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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Rete ridges form via evolutionarily distinct mechanisms in mammalian skin.
PMID 41639458 · PMC12959975 · Nature · 2026 · 8 claims · 8 setups
Rete ridges form through a mechanism independent from hair follicles and sweat glands, via interconnected epidermal invaginations
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The gene expression landscape of disease genes.
PMID 41664080 · PMC12983648 · Genome biology · 2026 · 8 claims · 8 setups
In tissues and cell types with established disease relevance, disease genes show higher and more specific gene expression than control genes
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ICE: robust detection of cellular senescence from weak single-cell signatures using imputation-based marker refinement.
PMID 41668152 · PMC12990438 · Genome biology · 2026 · 8 claims · 7 setups
Senescence-associated marker genes show weak, non-specific expression across human tissues and cell types compared to canonical tissue/cell-type markers
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High-throughput mapping of spontaneous mitotic crossover and genome instability events with sci-L3-Strand-seq.
PMID 41674384 · PMC12895072 · Nucleic acids research · 2026 · 8 claims · 6 setups
sci-L3-Strand-seq is a combinatorial indexing method with linear amplification for DNA template strand sequencing that cost-effectively scales to millions of single cells
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Heritable ER stress impairs mitochondrial metabolism and maintenance of hematopoietic stem cells after low-dose irradiation.
PMID 41675062 · PMC12886522 · iScience · 2026 · 8 claims · 8 setups
Proliferating 20 mGy-irradiated HSC exhibit oxidative stress and altered metabolism with increased mitochondrial ROS and mitochondrial Ca2+ overload compared to non-irradiated HSC
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ATRX loss couples genome instability at a G-rich repeat to dysregulation of human alpha-globin expression.
PMID 41688464 · PMC13018553 · Nature communications · 2026 · 8 claims · 8 setups
ATRX deficiency downregulates α-globin (HBM/HBA) selectively in a subset of cells that exhibit DNA damage, rather than uniformly across the population
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Oxaliplatin-induced cardiotoxicity in mice is connected to the changes in energy metabolism in the heart tissue.
PMID 41689157 · PMC13005559 · Cardio-oncology (London, England) · 2026 · 8 claims · 7 setups
Chronic oxaliplatin treatment causes direct cardiotoxicity in mice, evidenced by ECG, histology, and RNA-seq changes.
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Epigenetic profiling of hematopoietic stem cells from male mice identifies KDR and PU.1 as regulators of aging transcriptome and caloric restriction response.
PMID 41720793 · PMC13035812 · Nature communications · 2026 · 8 claims · 8 setups
Lifelong CR reduces white blood cell production and shifts hematopoiesis toward myeloid and thrombo-erythroid lineages while suppressing lymphoid output
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SLC25A37 as a novel therapeutic target for benign prostatic hyperplasia: integrative analyses of single-cell RNA sequencing and genome-wide association studies.
PMID 41726128 · PMC12917586 · Open medicine (Warsaw, Poland) · 2026 · 8 claims · 8 setups
SLC25A37 is causally associated with increased BPH risk, supported by MR, Bayesian colocalization, and reverse MR analyses
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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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pmid-41771874
PMID 41771874 · PMC13065974 · 8 claims · 8 setups
A chromosome-level genome assembly of C. yunnanensis was generated using PacBio HiFi sequencing and Hi-C scaffolding
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B lymphocytes of xeroderma pigmentosum or Cockayne syndrome patients with inherited defects in nucleotide excision repair are fully capable of somatic hypermutation of immunoglobulin genes.
PMID 9236193 · PMC2198998 · The Journal of experimental medicine · 1997 · 6 claims · 3 setups
EBV-transformed B cells from NER-defective patients (XP-B, XP-D, XP-V, CS-A) show a high frequency of point mutations in Ig heavy and light chain V regions but not in C regions
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Colorectal cancer genomics: evidence for multiple genotypes which influence survival.
PMID 11720434 · PMC2363933 · British journal of cancer · 2001 · 6 claims · 3 setups
Genetic grade (total number of CGH-detected gains+losses) varies greatly among Dukes' C CRC tumours and shows a multimodal (non-normal) distribution
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Measurement reproducibility in the early stages of biomarker development.
PMID 15665389 · PMC3839328 · Disease markers · 2004 · 6 claims · 3 setups
Functional PCA can be used as the basis for gauge R&R (repeatability and reproducibility) assessment of mass spectra without prior identification of which spectral features are biomarkers
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Detection of large deletions in the LDL receptor gene with quantitative PCR methods.
PMID 15842735 · PMC1087844 · BMC medical genetics · 2005 · 7 claims · 3 setups
MLPA was cheaper, more accurate and more precise than Real-Time PCR for detecting LDL receptor gene deletions
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Operon information improves gene expression estimation for cDNA microarrays.
PMID 16630355 · PMC1513396 · BMC genomics · 2006 · 7 claims · 3 setups
A hierarchical Bayesian model that borrows expression information from other genes within the same operon improves estimation of relative transcript levels.
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PrimerSeq: Design and visualization of RT-PCR primers for alternative splicing using RNA-seq data.
PMID 24747190 · PMC4411361 · Genomics, proteomics & bioinformatics · 2014 · 8 claims · 3 setups
PrimerSeq is a user-friendly stand-alone software with a GUI for systematic design and visualization of RT-PCR primers for alternative splicing analysis using user-provided RNA-seq data.
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Genetic association study and meta-analysis of the HTR2C Cys23Ser polymorphism and migraine.
PMID 17901921 · PMC3451673 · The journal of headache and pain · 2007 · 8 claims · 3 setups
The HTR2C Cys23Ser polymorphism is not significantly associated with migraine or migraine with aura in the case-control study
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FGF: a web tool for Fishing Gene Family in a whole genome database.
PMID 17584790 · PMC1933194 · Nucleic acids research · 2007 · 6 claims · 3 setups
FGF efficiently searches and identifies gene families in whole-genome databases and outputs visual phylogenetic trees annotated with gene structure, chromosome position, duplication fate, and selective pressure (Ka/Ks)
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Spontaneous symmetry breaking in genome evolution.
PMID 18367477 · PMC2377439 · Nucleic acids research · 2008 · 6 claims · 3 setups
Exon size distributions in sequenced genomes follow a lognormal pattern typical of a random Kolmogoroff fractioning process