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One or more keywords matched the following items that are connected to Agbaga, Martin-Paul
Item TypeName
Concept Cell Membrane
Concept Bruch Membrane
Concept Membrane 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 Mutant ELOVL4 that causes autosomal dominant stargardt-3 macular dystrophy is misrouted to rod outer segment disks.
Academic Article Altered photoreceptor metabolism in mouse causes late stage age-related macular degeneration-like pathologies.
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 Retinal very long-chain PUFAs: new insights from studies on ELOVL4 protein.
Academic Article Different Mutations in ELOVL4 Affect Very Long Chain Fatty Acid Biosynthesis to Cause Variable Neurological Disorders in Humans.
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 ELOVL4: Very long-chain fatty acids serve an eclectic role in mammalian health and function.
Academic Article W246G Mutant ELOVL4 Impairs Synaptic Plasticity in Parallel and Climbing Fibers and Causes Motor Defects in a Rat Model of SCA34.
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