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1 species, represented by pyroglutamylated amyloid-beta11-42, were enriched in these areas, consistent with ELISA results.
2 s found by WES and WGS, to determine whether mutant alleles were enriched in endothelial or non-endothelial cells, and to
3 e associated with AT while Microbacteriaceae and Ascomycota were enriched in DT.
4                                       Murine and human CAFs were enriched in HTR tumors expressing high levels of CD133(h
5                                   In vivo, hepatic NK cells were enriched in proximity to the alpha-smooth muscle actin (
6                  We observed that sorted ROS-high NKT cells were enriched in NKT1 and NKT17 cells, whereas NKT2 cells wer
7                                    Memory CCR5(+) TH1 cells were enriched in BAL fluid versus blood, and pathogenic respi
8 e lymphoid cell 1 (ILC1) cells, but not ILC2 or ILC3 cells, were enriched in the expression profiles associated with CD4,
9 ls, which share phenotypic markers with regulatory T cells, were enriched in SIV DNA in blood, lymph nodes (LN), spleen,
10                               These transcriptional changes were enriched in signalling pathways in which the PI3K-Akt si
11 ptome analysis revealed that four nitrogen-related clusters were enriched in the differentially expressed genes of the cp
12                              Genes at lipid-associated CpGs were enriched in lipid and amino acid metabolism processes.
13              In contrast, DHS-diminished TEs under darkness were enriched in Copia, LINE, and MuDR dispersed across chrom
14 ccurring mutations in NRAS and other MAPK pathway effectors were enriched in nonresponding patients, consistent with RAS
15                                        These response eQTLs were enriched in disease-associated variants, particularly fo
16                                                These events were enriched in seed sequence (73.33%), which was not observ
17                                                    iPSC-EVs were enriched in miRNAs and proteins with proangiogenic and c
18                                Glycoprotein targets of FUT8 were enriched in cell migration proteins including the adhesi
19 d two or more known SM biosynthetic genes, and module genes were enriched in SM functions.
20                   Pathway analyses showed that target genes were enriched in processes crucial for renal function, identi
21 um (NGE), and between GE and the underlying mesenchyme (GM) were enriched in multiple GO terms and KEGG pathways, includi
22 nalyses indicated that gene targets of PI3K-Akt but not HIF were enriched in early transcriptional responses to hypoxia.
23                  Notably, these tandem-duplication hotspots were enriched in breast cancer germline susceptibility loci (
24 n long-term survivors, we discovered that these individuals were enriched in neoantigen qualities defined by a fitness mo
25                    Both amk2- and gsk3-specific interactors were enriched in phenotype categories related to abnormal cel
26    Known luminal lineage markers, such as NKX3.1 and KRT18, were enriched in luminal-like cancers, and the basal lineage
27 ecimens demonstrated that cathepsin B-producing macrophages were enriched in invaded nerves, which was associated with in
28 tion factors, enhancer regions, and different histone marks were enriched in the T2D-associated DMRs.
29 -1(high)CD11c(neg) myeloid-derived suppressor cells (MDSCs) were enriched in GVHD target organs.
30 9, Plau, and Wsb1 that promote invasiveness and metastasis, were enriched in mouse and human angiosarcoma.
31                            Kruppel-like factor (KLF) motifs were enriched in corneal epithelial enhancers, consistent wit
32                                 Activating NOTCH1 mutations were enriched in metastatic ACCs (8 of 36 tumors [22%]).
33                                        HDL from HD patients were enriched in SAA, LBP, ApoC-III, di-sialylated ApoC-III (
34 h no event (HD-) (n = 12) showed that HDL from HD+ patients were enriched in SAA but had lower levels of sialylation acro
35 xpression was acutely inhibited, 120 mitochondrial proteins were enriched in the cytoplasm, suggesting that the accumulat
36                     Within the podocyte, all three proteins were enriched in the plasma membrane and organelle membrane c
37       Mutational signatures inferring defects in DNA repair were enriched in those with the highest mutation burdens.
38                 Interestingly, 24-nt small interfering RNAs were enriched in the 5' and 3' flanking sequences of nonaddit
39  neck SCCs, and EVs isolated from sera of patients with SCC were enriched in Dsg2 C-terminal fragment and epidermal growt
40                           HDL that increased IL-6 secretion were enriched in ApoC-III, di-sialylated glycans at multiple
41                                             Genetic signals were enriched in neuronal genesis and differentiation pathway
42 ucing the bulk-cultured population, CSLC-eliminating siRNAs were enriched in a few functional categories, such as lipid m
43 ifs containing predicted transcription factor binding sites were enriched in genomic regions with regeneration-responsive
44 versus wild-type cases, differentially methylated CpG sites were enriched in regions marked by histone H3K4me1, histone H
45 ody variants isolated using weak selections for specificity were enriched in arginine CDR mutations and displayed low spe
46 ted with PD by a recent Genome Wide Association (GWA) study were enriched in genes containing PD-associated NS SNVs.
47  flagellar assembly, bacterial chemotaxis and LPS synthesis were enriched in the tumors while those responsible for DNA r
48    For rare exonic duplications, six of 19 gene sets tested were enriched in the schizophrenia group; genes associated wi
49 subset of these clusters of ethylene-responsive transcripts were enriched in targets of EIN3 and ERFs.
50 cially in the perivascular and peribronchial regions, which were enriched in infiltrating leukocytes.

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