ArticleScientific reports2025
TGF-beta coordinates changes in Keratin gene expression during complex tissue regeneration.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
1 citing paper in PubMed.
- Loss of tissue-state plasticity: a conceptual framework for age-associated regenerative failure.Inflammation and regeneration · 2026Review
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Zebrafish larval tail regeneration can be broadly broken down into three phases: wound repair, initiation of regeneration and redevelopment of the tail. We and others have shown that activation of the Hedgehog and TGF-beta signalling pathways is required to trigger tail regeneration. In this study we initially focus on these two pathways to better understand their role regeneration. We have found that Hedgehog signalling acts upstream of the TGF-beta pathway by activating transcription of the TGF-beta ligand tgfb1a. We have identified differentially expressed genes that are regulated after tail excision as well as those that are dependent upon TGF-beta signalling. From this analysis we found that Keratin genes fall into two categories of co-expression: one set that is upregulated by TGF-beta signalling after injury (krt
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