THEODORE WENSEL to Male
This is a "connection" page, showing publications THEODORE WENSEL has written about Male.
Connection Strength
0.067
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A Large Endoplasmic Reticulum-Resident Pool of TRPM1 in Retinal ON-Bipolar Cells. eNeuro. 2018 May-Jun; 5(3).
Score: 0.025
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Evaluating retinal toxicity of intravitreal caspofungin in the mouse eye. Invest Ophthalmol Vis Sci. 2010 Nov; 51(11):5796-803.
Score: 0.014
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Phagocytosed photoreceptor outer segments activate mTORC1 in the retinal pigment epithelium. Sci Signal. 2018 05 29; 11(532).
Score: 0.006
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Mutations of the opsin gene (Y102H and I307N) lead to light-induced degeneration of photoreceptors and constitutive activation of phototransduction in mice. J Biol Chem. 2010 May 07; 285(19):14521-33.
Score: 0.003
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New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a gene. Hum Mol Genet. 2009 Jan 01; 18(1):178-92.
Score: 0.003
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Chronic cold exposure increases RGS7 expression and decreases alpha(2)-autoreceptor-mediated inhibition of noradrenergic locus coeruleus neurons. Eur J Neurosci. 2008 May; 27(9):2433-43.
Score: 0.003
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Neural reprogramming in retinal degeneration. Invest Ophthalmol Vis Sci. 2007 Jul; 48(7):3364-71.
Score: 0.003
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ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies. Hum Mol Genet. 2005 Oct 01; 14(19):2769-78.
Score: 0.003
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Knock-in human rhodopsin-GFP fusions as mouse models for human disease and targets for gene therapy. Proc Natl Acad Sci U S A. 2004 Jun 15; 101(24):9109-14.
Score: 0.002
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Evolution of the regulators of G-protein signaling multigene family in mouse and human. Genomics. 2002 Feb; 79(2):177-85.
Score: 0.002
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Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degeneration. Hum Mol Genet. 2001 Nov 01; 10(23):2671-8.
Score: 0.002