sci; 1995 Jul; 36(8):1603-14. PubMed ID: 7601641
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
