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1 ssibility that inappropriate expression of a nonepithelial cadherin by an epithelial cell might also
2 other systems, inappropriate expression of a nonepithelial cadherin, such as N-cadherin, by an epithe
3 ial cells; i.e., inadvertent expression of a nonepithelial cadherin.
4  explored the possibility that expression of nonepithelial cadherins may be correlated with increased
5 pithelial cell adenocarcinomas as well as in nonepithelial cancer cell lines, as well as in hematolog
6 ceeds in at least two steps: Conversion of a nonepithelial cell into an epithelial sheet followed by
7 ative lung's complex tissue architecture and nonepithelial cell lineages are not preserved in these m
8 ll foster meaningful investigations into how nonepithelial cell populations are controlled during lun
9        The corneal stromal cell is the first nonepithelial cell type shown to synthesize maspin.
10 e growth factors, cytokines and a variety of nonepithelial cell types including endothelial cells, im
11                                 Of interest, nonepithelial cell types such as vascular smooth muscle,
12                         Low gene delivery to nonepithelial cell types was directly correlated to a de
13 gpen was absent or greatly attenuated in the nonepithelial cell types we examined, including fibrobla
14  marked age-related changes occurred in many nonepithelial cell types, including resident immune cell
15 scription factor previously characterized in nonepithelial cell types, shows highest expression in sk
16  host and enhances inflammatory signaling in nonepithelial cell types, which subsequently promotes le
17 elial cells to undergo EMT in vivo to become nonepithelial cell types.
18 stochemistry demonstrated VZV replication in nonepithelial cell types.
19 rular volume (IGV) and numbers of podocytes, nonepithelial cells (NECs; tuft cells other than podocyt
20 lls were separated from normal epithelia and nonepithelial cells by dissection and bivariate cytokera
21                                   Studies on nonepithelial cells have shown that this protein is loca
22 t BRCA1 deficiency in epithelial and certain nonepithelial cells may result in combined effects of ab
23  thymic stroma is composed of epithelial and nonepithelial cells providing separate microenvironments
24                                  Analyses in nonepithelial cells show that claudin-4, which is incapa
25 able diversity of clusters of epithelial and nonepithelial cells that reside in the SMG that is also
26 al species, but could not be detected in the nonepithelial cells we examined.
27 pression in hepatocytes, cholangiocytes, and nonepithelial cells within the liver.
28                                           In nonepithelial cells, activation of phospholipase C (PLC)
29  we demonstrate that type I IFNs act through nonepithelial cells, including macrophages, to promote i
30  an aPKC targeting and specificity factor in nonepithelial cells, our results reveal that it performs
31 h as those of the kidney tubule, but also on nonepithelial cells, such as chondrocytes, fibroblasts,
32 s the heat shock protein (hsp72) response in nonepithelial cells, the possibility that mesalamine con
33 ns of AA transporters in both epithelial and nonepithelial cells.
34 ible Siglec-F ligands by lung epithelial and nonepithelial cells.
35 keratins as has been shown for SV40 in other nonepithelial cells.
36     Expression of PGLYRP2 was not induced in nonepithelial cells.
37 nstration of the presence of this protein in nonepithelial cells.
38 ely to be regulated by other Ets proteins in nonepithelial cells.
39 ions in all tissues, to the exclusion of all nonepithelial cells.
40 annel (ENaC) currents in many epithelial and nonepithelial cells.
41 rved in a number of different epithelial and nonepithelial cells.
42 n-4 significantly enhances polymerization in nonepithelial cells.
43           In addition, introduction of other nonepithelial cellular components, such as immune, mesen
44 rols, suggesting that CCL22 is secreted by a nonepithelial component of the microenvironment.
45 uman pancreas cells including epithelial and nonepithelial constituents, and uncovered 3 distinct aci
46 lize with epithelial adherens junctions, and nonepithelial-derived proteases have junctional proteins
47   Low dose level (relative risk = 3.418) and nonepithelial histology (relative risk = 2.336) were ind
48  this anticolitic activity is independent of nonepithelial immune VDR actions.
49 thelial stem cells, but the role of LRIG1 in nonepithelial intestinal cells has not been identified.
50   The OSMR is expressed in nonhematopoietic, nonepithelial intestinal stromal cells, which respond to
51 a novel interaction for alpha(E)beta(7) at a nonepithelial location.
52 on of hnRNP A2/B1 may play a role in EMT, in nonepithelial lung cancer cell lines A549 and H1703, thr
53 t, lung, ovarian, and bladder cancers) and 5 nonepithelial malignancies (lymphoma, mesothelioma, medu
54 mosomal instability and cancer, particularly nonepithelial malignancies typical of Werner syndrome.
55 lay a role in homotypic interactions between nonepithelial migratory myocytes during trabecular forma
56   AHNAK is predominantly nuclear in cells of nonepithelial origin, but is cytoplasmic or associated w
57 he RNase IIIb domain were found in 30 of 102 nonepithelial ovarian tumors (29%), predominantly in Ser
58 ced the whole transcriptomes or exomes of 14 nonepithelial ovarian tumors and noted closely clustered
59            Mutation carriers are at risk for nonepithelial ovarian tumors, notably sex cord-stromal t
60 he RNase IIIb domain of DICER1 are common in nonepithelial ovarian tumors.
61 er tissue contains responsive sites that are nonepithelial, probably vascular, or perhaps stromal.
62 ymphoma, melanoma, and lung, pancreatic, and nonepithelial skin cancers (higher during function inter
63 ip cancer (HR, 3.4; 95% CI, 2.0 to 6.0), and nonepithelial skin cancers (HR, 3.8; 95% CI, 2.5 to 5.8)
64 ), esophagus (RR, 11.42; 95% CI, 1.40-93.3), nonepithelial skin cancers (RR, 10.52; 95% CI, 1.09-88.7
65 x, growth factors, and cytokines produced by nonepithelial stromal cells.
66 mplex composition and dynamic changes of the nonepithelial stromal compartment across different devel
67  censoring in the CM743 trial and in the ITT nonepithelial subset raised additional areas of concern.
68 ings highlight the dynamic complexity of the nonepithelial thymus stroma and link this to separate in
69 on of p63 led to up-regulation of markers of nonepithelial tissues (mesenchyme and neural tissue) in
70 ntribute to transmembrane Cl(-) transport in nonepithelial tissues such as the heart.
71 e essential for life, but lumen formation in nonepithelial tissues such as the vascular system or hea
72 ng evidence that ENaCs are also expressed in nonepithelial tissues where their activity influences bl
73 induced polyp formation has been ascribed to nonepithelial tissues, how LKB1 deficiency increases can
74 n the brain, heart, ovary, testis, and other nonepithelial tissues, suggesting that MR expression in
75 ession when compared to other epithelial and nonepithelial tissues, with several antioxidant, detoxif
76 nels are found in other epithelia as well as nonepithelial tissues.
77 high levels on colon, breast, lung, and some nonepithelial tumors.
78  stabilization in several patients who had a nonepithelial type of malignancy.
79 e anticolitic contribution of epithelial and nonepithelial VDR signaling is unknown.
80 nd development of organoid cultures, whereas nonepithelial Wnt signals could provide a secondary phys