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One or more keywords matched the following items that are connected to Brush, Richard
Item TypeName
Concept Eye Proteins
Academic Article ELOVL4 protein preferentially elongates 20:5n3 to very long chain PUFAs over 20:4n6 and 22:6n3.
Academic Article Endoplasmic reticulum microenvironment and conserved histidines govern ELOVL4 fatty acid elongase activity.
Academic Article In vivo effect of mutant ELOVL4 on the expression and function of wild-type ELOVL4.
Academic Article Biosynthesis of very long-chain polyunsaturated fatty acids in hepatocytes expressing ELOVL4.
Academic Article Deciphering mutant ELOVL4 activity in autosomal-dominant Stargardt macular dystrophy.
Academic Article Role of Stargardt-3 macular dystrophy protein (ELOVL4) in the biosynthesis of very long chain fatty acids.
Academic Article Role of Elovl4 protein in the biosynthesis of docosahexaenoic acid.
Academic Article Homozygous Expression of Mutant ELOVL4 Leads to Seizures and Death in a Novel Animal Model of Very Long-Chain Fatty Acid Deficiency.
Academic Article Elovl4 5-bp deletion does not accelerate cone photoreceptor degeneration in an all-cone mouse.
Academic Article The Elovl4 Spinocerebellar Ataxia-34 Mutation 736T>G (p.W246G) Impairs Retinal Function in the Absence of Photoreceptor Degeneration.
Academic Article DHA does not protect ELOVL4 transgenic mice from retinal degeneration.
Academic Article Very long chain polyunsaturated fatty acids and rod cell structure and function.
Academic Article Effect of reduced retinal VLC-PUFA on rod and cone photoreceptors.
Academic Article Loss of human disease protein retinitis pigmentosa GTPase regulator (RPGR) differentially affects rod or cone-enriched retina.
Academic Article Examination of VLC-PUFA-deficient photoreceptor terminals.
Academic Article W246G Mutant ELOVL4 Impairs Synaptic Plasticity in Parallel and Climbing Fibers and Causes Motor Defects in a Rat Model of SCA34.
Academic Article ELOVL4 Mutations That Cause Spinocerebellar Ataxia-34 Differentially Alter Very Long Chain Fatty Acid Biosynthesis.
Academic Article A novel ELOVL4 variant, L168S, causes early childhood-onset Spinocerebellar ataxia-34 and retinal dysfunction: a case report.
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