Component

Mouse peripheral-tissue ATP7A abundance

Mouse peripheral-tissue ATP7A abundance. Species, exposure and limitations are retained in each linked claim.

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 acts on it

  1. Copper deficiency lowered ATP7A abundance in mouse peripheral tissues; subcutaneous copper restored it.

    Copper → Mouse peripheral-tissue ATP7A abundance source_derived_draftungraded
    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/copper-research/28931909.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "040f84f61342770e57eec0c3e82a0165c000bc5592a54344f92378b48e626c9f", "start_char": 0, "end_char": 1284, "text_sha256": "040f84f61342770e57eec0c3e82a0165c000bc5592a54344f92378b48e626c9f"}
    experimental_model
    Copper-deficient mouse models and subcutaneous copper administration
    exposure
    Systemic copper depletion and restoration
    limitations
    Opposite tissue responses are reported regulatory context, not a contradiction in the source.
    nutrient_topic
    Copper research collection; topical membership is not evidence of a direct dietary effect. · Copper
    organism
    Mouse
    plain_language
    Tissues adjusted their copper-export machinery as supply changed.
    primary_references
    [copper-p28931909] Organ-specific regulation of ATP7A abundance is coordinated with systemic copper homeostasis. (2017). https://pubmed.ncbi.nlm.nih.gov/28931909/ DOI: 10.1038/s41598-017-11961-z
    tissue_or_cell_type
    Intestine, heart, spleen and liver

    Copper: transport, cuproenzymes, deficiency, excess and nutrient interactions (2026-09-17) · lines 494–505

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Copper-deficient mouse models and subcutaneous copper administration · source_derived_draft · unverified_draft

    ### copper-atp7a-peripheral-response Copper deficiency lowered ATP7A abundance in mouse peripheral tissues; subcutaneous copper restored it. Condition category: normal nutrient_topic: Copper research collection; topical membership is not evidence of a direct dietary effect. plain_language: Tissues adjusted their copper-export machinery as supply changed. organism: Mouse tissue_or_cell_type: Intestine, heart, spleen and liver experimental_model: Copper-deficient mouse models and subcutaneous copper administration limitations: Opposite tissue responses are reported regulatory context, not a contradiction in the source. exposure: Systemic copper depletion and restoration evidence_span: {"source_cache": "artifacts/copper-research/28931909.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "040f84f61342770e57eec0c3e82a0165c000bc5592a54344f92378b48e626c9f", "start_char": 0, "end_char": 1284, "text_sha256": "040f84f61342770e57eec0c3e82a0165c000bc5592a54344f92378b48e626c9f"} [copper-p28931909] Organ-specific regulation of ATP7A abundance is coordinated with systemic copper homeostasis. (2017). https://pubmed.ncbi.nlm.nih.gov/28931909/ DOI: 10.1038/s41598-017-11961-z
    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