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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Discovery and characterization of gene-by-environment and epistatic genetic effects in a vertebrate model.
PMID 41672067 · PMC13174225 · Cell genomics · 2026 · 7 claims · 7 setups
A segregation analysis in an F2 medaka cross identified 16 QTLs linked to embryonic heart rate variation across temperatures
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Unraveling Cefiderocol Resistance in NDM- and OXA-48-like Co-Producing Klebsiella pneumoniae Isolates Through Integrated Genomic and Phenotypic Analysis.
PMID 42192735 · PMC13203471 · Antibiotics (Basel, Switzerland) · 2026 · 8 claims · 6 setups
K. pneumoniae isolates co-producing NDM and OXA-48-like carbapenemases are predominantly clonal, belonging to the high-risk ST147 lineage.
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Stenotrophomonas maltophilia Bloodstream Infection Outbreak in Acute Care Hospital, California, USA, 2022-2023(1).
PMID 41863496 · PMC13016006 · Emerging infectious diseases · 2026 · 8 claims · 5 setups
13 S. maltophilia bloodstream infections occurred among ICU patients from May 2022–September 2023, with whole-genome sequencing showing the isolates were highly related (ST239).
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Geographically Distinct Circulation of Genotype II and III St. Louis Encephalitis Virus, Texas, USA, 2009-2024.
PMID 41986946 · PMC13094854 · Emerging infectious diseases · 2026 · 7 claims · 7 setups
Genotype II and genotype III SLEV circulated concurrently in Texas during 2009–2024 but were geographically segregated, with no county having both.
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Combinatorial Mismatch Scan (CMS) for loci associated with dementia in the Amish.
PMID 16515697 · PMC1448207 · BMC medical genetics · 2006 · 8 claims · 7 setups
CMS compares IBS allele/genotype sharing between distantly related (beyond grandparental) affected and unaffected individuals from founder populations to detect disease loci while reducing confounding from population stratification and genetic heterogeneity.