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