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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Gene regulatory network determinants of rapid recall in human memory CD4(+) T cells.
PMID 41865369 · PMC13207208 · Cell reports · 2026 · 8 claims · 6 setups
Memory CD4+ T cells show enhanced chromatin accessibility proximal to rapid-recall genes compared to naive cells
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Multiomics combined drugs to explore the potential mechanism and treatment of ankylosing spondylitis.
PMID 41673882 · PMC13047816 · Journal of orthopaedic surgery and research · 2026 · 8 claims · 8 setups
Effector CD8+ memory T (Tem) cells are significantly elevated in AS patients compared to healthy controls
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Prominent neuroleptic sensitivity in a case of early-onset Alzheimer disease due to presenilin-1 G206A mutation.
PMID 18797263 · PMC4867177 · Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology · 2008 · 8 claims · 8 setups
A patient with the PS-1 G206A mutation developed prominent extrapyramidal signs (EPS) shortly after starting the atypical neuroleptic risperidone, which resolved completely after the drug was discontinued.
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Integrin β1 Demarks Precursors of Brain-Residing Antibody-Secreting Cells in Multiple Sclerosis.
PMID 41698162 · PMC12912196 · Neurology(R) neuroimmunology & neuroinflammation · 2026 · 7 claims · 6 setups
ITGB1 (integrin β1/CD29) is a major transcriptomic and protein-level discriminator of CXCR3+ memory B cells in blood
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Development of a pediatric immune cell atlas and characterization of CD4+ T cells in food allergy.
PMID 42025535 · PMC13105851 · Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2026 · 8 claims · 8 setups
A pediatric single-cell PBMC reference atlas was developed from 57 healthy children across 8 public scRNA-seq studies.
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Synaptic dysfunction and oxidative stress in Alzheimer's disease: emerging mechanisms.
PMID 16989739 · PMC3933161 · Journal of cellular and molecular medicine · 2006 · 6 claims · 8 setups
Mutations in APP, PS1 and PS2 genes and polymorphisms in the APOE gene are implicated in AD pathogenesis
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The spectrum of parkinsonian manifestations associated with glucocerebrosidase mutations.
PMID 18852351 · PMC2629407 · Archives of neurology · 2008 · 8 claims · 8 setups
GBA mutations are associated with a spectrum of parkinsonian phenotypes ranging from Parkinson disease to Lewy body dementia
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Clonal CD8(+) T cells populate the leptomeninges and coordinate with immune cells in human degenerative brain diseases.
PMID 41593242 · PMC12864034 · Nature immunology · 2026 · 8 claims · 6 setups
The human leptomeninges harbor substantial numbers of clonally expanded, tissue-resident memory CD8 T cells (ZNF683-high, CXCR6+, PD-1+)
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UBD: incorporating uncertainty in cell type proportion estimates from bulk samples to infer cell-type-specific profiles.
PMID 41520227 · PMC12895075 · Briefings in bioinformatics · 2026 · 7 claims · 4 setups
Existing CTS deconvolution methods (e.g., CIBERSORTx, TCA, bMIND, CellDMC, HBI) require cell type proportions that are in practice only estimated, not known, introducing unaccounted uncertainty into CTS inference.
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Has reproduction · 95
nf-rnaSeqCount: A Nextflow pipeline for obtaining raw read counts from RNA-seq data.
PMID 35574063 · PMC9097006 · South African computer journal = Suid-Afrikaanse rekenaartydskrif · 2021 · 7 claims · 5 setups
nf-rnaSeqCount is a portable, reproducible Nextflow pipeline that maps RNA-seq reads to a reference genome and quantifies gene abundance for differential expression analysis
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FLASH-MM: fast and scalable single-cell differential expression analysis using linear mixed-effects models.
PMID 41644528 · PMC12982622 · Nature communications · 2026 · 8 claims · 6 setups
FLASH-MM produces LMM parameter estimates identical to lmer (lme4) up to the sixth decimal place while being 50- to 140-fold faster as sample size increases from 20,000 to 120,000 cells
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scMILD: Single-cell multiple instance learning for sample classification and associated subpopulation discovery.
PMID 41907409 · PMC13019583 · iScience · 2026 · 8 claims · 8 setups
scMILD identifies condition-associated cells using only sample-level labels via a dual-branch MIL architecture with a shared encoder
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Has reproduction
Dissection of multiple sclerosis genetics identifies B and CD4+ T cells as driver cell subsets.
PMID 35672799 · PMC9175345 · Genome biology · 2022 · 8 claims · 7 setups
CD4+ T cells and B cells independently and significantly contribute to MS GWAS heritability enrichment, distinct from a merely shared immune regulatory landscape.
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Transcription network construction for large-scale microarray datasets using a high-performance computing approach.
PMID 18366618 · PMC2386070 · BMC genomics · 2008 · 8 claims · 7 setups
RMT removes the random noise component of the gene expression correlation matrix by testing its eigenvalue statistics against a null hypothesis derived from a truly random correlation matrix
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Cell neighborhood topology directs rare cell population identification.
PMID 41912521 · PMC13199379 · Nature communications · 2026 · 8 claims · 8 setups
RareQ is a framework that quantifies neighborhood connectivity (Q), a cell-specific measure of kNN-graph cliquishness, to detect rare cell populations from single-cell and spatial omics data
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Spatiotemporal Transcriptomics Characterizes Immune Microenvironment During Mouse Liver Aging.
PMID 42010880 · PMC13096584 · Aging cell · 2026 · 8 claims · 8 setups
T cells are the immune cell population with the most pronounced transcriptomic alterations during liver aging
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A comprehensive toolkit for analyzing cell-free DNA genomic sequencing data in liquid biopsy.
PMID 42111187 · PMC13157187 · iScience · 2026 · 8 claims · 8 setups
cfDNAanalyzer integrates feature extraction, feature processing/selection, and machine learning model building into a single one-command-line toolkit for cfDNA genomic sequencing data