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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MEIOC prevents continued mitotic cycling and promotes meiotic entry during mouse oogenesis.
PMID 41287933 · PMC12848572 · Development (Cambridge, England) · 2026 · 8 claims · 4 setups
MEIOC prevents continued mitotic cycling in preleptotene oocytes prior to meiotic entry
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Integrated proteomic and transcriptomic profiling of mouse lung development and Nmyc target genes.
PMID 17486137 · PMC2673710 · Molecular systems biology · 2007 · 8 claims · 7 setups
Global MudPIT-based proteomic profiling across six mouse lung developmental time points (E13.5–P56) identifies thousands of proteins and captures developmental/cell-biological expression patterns.
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Epigenetic regulation of serine biosynthesis by PHF8 during neurogenesis.
PMID 41714361 · PMC13022353 · EMBO reports · 2026 · 8 claims · 8 setups
PHF8 is required for neural stem cell (NSC) proliferation in vitro
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Identification of a new population of Tnn(+) progenitors to form tendon enthesis fibrocartilage.
PMID 42009636 · PMC13096267 · Bone research · 2026 · 8 claims · 8 setups
A novel Tnn+ progenitor cell population resides in the tendon enthesis and serves as a cellular origin of fibrocartilage lineages
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Has reproduction · 70
Predicting enhancers in mammalian genomes using supervised hidden Markov models.
PMID 30917778 · PMC6437899 · BMC bioinformatics · 2019 · 8 claims · 8 setups
eHMM predicts enhancers with high precision and recall comparable to state-of-the-art methods and consistently outperforms them in accuracy and resolution
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Unveiling critical signaling pathways in the murine salivary gland and the role of midkine.
PMID 41732276 · PMC12925232 · iScience · 2026 · 8 claims · 6 setups
CellChat analysis of scRNA-seq data from E12, E14, and E16 murine SMG reveals distinct and evolving ligand-receptor signaling networks across developmental stages
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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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Ontogeny and transcriptional regulation of Thetis cells.
PMID 41634202 · PMC13171621 · Nature · 2026 · 8 claims · 8 setups
TCs are radiosensitive haematopoietic cells derived from an IL7R+ progenitor, enriched in fetal liver
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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
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Developmental stage dominates cell-type identity and reveals a chromatin regulatory function for Rad50 in Drosophila.
PMID 41978263 · PMC13076223 · Nucleic acids research · 2026 · 8 claims · 8 setups
Developmental stage is a stronger determinant of transcriptional identity than cell type across Drosophila neurons, glia, and hemocytes
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A multi-omic single-cell landscape of perinatal mouse skin maps lineage specification and reveals shared dynamics in human fetal skin.
PMID 41998142 · PMC13144478 · Experimental & molecular medicine · 2026 · 7 claims · 8 setups
Integrated scATAC/scRNA multi-omics analysis of developing mouse skin identifies gene network axes underlying skin lineage specification
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Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans.
PMID 17218254 · PMC1885944 · Cell · 2007 · 8 claims · 8 setups
A semidominant ENU-induced S140G mutation in α-1 tubulin (Tuba1) causes hyperactivity and impaired neuronal migration in Jna/+ mice
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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.