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189 related items for PubMed ID: 39089885
1. Synchronized Photoactivation of T4K Rhodopsin Causes a Chromophore-Dependent Retinal Degeneration That Is Moderated by Interaction with Phototransduction Cascade Components. Tam BM, Burns P, Chiu CN, Moritz OL. J Neurosci; 2024 Sep 04; 44(36):. PubMed ID: 39089885 [Abstract] [Full Text] [Related]
2. Autophagy in Xenopus laevis rod photoreceptors is independently regulated by phototransduction and misfolded RHOP23H. Wen RH, Stanar P, Tam B, Moritz OL. Autophagy; 2019 Nov 04; 15(11):1970-1989. PubMed ID: 30975014 [Abstract] [Full Text] [Related]
9. Light Induces Ultrastructural Changes in Rod Outer and Inner Segments, Including Autophagy, in a Transgenic Xenopus laevis P23H Rhodopsin Model of Retinitis Pigmentosa. Bogéa TH, Wen RH, Moritz OL. Invest Ophthalmol Vis Sci; 2015 Dec 25; 56(13):7947-55. PubMed ID: 26720441 [Abstract] [Full Text] [Related]
10. Xenopus laevis P23H rhodopsin transgene causes rod photoreceptor degeneration that is more severe in the ventral retina and is modulated by light. Zhang R, Oglesby E, Marsh-Armstrong N. Exp Eye Res; 2008 Apr 25; 86(4):612-21. PubMed ID: 18291367 [Abstract] [Full Text] [Related]
12. Dysmorphic photoreceptors in a P23H mutant rhodopsin model of retinitis pigmentosa are metabolically active and capable of regenerating to reverse retinal degeneration. Lee DC, Vazquez-Chona FR, Ferrell WD, Tam BM, Jones BW, Marc RE, Moritz OL. J Neurosci; 2012 Feb 08; 32(6):2121-8. PubMed ID: 22323724 [Abstract] [Full Text] [Related]
15. Recent insights into the mechanisms underlying light-dependent retinal degeneration from X. laevis models of retinitis pigmentosa. Moritz OL, Tam BM. Adv Exp Med Biol; 2010 Feb 08; 664():509-15. PubMed ID: 20238053 [Abstract] [Full Text] [Related]
18. A novel form of transducin-dependent retinal degeneration: accelerated retinal degeneration in the absence of rod transducin. Brill E, Malanson KM, Radu RA, Boukharov NV, Wang Z, Chung HY, Lloyd MB, Bok D, Travis GH, Obin M, Lem J. Invest Ophthalmol Vis Sci; 2007 Dec 08; 48(12):5445-53. PubMed ID: 18055791 [Abstract] [Full Text] [Related]
19. Rpe65 as a modifier gene for inherited retinal degeneration. Samardzija M, Wenzel A, Naash M, Remé CE, Grimm C. Eur J Neurosci; 2006 Feb 08; 23(4):1028-34. PubMed ID: 16519667 [Abstract] [Full Text] [Related]
20. Disrupted Plasma Membrane Protein Homeostasis in a Xenopus Laevis Model of Retinitis Pigmentosa. Ropelewski P, Imanishi Y. J Neurosci; 2019 Jul 10; 39(28):5581-5593. PubMed ID: 31061086 [Abstract] [Full Text] [Related] Page: [Next] [New Search]