Experiments
Searchable full-text extractions: founding hypothesis, core claims, experimental setups, key results and statistics — pulled out of each paper as structure. Search a cell line, an assay or an entity (e.g. HUH7) and find every paper that worked with it. This corpus stands on its own: most entries carry no reproduction assessment (yet).
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Spatial cartography of human thymus enables the geopositioning of lineage transcription factors in rare mimetic thymic epithelial cells.
PMID 41807357 · PMC13102919 · Nature communications · 2026 · 7 claims · 7 setups
Generated a high-resolution spatial transcriptomic atlas of human fetal (13,14,17,18w) and paediatric (7w,2y,5y,6y) thymi using Stereo-seq, integrated with scRNA-seq and MACSima/Stereo-CITE proteomics
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An in vivo and in vitro spatiotemporal profile of human midbrain development.
PMID 41633979 · PMC12877092 · Nature communications · 2026 · 8 claims · 6 setups
By 22 post-conceptional weeks (PCW), fetal ventral midbrain tissue exhibits structural complexity comparable to adult tissue
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Rete ridges form via evolutionarily distinct mechanisms in mammalian skin.
PMID 41639458 · PMC12959975 · Nature · 2026 · 8 claims · 8 setups
Rete ridges form through a mechanism independent from hair follicles and sweat glands, via interconnected epidermal invaginations
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Has reproduction · 94
Eye in a Disk: eyeIntegration Human Pan-Eye and Body Transcriptome Database Version 1.0.
PMID 31343654 · PMC6660187 · Investigative ophthalmology & visual science · 2019 · 8 claims · 5 setups
EiaD is a reproducible, versioned RNA-seq transcriptome dataset combining 916 healthy human eye samples and 1375 GTEx body samples across 19 eye and 54 body tissues, built with a Snakemake pipeline and served as a single SQLite database.
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Development of a split-toxin CRISPR screening platform to systematically identify regulators of human myoblast fusion.
PMID 41540035 · PMC12808753 · Nature communications · 2026 · 8 claims · 7 setups
A CRISPR screening platform combining human myoblast models, a custom muscle-targeted gRNA library (MyoCRISPR-KO Lib), and a split-toxin selection system enables quantitative enrichment of fusion-defective myocytes.