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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Single-cell landscape of piglet lung response with Actinobacillus pleuropneumoniae.
PMID 41843736 · PMC13014559 · Virulence · 2026 · 8 claims · 8 setups
scRNA-seq of piglet lungs identified 18 cell subpopulations with distinct phenotypes in infected vs control lungs
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Migratory Tumor Cells Cooperate with Cancer Associated Fibroblasts in Hormone Receptor-Positive and HER2-Negative Breast Cancer.
PMID 38892065 · PMC11172245 · International journal of molecular sciences · 2024 · 8 claims · 8 setups
HR+/HER2-BC tumor epithelial cells comprise four single-cell-defined functional (SC-f) subtypes: migratory, secretory, proliferating, and dysfunctional.
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Single-cell transcriptome analysis reveals DNMT1(+) epithelial cells promote lymphatic metastasis via CXCL17-mediated TAM infiltration.
PMID 41845371 · PMC13107741 · Journal of translational medicine · 2026 · 8 claims · 8 setups
DNMT1+ epithelial cells, characterized by high epithelial-mesenchymal transition potential, show a propensity for lymph node metastasis in bladder cancer
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Dual mechanisms of supporting cell regeneration in the neonatal mouse cochlea.
PMID 41867623 · PMC13000480 · iScience · 2026 · 8 claims · 8 setups
GER cells regenerate IPhCs through both mitotic and non-mitotic mechanisms
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Notch3 regulates pericyte phenotypic plasticity in colorectal cancer.
PMID 41618002 · PMC12960917 · Communications biology · 2026 · 8 claims · 8 setups
Murine tumor pericytes originate from normal tissue-resident pericytes that proliferate inside tumors
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Multi-Transcriptomic Analysis Reveals That EREG-Driven TME Crosstalk Defines Anti-EGFR Response in Colorectal Cancer.
PMID 42043480 · PMC13115984 · Cancer medicine · 2026 · 8 claims · 8 setups
EGFRI eligibility (defined by left-sidedness, RAS/BRAF wild-type, MSS) stratifies cancer cell transcriptomic characteristics more strongly than sidedness alone.