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1 olate siderophore, binds to the host protein lipocalin 2.
2 ounter-regulated by the presence of iron and lipocalin 2.
3 h a striking structural resemblance to human lipocalin 2.
4 IL-1beta and IL-17 also individually induce lipocalin 2.
5 (neutrophil gelatinase-associated lipocalin/lipocalin 2), a secreted glycoprotein that binds to MMP-
6 ain Salmonella by promoting the induction of lipocalin 2, a host antimicrobial factor that inhibits b
7 s survival advantage is counter-regulated by lipocalin 2, a siderophore-binding host protein, which r
11 skin lesions, protein and mRNA expression of lipocalin 2 and other innate defense genes (hBD2, elafin
12 an overcome metal ion starvation mediated by lipocalin-2 and calprotectin via alternative pathways, I
13 ression of antimicrobial proteins, including lipocalin-2 and calprotectin, which sequester essential
15 xpressed at the RNA level (TFF1, TFF2, TFF3, lipocalin 2, and galectin 3) showed a good concordance b
16 eries of the roles of ferroportin, hepcidin, lipocalin 2, and members of the six transmembrane epithe
17 F9, IL-6, IL-19, CCL20, S100A7/A8/A9, DEFB4, lipocalin 2, and peptidase inhibitor 3 (p < 0.05), indic
20 id-A3, chemokine ligands (Ccl2, Ccl7, Ccl9), lipocalin-2, and matrix metalloproteinase-3 and -12 of i
22 ed by the immobilization of rabbit polygonal lipocalin-2 antibody on gold nanoparticles attached on g
24 m of MMA-associated kidney disease, identify lipocalin-2 as a biomarker of increased oxidative stress
25 sion of the IL-17 target genes IL-6 and 24p3/lipocalin-2 as a readout, functional reconstitution of s
29 d hypomethylated genes (trefoil factor 2 and lipocalin 2) between pancreatic and breast cancer cell l
31 ion of IL-1beta alone could reconstitute the lipocalin 2 deficiency in TLR4 knockout animals and resc
33 observed to be Dectin-1 and IL-22 dependent, lipocalin 2-deficient mice did not demonstrate impaired
36 ion of Tfrc (transferrin receptor) and Lcn2 (lipocalin 2)), facilitate glucose import (e.g. Hk2 (hexo
37 8; CCL20/FCH, 8.36; PI3 [elafin]/FCH, 15.40; lipocalin 2/FCH, 6.94, human beta-defensin 2 [DEFB4A]/FC
38 d in classical pancreatic carcinomas such as lipocalin 2, galectin 3, claudin 4, and cathepsin E.
41 (C5) that secretes relatively high levels of lipocalin 2 (human NGAL) induced suppression of hematopo
42 cornea and, in the conjunctiva, sPLA(2)-IIA, lipocalin 2, IGFBP3, multiple MCH class II proteins, and
45 g/ml, IQR 0-11.1; n = 14), urinary levels of lipocalin-2 in SLE patients were significantly higher (n
46 NA antibodies promote the local secretion of lipocalin-2 in the kidneys of patients with systemic lup
49 inct at the molecular level and suggest that lipocalin 2 is a new therapeutic target for breast cance
55 usly secretion of the iron chelating protein lipocalin 2 (LCN2) and protons, which acidify the urine.
58 We have recently characterized the role of lipocalin 2 (Lcn2) as a new adipose-derived cytokine in
60 ough molecular and genetic analyses in mice, lipocalin 2 (LCN2) as an osteoblast-enriched, secreted p
66 how that a mutant form (K3Cys) of endogenous lipocalin 2 (LCN2) is filtered by the kidney but can byp
73 ulating levels of the secreted glycoprotein, lipocalin 2 (Lcn2), an adipokine previously associated w
75 However, Ent is bound by the host protein lipocalin 2 (Lcn2), preventing bacterial reuptake of afe
76 oprotection markers, including COX-2 itself, lipocalin 2 (LCN2), tissue inhibitor of metalloproteinas
82 he antimicrobial siderophore-binding peptide Lipocalin-2 (Lcn2) are observed in inflammatory bowel di
83 ich immunoassay (IA) was developed for human lipocalin-2 (LCN2) by functionalizing a KOH-treated poly
87 thelicidin antimicrobial protein (Camp), and lipocalin-2 (Lcn2) mRNA expression giving rise to cells
90 over 100 different cytokines, we found that Lipocalin-2 (LCN2) was the most substantially elevated p
91 -2), inducible nitric oxide synthase (Nos2), lipocalin-2 (Lcn2), MIP-1alpha, MIP-1beta, and keratinoc
92 levels of a specific inflammatory cytokine, lipocalin-2 (LCN2), were elevated in the plasmas of pati
94 ukemic mice and CML patients showed elevated lipocalin 2 levels compared with healthy individuals.
97 rtened colons, and increased fecal levels of lipocalin 2), metabolic syndrome, and an inability to cl
98 bulin, ceruloplasmin, complement components, lipocalin-2, metallothionein, serine protease inhibitor-
99 that use catecholate-type siderophores, and lipocalin 2(-/-) mice are highly susceptible to infectio
100 previous studies indicate that reduction of lipocalin 2 (mouse 24p3) expression by either anti-sense
101 bial protein siderocalin (SCN; also known as lipocalin 2, neutrophil gelatinase-associated lipocalin/
103 bial protein siderocalin (SCN; also known as lipocalin-2, neutrophil gelatinase-associated lipocalin,
106 in this model and mucosal reconstitution of lipocalin 2 protein in these animals resulted in rescue
107 pus erythematosus (SLE), and whether urinary lipocalin-2 represents a marker of kidney involvement in
109 e neutrophil peptides cathelicidin LL-37 and lipocalin 2 restricted growth of the organism, the latte
110 transcription, translation and secretion of lipocalin 2; secreted lipocalin 2 then limits bacterial
111 8 signaling is required for the induction of lipocalin 2 secretion and iron sequestration in the sple
112 ory factors such as dietary iron and luminal lipocalin 2 should be taken into consideration for optim
114 s unique genes, such as guanosine deaminase, lipocalin 2, synaptotagmin 4, and latrophilin 2, whose t
115 wer circulating concentrations of HNP1-3 and lipocalin 2 than south Asian and white participants.
116 ation and secretion of lipocalin 2; secreted lipocalin 2 then limits bacterial growth by sequestratin
118 vercome iron restriction by the host protein lipocalin 2, which counteracts some siderophores, is ess
119 ys identified numerous biomarkers, including lipocalin-2, which was then used to monitor the response
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