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).

• Metabolism as a complex genetic trait, a systems biology approach: implications for inborn errors of metabolism and clinical diseases.

  PMID 18836848 · PMC4319114 · Journal of inherited metabolic disease · 2008 · 7 claims · 8 setups

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  Synergistic heterozygosity — cumulative heterozygous mutations at multiple loci in functionally related metabolic pathways — can cause physiologically relevant reduction of pathway flux and disease.

  models liver sucrose vlcad-deficient physiological blue sucrose

• Characterizing gene perturbations in single cells via network divergence analysis.

  PMID 41965857 · PMC13249949 · Nature communications · 2026 · 8 claims · 8 setups

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  scDNS quantifies gene-specific functional perturbations by measuring Jensen-Shannon divergence between condition-specific gene interaction network configurations

  ipsc-derived embryonic panc-1 triple scrna-seq single-nucleus

• LBR and LAP2 mediate heterochromatin tethering to the nuclear periphery to preserve genome homeostasis.

  PMID 41735607 · PMC12992122 · Nature cell biology · 2026 · 7 claims · 8 setups

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  Combined downregulation of 12 abundant, ubiquitously expressed nuclear envelope proteins (si-11) causes global detachment of constitutive heterochromatin from the nuclear envelope and its relocation to the nuclear interior in multiple mammalian cell types

  hct116 rpe-1 nih immunofluorescence immunoblot sequencing