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1 ggressive metastatic cancer phenotype (SPP1, CHI3L1).
2 red genetically to overexpress or lack mouse CHI3L1.
3 augment the expression of WAT and pulmonary Chi3l1.
4 lens epithelium, and TM and did not express CHI3L1.
5 ted TMSCs began expressing TM marker protein CHI3L1.
9 pe (MUM1), lymphoproliferation (SPP1, TCL1A, CHI3L1), aggressive clinical behavior (SPP1, CHI3L1, MUM
11 mal human bronchial epithelial cells express CHI3L1 and secrete YKL-40 under base-line culture condit
12 t RLH activation inhibits tumor induction of Chi3l1 and the expression of receptor IL-13Ralpha2 and p
13 the fibrosis was due to interactions between CHI3L1 and the receptor CRTH2, which trafficked normally
14 (BRP-39), also known as chitinase 3-like 1 (CHI3L1) and encoded by the Chi3l1 gene, is expressed at
15 Mouse breast regression protein 39 (BRP-39; Chi3l1) and its human homologue YKL-40 are chitinase-lik
17 on in its encoding gene (chitinase 3-like 1 [CHI3L1]) and are increased in patients with several dise
18 the functional role of CHI3L1 in vivo, anti-CHI3L1 antibody was administered into the dextran sulfat
19 ys exacerbate pulmonary fibrosis and suggest CHI3L1 as a potential biomarker for pulmonary fibrosis p
21 NA (siRNA), corneas treated with recombinant CHI3L1 before C. albicans inoculation had markedly ameli
23 between the degree of kidney injury and both Chi3l1/Brp-39 expression in the kidney and its levels in
25 eased release of chitinase 3-like protein 1 (CHI3L1), CHI3L2, complement factor B, matrix metalloprot
27 3Ralpha2, a recently identified receptor for Chi3l1, consistent with a key role for Chi3l1 in melanom
28 vivo neutralization experiments showed that CHI3L1 contributes to the facilitation of bacterial inva
29 een 68 CHI3L1 SNPs, methylation levels at 14 CHI3L1 CpG sites in whole-blood DNA, and circulating YKL
30 determine (1) whether methylation levels at CHI3L1 CpG sites mediate the association of CHI3L1 singl
32 epithelial apoptosis but exhibit exaggerated CHI3L1-driven fibroproliferation, which together promote
35 compressive stress) applied for 3 h induces CHI3L1 expression by approximately 4-fold compared with
37 and RT-PCR analyses significantly increased CHI3L1 expression in non-dysplastic mucosa from patients
38 s mechanical stress-induced up-regulation of CHI3L1 expression in normal human bronchial epithelial c
39 rate that mechanical stress potently induces CHI3L1 expression leading to increased secretion of YKL-
42 hitinase-like protein YKL-40, encoded by the CHI3L1 gene, is a biomarker and functional effector of c
43 itinase 3-like 1 (CHI3L1) and encoded by the Chi3l1 gene, is expressed at high levels by macrophages
49 factor-related activation-induced cytokine, CHI3L1, IL-16, and matrix metalloproteinase-12 were card
50 This study sought to elucidate the role of CHI3L1 in augmenting the corneal innate immune response
54 at the protein level of ECM-related SPP1 and CHI3L1 in PCNSL cells was demonstrated by immunohistoche
58 tically modified mice to define the roles of Chi3l1 in white adipose tissue (WAT) accumulation and Th
59 strate that TMEM219 plays a critical role in Chi3l1-induced IL-13Ralpha2 mediated signalling and tiss
60 hese responses and the pathways that control Chi3l1-induced tumor responses are poorly understood.
65 NP rs4950928, the intronic SNP rs12141494 in CHI3L1 is associated with asthma severity, lung function
68 This is the first report demonstrating that CHI3L1 is induced during fungal infection, where it acts
71 ays using intracellular bacteria showed that CHI3L1 is required for the enhancement of adhesion and i
79 on injury (U-IRI) led to sustained low-level Chi3l1 mRNA expression by renal cells and promoted macro
80 CHI3L1), aggressive clinical behavior (SPP1, CHI3L1, MUM1), and aggressive metastatic cancer phenotyp
85 determine the effect of genetic variation in CHI3L1 on asthma severity and YKL-40 expression in subje
86 In this study, we investigated the role of CHI3L1 on CECs during the development of colitis-associa
89 In mouse strains with genetic deletions of Chi3l1 or Sema7a, there was a significant reduction in p
94 c chitinase-like protein chitinase 3-like-1 (CHI3L1) plays a protective role in the lung by ameliorat
95 all asthmatic children were genotyped for a CHI3L1 promoter single nucleotide polymorphism (rs495092
96 ymorphisms (SNPs) in the chitinase 3-like 1 (CHI3L1) promoter, the gene encoding YKL-40, are associat
97 ochemical staining showed strong staining of CHI3L1 protein around tumor areas in these mouse models.
99 patients revealed a significant elevation of CHI3L1 protein concentration in human serum samples from
100 mation-induced lung cancer mouse models, the CHI3L1 protein concentration was also highly increased i
101 wnstream genes products, chitinase 3-like 1 (CHI3L1) protein, showed increased concentration in both
102 ten candidate genes (ORMDL1, ORMDL2, ORMDL3, CHI3L1, RAD50, IL13, IL4, STAT6, FOXP3, and RUNX3) was a
104 ession in animal models, and that miR-24 and CHI3L1 represent novel plasma biomarkers of AAA disease
105 rough which Sem7a and its receptors regulate Chi3l1, revealing a host axis involving IL13Ralpha2 that
106 CHI3L1 CpG sites mediate the association of CHI3L1 single nucleotide polymorphisms (SNPs) with YKL-4
107 was more severe in the corneas treated with Chi3l1 small interfering RNA (siRNA), corneas treated wi
110 the blood and (2) whether these biomarkers (CHI3L1 SNPs, methylation profiles, and YKL-40 levels) ar
111 TMEM219 or IL-13Ralpha2 similarly decreased Chi3l1-stimulated epithelial cell HB-EGF production and
113 hese animals have a defect in the ability of CHI3L1 to inhibit epithelial apoptosis but exhibit exagg
114 copied one another as regards the ability of Chi3l1 to inhibit oxidant-induced apoptosis and lung inj
116 in vitro studies reveal chitinase 3-like 1 (Chi3l1) to be a major target and effector under the cont
120 associated with truncal adiposity, and serum Chi3l1 was associated with persistent asthma and low lun
126 n of chilectins is pronounced in mammals and CHI3L1 (with a proposed function in immunity) is found i
127 zed human astrocytes stably transfected with CHI3L1/YKL-40 exhibited changes in gene expression simil
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