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107 related items for PubMed ID: 2141327

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  • 3. 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 03; 6():204-15. PubMed ID: 11063754
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  • 4. 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 03; 142(3):515-8. PubMed ID: 16935610
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  • 5. Identification of proteins in retinas and IPM from eyes with retinitis pigmentosa.
    Schmidt SY, Heth CA, Edwards RB, Brandt JT, Adler AJ, Spiegel A, Shichi H, Berson EL.
    Invest Ophthalmol Vis Sci; 1988 Nov 03; 29(11):1585-93. PubMed ID: 2972663
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  • 10. 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 03; 58(4):397-408. PubMed ID: 7925677
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  • 11. Distribution patterns of photoreceptors, protein, and cyclic nucleotides in the human retina.
    Farber DB, Flannery JG, Lolley RN, Bok D.
    Invest Ophthalmol Vis Sci; 1985 Nov 03; 26(11):1558-68. PubMed ID: 2997074
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  • 12. 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 03; 47(4):1669-81. PubMed ID: 16565408
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  • 16. Pharmacological manipulation of gain-of-function and dominant-negative mechanisms in rhodopsin retinitis pigmentosa.
    Mendes HF, Cheetham ME.
    Hum Mol Genet; 2008 Oct 01; 17(19):3043-54. PubMed ID: 18635576
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  • 17. Opsin, G-protein and 48-kDa protein in normal and rd mouse retinas: developmental expression of mRNAs and proteins and light/dark cycling of mRNAs.
    Bowes C, van Veen T, Farber DB.
    Exp Eye Res; 1988 Sep 01; 47(3):369-90. PubMed ID: 2846333
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  • 18. Hammerhead ribozymes designed to cleave all human rod opsin mRNAs which cause autosomal dominant retinitis pigmentosa.
    Sullivan JM, Pietras KM, Shin BJ, Misasi JN.
    Mol Vis; 2002 Apr 08; 8():102-13. PubMed ID: 11961505
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  • 19. A diffusible factor from normal retinal cells promotes rod photoreceptor survival in an in vitro model of retinitis pigmentosa.
    Streichert LC, Birnbach CD, Reh TA.
    J Neurobiol; 1999 Jun 15; 39(4):475-90. PubMed ID: 10380070
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  • 20. Differential expression of cone opsin mRNA levels following experimental retinal detachment and reattachment.
    Rex TS, Lewis GP, Geller SF, Fisher SK.
    Mol Vis; 2002 Apr 16; 8():114-8. PubMed ID: 11979236
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