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1 E3 in opossum kidney (OK) and Xenopus laevis uroepithelial (A6) cells.
2 tations increasing monomannose (1M)-specific uroepithelial adhesion are commonly found in uropathogen
3 oma, glioma, non-Hodgkin lymphoma, melanoma, uroepithelial cancer, and head and neck cancers.
4 an prostate epithelial cell (HPEC) and human uroepithelial cell (HUC) cultures.
5 ere analysed in six newly immortalized human uroepithelial cell (HUC) lines transformed by Human Papi
6 ngagement of toll-like receptors can lead to uroepithelial cell activation and production of inflamma
7                                      Limited uroepithelial cell adherence was observed in vivo, and w
8                            We identified one uroepithelial cell line that exhibited a distinctly diff
9 at arsenic activates EGFR and ERK in a human uroepithelial cell line.
10             We used murine and human bladder uroepithelial cell models of UTI and S. agalactiae mutan
11 n toxicity to SV40 immortalized normal human uroepithelial cell-1.
12 ility of E6-, versus E7-, immortalized human uroepithelial cells (HUC) to undergo apoptosis in respon
13 roduct, occurs at senescence in normal human uroepithelial cells (HUC).
14 vels are low to undetectable in normal human uroepithelial cells (HUCs) and in immortalized uroepithe
15 tured and cultured specimens of normal human uroepithelial cells (HUCs) and in uncultured and culture
16 ras in NIH3T3 and in SV40 immortalized human uroepithelial cells (SVHUC) enhanced their sensitivity t
17 ens in promoting malignant transformation of uroepithelial cells and bladder cancer tumorigenesis in
18 niae, and Salmonella typhimurium for gut and uroepithelial cells and for various soluble mannosylated
19         UPEC induced IDO expression in human uroepithelial cells and polymorphonuclear leukocytes (PM
20  literature regarding the mechanism by which uroepithelial cells are activated by type 1 piliated E.
21           Hierarchical clustering classified uroepithelial cells based on their histopathogenesis and
22 ount for the increased binding of E. coli to uroepithelial cells from nonsecretors and for the increa
23 unctionally equivalent cell culture model of uroepithelial cells has eluded investigators.
24 th acute cystitis bound to human T24 bladder uroepithelial cells in close association with F-actin in
25 owth in human urine ex vivo and adherence to uroepithelial cells in vitro were equivalent for an isog
26 litate the attachment of Escherichia coli to uroepithelial cells is shut off outside the host at temp
27 proliferation-enhancing effect of arsenic on uroepithelial cells likely contributes to its ability to
28  Archetype JCV is present in bone marrow and uroepithelial cells of most adults.
29 to a greater extent during UPEC infection of uroepithelial cells than during that of neutrophils.
30  and primary tumors, as well as in oncogenic uroepithelial cells transformed with human papillomaviru
31                        Acute cytotoxicity in uroepithelial cells triggered by covR-deficient but not
32 oepithelial cells (HUCs) and in immortalized uroepithelial cells with functional pRb, whereas p16 lev
33 coli and dramatically increases adherence to uroepithelial cells).
34  and decreases viability in primary cultured uroepithelial cells.
35 o induce the death and exfoliation of target uroepithelial cells.
36 a to adhere to specific receptors present on uroepithelial cells.
37 osmotic stress, human urine, and exposure to uroepithelial cells.
38 the ability to adhere to cultured T-24 human uroepithelial cells.
39 uced alpha-hemolysin-mediated exfoliation of uroepithelial cells.
40 chia coli bacteria that mediate adherence to uroepithelial cells.
41 bmucosa while CRHR2 expression was mainly in uroepithelial cells.
42 ted for colonization in mice and adhesion to uroepithelial cells.
43 scopy to be densely packed on the surface of uroepithelial cells.
44 their ability to mediate E. coli adhesion to uroepithelial cells.
45 phenotypes to adhere to glycoproteins and to uroepithelial cells.
46 ion, as well as adhesion to and viability of uroepithelial cells.
47 g surface growth adaptation and infection of uroepithelial cells.
48 mucosa epithelial layer yet fail to complete uroepithelial differentiation, producing a nontransition
49 uld serve as a useful tool to explore normal uroepithelial function as well as dysfunction as a resul
50 gh-mannose type N-glycan binding epitopes on uroepithelial glycoproteins.
51                        Cumulatively, E. coli uroepithelial invasion occurs through lipid rafts, which
52 is isolate UTI89, required the presence of a uroepithelial layer; YbcL(UTI) did not inhibit neutrophi
53 istochemical studies revealed that the human uroepithelial lining of the ureterovesical junction expr
54 nary tract abnormalities, including 15 of 16 uroepithelial malignancies, five congenital anomalies, f
55 n event associated with tumor progression in uroepithelial neoplasms.
56  tract to ensure access to the intracellular uroepithelial niche that supports the propagation of inf
57 d neoplasia but did increase arsenic-induced uroepithelial proliferative lesions.
58 hed neutrophil infiltration, and accelerated uroepithelial recovery.
59  the progenitor cell population required for uroepithelial renewal during tubular morphogenesis.
60 lla" cells expressed uroplakins and a 27-kDa uroepithelial specific antigen that assembled into deter
61 o baseline alterations in immune activation, uroepithelial structure, apical expression of uroplakins
62 adhesins were capable of binding strongly to uroepithelial tissue culture cells and guinea pig erythr
63  p53, pRB, and INK4A (p16), is necessary for uroepithelial transformation.
64 ullary cell death in vivo and development of uroepithelial tumors from surviving cells that have chro