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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Pseudotimecascade Visualizes Gene Expression Cascade in Pseudotime Analysis.
PMID 41939293 · PMC13047748 · Computational and structural biotechnology journal · 2026 · 8 claims · 6 setups
Pseudotimecascade jointly analyzes multiple genes to uncover their relative temporal ordering and stage-specific activation patterns along pseudotime.
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Interpretable learning of temporal cellular dynamics from single-cell data.
PMID 41875867 · PMC13030976 · Cell reports methods · 2026 · 7 claims · 7 setups
NeuroVelo couples a linear latent phase-space projection with a non-linear neural ODE, using RNA velocity as a physics-informed loss penalty, to jointly model cellular dynamics and enable gene-level interpretability
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Gene expression profiling identifies potential biomarkers for vaso-occlusive episodes in sickle cell disease.
PMID 41797711 · PMC13041688 · JCI insight · 2026 · 8 claims · 5 setups
Pathways linked to complement activation, coagulation, and IL-6/JAK/STAT3 signaling are enriched during VOEs in CD45+ leukocytes
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RPS19 and RPL5 haploinsufficient models reveal divergent ribosomal subunit controls of fetal hematopoiesis.
PMID 41951665 · PMC13237010 · Nature communications · 2026 · 8 claims · 8 setups
RPL5 haploinsufficiency causes HSPC accumulation and prenatal lethality via p53-mediated ferroptosis of mature erythroid progenitors
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Functional analysis of human hematopoietic stem cell gene expression using zebrafish.
PMID 16089502 · PMC1166352 · PLoS biology · 2005 · 8 claims · 8 setups
277 unique transcripts are differentially expressed between Rho lo and Rho hi HSC-enriched/depleted populations, conserved across both umbilical cord blood and bone marrow
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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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Glia maturation factor gamma (GMFG): a cytokine-responsive protein during hematopoietic lineage development and its functional genomics analysis.
PMID 17127212 · PMC5054077 · Genomics, proteomics & bioinformatics · 2006 · 8 claims · 6 setups
GMFG is a cytokine-responsive protein in EPO-induced (erythroid) and G-CSF-induced (myeloid) hematopoietic lineage development
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Alternative polyadenylation links RNA processing to iron metabolism in human erythropoiesis.
PMID 41805127 · PMC12972907 · Nucleic acids research · 2026 · 8 claims · 8 setups
CPSF6 facilitates erythropoiesis; its depletion impairs heme synthesis and causes intracellular iron deficiency
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Combining transcriptional profiling and genetic linkage analysis to uncover gene networks operating in hematopoietic stem cells and their progeny.
PMID 18560825 · PMC2493868 · Immunogenetics · 2008 · 8 claims · 8 setups
Neither transcriptional profiling alone nor genetic linkage analysis alone has been an effective approach to identify genes or gene networks that specify stemness or initiate differentiation/lineage specification.
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Functional correction and genome integrity with duplex base editing of β-thalassemic hematopoietic stem cells.
PMID 41629994 · PMC12952134 · Genome biology · 2026 · 8 claims · 8 setups
Duplex base editing (2×BE) of BCL11A enhancer and HBG promoter produces significantly higher HbF and γ-globin induction than simplex BE or DSB-Cas9 editing
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Integrating natural and engineered genetic variations to decode regulatory influence on blood traits.
PMID 41637188 · PMC12932927 · Cell reports · 2026 · 8 claims · 8 setups
Combined MPRA enhancer assays, RNA-seq (DE/ATU) analysis, and CRISPR-Cas9 engineering to dissect the function of 94 rare non-coding variants (RNVs) associated with blood traits
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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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Bayesian inference of RNA velocity incorporating timepoints, lineage bifurcations, and count data.
PMID 41860983 · PMC13021174 · PLoS computational biology · 2026 · 8 claims · 8 setups
VeloVAE significantly outperforms previous RNA velocity methods in data fit, accuracy of inferred differentiation directions, and transcription rate estimation.
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Transcriptional readthrough precedes alternative splicing programs triggered in CML cells by imatinib.
PMID 41860998 · PMC13004010 · Science advances · 2026 · 8 claims · 6 setups
Imatinib treatment induces transcriptional readthrough in K562 CML cells within 1 hour, before detectable gene expression or alternative splicing changes
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Neural network-assisted RNA velocity imputation for empowering transcript dynamics-based analyses.
PMID 41736867 · PMC12927306 · iScience · 2026 · 8 claims · 8 setups
NARVI, a deep neural network trained on expression-velocity relationships of passed genes, can impute RNA velocity for dropped genes that conventional tools (e.g., scVelo, UniTVelo) fail to calculate
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Prediction of myeloid malignant cells in Fanconi anemia using machine learning.
PMID 41557613 · PMC12818649 · PloS one · 2026 · 6 claims · 7 setups
A DNN classifier trained on AML scRNA-seq data accurately predicts AML-like transcriptional profiles at single-cell resolution
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Interactive analysis of single-cell trajectories in 3D space with Cell Journey.
PMID 41773942 · PMC13042281 · GigaScience · 2026 · 7 claims · 3 setups
Cell Journey is an interactive platform for computing and visualizing RNA velocity-based single-cell trajectories in 3D space.
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Development of double-positive thymocytes at single-cell resolution.
PMID 33771202 · PMC8004397 · Genome medicine · 2021 · 7 claims · 8 setups
DP thymocytes can be classified into blast, rearrangement, and selection subtypes, distinguishable by surface markers CD2 and Ly6d
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Systematic background selection with BasCoD enhances contrastive dimension reduction in single cell genomics.
PMID 41844632 · PMC13144610 · Nature communications · 2026 · 8 claims · 7 setups
BasCoD is a statistical testing framework using spectral subspace inclusion theory to evaluate whether a candidate background dataset is suitable for contrastive dimension reduction of a target dataset