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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GeneSpeed Beta Cell: an online genomics data repository and analysis resource tailored for the islet cell biologist.
PMID 18795106 · PMC2532782 · Experimental diabetes research · 2008 · 6 claims · 4 setups
GeneSpeed Beta Cell is an online genomics data repository allowing simultaneous multiexperiment viewing and multidimensional (Boolean intersection/union) querying of pancreas- and islet-relevant datasets, integrated with GeneSpeed's domain-based gene categorization.
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The RNA-binding protein SRSF3 controls epicardial formation by regulating splicing and proliferation.
PMID 41601313 · PMC13006530 · Development (Cambridge, England) · 2026 · 8 claims · 8 setups
SRSF3 is highly expressed in the proepicardial organ and early epicardium, declining after E11.5 and remaining low postnatally
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Modular genetic architecture underlies human hand and foot evolution.
PMID 42118837 · PMC13187773 · Proceedings of the National Academy of Sciences of the United States of America · 2026 · 8 claims · 8 setups
Gene expression and regulatory modules strongly separate metapodials from phalanges, and separate tissues to a lesser extent along the anterior-posterior axis or between limb types
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A single-nucleotide enhancer mutation overrides chromosomal sex to drive XX male development.
PMID 41957362 · PMC13066550 · Nature communications · 2026 · 8 claims · 7 setups
A 3 bp deletion or a 1 bp insertion in the Enh13 SOX9 binding site causes complete XX female-to-male sex reversal in adult homozygous mice
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Novel mutations in GJA1 cause oculodentodigital syndrome.
PMID 18946008 · PMC2588666 · Journal of dental research · 2008 · 8 claims · 3 setups
Heterozygous missense mutations in GJA1 were found in all analyzed ODD-affected individuals across ten unrelated families
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Has reproduction · 87
High-resolution mapping of transcriptional dynamics across tissue development reveals a stable mRNA-tRNA interface.
PMID 25122613 · PMC4216921 · Genome research · 2014 · 8 claims · 7 setups
mRNA codon and amino acid pools are highly stable across mouse development and across tissues, simply reflecting the genomic background distribution of any possible transcriptome.
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Splicing variants in MYRF cause partial loss of function in the retinal pigment epithelium leading to nanophthalmos.
PMID 41746734 · PMC13043084 · JCI insight · 2026 · 8 claims · 8 setups
The dG-MYRF C-terminal frameshift variant undergoes normal homotrimerization, cleavage, and nuclear localization but shows reduced steady-state levels of the C-terminal cleavage product and decreased transcriptional activation of target genes.
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Has reproduction · 82
Temporal control of progenitor competence shapes maturation in GABAergic neuron development in mice.
PMID 40629142 · PMC12321585 · Nature neuroscience · 2025 · 8 claims · 8 setups
Ganglionic eminence (ventral) progenitors maintain stable differentiation competence throughout neurogenesis, generating a consistent set of postmitotic precursor states at all stages, unlike dorsal cortical progenitors whose differentiation competence changes gradually.
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Has reproduction · 68
Microglia maintain structural integrity during fetal brain morphogenesis.
PMID 38309258 · PMC10869139 · Cell · 2024 · 8 claims · 8 setups
Embryonic ATM-like microglia accumulate at two fetal cortical boundaries, the cortico-striato-amygdalar boundary (CSA) and cortico-septal boundary (CSB), resembling post-natal axon-tract-associated microglia (ATM)
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Base barrier cells provide compartmentalization of choroid plexus, brain and CSF.
PMID 41680326 · PMC12971494 · Nature neuroscience · 2026 · 8 claims · 8 setups
A distinct fibroblast population, ChP base barrier cells (BBCs, formerly type II fibroblasts), exists at the base of the choroid plexus, separate from ChP stromal (type I) fibroblasts