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).

• Single-cell epigenomics uncovers heterochromatin instability and transcription factor dysfunction during mouse brain aging.

  PMID 41824460 · PMC13189690 · Cell reports · 2026 · 8 claims · 6 setups

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  Aging causes widespread, concordant changes in chromatin accessibility and gene expression across neuronal and glial cell types in the mouse brain

  brain snatac-seq single-nucleus merfish

• Shared genetic and neuroimmune architecture links type 1 diabetes with neurocognitive traits.

  PMID 41826324 · PMC13139607 · Nature communications · 2026 · 8 claims · 8 setups

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  T1D GWAS heritability is enriched in accessible chromatin of brain-resident cells, most notably microglia, across neurodevelopment into adulthood

  cortex single-nucleus gwas gtex stratified scavenge s-ldsc

• Single-nucleus multiomic profiling of the aging mouse substantia nigra reveals conserved gene alterations linked to Parkinson's disease.

  PMID 41781332 · PMC13138337 · Genome research · 2026 · 8 claims · 7 setups

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  Single-nucleus multiome (RNA+ATAC) sequencing of mouse substantia nigra across four age stages (2, 6, 12, 18 months) yields a 40,125-cell atlas spanning 27 cell subclasses

  substantia allen five oligodendrocyte single-nucleus scrna-seq single-cell

• Dominant clones leverage developmental epigenomic states to drive ependymoma.

  PMID 41882368 · PMC13102692 · Nature · 2026 · 8 claims · 8 setups

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  Chromatin accessibility patterns in neural progenitor cells are pre-established during normal development and are subsequently commissioned (not created) by ZR binding to drive oncogene expression

  rgcs ha-tagged developing native-forming bulk csi snmultiome

• A unique malignant cell type per patient tumor encoded in each cancer cell transcriptome.

  PMID 41884004 · PMC13010111 · iScience · 2026 · 8 claims · 8 setups

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  Malignant cells cluster predominantly by tumor of origin, while non-malignant cells from the same tumors cluster by cell type independent of patient

  malignant non-malignant ovarian normal scrna-seq alternative paired