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