戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ycles of active proliferation of the ovarian surface epithelium.
2 ression compared to the brushings of ovarian surface epithelium.
3 an either c-MYC or N-MYC relative to ovarian surface epithelium.
4  from the fallopian tube or from the ovarian surface epithelium.
5 m targets of regulation by PR in the uterine surface epithelium.
6 n-regulation of E-cadherin expression in the surface epithelium.
7 XA7 expression is absent from normal ovarian surface epithelium.
8 ntiation and immune activation of the ocular surface epithelium.
9 basal and the suprabasal cells of the ocular surface epithelium.
10 ostatic cellular renewal processes in ocular surface epithelium.
11 hral epithelium and the ectodermally derived surface epithelium.
12 and demonstrated expression in the papillary surface epithelium.
13 ting restoration of the ischemically damaged surface epithelium.
14 ts the crypts of the tonsils rather than the surface epithelium.
15 er are strategically positioned close to the surface epithelium.
16 derm-derived mesenchyme and ectoderm-derived surface epithelium.
17 cally expressed in the basal cells of ocular-surface epithelium.
18 inal epithelium, hair follicles, and ovarian surface epithelium.
19     There was absence of cytologic atypia of surface epithelium.
20 eted crypts hypertrophy to later replace the surface epithelium.
21 tube (FT) epithelium rather than the ovarian surface epithelium.
22 ith neoplastic transformation of the ovarian surface epithelium.
23 of this channel in Cl(-) secretion in airway surface epithelium.
24 MUC4, and MUC16--are expressed at the ocular surface epithelium.
25 ell lines (OCC) compared with normal ovarian surface epithelium.
26 otection of pathogen adherence on the ocular surface epithelium.
27 cancer cell lines, but not in normal ovarian surface epithelium.
28 lpha) is characteristic of malignant ovarian surface epithelium.
29 n the absence of Pten locally in the ovarian surface epithelium.
30  corneal versus epidermal fate of the ocular surface epithelium.
31 arcinoma cell lines relative to immortalized surface epithelium.
32  serous borderline tumors and normal ovarian surface epithelium.
33  ovarian cancer specimens and normal ovarian surface epithelium.
34 ormation and tumor initiation of the ovarian surface epithelium.
35               Cell lines transformed ovarian surface epithelium 1 and 4 (TOSE 1 and 4) established fr
36 deletion of Trp53 and Pten in murine ovarian surface epithelium accelerated ovarian tumorigenesis and
37  isolate colonic crypt cells, differentiated surface epithelium, adenomas, carcinomas and metastases,
38 ASGP mRNA was localized in the entire ocular surface epithelium after 1 week of feeding, was diminish
39          Changes in WGA binding to the human surface epithelium allowed regions containing normal epi
40  HGSOC research to modeling based on ovarian surface epithelium alone is inadequate.
41 e viruses replicate extremely rapidly in the surface epithelium and are quickly transmitted to other
42 CC) TMEM16A is expressed in the adult airway surface epithelium and ASM.
43 ls of GC UNC-45 compared with normal ovarian surface epithelium and benign cystadenoma.
44  destruction with a loss of small intestinal surface epithelium and death.
45 ate microscopic lesions in the mouse gastric surface epithelium and directly measure epithelial resti
46                                      Ovarian surface epithelium and fallopian tube epithelium, not pr
47              Although the sources of ovarian surface epithelium and granulosa cells are known, the or
48 ls of the descending thin limb and papillary surface epithelium and is induced throughout the distal
49 nies malignant transformation of the ovarian surface epithelium and is maintained in peritoneal metas
50  of the gene encoding BMP receptor 1A in the surface epithelium and its derivatives causes arrest of
51  cytopathic damage on nontransformed ovarian surface epithelium and mesothelium.
52 n the human airways, MUC5AC localizes to the surface epithelium and MUC5B to submucosal glands, the f
53              The presence of FSHR in ovarian surface epithelium and of gonadotropin-binding sites in
54  that Wnt signaling is present in the ocular surface epithelium and plays an important role in the re
55 g characterised by piecemeal shedding of the surface epithelium and rapid restoration of tissue homeo
56 rt that ovulation, by disrupting the ovarian surface epithelium and releasing chemokines/cytokines, p
57 ates stress signaling pathways in the ocular surface epithelium and resident immune cells.
58 vation of epithelial ovarian tumors from the surface epithelium and should promote heightened interes
59 ined from the distance between images of the surface epithelium and subbasal nerve plexus.
60 l, and immature secretory populations within surface epithelium and submucosal glands, residing in ni
61 ne expression was greatly enhanced in airway surface epithelium and the submucosal gland region in ov
62  thickened bud initially protrudes above the surface epithelium and then transforms to a bulb and sin
63 t inducer of COX-2 expression in the ovarian surface epithelium and this regulation is a critical ste
64 t bacteria or their products exist below the surface epithelium and thus permit physical interaction
65 s hair follicles and teeth, develop from the surface epithelium and underlying mesenchyme; however, t
66 xpression of this molecule was restricted in surface epithelium and upper crypts but not lower crypts
67 ssection of distinct anatomic areas (crypts, surface epithelium, and germinal centers) of the tonsil,
68 HE2 remains localized to apical membranes of surface epithelium, and NHE1 protein amount or localizat
69  outer medulla, inner medulla, the papillary surface epithelium, and the transitional urinary epithel
70 rs, evidence of enhanced DNA damage in tumor surface epithelium, and to significant alteration in the
71 ric parietal cells, AQP3 and AQP4 in colonic surface epithelium, AQP5 in salivary gland, AQP7 in smal
72 veral Wnt genes are broadly expressed in the surface epithelium at the time of mammary initiation, an
73 flammatory stress depleted CLU in the ocular surface epithelium but allowed MMP-9 to prevail therein.
74 uced premalignant hyperplasia of the ovarian surface epithelium but no tumors.
75 ne had no demonstrable effect on the ovarian surface epithelium but resulted in papillary hyperplasia
76  treatment caused exfoliation of the mucosal surface epithelium, but neither caused deep erosions or
77 ylori colocalizes with MUC5AC at the gastric surface epithelium, but not with MUC6 secreted in concer
78 e thought to arise from cells of the ovarian surface epithelium by mechanisms that are poorly underst
79 ar and nose develop from discrete patches of surface epithelium, called placodes, which fold into sph
80                 By using the primary ovarian surface epithelium cell culture, we show that conditiona
81 egulated in HGSOC compared to normal ovarian surface epithelium cells and/or FTSECs.
82 inactivation of p53 in primary mouse ovarian surface epithelium cells.
83 pression of Ihh and proliferation within the surface epithelium compared with mice given infusions of
84  coalesce, and radially intercalate into the surface epithelium, converting mesenchymal-epithelial tr
85               Expression of ICAM-1 by ocular surface epithelium decreased significantly in both group
86 absence of an external phenotype, the ocular surface epithelium develops properly, but young mice dis
87 potent progenitors within the single-layered surface epithelium differentiate to form the epidermis a
88                  RhoA knockout in the ocular surface epithelium disturbs this network by decreasing M
89 oth instances, lymphoid follicles covered by surface epithelium (dome-formation) were found.
90 a thick, protective mucus plug overlying the surface epithelium, entrapping Eh.
91       These data indicate that the CF airway surface epithelium, even without hyperviscous secretions
92 strated to concentrate and persist in ocular surface epithelium, exhibit significant antiacanthamoeba
93 ylori-positive patients, whereas less of the surface epithelium expresses normal surface-type gastric
94         Laser capture microdissection of the surface epithelium, followed by quantitative reverse-tra
95 munohistochemical analysis revealed that the surface epithelium from all benign ovarian samples had w
96              DPP4 was rarely detected in the surface epithelium from nasal cavity to conducting airwa
97 conditional Pten deletion within the ovarian surface epithelium gives rise to preneoplastic ovarian l
98 ng multiple lineage determination of ovarian surface epithelium, granulosa cells and theca cells.
99 oma cell lines (human 'immortalized' ovarian surface epithelium (HIO)-117, HIO-114, A2780, SKOV3 and
100 y cultures derived from normal human ovarian surface epithelium (HOSE) and from ovarian carcinomas (C
101  in primary cultures of normal human ovarian surface epithelium (HOSE) and ovarian tumor-derived epit
102 varian cancer derived from the human ovarian surface epithelium (HOSE) is the leading cause of death
103 reased binding of WGA and HPA to the luminal surface epithelium in human dysplasia suggests that thes
104 (-) /SOX9(+) ) is involved in the renewal of surface epithelium in injured EHBT.
105 ly positioned cholangiocytes replenished the surface epithelium in mural glands.
106 onic dye used to assess damage of the ocular surface epithelium in ocular surface disease.
107  of rMuc5AC was detected by RT-PCR in ocular surface epithelium in rat pups 1 day after birth.
108 3, the predominant apical isoform in colonic surface epithelium in the pathogenesis of colon cancer h
109 o modulate the homeostatic renewal of ocular surface epithelium in the rat.
110 NT inhibitor Dickkopf 1 in transgenic embryo surface epithelium in vivo completely blocks mammary pla
111 , highly efficient selective transduction of surface epithelium, in which progenitors stably incorpor
112 granulosa (EPG) cells, arises in the ovarian surface epithelium, ingresses cortically by E12.5 or ear
113 ng the tear-film layer at the air and ocular surface epithelium interface.
114 r cells destroy the basement membrane of the surface epithelium, invade, and metastasize is essential
115  of this relationship is threatened when the surface epithelium is injured, yet little is known about
116 Ts, the cystadenoma epithelium, like ovarian surface epithelium, lacks cytological atypia.
117 mpensated for the absence of ENaC in colonic surface epithelium, leading to colon-specific pseudohypo
118                                          The surface epithelium lining the intestinal tract renews it
119 demonstrate that lactoferrin adherent to the surface epithelium may contribute to the activation of e
120 in the angiogenic characteristics of ovarian surface epithelium may play an important role in the eti
121 ns present in the apical cells of the ocular surface epithelium (MUC1, -4, and -16) are believed to c
122 n = 130) compared with either normal ovarian surface epithelium (n = 31; P = 0.039) or fallopian tube
123  fluid and a redistribution of HB-EGF in the surface epithelium near the wound site.
124 revents the delay in wound healing of ocular surface epithelium observed in poorly controlled diabeti
125 ose expression is localized to the placental surface epithelium of artiodactyl species.
126 n the descending thin limb and the papillary surface epithelium of both control and LPS-treated anima
127 uct, and its expression is restricted to the surface epithelium of both of these tissues.
128                                HB-EGF in the surface epithelium of burn wounds was uniformally distri
129 ur findings suggest that loss of NHE3 in the surface epithelium of colonic tumors has profound conseq
130 normal tissue when sprayed on to the luminal surface epithelium of freshly resected colon tissue from
131 calized mainly at the apical membrane in the surface epithelium of normal human colon with less distr
132                                          The surface epithelium of the colon is being replaced consta
133  villous tips of the small intestine and the surface epithelium of the colon.
134           Essential for the viability of the surface epithelium of the eye and for normal vision is t
135      The receptor is highly expressed on the surface epithelium of the human colon and was observed t
136 expression to specific, limited areas of the surface epithelium of the nasopharynx may have important
137 oscopy localized alpha-GalCer to the colonic surface epithelium of WT but not CD1d(-/-) mice, indicat
138 erized by rapid progression from the ovarian surface epithelium or inclusion cysts to a conventional
139 ormal fallopian tube epithelium than ovarian surface epithelium or peritoneum.
140 ed salivary glands, and the non-taste tongue surface epithelium originate from a common Lgr5 cell.
141 ly expressed Yap isoform in both the ovarian surface epithelium (OSE) and epithelial ovarian cancers.
142  fallopian tube epithelium (FTE) and ovarian surface epithelium (OSE) both considered candidates.
143 e ovarian malignancies along with 10 ovarian surface epithelium (OSE) brushings.
144            Estrogens regulate normal ovarian surface epithelium (OSE) cell functions but also affect
145 we tested PI3K isoform dependence in ovarian surface epithelium (OSE) cells deficient in both PTEN an
146 tiation, are not expressed in normal ovarian surface epithelium (OSE), but are expressed in different
147  fallopian tube epithelium (FTE) and ovarian surface epithelium (OSE), has hampered development of ta
148           The stem cell niche of the ovarian surface epithelium (OSE), which is ruptured and regenera
149 genetic alterations sustained by the ovarian surface epithelium (OSE).
150  ovarian cancers (EOCs) arise in the Ovarian Surface Epithelium (OSE).
151                 Fgfr2 deletion in the ocular surface epithelium reduced Sox9 and eliminated Sox10 exp
152                                          Its surface epithelium, specialized for transport, forms by
153 t markedly higher levels than normal ovarian surface epithelium, suggesting that immunogenicity of HO
154 a transcriptional atlas of cells from tongue surface epithelium, taste buds, and the associated and n
155 rial dysfunction in the apical domain of the surface epithelium that may reduce the consumption of fa
156 rotein is expressed in the micromere-derived surface epithelium that undergoes epiboly and in the lar
157                                  Beneath the surface epithelium, the fibrous tissue was virtually rep
158 biliary tree have glands that connect to the surface epithelium through narrow pits.
159 ion was to examine the progression of ocular surface epithelium through the G1/S transition of the ce
160 cteria were apparent in the lumen and on the surface epithelium throughout the gut initially, but sev
161 initiated the endoreplication of the uterine surface epithelium to form distinct epithelial plaques.
162 uggests a compensatory attempt of the ocular surface epithelium to synthesize mucin-type O-glycans to
163 ion of PKCiota contributed to murine ovarian surface epithelium transformation in cooperation with mu
164 egulation in small intestine villi and colon surface epithelium using a conditional epithelium-specif
165 ssion of the three mucin genes by the ocular surface epithelium was assayed by reverse transcription-
166  given gastrin infusions for 7 days; gastric surface epithelium was collected and expression of Ihh w
167                                         When surface epithelium was conditionally targeted for ablati
168        An electrokinetic model of the ocular surface epithelium was developed to simulate PD measurem
169            At 18 days in culture, the ocular surface epithelium was markedly reduced in thickness and
170 ian tumors and cell lines and normal ovarian surface epithelium, we identified hundreds of potential
171 jor role for Fgfr2 in the developing genital surface epithelium, where epithelial maturation is requi
172  apoptosis was limited to scattered cells in surface epithelium, whereas apoptosis was clearly observ
173 langiocytes of extramural glands renewed the surface epithelium, whereas basally oriented cholangiocy
174 was distributed throughout the entire ocular surface epithelium, whereas GalNAc-T1 was found in scatt
175 irectly regulated by vitamin A in the ocular surface epithelium, whereas the membrane-spanning mucin
176 plastic morphological changes of the ovarian surface epithelium, which can be reversed by a reduction
177                    In comparison with normal surface epithelium, which does not express HE4, we found
178  and a cell line derived from normal ovarian surface epithelium, which is the origin of human epithel
179  homeostasis and wound healing of the ocular surface epithelium, which necessitates normal architectu
180  a neoplastic papillary proliferation of the surface epithelium with a thick layer of parakeratin, de
181 as comparable in magnitude across the ocular surface epithelium, with the exception of a few mitotic
182 uces the PED area and accelerates the ocular surface epithelium wound healing.

 
Page Top