880 related articles for article (PubMed ID: 7925677)
1. 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]
2. 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]
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. 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]
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. 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]
7. Degenerative changes in a retina affected with autosomal dominant retinitis pigmentosa.
Flannery JG; Farber DB; Bird AC; Bok D
Invest Ophthalmol Vis Sci; 1989 Feb; 30(2):191-211. PubMed ID: 2914751
[TBL] [Abstract][Full Text] [Related]
8. Rod photoreceptor neurite sprouting in retinitis pigmentosa.
Li ZY; Kljavin IJ; Milam AH
J Neurosci; 1995 Aug; 15(8):5429-38. PubMed ID: 7643192
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Clinical-ultrastructural study of a retinal dystrophy.
Bunt-Milam AH; Kalina RE; Pagon RA
Invest Ophthalmol Vis Sci; 1983 Apr; 24(4):458-69. PubMed ID: 6682096
[TBL] [Abstract][Full Text] [Related]
11. Histologic study of retinitis pigmentosa due to a mutation in the RP13 gene (PRPC8): comparison with rhodopsin Pro23His, Cys110Arg, and Glu181Lys.
To K; Adamian M; Berson EL
Am J Ophthalmol; 2004 May; 137(5):946-8. PubMed ID: 15126168
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Life history of cones in the rhodopsin-mutant P23H-3 rat: evidence of long-term survival.
Chrysostomou V; Stone J; Valter K
Invest Ophthalmol Vis Sci; 2009 May; 50(5):2407-16. PubMed ID: 19117918
[TBL] [Abstract][Full Text] [Related]
16. Retinopathy induced in mice by targeted disruption of the rhodopsin gene.
Humphries MM; Rancourt D; Farrar GJ; Kenna P; Hazel M; Bush RA; Sieving PA; Sheils DM; McNally N; Creighton P; Erven A; Boros A; Gulya K; Capecchi MR; Humphries P
Nat Genet; 1997 Feb; 15(2):216-9. PubMed ID: 9020854
[TBL] [Abstract][Full Text] [Related]
17. Histopathologic study of an unusual form of retinitis pigmentosa.
Szamier RB; Berson EL
Invest Ophthalmol Vis Sci; 1982 May; 22(5):559-70. PubMed ID: 7076403
[TBL] [Abstract][Full Text] [Related]
18. Autosomal dominant retinitis pigmentosa in a large family: a clinical and molecular genetic study.
Rosas DJ; Roman AJ; Weissbrod P; Macke JP; Nathans J
Invest Ophthalmol Vis Sci; 1994 Jul; 35(8):3134-44. PubMed ID: 8045708
[TBL] [Abstract][Full Text] [Related]
19. Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosa.
Jacobson SG; Kemp CM; Cideciyan AV; Macke JP; Sung CH; Nathans J
Invest Ophthalmol Vis Sci; 1994 Apr; 35(5):2521-34. PubMed ID: 8163341
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
