These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. Detailed histopathologic characterization of the retinopathy, globe enlarged (rge) chick phenotype. Montiani-Ferreira F; Fischer A; Cernuda-Cernuda R; Kiupel M; DeGrip WJ; Sherry D; Cho SS; Shaw GC; Evans MG; Hocking PM; Petersen-Jones SM Mol Vis; 2005 Jan; 11():11-27. PubMed ID: 15660021 [TBL] [Abstract][Full Text] [Related]
3. Concentric retinitis pigmentosa: clinicopathologic correlations. Milam AH; De Castro EB; Smith JE; Tang WX; John SK; Gorin MB; Stone EM; Aguirre GD; Jacobson SG Exp Eye Res; 2001 Oct; 73(4):493-508. PubMed ID: 11825021 [TBL] [Abstract][Full Text] [Related]
4. Autosomal dominant retinitis pigmentosa caused by the threonine-17-methionine rhodopsin mutation: retinal histopathology and immunocytochemistry. Li ZY; Jacobson SG; Milam AH Exp Eye Res; 1994 Apr; 58(4):397-408. PubMed ID: 7925677 [TBL] [Abstract][Full Text] [Related]
5. Rhodopsin transgenic pigs as a model for human retinitis pigmentosa. Li ZY; Wong F; Chang JH; Possin DE; Hao Y; Petters RM; Milam AH Invest Ophthalmol Vis Sci; 1998 Apr; 39(5):808-19. PubMed ID: 9538889 [TBL] [Abstract][Full Text] [Related]
6. Functional and structural changes in the retina of wire-haired dachshunds with early-onset cone-rod dystrophy. Ropstad EO; Narfström K; Lingaas F; Wiik C; Bruun A; Bjerkås E Invest Ophthalmol Vis Sci; 2008 Mar; 49(3):1106-15. PubMed ID: 18326738 [TBL] [Abstract][Full Text] [Related]
7. Loss of cone molecular markers in rhodopsin-mutant human retinas with retinitis pigmentosa. John SK; Smith JE; Aguirre GD; Milam AH Mol Vis; 2000 Nov; 6():204-15. PubMed ID: 11063754 [TBL] [Abstract][Full Text] [Related]
8. Predominant rod photoreceptor degeneration in Leber congenital amaurosis. van der Spuy J; Munro PM; Luthert PJ; Preising MN; Bek T; Heegaard S; Cheetham ME Mol Vis; 2005 Jul; 11():542-53. PubMed ID: 16052170 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Yearly rates of rod and cone functional loss in retinitis pigmentosa and cone-rod dystrophy. Birch DG; Anderson JL; Fish GE Ophthalmology; 1999 Feb; 106(2):258-68. PubMed ID: 9951474 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. High-resolution imaging with adaptive optics in patients with inherited retinal degeneration. Duncan JL; Zhang Y; Gandhi J; Nakanishi C; Othman M; Branham KE; Swaroop A; Roorda A Invest Ophthalmol Vis Sci; 2007 Jul; 48(7):3283-91. PubMed ID: 17591900 [TBL] [Abstract][Full Text] [Related]
13. Clinicopathologic effects of the Q64ter rhodopsin mutation in retinitis pigmentosa. Milam AH; Li ZY; Cideciyan AV; Jacobson SG Invest Ophthalmol Vis Sci; 1996 Apr; 37(5):753-65. PubMed ID: 8603860 [TBL] [Abstract][Full Text] [Related]
14. Double cone dystrophy and RPE degeneration in the retina of the zebrafish gnn mutant. Biehlmaier O; Neuhauss SC; Kohler K Invest Ophthalmol Vis Sci; 2003 Mar; 44(3):1287-98. PubMed ID: 12601061 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Cone neurite sprouting: an early onset abnormality of the cone photoreceptors in the retinal degeneration mouse. Fei Y Mol Vis; 2002 Aug; 8():306-14. PubMed ID: 12355062 [TBL] [Abstract][Full Text] [Related]
17. Photoreceptor loss in age-related macular degeneration. Curcio CA; Medeiros NE; Millican CL Invest Ophthalmol Vis Sci; 1996 Jun; 37(7):1236-49. PubMed ID: 8641827 [TBL] [Abstract][Full Text] [Related]
18. Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15. Demirci FY; Gupta N; Radak AL; Rigatti BW; Mah TS; Milam AH; Gorin MB Am J Ophthalmol; 2005 Feb; 139(2):386-8. PubMed ID: 15734019 [TBL] [Abstract][Full Text] [Related]
19. Localization of tubby-like protein 1 in developing and adult human retinas. Milam AH; Hendrickson AE; Xiao M; Smith JE; Possin DE; John SK; Nishina PM Invest Ophthalmol Vis Sci; 2000 Jul; 41(8):2352-6. PubMed ID: 10892883 [TBL] [Abstract][Full Text] [Related]
20. Ectopic synaptogenesis during retinal degeneration in the royal college of surgeons rat. Peng YW; Senda T; Hao Y; Matsuno K; Wong F Neuroscience; 2003; 119(3):813-20. PubMed ID: 12809702 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]