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1 e profiles of patients who recovered from moderate COVID-19 were enriched in tissue reparative growth factor signature A,
2 esting that these cells are primed to grow in the bone, and were enriched in skeletal sites of metastasis over soft tissu
3 ions and mRNA abundance associations with target genes, and were enriched in motif-rewiring mutations and structural vari
4 start sites and accessible chromatin of the host genome and were enriched in repressive chromatin marks.
5                           Genes disrupted by SV breakpoints were enriched in neuronal lineages and associated with phenot
6          Mass cytometry showed that switched memory B cells were enriched in the tumours of responders.
7 II and in chronically infected individuals, beta7high cells were enriched in integrated and total HIV-1 DNA compared to b
8 e Gene Ontology proteome analysis revealed that SUM52 cells were enriched in proteins associated with cell metabolism and
9                        In all groups, pulmonary CD8 T cells were enriched in effector memory subsets compared with blood
10                             New surface marker combinations were enriched in transcriptional subclusters, including a sub
11                                           In particular, ET were enriched in polyfunctional T cells.
12                                        The identified genes were enriched in pathways activated by associative conditioni
13                                      Infant chimpanzee guts were enriched in some of the same taxa prevalent in infant hu
14 Compared with controls, uniquely upregulated genes in HFpEF were enriched in mitochondrial adenosine triphosphate synthes
15 HIF2alpha) and hypoxia-inducible factor 1alpha (HIF1alpha), were enriched in the DhMRs.
16                                  Regulatory SNPs identified were enriched in coronary artery disease (CAD) loci, and this
17 nile acinar and islet cells in donors without diabetes, LDs were enriched in islet alpha- and beta-cells from donors with
18           Only CD8alphaalpha IELs established in early life were enriched in cells bearing type B IELp TCR usage.
19 ets and mRNAs expressed at low levels with short half-lives were enriched in the polysomes of upf1 mutants, indicating th
20 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
21                                   Liver tumors in male mice were enriched in pathways and gene signatures associated with
22  The resulting transcriptome datasets from LCM microvessels were enriched in known brain endothelial and pericyte markers
23                                                     TR-Mphi were enriched in TAC3 and associated with mitochondrial funct
24                                                        MTEX were enriched in immunosuppressive proteins (P = 0.03).
25                                                    Non-MTEX were enriched in immunostimulatory proteins (P = 0.002) and w
26                                        Identified mutations were enriched in essential protein domains and genes identifi
27 h anemia compared with control individuals, other mutations were enriched in the anemia cohort, including TP53 and SF3B1.
28 revealed that gene sets of layer 5b and 6 pyramidal neurons were enriched in DEGs of the mPFC downregulated in both NAc D
29 nts of the Fibroblast Growth Factor (FGF) signaling pathway were enriched in nascent myotubes in Drosophila embryos.
30             Cell proliferation and immune activity pathways were enriched in BCs with high mutation rates.
31 gment biosynthesis, and other secondary metabolite pathways were enriched in control and drought stressed PRLT2/89-33 at
32 osing solution, C6 and C7 perfluoroalkyl sulfonates (PFSAs) were enriched in dosed mouse serum, suggesting in vivo transf
33                                     Among them, 42 proteins were enriched in the cells exposed to low oxygen, whereas 28
34 uding TRAIL (TNFSF10), TL1A (TNFSF15), and their receptors, were enriched in E2F1(high) While TRAIL was equally expressed
35                                            Foxp3 regulators were enriched in genes encoding subunits of the SWI/SNF nucle
36 und the genes most informative for predicting drug response were enriched in well-known cancer signaling pathways and hig
37 whereas N. aquilinus (a wood-feeder) gut microbiome samples were enriched in genes involved in carbohydrate metabolism an
38 es of 1,024 metastatic samples revealed that 13 focal SCNAs were enriched in metastatic samples, including gains in chrom
39 or tyrosine kinase (Erbb), and Toll-like receptor signaling were enriched in lysates of podocytes treated with the TrkC l
40 ia targeted expression profiling(17) that B cell signatures were enriched in the tumours of patients who respond to treat
41                                               Eighteen taxa were enriched in fetal meconium, with Micrococcaceae (n = 9)
42                                       Rare variants in TET2 were enriched in the discovery combined EOAD and FTD cohort (
43 s variants in the genes EBNA1, EBNA2, BcLF1, and BARF1 that were enriched in eBL patients.
44              In the presence of inflammation, portal tracts were enriched in CD3+, CD20+ but displayed fewer CD68+.
45                      In humans and mice, sTDP43 transcripts were enriched in vulnerable motor neurons, and we observed a
46 coding for ribosomal proteins and regulators of translation were enriched in this screen.
47                          Platinum-tolerant cells and tumors were enriched in ALDH(+) cells, formed more spheroids, and ex
48                                                    Variants were enriched in genes involved in carbohydrate metabolism, a
49       Interestingly, rare, predicted-damaging LRP2 variants were enriched in a HLHS cohort; however, understanding their
50 d, strikingly, found that only two PATs, ZDHHC5 and ZDHHC8, were enriched in DRG axons.