Richard Brush to Mutation
This is a "connection" page, showing publications Richard Brush has written about Mutation.
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W246G Mutant ELOVL4 Impairs Synaptic Plasticity in Parallel and Climbing Fibers and Causes Motor Defects in a Rat Model of SCA34. Mol Neurobiol. 2021 Oct; 58(10):4921-4943.
Score: 0.144
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The Elovl4 Spinocerebellar Ataxia-34 Mutation 736T>G (p.W246G) Impairs Retinal Function in the Absence of Photoreceptor Degeneration. Mol Neurobiol. 2020 Nov; 57(11):4735-4753.
Score: 0.135
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Homozygous Expression of Mutant ELOVL4 Leads to Seizures and Death in a Novel Animal Model of Very Long-Chain Fatty Acid Deficiency. Mol Neurobiol. 2018 02; 55(2):1795-1813.
Score: 0.112
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Examination of VLC-PUFA-deficient photoreceptor terminals. Invest Ophthalmol Vis Sci. 2014 Apr 24; 55(7):4063-72.
Score: 0.087
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High levels of retinal docosahexaenoic acid do not protect photoreceptor degeneration in VPP transgenic mice. Mol Vis. 2010 Aug 18; 16:1669-79.
Score: 0.068
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Lipid differences in rod outer segment membranes of rats with P23H and S334ter opsin mutations. Mol Vis. 2005 May 12; 11:338-46.
Score: 0.047
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P23H and S334ter opsin mutations: Increasing photoreceptor outer segment n-3 fatty acid content does not affect the course of retinal degeneration. Mol Vis. 2004 Mar 26; 10:199-207.
Score: 0.043
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ELOVL4 Mutations That Cause Spinocerebellar Ataxia-34 Differentially Alter Very Long Chain Fatty Acid Biosynthesis. J Lipid Res. 2023 01; 64(1):100317.
Score: 0.040
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Elovl4 5-bp deletion does not accelerate cone photoreceptor degeneration in an all-cone mouse. PLoS One. 2018; 13(1):e0190514.
Score: 0.028
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Deciphering mutant ELOVL4 activity in autosomal-dominant Stargardt macular dystrophy. Proc Natl Acad Sci U S A. 2013 Apr 02; 110(14):5446-51.
Score: 0.020