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Article

Elovl4 haploinsufficiency does not induce early onset retinal degeneration in mice

25 Jan 2007

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Share to Photosynthetic Processes and Mechanisms
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 17254625
DOI: 10.1016/j.visres.2006.10.023

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Elovl4 haploinsufficiency does not induce early onset retinal degeneration in micePMID 17254625Read ↗

Haploinsufficiency is not the key mechanism of pathogenesis in a heterozygous Elovl4 knockout mouse model of STGD3 disease.Semantic proximity Read ↗

A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophySemantic proximity Read ↗

Elovl4 5-bp deletion does not accelerate cone photoreceptor degeneration in an all-cone mouse.Semantic proximity Read ↗

Elovl4 5-bp-deletion knock-in mice develop progressive photoreceptor degeneration.Semantic proximity Read ↗

Mutant ELOVL4 that causes autosomal dominant stargardt-3 macular dystrophy is misrouted to rod outer segment disks.Semantic proximity Read ↗

In vivo effect of mutant ELOVL4 on the expression and function of wild-type ELOVL4.Semantic proximity Read ↗

A novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophy.Semantic proximity Read ↗

Characterization of mouse orthologue of ELOVL4: genomic organization and spatial and temporal expressionSemantic proximity Read ↗

Depletion of ceramides with very long chain fatty acids causes defective skin permeability barrier function, and neonatal lethality in ELOVL4 deficient miceSemantic proximity Read ↗

The Lipid Elongation Enzyme ELOVL2 is a molecular regulator of aging in the retinaSemantic proximity Read ↗

Mouse Models of Stargardt 3 Dominant Macular Degeneration.Semantic proximity Read ↗

The Elovl4 Spinocerebellar Ataxia-34 Mutation 736T>G (p.W246G) Impairs Retinal Function in the Absence of Photoreceptor Degeneration.Semantic proximity Read ↗

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