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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.
Mutant ELOVL4 that causes autosomal dominant stargardt-3 macular dystrophy is misrouted to rod outer segment disks.
Deciphering mutant ELOVL4 activity in autosomal-dominant Stargardt macular dystrophy.
Insulin receptor signaling in cones.
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.
Retinal very long-chain PUFAs: new insights from studies on ELOVL4 protein.
Different Mutations in ELOVL4 Affect Very Long Chain Fatty Acid Biosynthesis to Cause Variable Neurological Disorders in Humans.
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.
ELOVL4: Very long-chain fatty acids serve an eclectic role in mammalian health and function.
W246G Mutant ELOVL4 Impairs Synaptic Plasticity in Parallel and Climbing Fibers and Causes Motor Defects in a Rat Model of SCA34.