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1                           Immune and inflammatory functions were enriched among the genes downregulated in response to st
2                                             Causal variants were enriched at conserved nucleotides, tended to have low de
3 tine, polyunsaturated)' and 'hexosylceramides' sub-pathways were enriched by all methods, and 'sphingomyelins' by all but
4                  Plasma endothelial-derived exosomes (EDEs) were enriched by two-step immunoabsorption from four groups o
5                            Furthermore, tissue-specific NFR were enriched for binding motifs of transcription factors rel
6 orrelates of depression-linked brain function and structure were enriched for disorder-relevant molecular pathways.
7                       The fusion transcripts in fetal brain were enriched for genes for long-term depression; while those
8 eover, the DEGs associated with parental Holocaust exposure were enriched for glucocorticoid-regulated genes and immune p
9     Genes abnormally expressed in major depressive disorder were enriched for innate immune-related functions, coded for
10 that fetal-enhancer regions methylated by Dnmt3a and Dnmt3b were enriched for kidney disease genetic risk loci.
11                   Positively weighted (downregulated) genes were enriched for neuronal, specifically interneuronal, affil
12       The genes under genetic regulation in human and mouse were enriched for oxidative phosphorylation and adipogenesis.
13 al profiling by mass spectrometry showed that placental EVs were enriched for proteins that function in transport and vir
14 gnatures in non-progressors, and found that non-progressors were enriched for proteomic processes involving regulation of
15                                             These same loci were enriched for signatures of long-term balancing selection
16 own to have breast cancer, two of them contained cells that were enriched for the CSC phenotype and carried mutations in
17         Genes whose expression correlate with schizophrenia were enriched for those involved in abnormal CNS synaptic tra
18                     Cells with inactive pgRNA transcription were enriched from 0% (HB1) to 14.3% (HB5) of infected hepato
19                          Platinum-tolerant cells and tumors were enriched in ALDH(+) cells, formed more spheroids, and ex
20             Cell proliferation and immune activity pathways were enriched in BCs with high mutation rates.
21              In the presence of inflammation, portal tracts were enriched in CD3+, CD20+ but displayed fewer CD68+.
22 revealed that gene sets of layer 5b and 6 pyramidal neurons were enriched in DEGs of the mPFC downregulated in both NAc D
23 osing solution, C6 and C7 perfluoroalkyl sulfonates (PFSAs) were enriched in dosed mouse serum, suggesting in vivo transf
24 d, strikingly, found that only two PATs, ZDHHC5 and ZDHHC8, were enriched in DRG axons.
25 uding TRAIL (TNFSF10), TL1A (TNFSF15), and their receptors, were enriched in E2F1(high) While TRAIL was equally expressed
26                                        Identified mutations were enriched in essential protein domains and genes identifi
27                                            Foxp3 regulators were enriched in genes encoding subunits of the SWI/SNF nucle
28                                                    Non-MTEX were enriched in immunostimulatory proteins (P = 0.002) and w
29                                                        MTEX were enriched in immunosuppressive proteins (P = 0.03).
30 s 53 tissues, genes in kidney function-associated GWAS loci were enriched in kidney (P=9.1E-8 for eGFR; P=1.2E-5 for urat
31 or tyrosine kinase (Erbb), and Toll-like receptor signaling were enriched in lysates of podocytes treated with the TrkC l
32 ions and mRNA abundance associations with target genes, and were enriched in motif-rewiring mutations and structural vari
33 nts of the Fibroblast Growth Factor (FGF) signaling pathway were enriched in nascent myotubes in Drosophila embryos.
34                                           In particular, ET were enriched in polyfunctional T cells.
35 e Gene Ontology proteome analysis revealed that SUM52 cells were enriched in proteins associated with cell metabolism and
36                                      Infant chimpanzee guts were enriched in some of the same taxa prevalent in infant hu
37 h anemia compared with control individuals, other mutations were enriched in the anemia cohort, including TP53 and SF3B1.
38 HIF2alpha) and hypoxia-inducible factor 1alpha (HIF1alpha), were enriched in the DhMRs.
39 ets and mRNAs expressed at low levels with short half-lives were enriched in the polysomes of upf1 mutants, indicating th
40 ia targeted expression profiling(17) that B cell signatures were enriched in the tumours of patients who respond to treat
41 e profiles of patients who recovered from moderate COVID-19 were enriched in tissue reparative growth factor signature A,
42                      In humans and mice, sTDP43 transcripts were enriched in vulnerable motor neurons, and we observed a
43 d trisome footprint profiling in yeast and found collisions were enriched on diverse sequence motifs known to slow transl
44 nscription factors (TF) were identified whose binding sites were enriched or depleted in mutations.
45                     Prior to trypsin digestion, IgG and IgA were enriched simultaneously, followed by a one-step denatura
46                                            Top MWAS results were enriched specific pathways, overlapped with genes found
47 atched non-invading SUM149 inflammatory breast cancer cells were enriched using this device and these two functionally di
48        Macrophages from both human and murine tumor tissues were enriched with lipids due to increased lipid uptake by ma
49 kin and nasal samples from workers in the machine shop area were enriched with Pseudomonas, the dominant taxa in MWF.
50    As for functional characteristics, such control proteins were enriched with regulatory and signaling genes, disease ge