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1 pathway, metabolic pathways (pathway IDs: 5200, 4151, 1100) were significantly enriched.
3 In this new data, loss-of-function (LoF) DNVs were significantly enriched among 3,471 LoF-intolerant genes,
4 ation tests were used to determine if obesity-related genes were significantly enriched among all intragenic sites that a
5 e, the targets of drug candidates predicted by our approach were significantly enriched among genes differentially expres
6 KEGG pathway analysis showed 20 pathways were significantly enriched and the most significantly enrich
8 PM(2.5) levels of lead, arsenic, chromium, and zinc were significantly enriched at some locations by factors of 1
9 SNP-containing enhancers from inflammatory skin conditions were significantly enriched at the HLA locus and also targete
11 of ice cover as sequences related to known nitrifying taxa were significantly enriched during ice cover.
13 hippocampus, thalamus, cortex, pons, medulla, pallidum that were significantly enriched for BMI heritability (p<1.6x10(-4
14 disinhibition-related brain regions were identified, which were significantly enriched for functional biological interac
16 The genes associated with mortality in BAL cells were significantly enriched for genes expressed in airway bas
17 observed that susceptibility variants for HIV-1 acquisition were significantly enriched for genes expressed in T-cells, b
18 enes associated with neurodevelopmental disorders (n = 159) were significantly enriched for LoF DNVs.
22 Furthermore, 4 of 220 gene co-expression modules tested were significantly enriched for the dystonia-associated genes
23 renia group, 83% of DEGs showed lower expression, and these were significantly enriched for three functional pathways, ea
24 Most of the distribution categories contained genes that were significantly enriched for unique biological processes.
25 RNAs which aligned to known microbial taxa, were significantly enriched in 10 of 12 primary demyelination
26 Bioinformatics analysis showed that the nearby genes were significantly enriched in 36 GO terms and 6 KEGG pathway
30 gnal transducer and activator of transcription 5) signaling were significantly enriched in AMs isolated on Day 1 in alive
31 ; 13 pathways including branched chain amino acid synthesis were significantly enriched in baseline samples from CD patie
32 G pathway analysis, genes associated with 'cancer' pathways were significantly enriched in both bioinformatic analysis of
33 Pathway enrichment analysis showed that relevant genes were significantly enriched in cancer-related pathways.
34 We found that reproductive gene ontology categories were significantly enriched in developing galls, and that exp
35 stly, since microhomologies between human and BKPyV genomes were significantly enriched in flanking regions of 84% of the
37 Genes showing reduced expression in Sox2-deleted cells were significantly enriched in interactions between promoters
38 induced versus schizophrenia-associated expression profiles were significantly enriched in pathways relevant to schizophr
39 profiles between subspecies, and genes with those APA sites were significantly enriched in quantitative trait loci (QTL)
40 , LMNA, BAG3, TNNT2, TNNC1, PLN, ACTC1, NEXN, TPM1, and VCL were significantly enriched in specific patient subsets, with
41 ponsive genes in immature dendritic cells and naive B cells were significantly enriched in synovial tissues from UA, earl
42 equence contexts of indels targeting lineage-defining genes were significantly enriched in the AATAATD DNA motif and spec
43 plementarity determining region 3 sequences and motifs that were significantly enriched in the activated cells and 17% of
44 The microhomologies between human and BKPyV genomes were significantly enriched in the flanking regions of 84.5%
45 including glycerophospholipid and sphingolipid metabolisms were significantly enriched in the LCKD samples.
46 mature and more activated phenotype: 1) reappearing B cells were significantly enriched in transitional (before: 10.1 +/-
47 chromosome-sorted samples reveals a cohort of proteins that were significantly enriched on mitotic ESC chromosomes.
49 The genomic regions spanning crossovers were significantly enriched with the Stowaway family of minia