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14 matching publication(s)

Publication	Journal	Year	Score	Verdict
Neuronal Small RNAs Control Behavior Transgenerationally. PMID 31178120	Cell	2019	49	L1 49/100
Starvation-induced transgenerational inheritance of small RNAs in C. elegans. PMID 25018105	Cell	2014	64	L1 64/100
Histone deacetylase SIRT6 regulates tryptophan catabolism and prevents metabolite imbalance associated with neurodegeneration. PMID 41345108	Nat Commun	2025	93	L1 93/100
The Multi-State Epigenetic Pacemaker enables the identification of combinations of factors that influence DNA methylation. PMID 39549198	Geroscience	2024	54	L1 54/100
Complete human day 14 post-implantation embryo models from naive ES cells. PMID 37673118	Nature	2023	100	L1 100/100
Intrinsic suppression of type I interferon production underlies the therapeutic efficacy of IL-15-producing natural killer cells in B-cell acute lymphoblastic l PMID 37217248	J Immunother Cancer	2023	76	L1 76/100
LMAS: evaluating metagenomic short de novo assembly methods through defined communities. PMID 36576131	Gigascience	2022	86	L1 86/100
Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs. PMID 36414417	—	2023	85	L1 85/100
Identification and functional implications of pseudouridine RNA modification on small noncoding RNAs in the mammalian pathogen Trypanosoma brucei. PMID 35714765	J Biol Chem	2022	80	80/100
Experimental identification and in silico prediction of bacterivory in green algae. PMID 33649548	ISME J	2021	93	L1 93/100
Comparing the utility of in vivo transposon mutagenesis approaches in yeast species to infer gene essentiality. PMID 32681306	Curr Genet	2020	81	L1 81/100
The exonuclease Xrn1 activates transcription and translation of mRNAs encoding membrane proteins. PMID 30899024	Nat Commun	2019	85	L1 85/100
Benefit from decline: the primary transcriptome of Alteromonas macleodii str. Te101 during Trichodesmium demise. ⚑ PMID 29335641	ISME J	2018	—	L1 No data access ⚑
Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome. PMID 17033964	—	2006	75	L1 75/100