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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pmid-41807033
PMID 41807033 · PMC12983827 · 8 claims · 8 setups
A ferroptosis-driver gene signature (FD.sig) and machine learning model (FD.model) can predict ICI response
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Simultaneous epigenomic profiling and regulatory activity measurement using e2MPRA.
PMID 41535307 · PMC12913623 · Nature communications · 2026 · 8 claims · 8 setups
e2MPRA, combining lentiviral integration-based MPRA with CUT&Tag or ATAC-seq, enables simultaneous measurement of regulatory activity, protein binding, and epigenetic modification of the same synthetic CRE sequences.
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Mechanisms of gene regulation by SRCAP and H2A.Z.
PMID 41792122 · PMC13087030 · Nature communications · 2026 · 8 claims · 8 setups
Acute SRCAP degradation causes rapid, genome-wide replacement of H2A.Z by canonical H2A, with turnover fastest at active promoters/enhancers and slower at bivalent loci
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Feed-forward loops by NR5A2 ensure robust gene activation during pre-implantation development.
PMID 41355514 · PMC12848575 · Development (Cambridge, England) · 2026 · 8 claims · 8 setups
NR5A2 chromatin binding is dynamic, changing genome-wide from the 2-cell to the morula stage, with peak numbers and target regions (e.g. SINE B1/Alu) shifting over developmental time
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Distal enhancers regulate mammalian early embryonic lineage differentiation through long-range interactions.
PMID 41562256 · PMC12820533 · Nucleic acids research · 2026 · 8 claims · 8 setups
Lineage-specific H3K27ac is predominantly enriched at distal enhancers rather than promoters, indicating first-lineage differentiation relies on distal enhancer activity
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ZFHX4 is necessary for dopaminergic neuron differentiation and controls cell cycle by regulating LIN28A.
PMID 42208531 · PMC13261933 · Stem cell reports · 2026 · 8 claims · 8 setups
ZFHX4 is a super-enhancer-controlled transcription factor induced during mDAN specification
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Bromodomain protein IBD1 bridges histone acetylation and H2A.Z deposition to fine-tune transcription.
PMID 41728948 · PMC12926916 · Nucleic acids research · 2026 · 8 claims · 8 setups
IBD1's bromodomain recognizes H3K9/K14 di-acetylation to recruit the SWR complex subunit ARP6, ensuring precise H2A.Z incorporation into chromatin
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Pre-implantation embryo metabolism identified by PEMA reveals endogenous lactate insufficiency contributes to pre-implantation development arrest.
PMID 42272466 · PMC13247451 · Fundamental research · 2026 · 6 claims · 7 setups
PEMA, a computational tool that weights metabolic reactions using Ribo-seq data combined with RNA-seq-derived flux balance analysis, can characterize metabolic states of human and mouse pre-implantation embryos more precisely than existing methods like Compass.
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Ectopic expression of BEX genes in T-cell acute lymphoblastic leukemia.
PMID 40811813 · PMC12830129 · Blood advances · 2026 · 6 claims · 8 setups
Bex1 (and to a lesser extent Bex4) is ectopically expressed in Pten-deficient mouse T-ALL blasts
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YAP/TAZ-VGLL3 governs adipocyte fate via epigenetic reprogramming of PPARγ and its target enhancers.
PMID 41533786 · PMC12802833 · Science advances · 2026 · 8 claims · 8 setups
TAZ represses PPARγ-bound target enhancers, evidenced by markedly reduced H3K27ac occupancy, leading to transcriptional repression of adipogenic genes including Pparg2
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Af-CUT&Tag: a sensitive and antibody-free chromatin profiling method using genetically encoded tags and high-affinity binders fused to Tn5.
PMID 41547832 · PMC12914055 · Nature communications · 2026 · 8 claims · 8 setups
Af-CUT&Tag eliminates dependence on conventional target antibodies by using CRISPR-integrated HiBiT/ALFA-tags recognized by LgBiT/NbALFA-Tn5 fusion proteins
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Evolutionary innovation within conserved gene regulatory networks underlying biomineralized skeletons in Bilateria.
PMID 41556888 · PMC12862220 · Molecular biology and evolution · 2026 · 8 claims · 6 setups
A biphasic regulatory program orchestrates larval and adult shell formation in Crassostrea nippona, involving coordinated activity of ancient transcription factors and dynamic chromatin remodeling
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Sequencing DNA methylation and hydroxymethylation at co-occurring chromatin features.
PMID 41667493 · PMC13002996 · Nature communications · 2026 · 8 claims · 8 setups
6-base-CUT&Tag (6B-C&T) simultaneously maps G, A, T, C, 5mC, and 5hmC at antibody-targeted chromatin features on the same DNA fragment
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Loss of SOCS1 in Donor T Cells Exacerbates Intestinal GVHD by Driving a Chemokine-Dependent Pro-Inflammatory Immune Microenvironment.
PMID 41580972 · PMC13042394 · Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026 · 8 claims · 8 setups
T cell-specific Socs1 loss intrinsically drives pro-inflammatory T cell differentiation independent of antigen stimulation, with the strongest effects in CD8+ T cells
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The chromatin remodeller CHD4 regulates transcription factor binding to both prevent activation of silent enhancers and maintain active regulatory elements.
PMID 41632506 · PMC12867480 · eLife · 2026 · 8 claims · 8 setups
CHD4 acts via a second mechanism beyond nucleosome sliding: actively restricting the residence time of transcription factors on chromatin
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Sequential RNA polymerase II activation drives human hematopoiesis.
PMID 41520338 · PMC13067999 · Cell reports · 2026 · 7 claims · 7 setups
sciCUT&Tag2in1 enables simultaneous single-cell combinatorial-indexing profiling of Pol II occupancy (Ser5/Ser2-phospho CTD) together with histone modifications (H3K4me1-2-3 or H3K27me3) in up to 50,000 cells per experiment
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PRDM1+ Malignant Cells Mediate an Immunosuppressive Landscape and Resistance to Neoadjuvant Chemoradiotherapy and Immunotherapy in Esophageal Squamous Cell Carcinoma.
PMID 41556358 · PMC13042517 · Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026 · 8 claims · 8 setups
A PRDM1+ malignant epithelial cell subcluster (Epi_C4) is enriched in NMPR patients and is associated with nICRT treatment resistance