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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Ectopic CD11c Drives SMAD3-Mediated Aberrant Antigen Presentation and Epithelial-Mesenchymal Transition in Esophageal Squamous Cell Carcinoma.
PMID 41799568 · PMC12963642 · Cancer communications (London, England) · 2026 · 8 claims · 13 setups
An ESCC epithelial cell subcluster with ectopic CD11c (ITGAX) expression, found in both mice and humans, exhibits concurrent impaired antigen presentation and EMT phenotypes
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Ectopic NMDAR expression in cancer unmasks germline-encoded autoimmunity.
PMID 41882353 · PMC13216075 · Nature · 2026 · 8 claims · 8 setups
GluN1 and GluN2B NMDAR subunits are ectopically expressed in cancer cells of human TNBC tumours
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Multi-cohort and single-cell profiling of aging genes reveals prognostic and therapeutic targets in breast cancer.
PMID 41732271 · PMC12924738 · iScience · 2026 · 8 claims · 7 setups
The eight-gene MLAG signature outperforms 100 previously published prognostic models across 12 independent breast cancer cohorts
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Multi-omics integration and machine learning reveal gut-immune signatures in idiopathic pulmonary fibrosis: insights from bulk RNA-seq, single-cell profiles, spatial transcriptomics, and experimental validation.
PMID 41939867 · PMC13043422 · Frontiers in immunology · 2026 · 7 claims · 8 setups
CXCL13, IL33, TLR4, and IGF1 are core IPF genes consistently linked to immune infiltration and fibrotic remodeling across bulk, single-cell, spatial, and blood multi-omics data
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Has reproduction · 67
Integrative analyses reveal signaling pathways underlying familial breast cancer susceptibility.
PMID 26969729 · PMC4812528 · Molecular systems biology · 2016 · 8 claims · 6 setups
Cell adhesion pathways are significantly and consistently dysregulated in women who develop familial breast cancer (FBC)
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Estropausal gut microbiota transplant improves measures of ovarian function in adult mice.
PMID 41776310 · PMC13004687 · Nature aging · 2026 · 8 claims · 7 setups
Young and estropausal female mice have distinct, separable gut microbial profiles (beta and alpha diversity) across multiple cohorts.
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Identification of cycling regulatory T cell precursors as conductors of immune escape during breast carcinoma progression.
PMID 41997138 · PMC13213619 · Cancer cell · 2026 · 8 claims · 8 setups
A novel proliferative Treg precursor state, cycling Treg (cycTreg: FOXP3^int, MKI67^hi, IKZF2/4^int-hi), is absent in normal breast, low in DCIS, and strongly expanded in IBC
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Has reproduction · 87
RNA-Seq transcriptome profiling identifies CRISPLD2 as a glucocorticoid responsive gene that modulates cytokine function in airway smooth muscle cells.
PMID 24926665 · PMC4057123 · PloS one · 2014 · 8 claims · 8 setups
Dexamethasone treatment (1 µM, 18 h) of primary human ASM cells differentially regulates 316 genes, including both known and previously uninvestigated glucocorticoid-responsive genes.
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SMARCB1 missense mutants disrupt SWI/SNF complex stability and remodeling activity.
PMID 41951591 · PMC13237135 · Nature communications · 2026 · 8 claims · 8 setups
RPT2 domain missense mutations disrupt SMARCB1 antiproliferative function by destabilizing the SWI/SNF complex and impairing chromatin remodeling and transcriptional regulation, comparable to nonsense mutations
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Single-cell transcriptomics reveals heterogeneous neutrophil populations and diagnostic biomarkers in atherosclerosis.
PMID 41847341 · PMC12989409 · Frontiers in physiology · 2026 · 8 claims · 8 setups
Integration of scRNA-seq data from six human carotid samples identified 16 distinct cell subtypes after batch effect correction with Harmony
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A Chronic Fatigue Syndrome - related proteome in human cerebrospinal fluid.
PMID 16321154 · PMC1326206 · BMC neurology · 2005 · 7 claims · 6 setups
CFS, PGI and fibromyalgia are highly overlapping symptom complexes likely reflecting a shared underlying pathophysiological mechanism rather than distinct diseases