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1 s or spontaneously transformed human ovarian surface epithelial cells.
2  in the macroscopic apical K+ conductance of surface epithelial cells.
3  the mucosal layer to interact directly with surface epithelial cells.
4 t transformation of Kras/Pten-mutant ovarian surface epithelial cells.
5  IL-17A, which directly or indirectly damage surface epithelial cells.
6 c fallopian tube secretory cells and ovarian surface epithelial cells.
7 airs mucus secretion in primary human airway surface epithelial cells.
8 he hypothesis that HGSOC arises from ovarian surface epithelial cells.
9 t with the increased number of Klf5CN ocular surface epithelial cells.
10  periciliary fluid layer (PCL) that contacts surface epithelial cells.
11 iferation of telomerase-immortalized ovarian surface epithelial cells.
12  HRAS in the transformation of human ovarian surface epithelial cells.
13  recombination of oncogenic genes in ovarian surface epithelial cells.
14 ce bearing tumors derived from mouse ovarian surface epithelial cells.
15  repetitive domains and expressed by various surface epithelial cells.
16 pressed at high levels in airway and gastric surface epithelial cells.
17 rian cell lines than in immortalized ovarian surface epithelial cells.
18 teasome inhibitors than immortalized ovarian surface epithelial cells.
19 line OSE137 and two additional human ovarian surface epithelial cells.
20 enting rose bengal staining of normal ocular surface epithelial cells.
21 of nuclear BCL-2 expression in TUNEL-labeled surface epithelial cells.
22 OX-2 expression in normal and cancer ovarian surface epithelial cells.
23  cells but not in immortalized human ovarian surface epithelial cells.
24 nces the physiological properties of ovarian surface epithelial cells.
25 g in the primary mesenchyme cells and in the surface epithelial cells.
26 cascade for telomerase regulation in ovarian surface epithelial cells.
27 al cell function but stimulate the growth of surface epithelial cells.
28 ely with morphological transformation of the surface epithelial cells.
29 nctions of phagocytic leukocytes and certain surface epithelial cells.
30 pression in normal and malignant rat ovarian surface epithelial cells.
31 arise from the transformation of the ovarian surface epithelial cells, a single layer of cells surrou
32 that transform ovarian and/or fallopian tube surface epithelial cells, allowing for their abnormal gr
33 at Gal3 was selectively expressed by gastric surface epithelial cells and abundantly secreted into th
34 les of human HRAS or KRAS into human ovarian surface epithelial cells and examined the phenotype and
35 l lines, HGSOC tumours, immortalized ovarian surface epithelial cells and fallopian tube epithelial c
36 the primary cultures of normal human ovarian surface epithelial cells and immortalized cell lines, fo
37 Expression was increased particularly in the surface epithelial cells and infiltrating inflammatory c
38 gth NAC-1 enhanced tumorigenicity of ovarian surface epithelial cells and NIH 3T3 cells in athymic nu
39                       Treating human ovarian surface epithelial cells and ovarian cancer cells with S
40 nes relative to those in immortalized normal surface epithelial cells and that suppression of FER att
41 rties of this DeltapslAB mutant using biotic surfaces (epithelial cells and mucin-coated surfaces) an
42  (three SDs above the mean of normal ovarian surface epithelial cells) and high-grade primary ovarian
43 ulosa and thecal cells of growing follicles, surface epithelial cells, and epithelial cells lining si
44 formation and tumorigenesis in human ovarian surface epithelial cells, and promotes growth of cancer
45 or most cell growth and expansion in ovarian surface epithelial cells, and the AMHR2 lineage-derived
46  reflux esophagitis develops when esophageal surface epithelial cells are exposed to lethal chemical
47                                  The ovarian surface epithelial cells are organized by a sheet of bas
48                                        Human surface epithelial cells are situated at host-environmen
49 were expressed in a distinct distribution by surface epithelial cells as well as chief and parietal c
50 varian cancer compared to cultivated ovarian surface epithelial cells, as concluded by real-time reve
51 epithelial phenotype of immortalized ovarian surface epithelial cells, as indicated by the appearance
52 s not expressed in normal mammary or ovarian surface epithelial cells but is highly expressed in the
53  of normal tissues, including normal ovarian surface epithelial cells, but is undetectable in 5 of 7
54 ssion was shown to be induced in the uterine surface epithelial cells by treatment of prepubertal rat
55 terleukin-1beta (P = 0.025), in their ocular surface epithelial cells compared with homozygous major
56     The lytic effect in immortalized ovarian surface epithelial cells confirmed that cellular retinob
57 holipid "barrier"), an epithelial "barrier" (surface epithelial cells connected by tight junctions an
58 face and crypt epithelial cell colonization, surface epithelial cell damage, and systemic disseminati
59 ing ability in response to NE, while ovarian surface epithelial cells displayed a p53-independent dec
60 sion of HOXB7 in immortalized normal ovarian surface epithelial cells dramatically enhanced cellular
61 mpared to resistant and immortalized ovarian surface epithelial cells (e.g., 70-fold with malignant 2
62 , while in the lung, P. aeruginosa uptake by surface epithelial cells enhances P. aeruginosa clearanc
63                  In contrast, normal ovarian surface epithelial cells express, but do not secrete, Fa
64 ovarian cancer cells, but not normal ovarian surface epithelial cells, formed patterned networks cont
65  risk of ovarian cancer, we screened ovarian surface epithelial cells from 25 primary cultures establ
66 e modification in fallopian tube and ovarian surface epithelial cells (FTSECs, OSECs), the debated ce
67  cultured normal and malignant human ovarian surface epithelial cells(HOSE) and in invasive and borde
68 ial ultrastructure and metabolism in mucosal surface epithelial cells; however, this appears to be co
69 growth and modulated Myc activity in ovarian surface epithelial cells immortalized with temperature-s
70              To determine the fate of ocular surface epithelial cells in response to corneal injury,
71                           The fate of ocular surface epithelial cells in response to injury of the co
72                            The percentage of surface epithelial cells in S-phase is increased in tran
73 he intestinal tract is largely restricted to surface epithelial cells in the colon.
74        FN protein is abundantly expressed by surface epithelial cells in the normal colon.
75  and are localized in the nucleus in ovarian surface epithelial cells in tissues or primary cell cult
76 verexpression in nontumorigenic immortalized surface epithelial cells (IOSE cells) promoted constitut
77 ls as compared with the normal human ovarian surface epithelial cells is critical for cell growth.
78  prevented HGSOC cells from invading ovarian surface epithelial cell layers in culture.
79 ng VEGF165 into a nontumorigenic rat ovarian surface epithelial cell line (ROSE199), we investigated
80 ease in IC(50) for carboplatin in an ovarian surface epithelial cell line and in a low-grade serous c
81 ing a spontaneously immortalized rat ovarian surface epithelial cell line in culture with ecotropic r
82 e immortalized non-tumorigenic human ovarian surface epithelial cell line T80 and retroviral infectio
83                         A second rat ovarian surface epithelial cell line was similarly transduced wi
84 lls (a genetically transformed human ovarian surface epithelial cell line whose tumorigenicity depend
85 nes as compared with an immortalized ovarian surface epithelial cell line; and in 55% of ovarian tumo
86  eight independently transformed rat ovarian surface epithelial cell lines compared to the normal pro
87 ion in independently transformed rat ovarian surface epithelial cell lines compared to the normal pro
88 es, compared with immortalized human ovarian surface epithelial cell lines.
89 odamine 800 incubated with two human ovarian surface epithelial cell lines: OSE(tsT)-14 normal cells
90 tionally, we show that in normal rat ovarian surface epithelial cells Lot1 gene expression is respons
91 e, we show that calcium signaling in ovarian surface epithelial cells not only induces telomerase act
92 d in lymphocytes, macrophages, and crypt and surface epithelial cells of the colon.
93 drives the synthesis of u-PAR in the luminal surface epithelial cells of the colon.
94 LF4 expression is predominant in the luminal surface epithelial cells of the colonic crypt, and we hy
95 ocalized high levels of LL-37/hCAP-18 RNA to surface epithelial cells of the conducting airway as wel
96 VCA1 and OVCA2 mRNA were expressed in normal surface epithelial cells of the ovary, but the level of
97 NC1 in serous cells of submucosal glands and surface epithelial cells of the upper respiratory tract,
98 s used to map the protein content of ovarian surface epithelial cells (OSE) and an ovarian carcinoma-
99  were experimentally engineered into ovarian surface epithelial cells (OSE) thought to be the cells o
100 (OCCs) as compared with nonmalignant ovarian surface epithelial cells (OSEs).
101  growing fibroblasts and established ovarian surface epithelial cells, p150(Sal2) undergoes polyubiqu
102  epithelium, loss of DeltaNp63 occurs in all surface epithelial cells preparing to undergo desquamati
103                                   At mucosal surfaces, epithelial cells provide a structural barrier
104          Thus, the transformed human ovarian surface epithelial cells recapitulated many features of
105 ry2, but not either one alone, in the ocular surface epithelial cells result in the "EOB" (eyes open
106 all interfering RNA (siRNA) in human ovarian surface epithelial cells resulted in deformation of the
107 rhabditis elegans, the concerted movement of surface epithelial cells results in enclosure of the emb
108 n of the encoded glycoprotein TSP1 in ocular surface epithelial cells significantly increases the sus
109                                              Surface epithelial cells, such as the epidermal keratino
110     Their levels are higher in human ovarian surface epithelial cells than cancer cells.
111 ;Amhr2-Cre mice developed aggressive ovarian surface epithelial cell tumors that did not occur in the
112 va may be related to replenishment of ocular surface epithelial cells used in the repair process rath
113  conjectured to serve in replenishing ocular surface epithelial cells used in the repair process.
114         Most existing immortal human ovarian surface epithelial cells were achieved by using viral pr
115 ermeabilities (P(f)(mem)) of calcein-stained surface epithelial cells were measured from the kinetics
116 ovarian cancer cells, but not normal ovarian surface epithelial cells, were proven to express LPA(2)
117  (ASL) is the thin fluid layer lining airway surface epithelial cells, whose volume and composition a
118           The ovarian cell lines are ovarian surface epithelial cells with temperature-sensitive larg

 
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