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140 related items for PubMed ID: 7488190
1. Altered cAMP levels in retinas from transgenic mice expressing a rhodopsin mutant. Weiss ER, Hao Y, Dickerson CD, Osawa S, Shi W, Zhang L, Wong F. Biochem Biophys Res Commun; 1995 Nov 22; 216(3):755-61. PubMed ID: 7488190 [Abstract] [Full Text] [Related]
2. Characterization of rhodopsin P23H-induced retinal degeneration in a Xenopus laevis model of retinitis pigmentosa. Tam BM, Moritz OL. Invest Ophthalmol Vis Sci; 2006 Aug 22; 47(8):3234-41. PubMed ID: 16877386 [Abstract] [Full Text] [Related]
8. 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 [Abstract] [Full Text] [Related]
10. Mislocalized rhodopsin does not require activation to cause retinal degeneration and neurite outgrowth in Xenopus laevis. Tam BM, Xie G, Oprian DD, Moritz OL. J Neurosci; 2006 Jan 04; 26(1):203-9. PubMed ID: 16399688 [Abstract] [Full Text] [Related]
12. Overexpression of Bcl-2 or Bcl-XL transgenes and photoreceptor degeneration. Joseph RM, Li T. Invest Ophthalmol Vis Sci; 1996 Nov 04; 37(12):2434-46. PubMed ID: 8933760 [Abstract] [Full Text] [Related]
13. Defective trafficking of rhodopsin and its role in retinal degenerations. Hollingsworth TJ, Gross AK. Int Rev Cell Mol Biol; 2012 Nov 04; 293():1-44. PubMed ID: 22251557 [Abstract] [Full Text] [Related]
17. High levels of retinal docosahexaenoic acid do not protect photoreceptor degeneration in VPP transgenic mice. Li F, Marchette LD, Brush RS, Elliott MH, Davis KR, Anderson AG, Anderson RE. Mol Vis; 2010 Aug 18; 16():1669-79. PubMed ID: 20806040 [Abstract] [Full Text] [Related]
18. 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 [Abstract] [Full Text] [Related]
19. A rhodopsin gene mutation responsible for autosomal dominant retinitis pigmentosa results in a protein that is defective in localization to the photoreceptor outer segment. Sung CH, Makino C, Baylor D, Nathans J. J Neurosci; 1994 Oct 03; 14(10):5818-33. PubMed ID: 7523628 [Abstract] [Full Text] [Related]
20. Aggregation of rhodopsin mutants in mouse models of autosomal dominant retinitis pigmentosa. Vasudevan S, Senapati S, Pendergast M, Park PS. Nat Commun; 2024 Feb 16; 15(1):1451. PubMed ID: 38365903 [Abstract] [Full Text] [Related] Page: [Next] [New Search]