Component

Mouse PKC beta I isoform

Mouse PKC beta I isoform. Species, exposure and limitations are retained in each linked claim.

2 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. Blocking PKC beta I prevented the inositol-mediated reduction of neural tube defects in curly-tail mouse embryos.

    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    evidence_span
    {"source_cache": "artifacts/inositol-research/14613966.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "670b8f0a36bfbecfb417fe28f8748e65994ac47b153ffcf66c42c21e7489f9cc", "start_char": 0, "end_char": 1735, "text_sha256": "670b8f0a36bfbecfb417fe28f8748e65994ac47b153ffcf66c42c21e7489f9cc"}
    experimental_model
    Embryo culture with selective PKC inhibition
    exposure
    Inositol exposure in a folate-resistant neural-tube-defect model
    limitations
    Mechanistic mouse prevention does not establish human efficacy or permit replacing folic acid.
    nutrient_topic
    Inositol research collection; topical membership is not evidence of a direct dietary effect. · Inositol (stereoisomer family)
    organism
    Curly-tail mutant mice
    plain_language
    Adding inositol could not overcome failure of this downstream signaling step.
    primary_references
    [ino-p14613966] Specific isoforms of protein kinase C are essential for prevention of folate-resistant neural tube defects by inositol. (2004). https://pubmed.ncbi.nlm.nih.gov/14613966/ DOI: 10.1093/hmg/ddh003
    tissue_or_cell_type
    Neurulation-stage embryos and hindgut
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    Inositol: synthesis, signaling, mineral interactions and conditional deficiency (2026-09-17) · lines 1367–1378

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Embryo culture with selective PKC inhibition · source_derived_draft · unverified_draft

    ### ino-ntd-pkc-beta Blocking PKC beta I prevented the inositol-mediated reduction of neural tube defects in curly-tail mouse embryos. Condition category: machinery_impairment nutrient_topic: Inositol research collection; topical membership is not evidence of a direct dietary effect. plain_language: Adding inositol could not overcome failure of this downstream signaling step. organism: Curly-tail mutant mice tissue_or_cell_type: Neurulation-stage embryos and hindgut experimental_model: Embryo culture with selective PKC inhibition limitations: Mechanistic mouse prevention does not establish human efficacy or permit replacing folic acid. exposure: Inositol exposure in a folate-resistant neural-tube-defect model evidence_span: {"source_cache": "artifacts/inositol-research/14613966.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "670b8f0a36bfbecfb417fe28f8748e65994ac47b153ffcf66c42c21e7489f9cc", "start_char": 0, "end_char": 1735, "text_sha256": "670b8f0a36bfbecfb417fe28f8748e65994ac47b153ffcf66c42c21e7489f9cc"} [ino-p14613966] Specific isoforms of protein kinase C are essential for prevention of folate-resistant neural tube defects by inositol. (2004). https://pubmed.ncbi.nlm.nih.gov/14613966/ DOI: 10.1093/hmg/ddh003
    Complete structured claim and evidence

Where it participates (unsigned role)

  1. Inositol stimulated hindgut-cell proliferation in curly-tail embryos, and this effect required PKC beta I.

    Myo-inositol → Embryonic hindgut cell proliferation source_derived_draftungraded
    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/inositol-research/14613966.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "670b8f0a36bfbecfb417fe28f8748e65994ac47b153ffcf66c42c21e7489f9cc", "start_char": 0, "end_char": 1735, "text_sha256": "670b8f0a36bfbecfb417fe28f8748e65994ac47b153ffcf66c42c21e7489f9cc"}
    experimental_model
    Embryo culture with selective PKC inhibition
    exposure
    Inositol exposure in a folate-resistant neural-tube-defect model
    limitations
    Mechanistic mouse prevention does not establish human efficacy or permit replacing folic acid.
    nutrient_topic
    Inositol research collection; topical membership is not evidence of a direct dietary effect. · Inositol (stereoisomer family)
    organism
    Curly-tail mutant mice
    plain_language
    The rescue involved growth of a particular embryonic tissue, not just a general vitamin effect.
    primary_references
    [ino-p14613966] Specific isoforms of protein kinase C are essential for prevention of folate-resistant neural tube defects by inositol. (2004). https://pubmed.ncbi.nlm.nih.gov/14613966/ DOI: 10.1093/hmg/ddh003
    tissue_or_cell_type
    Neurulation-stage embryos and hindgut

    Inositol: synthesis, signaling, mineral interactions and conditional deficiency (2026-09-17) · lines 1393–1404

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Embryo culture with selective PKC inhibition · source_derived_draft · unverified_draft

    ### ino-ntd-hindgut Inositol stimulated hindgut-cell proliferation in curly-tail embryos, and this effect required PKC beta I. Condition category: normal nutrient_topic: Inositol research collection; topical membership is not evidence of a direct dietary effect. plain_language: The rescue involved growth of a particular embryonic tissue, not just a general vitamin effect. organism: Curly-tail mutant mice tissue_or_cell_type: Neurulation-stage embryos and hindgut experimental_model: Embryo culture with selective PKC inhibition limitations: Mechanistic mouse prevention does not establish human efficacy or permit replacing folic acid. exposure: Inositol exposure in a folate-resistant neural-tube-defect model evidence_span: {"source_cache": "artifacts/inositol-research/14613966.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "670b8f0a36bfbecfb417fe28f8748e65994ac47b153ffcf66c42c21e7489f9cc", "start_char": 0, "end_char": 1735, "text_sha256": "670b8f0a36bfbecfb417fe28f8748e65994ac47b153ffcf66c42c21e7489f9cc"} [ino-p14613966] Specific isoforms of protein kinase C are essential for prevention of folate-resistant neural tube defects by inositol. (2004). https://pubmed.ncbi.nlm.nih.gov/14613966/ DOI: 10.1093/hmg/ddh003
    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