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 spatial transcriptomics reveals tumor microenvironment heterogeneity in primary and lymph node-metastatic small cell lung cancer.
PMID 41916294 · PMC13130650 · Cell reports. Medicine · 2026 · 8 claims · 8 setups
Three malignant subclusters (C5, C6, C9) are enriched in LNM tumors and display distinct metabolic and angiogenic programs alongside spatial immune exclusion
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SpaNiche: spatial niche analysis to explore colocalization patterns and cellular interactions in spatial transcriptomics data.
PMID 42015285 · PMC13231777 · Genome biology · 2026 · 8 claims · 6 setups
SpaNiche integrates smoothed cell-type abundance and ligand-receptor expression matrices via graph-regularized joint NMF, across multiple spatial views, to identify colocalization patterns
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Single cell profiling reveals malignant states and immune landscapes in PCNSL and systemic DLBCL.
PMID 42023148 · PMC13097095 · iScience · 2026 · 8 claims · 8 setups
PCNSL and sDLBCL contain five distinct malignant B-cell subtypes (B0-B4) with discrete differentiation trajectories
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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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Reprogramming of stroma-derived chemokine networks drives the loss of tissue organization in nodal B cell lymphoma.
PMID 41882179 · PMC13035477 · Nature cancer · 2026 · 8 claims · 8 setups
LN-resident stromal cells (FRCs, BECs, LECs) drive chemokine-based lymphocyte zonation, and disruption of this system underlies the loss of tissue organization in nodal B cell lymphoma