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 transcriptomics of human embryos identifies multiple sympathoblast lineages with potential implications for neuroblastoma origin.
PMID 33833454 · PMC7610777 · Nature genetics · 2021 · 8 claims · 8 setups
In human embryos, intra-adrenal sympathoblasts are directly derived from nerve-associated Schwann cell precursors (SCPs), similarly to chromaffin cells
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Gene regulatory network determinants of rapid recall in human memory CD4(+) T cells.
PMID 41865369 · PMC13207208 · Cell reports · 2026 · 8 claims · 6 setups
Memory CD4+ T cells show enhanced chromatin accessibility proximal to rapid-recall genes compared to naive cells
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Single-cell atlas of the developing Down syndrome brain cortex.
PMID 41545595 · PMC13004680 · Nature medicine · 2026 · 8 claims · 8 setups
RORB/FOXP1-expressing L4-like excitatory neurons are subtype-specifically and dramatically reduced in Down syndrome fetal cortex, especially at later stages (PCW16-20)
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Tumour-brain crosstalk restrains cancer immunity via a sensory-sympathetic axis.
PMID 41639447 · PMC12935554 · Nature · 2026 · 8 claims · 8 setups
Lung adenocarcinoma (LUAD) induces increased innervation and functional/transcriptional engagement of vagal sensory neurons (VSNs)
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Has reproduction · 74
Evaluation of classification and forecasting methods on time series gene expression data.
PMID 33156855 · PMC7647064 · PloS one · 2020 · 8 claims · 4 setups
Deep learning based methods generally outperform traditional approaches for time series gene expression classification.
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GeneExt: a gene model extension tool for enhanced single-cell RNA-seq analysis.
PMID 41769841 · PMC12970594 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 8 setups
Incomplete/inaccurate gene annotations, especially missing or truncated 3' UTRs, cause reads to map to non-genic regions and genes to be under-quantified or missing from scRNA-seq expression matrices in non-model species
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MECP2 mutations rewire human ESC fate and bias cortical lineage commitment.
PMID 42030940 · PMC13163216 · Stem cell reports · 2026 · 8 claims · 8 setups
MECP2 mutations induce an early naïve-like transcriptional drift in human ESCs, marked by upregulation of ZFP42/REX1 and other naïve-enriched markers