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1 hral epithelium and the ectodermally derived surface epithelium.
2 an either c-MYC or N-MYC relative to ovarian surface epithelium.
3 m targets of regulation by PR in the uterine surface epithelium.
4 n-regulation of E-cadherin expression in the surface epithelium.
5 XA7 expression is absent from normal ovarian surface epithelium.
6 ntiation and immune activation of the ocular surface epithelium.
7 basal and the suprabasal cells of the ocular surface epithelium.
8 ostatic cellular renewal processes in ocular surface epithelium.
9 and demonstrated expression in the papillary surface epithelium.
10 cally expressed in the basal cells of ocular-surface epithelium.
11 inal epithelium, hair follicles, and ovarian surface epithelium.
12 There was absence of cytologic atypia of surface epithelium.
13 eted crypts hypertrophy to later replace the surface epithelium.
14 tube (FT) epithelium rather than the ovarian surface epithelium.
15 ith neoplastic transformation of the ovarian surface epithelium.
16 of this channel in Cl(-) secretion in airway surface epithelium.
17 from the fallopian tube or from the ovarian surface epithelium.
18 MUC4, and MUC16--are expressed at the ocular surface epithelium.
19 ell lines (OCC) compared with normal ovarian surface epithelium.
20 otection of pathogen adherence on the ocular surface epithelium.
21 cancer cell lines, but not in normal ovarian surface epithelium.
22 lpha) is characteristic of malignant ovarian surface epithelium.
23 n the absence of Pten locally in the ovarian surface epithelium.
24 corneal versus epidermal fate of the ocular surface epithelium.
25 arcinoma cell lines relative to immortalized surface epithelium.
26 serous borderline tumors and normal ovarian surface epithelium.
27 ovarian cancer specimens and normal ovarian surface epithelium.
28 ormation and tumor initiation of the ovarian surface epithelium.
29 ycles of active proliferation of the ovarian surface epithelium.
30 ression compared to the brushings of ovarian surface epithelium.
32 isolate colonic crypt cells, differentiated surface epithelium, adenomas, carcinomas and metastases,
33 ASGP mRNA was localized in the entire ocular surface epithelium after 1 week of feeding, was diminish
39 ate microscopic lesions in the mouse gastric surface epithelium and directly measure epithelial resti
42 ls of the descending thin limb and papillary surface epithelium and is induced throughout the distal
43 nies malignant transformation of the ovarian surface epithelium and is maintained in peritoneal metas
44 of the gene encoding BMP receptor 1A in the surface epithelium and its derivatives causes arrest of
46 n the human airways, MUC5AC localizes to the surface epithelium and MUC5B to submucosal glands, the f
48 that Wnt signaling is present in the ocular surface epithelium and plays an important role in the re
49 rt that ovulation, by disrupting the ovarian surface epithelium and releasing chemokines/cytokines, p
51 vation of epithelial ovarian tumors from the surface epithelium and should promote heightened interes
53 ne expression was greatly enhanced in airway surface epithelium and the submucosal gland region in ov
54 t inducer of COX-2 expression in the ovarian surface epithelium and this regulation is a critical ste
55 t bacteria or their products exist below the surface epithelium and thus permit physical interaction
56 s hair follicles and teeth, develop from the surface epithelium and underlying mesenchyme; however, t
57 xpression of this molecule was restricted in surface epithelium and upper crypts but not lower crypts
58 HE2 remains localized to apical membranes of surface epithelium, and NHE1 protein amount or localizat
59 outer medulla, inner medulla, the papillary surface epithelium, and the transitional urinary epithel
60 ric parietal cells, AQP3 and AQP4 in colonic surface epithelium, AQP5 in salivary gland, AQP7 in smal
61 veral Wnt genes are broadly expressed in the surface epithelium at the time of mammary initiation, an
62 flammatory stress depleted CLU in the ocular surface epithelium but allowed MMP-9 to prevail therein.
64 ne had no demonstrable effect on the ovarian surface epithelium but resulted in papillary hyperplasia
65 treatment caused exfoliation of the mucosal surface epithelium, but neither caused deep erosions or
66 ylori colocalizes with MUC5AC at the gastric surface epithelium, but not with MUC6 secreted in concer
67 e thought to arise from cells of the ovarian surface epithelium by mechanisms that are poorly underst
68 ar and nose develop from discrete patches of surface epithelium, called placodes, which fold into sph
71 pression of Ihh and proliferation within the surface epithelium compared with mice given infusions of
73 absence of an external phenotype, the ocular surface epithelium develops properly, but young mice dis
74 potent progenitors within the single-layered surface epithelium differentiate to form the epidermis a
79 strated to concentrate and persist in ocular surface epithelium, exhibit significant antiacanthamoeba
80 ylori-positive patients, whereas less of the surface epithelium expresses normal surface-type gastric
82 munohistochemical analysis revealed that the surface epithelium from all benign ovarian samples had w
84 conditional Pten deletion within the ovarian surface epithelium gives rise to preneoplastic ovarian l
85 ng multiple lineage determination of ovarian surface epithelium, granulosa cells and theca cells.
86 oma cell lines (human 'immortalized' ovarian surface epithelium (HIO)-117, HIO-114, A2780, SKOV3 and
87 y cultures derived from normal human ovarian surface epithelium (HOSE) and from ovarian carcinomas (C
88 in primary cultures of normal human ovarian surface epithelium (HOSE) and ovarian tumor-derived epit
89 varian cancer derived from the human ovarian surface epithelium (HOSE) is the leading cause of death
90 reased binding of WGA and HPA to the luminal surface epithelium in human dysplasia suggests that thes
94 NT inhibitor Dickkopf 1 in transgenic embryo surface epithelium in vivo completely blocks mammary pla
95 , highly efficient selective transduction of surface epithelium, in which progenitors stably incorpor
97 r cells destroy the basement membrane of the surface epithelium, invade, and metastasize is essential
98 of this relationship is threatened when the surface epithelium is injured, yet little is known about
100 mpensated for the absence of ENaC in colonic surface epithelium, leading to colon-specific pseudohypo
102 demonstrate that lactoferrin adherent to the surface epithelium may contribute to the activation of e
103 in the angiogenic characteristics of ovarian surface epithelium may play an important role in the eti
104 ns present in the apical cells of the ocular surface epithelium (MUC1, -4, and -16) are believed to c
105 n = 130) compared with either normal ovarian surface epithelium (n = 31; P = 0.039) or fallopian tube
107 revents the delay in wound healing of ocular surface epithelium observed in poorly controlled diabeti
109 n the descending thin limb and the papillary surface epithelium of both control and LPS-treated anima
112 normal tissue when sprayed on to the luminal surface epithelium of freshly resected colon tissue from
113 calized mainly at the apical membrane in the surface epithelium of normal human colon with less distr
117 The receptor is highly expressed on the surface epithelium of the human colon and was observed t
118 expression to specific, limited areas of the surface epithelium of the nasopharynx may have important
119 oscopy localized alpha-GalCer to the colonic surface epithelium of WT but not CD1d(-/-) mice, indicat
120 erized by rapid progression from the ovarian surface epithelium or inclusion cysts to a conventional
122 ly expressed Yap isoform in both the ovarian surface epithelium (OSE) and epithelial ovarian cancers.
125 we tested PI3K isoform dependence in ovarian surface epithelium (OSE) cells deficient in both PTEN an
126 tiation, are not expressed in normal ovarian surface epithelium (OSE), but are expressed in different
131 t markedly higher levels than normal ovarian surface epithelium, suggesting that immunogenicity of HO
132 rotein is expressed in the micromere-derived surface epithelium that undergoes epiboly and in the lar
134 ion was to examine the progression of ocular surface epithelium through the G1/S transition of the ce
135 cteria were apparent in the lumen and on the surface epithelium throughout the gut initially, but sev
136 initiated the endoreplication of the uterine surface epithelium to form distinct epithelial plaques.
137 uggests a compensatory attempt of the ocular surface epithelium to synthesize mucin-type O-glycans to
138 ion of PKCiota contributed to murine ovarian surface epithelium transformation in cooperation with mu
139 egulation in small intestine villi and colon surface epithelium using a conditional epithelium-specif
140 ssion of the three mucin genes by the ocular surface epithelium was assayed by reverse transcription-
141 given gastrin infusions for 7 days; gastric surface epithelium was collected and expression of Ihh w
145 ian tumors and cell lines and normal ovarian surface epithelium, we identified hundreds of potential
146 jor role for Fgfr2 in the developing genital surface epithelium, where epithelial maturation is requi
147 apoptosis was limited to scattered cells in surface epithelium, whereas apoptosis was clearly observ
148 was distributed throughout the entire ocular surface epithelium, whereas GalNAc-T1 was found in scatt
149 irectly regulated by vitamin A in the ocular surface epithelium, whereas the membrane-spanning mucin
150 plastic morphological changes of the ovarian surface epithelium, which can be reversed by a reduction
152 and a cell line derived from normal ovarian surface epithelium, which is the origin of human epithel
153 homeostasis and wound healing of the ocular surface epithelium, which necessitates normal architectu
154 a neoplastic papillary proliferation of the surface epithelium with a thick layer of parakeratin, de
155 as comparable in magnitude across the ocular surface epithelium, with the exception of a few mitotic
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