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 spatiotemporal dissection of the human maternal-fetal interface.
PMID 41951740 · PMC13149032 · Nature · 2026 · 8 claims · 8 setups
Generated a comprehensive single-cell multiomic and spatial atlas of the human maternal-fetal interface from early gestation to term
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Unique phenotypic and T cell receptor characteristics of CD8(+) T cells accumulated in the brains of Alzheimer's disease mice.
PMID 41794902 · PMC13087195 · Scientific reports · 2026 · 8 claims · 5 setups
Brain CD8+ T cells segregate into two major, mutually exclusive Trm populations: a CXCR6-related immunosuppressive cluster (cd8_c0) present in both aged non-Tg and 5xFAD_WT mice, and an AD-associated stem-like cluster (cd8_c1) present only in 5xFAD mice.
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Androgen activity in the male embryonic hindbrain drives lethal PFA ependymoma.
PMID 41882358 · PMC13083265 · Nature · 2026 · 8 claims · 8 setups
The cellular hierarchy of PFA ependymoma is less differentiated in male than in female patients
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Has reproduction · 100
Lipopolysaccharide distinctively alters human microglia transcriptomes to resemble microglia from Alzheimer's disease mouse models.
PMID 36254682 · PMC9612871 · Disease models & mechanisms · 2022 · 8 claims · 8 setups
iPSC-microglia show a shared core transcriptional response to ATPγS and to LPS+IFN-γ, suggesting a convergent mechanism of action
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Homeodomain protein Sxi1α independently controls cell-cell fusion and gene expression during sexual reproduction in Cryptococcus deneoformans.
PMID 41818280 · PMC13001979 · PLoS genetics · 2026 · 8 claims · 8 setups
Sxi1α has a previously unrecognized inhibitory role in same-sex (α-α) cell-cell fusion during unisexual reproduction
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A new form of diabetes caused by INS mutations defined by zygosity, stem cell and population data.
PMID 41484206 · PMC12905373 · EMBO molecular medicine · 2026 · 6 claims · 7 setups
INS R6C is a recessive loss-of-function mutation causing diabetes only in homozygous individuals, not a dominant mutation as previously classified.