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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Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis.
PMID 20023659 · PMC2980844 · Nature genetics · 2010 · 8 claims · 8 setups
Mutations in INF2, a formin family actin-regulating protein, cause autosomal dominant focal segmental glomerulosclerosis (FSGS)
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Science star over Asia.
PMID 16149850 · PMC1201306 · PLoS biology · 2005 · 8 claims · 7 setups
Ariff Bongso and associates at Singapore's National University Hospital were the first to derive human embryonic stem cells, from a five-day-old discarded human embryo in 1994, and showed the cells were pluripotent with therapeutic transplant potential.
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CX-5461 and doxorubicin activate a shared DNA damage-associated transcriptional response in human cardiomyocytes.
PMID 41543508 · PMC12958809 · G3 (Bethesda, Md.) · 2026 · 6 claims · 7 setups
CX induces cell death in iPSC-derived cardiomyocytes at micromolar concentrations
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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
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The Proteomics Identifications database: 2010 update.
PMID 19906717 · PMC2808904 · Nucleic acids research · 2010 · 8 claims · 6 setups
PRIDE has become one of the main repositories for MS-based proteomics data, with substantial growth in data holdings over the last two years.