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Initial reports that a gain-of-function polymorphism (L503F variant, rs1050152) in SLC22A4 that increased transport efficiency of ergothioneine was associated with increased risk of Crohns disease (56) were subsequently shown to have been confounded by the SLC22A4 gene being in linkage disequilibrium with the interferon regulatory factor 1 ( IRF1 ) gene, which was the locus conferring Crohns disease susceptibility (57)

Tissue-Repair & Regenerative Research GHK-Cu is widely researched for its interaction with: Fibroblast-related signaling pathways Keratinocyte-related mechanisms Tissue-remodeling pathways Collagen-organization signaling Angiogenesis and vascular-support pathways Extracellular-matrix and dermal-maintenance mechanisms Research commonly investigates its interaction with: Tissue-maintenance mechanisms Recovery-focused regenerative pathways Skin-integrity and dermal-support research Scar-remodeling and extracellular-matrix signaling Connective-tissue and physiological-resilience pathways These pathways have contributed to broader research interest in GHK-Cu within regenerative, recovery-focused, and tissue-maintenance research models