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).

Publications 1.3k Datasets 392.5k Experiments 6

System / cell line: young ✕ Assay: biological ✕ Clear

Single-cell analysis of testicular bacterial microbiome changes during aging and effect on reproductive capacity in mice.

PMID 41438041 · PMC12719757 · iScience · 2025 · 8 claims · 8 setups

Has reproduction · 78

INVADE-seq (single-cell RNA-seq combined with 16S rRNA targeting) detects a sparse but widespread bacterial presence across diverse testicular cell types

testis young testicular invade-seq histology sperm
Cell-Type-Specific Gene Modules Related to the Regional Homogeneity of Spontaneous Brain Activity and Their Associations With Common Brain Disorders.

PMID 33958982 · PMC8093778 · Frontiers in neuroscience · 2021 · 7 claims · 8 setups

Has reproduction · 59

Fourteen gene modules were consistently associated with ReHo across three independent fMRI datasets.

healthy six ahba neurons resting-state microarray wgcna
Exploring candidate genes for pericarp russet pigmentation of sand pear (Pyrus pyrifolia) via RNA-Seq data in two genotypes contrasting for pericarp color.

PMID 24400075 · PMC3882208 · PloS one · 2014 · 8 claims · 5 setups

Has reproduction · 74

RNA-seq-based bulked segregant analysis of russet- vs green-pericarp F1 pools identified 29,100 unigenes, 206 of which were significantly differentially expressed (|log2 fold change| > 1).

pericarp green cuiguan illumina bulk qrt-pcr light
Significance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonism.

PMID 19087301 · PMC2635385 · BMC neurology · 2008 · 8 claims · 8 setups

Full-text index only

A parkin exon 4 deletion segregates with disease in a three-generation family (Family F), homozygous in both affected individuals

consanguineous same affected family sanger multiplex microsatellite
Age Deceleration and Reversal Gene Patterns in Dauer Diapause.

PMID 41104926 · PMC12686545 · Aging cell · 2025 · 8 claims · 8 setups

Has reproduction · 88

Dauer arrest, regardless of duration, does not cause lasting functional decline in lifespan, brood size, or developmental resumption

daf-2 wild-type same dauer developmental lifespan brood
Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.

PMID 18162506 · PMC7611804 · Diabetes · 2008 · 8 claims · 8 setups

Full-text index only

Heterozygous INS mutations are a common cause of permanent neonatal diabetes (PNDM) diagnosed before 6 months of age

peripheral patients mody young-onset pcr microsatellite variant

Experiments

Single-cell analysis of testicular bacterial microbiome changes during aging and effect on reproductive capacity in mice.

Cell-Type-Specific Gene Modules Related to the Regional Homogeneity of Spontaneous Brain Activity and Their Associations With Common Brain Disorders.

Exploring candidate genes for pericarp russet pigmentation of sand pear (Pyrus pyrifolia) via RNA-Seq data in two genotypes contrasting for pericarp color.

Significance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonism.

Age Deceleration and Reversal Gene Patterns in Dauer Diapause.

Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.