Component

Adenoviral DES1 expression

Human DES1 overexpression after intravitreal adenoviral delivery; cellular targeting was not exclusive.

1 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

Tracing routes…

What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What it acts on

  1. Intravitreal adenovirus expressing human DES1 increased retinal 9-cis-retinal in Rpe65-null mice relative to the RFP control virus.

    Adenoviral DES1 expression → 9-cis-retinal source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    cross_nutrient
    false
    evidence_location
    Figure 4a; Results: Gene therapy of rpe65-null mice
    experimental_model
    Adenoviral human DES1 versus RFP in Rpe65-null mice
    exposure
    Retinoids measured one day after injection; Figure 4a without added intravitreal retinol.
    limitations
    11-cis-retinoids remained undetectable in this comparison; viral cell targeting was not exclusive.
    nutrient
    Vitamin A · Vitamin A
    nutrient_topic
    Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. · Vitamin A
    organism
    Homo sapiens transgene in Mus musculus
    plain_language
    Extra DES1 increased an alternative cis-retinal isomer in the mutant eyes.
    primary_references
    [vav-kaylor2013] Identification of DES1 as a vitamin A isomerase in Müller glial cells of the retina. (2013). https://pubmed.ncbi.nlm.nih.gov/23143414/ DOI: 10.1038/nchembio.1114
    tissue_or_cell_type
    retina
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    Vitamin A expansion: reproduction, light-driven vision and shared mechanisms (2026-09-17) · lines 603–616

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Adenoviral human DES1 versus RFP in Rpe65-null mice · source_derived_draft · unverified_draft

    ### vae-des1-gene-transfer-9cis Intravitreal adenovirus expressing human DES1 increased retinal 9-cis-retinal in Rpe65-null mice relative to the RFP control virus. Condition category: machinery_impairment nutrient_topic: Vitamin A expansion research collection; topical membership is not evidence of a direct dietary effect. plain_language: Extra DES1 increased an alternative cis-retinal isomer in the mutant eyes. organism: Homo sapiens transgene in Mus musculus tissue_or_cell_type: retina experimental_model: Adenoviral human DES1 versus RFP in Rpe65-null mice limitations: 11-cis-retinoids remained undetectable in this comparison; viral cell targeting was not exclusive. exposure: Retinoids measured one day after injection; Figure 4a without added intravitreal retinol. cross_nutrient: false evidence_location: Figure 4a; Results: Gene therapy of rpe65-null mice nutrient: Vitamin A [vav-kaylor2013] Identification of DES1 as a vitamin A isomerase in Müller glial cells of the retina. (2013). https://pubmed.ncbi.nlm.nih.gov/23143414/ DOI: 10.1038/nchembio.1114
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.

    Evidence, AI assistance and curation standards