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Items: 1 to 20 of 87

1.

Development of a cellular model of rod opsin retinitis pigmentosa.

Adamowicz M, Song A, Wadsworth S, Scaria A, O'Riordan C.

Adv Exp Med Biol. 2012;723:573-9. doi: 10.1007/978-1-4614-0631-0_73. No abstract available.

PMID:
22183380
2.

Pharmacological manipulation of gain-of-function and dominant-negative mechanisms in rhodopsin retinitis pigmentosa.

Mendes HF, Cheetham ME.

Hum Mol Genet. 2008 Oct 1;17(19):3043-54. doi: 10.1093/hmg/ddn202. Epub 2008 Jul 17.

3.

Retinoids assist the cellular folding of the autosomal dominant retinitis pigmentosa opsin mutant P23H.

Noorwez SM, Malhotra R, McDowell JH, Smith KA, Krebs MP, Kaushal S.

J Biol Chem. 2004 Apr 16;279(16):16278-84. Epub 2004 Feb 9.

4.

P23H opsin knock-in mice reveal a novel step in retinal rod disc morphogenesis.

Sakami S, Kolesnikov AV, Kefalov VJ, Palczewski K.

Hum Mol Genet. 2014 Apr 1;23(7):1723-41. doi: 10.1093/hmg/ddt561. Epub 2013 Nov 7.

5.

Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations.

Sakami S, Maeda T, Bereta G, Okano K, Golczak M, Sumaroka A, Roman AJ, Cideciyan AV, Jacobson SG, Palczewski K.

J Biol Chem. 2011 Mar 25;286(12):10551-67. doi: 10.1074/jbc.M110.209759. Epub 2011 Jan 11.

6.

Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene.

Naash MI, Hollyfield JG, al-Ubaidi MR, Baehr W.

Proc Natl Acad Sci U S A. 1993 Jun 15;90(12):5499-503.

7.

Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa.

Olsson JE, Gordon JW, Pawlyk BS, Roof D, Hayes A, Molday RS, Mukai S, Cowley GS, Berson EL, Dryja TP.

Neuron. 1992 Nov;9(5):815-30.

PMID:
1418997
8.
10.

Mice with a D190N mutation in the gene encoding rhodopsin: a model for human autosomal-dominant retinitis pigmentosa.

Sancho-Pelluz J, Tosi J, Hsu CW, Lee F, Wolpert K, Tabacaru MR, Greenberg JP, Tsang SH, Lin CS.

Mol Med. 2012 May 9;18:549-55. doi: 10.2119/molmed.2011.00475.

11.

Inherent instability of the retinitis pigmentosa P23H mutant opsin.

Chen Y, Jastrzebska B, Cao P, Zhang J, Wang B, Sun W, Yuan Y, Feng Z, Palczewski K.

J Biol Chem. 2014 Mar 28;289(13):9288-303. doi: 10.1074/jbc.M114.551713. Epub 2014 Feb 10.

13.

The cellular fate of mutant rhodopsin: quality control, degradation and aggresome formation.

Saliba RS, Munro PM, Luthert PJ, Cheetham ME.

J Cell Sci. 2002 Jul 15;115(Pt 14):2907-18.

14.

Ribozyme rescue of photoreceptor cells in a transgenic rat model of autosomal dominant retinitis pigmentosa.

Lewin AS, Drenser KA, Hauswirth WW, Nishikawa S, Yasumura D, Flannery JG, LaVail MM.

Nat Med. 1998 Aug;4(8):967-71. Erratum in: Nat Med 1998 Sep;4(9):1081.

PMID:
9701253
16.

Electrostatic compensation restores trafficking of the autosomal recessive retinitis pigmentosa E150K opsin mutant to the plasma membrane.

Pulagam LP, Palczewski K.

J Biol Chem. 2010 Sep 17;285(38):29446-56. doi: 10.1074/jbc.M110.151407. Epub 2010 Jul 13.

17.

Photoreceptor rosettes in autosomal dominant retinitis pigmentosa with reduced penetrance.

Tulvatana W, Adamian M, Berson EL, Dryja TP.

Arch Ophthalmol. 1999 Mar;117(3):399-402.

PMID:
10088824
18.

Defective intracellular transport is the molecular basis of rhodopsin-dependent dominant retinal degeneration.

Colley NJ, Cassill JA, Baker EK, Zuker CS.

Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):3070-4.

19.

Acuity recovery and cone pigment regeneration after a bleach in patients with retinitis pigmentosa and rhodopsin mutations.

Sandberg MA, Pawlyk BS, Berson EL.

Invest Ophthalmol Vis Sci. 1999 Sep;40(10):2457-61.

PMID:
10476820
20.
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