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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Trisomy 21 Drives ADARB1 Overexpression and Premature RNA Recoding in the Developing Fetal Brain.
PMID 41917044 · PMC13039865 · Nature communications · 2026 · 8 claims · 8 setups
T21 causes widespread fetal brain gene expression dysregulation with significant enrichment for chromosome 21 genes and perturbation of neurodevelopmental, synaptic, and immune-related pathways
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Shared genetic and neuroimmune architecture links type 1 diabetes with neurocognitive traits.
PMID 41826324 · PMC13139607 · Nature communications · 2026 · 8 claims · 8 setups
T1D GWAS heritability is enriched in accessible chromatin of brain-resident cells, most notably microglia, across neurodevelopment into adulthood
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Annotation and analysis of 10,000 expressed sequence tags from developing mouse eye and adult retina.
PMID 14519200 · PMC328454 · Genome biology · 2003 · 8 claims · 5 setups
Annotation of 8,633 high-quality non-mitochondrial/non-ribosomal ESTs shows 57% represent known genes and 43% are unknown or novel, with M15E having the highest proportion of novel ESTs
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MultiSP deciphers tissue structure and multicellular communication from spatial multi-omics data.
PMID 41650976 · PMC13174227 · Cell genomics · 2026 · 7 claims · 5 setups
MultiSP outperforms existing spatial and single-cell multi-omics integration methods in detecting biologically accurate spatial domains across multiple spatial multi-omics technologies and tissue types
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FOXP1 is differentially active during development of murine vasopressin and oxytocin magnocellular neurons.
PMID 42088346 · PMC13138059 · iScience · 2026 · 8 claims · 7 setups
FOXP1 participates in MCN development and is differentially active in OXT MCNs relative to AVP MCNs
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Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes.
PMID 18775783 · PMC2729512 · Molecular and cellular neurosciences · 2008 · 8 claims · 8 setups
Six 22q11 genes (Mrpl40, Prodh, Slc25a1, Txnrd2, T10, Zdhhc8) encode proteins that localize to mitochondria, including neuronal/synaptic mitochondria.