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1 hylstilbestrol (DES) treatment in the mature uteri.
2 isolated longitudinal smooth muscle from rat uteri.
3 ial dysfunction-related genes in adenomyotic uteri.
4 hagy, fibrosis, and TGF-beta1 in adenomyotic uteri.
5  control were 49 age-matched nontransplanted uteri.
6  induced by 3-nitropropionic acid in control uteri.
7 affolds from adult human fallopian tubes and uteri.
8 n the luminal epithelium of PUGKO but not WT uteri.
9 ing tumor development in Cdh1(d/d)Trp53(d/d) uteri.
10 ic analyses of isolated GE and Foxa2-deleted uteri.
11  phosphatidylethanolamine levels in pregnant uteri.
12 reased both the level and function of LIF in uteri.
13 ration and differentiation in C/EBPbeta-null uteri.
14 tion patterns were counted in glands from 30 uteri.
15 sected from ethanol-fixed, paraffin-embedded uteri.
16 g those of the bladder, pancreas, and cervix uteri.
17 eudohermaphrodites that possess oviducts and uteri.
18 of these genes in wild-type and ERalpha(-/-) uteri.
19 ngitudinal oviductal-cervical axis of murine uteri.
20 parison to the same compartments in WT mouse uteri.
21 played underdeveloped external genitalia and uteri.
22 two that consisted of neonatally DES-exposed uteri.
23 ), breast (31%; 95% CI, 11%-51%), and corpus uteri (27%; 95% CI, 11%-43%).
24         The cure fraction was 69% for corpus uteri, 32% for ovarian, and 58% for cervical cancer pati
25  and HB-EGF appears unaffected in the mutant uteri, a decrease is observed in the intensity and numbe
26 ncluding infertility, relatively hypoplastic uteri, abnormal ovaries, stunted mammary gland ductal de
27 c mediators were sustained in UtEpialphaERKO uteri after E(2) treatment.
28 ations among the cPten(f/f)Grp78(f/f) murine uteri also corresponded to abrogation of AKT activation
29 ed orthologous genes also found in mammalian uteri and co-option of specific cells for sticky eggs at
30 ganoids from human fetal fallopian tubes and uteri and compared them with their adult counterparts.
31 ymphoma, and leukemia for both sexes; corpus uteri and female breast cancer; prostate cancer), for th
32            We also show that APC(cKO) mutant uteri and human endometrial cancer have decreased stroma
33   Participants, aged 25-42 years, had intact uteri and no history of cancer or fibroids at enrollment
34 lowed 22,895 premenopausal women with intact uteri and no prior self-reported diagnosis of uterine le
35 xamination showed severe inflammation in the uteri and vaginae of progesterone-treated animals, where
36  anus, liver, pancreas, lung, breast, cervix uteri, and prostate) comprising 60% of global diagnosed
37  anus, liver, pancreas, lung, breast, cervix uteri, and prostate) representing 60% of all cancer diag
38  anus, liver, pancreas, lung, breast, cervix uteri, and prostate).
39 d OSR1/OSR1 expression in postpubertal human uteri, and the prenatal and postnatal expression pattern
40                                  Rudimentary uteri are common in patients with MRKH syndrome.
41 h is expressed in gestation day 8.5 pregnant uteri, as well as in uterine stromal cells and endotheli
42 y reduced in both single and double knockout uteri at 3.5 dpc.
43 istributions of uNK cells in WT and NOS-2-/- uteri at any stage of gestation.
44 eased PR, and elevated AKR1C18 expression in uteri at E17.25 followed by reduced P4 levels and increa
45 mic profiling of mouse neonatal oviducts and uteri at the initiation of MD epithelial differentiation
46 ver cancer among men, lung cancer and corpus uteri cancer among women, and pancreatic cancer in both
47                           The risk of corpus uteri cancer was significantly increased at ages 15-44 y
48 n women were alive after diagnosis of corpus uteri cancer, 0.2% (52 551) after cervical cancer, and 0
49 tients with cervical cancer, 63% with corpus uteri cancer, and 55% with ovarian cancer were already c
50 ossibly bladder cancer, melanoma, and corpus uteri cancer, but are at a decreased risk for breast can
51 topoietic cancers in men and lung and cervix uteri cancers in women were elevated y 10%, 9%, and 17%,
52 cy to term and deliver, while four had their uteri collected at the end of gestation.
53                                          Two uteri contained intraluminal blood, and two showed signs
54 oluble extracts prepared from day 7 pregnant uteri containing implanted embryos.
55                                              Uteri deprived of Notch1 signaling demonstrated decrease
56                                              Uteri derived from adult female mice homozygous for a fl
57  in the presence of males, their ovaries and uteri develop normally and they are fertile.
58 myomatous, Med12 c.131G>A variant-expressing uteri developed chromosomal rearrangements.
59 mplantation, only the cell-seeded engineered uteri developed native tissue-like structures, including
60 ype blastocysts were transferred into mutant uteri distal to the transformed region on day 2.5 of pse
61                  Additionally, Wnt-7a mutant uteri do not form glands.
62           Microarray analysis of GEN-exposed uteri during early pregnancy revealed significant overla
63 K) cells were the predominant populations in uteri during early to midgestation, whereas T and B cell
64  (COX2), was downregulated in LPA3-deficient uteri during pre-implantation.
65                                     In mouse uteri, early- and late-phase estrogen-regulated gene res
66                          In addition, mutant uteri exhibited decreased decidualization in response to
67 netic protein activities and that the mutant uteri failed to respond to exogenous estradiol stimulati
68 ther probe the mechanism of this phenomenon, uteri from 7-day-old control or DES-exposed donors were
69 etrial tissues from women were compared with uteri from a mouse model (tissue recovered 0, 4, 8, 24 a
70                                        Whole uteri from a separate cohort of animals were injected wi
71 us indirectly via ER-positive stromal cells, uteri from adult ER-deficient ER knockout (ko) mice and
72                                              Uteri from Chst10(-/-) females at the pro-estrus stage w
73                    Histologic examination of uteri from cPten(f/f)Grp78(f/f) mice also revealed no co
74                 Eighteen recipients received uteri from living donors and 2 from deceased donors.
75 activated in vivo by 17 beta-estradiol (E2), uteri from ovariectomized mice were examined for enhance
76                                              Uteri from pregnant GEN-exposed mice were posteriorized
77 and epithelial cells were then cultured from uteri from such animals and provided with retinol or wit
78                               Examination of uteri from time pregnant mutant females revealed defects
79                                              Uteri from wild-type (WT) and NOS-2-/- mice were collect
80 lume was 6.4 mL (range, 0.4-80.2 mL), and 18 uteri had a volume greater than 10 mL.
81 report that, after PMSG treatment, collected uteri had markedly higher levels of retinoic acid than d
82 eir blood and tissues, including ovaries and uteri harvested.
83                                              Uteri have a constant caudal relationship to ovaries.
84 aginas have stratified epithelium and normal uteri have simple columnar epithelium, however, mutant u
85  simple columnar epithelium, however, mutant uteri have stratified epithelium.
86 ian ducts leads to retention of oviducts and uteri in males.
87 uction, the diminished endometrial growth in uteri in response to exogenous gonadotropins indicates t
88 of 24 surgical specimens of ovary and adnexa uteri in the fresh state from 15 patients was performed
89 radiol (E(2)), but not in KIKO or alpha ERKO uteri, indicating ER alpha- and ERE-dependent regulation
90 uces proliferation in wild type but not KIKO uteri, indicating that IGF1 replacement does not rescue
91 cancer, the malignant neoplasm of the cervix uteri is the second most common cancer among women world
92 n complete absence of embryo implantation in uteri lacking both receptors.
93 pe II carcinomas, we hypothesized that mouse uteri lacking both Trp53 and Cdh1 would exhibit a phenot
94                                     In mouse uteri lacking Hand2, continued induction of these FGFs i
95 y compared for efficacy and potency in hone, uteri, lipids, and adipose tissues in an ovariectomized
96 provides a proof of concept that nulliparous uteri may present a suitable source of uterine grafts fo
97 uded 102,164 premenopausal women with intact uteri, no prior history of UL or cancer, and prenatal DE
98 eosinophils and BM8+, Ia+, and CD4+ cells in uteri obtained from adult Ovx control and E2-treated C57
99                      Cytosolic proteins from uteri of 19-day-old rats were analyzed by an electrophor
100                                          The uteri of adult conditional beta-catenin mutants are gros
101                                          The uteri of adult FOXA2-deleted mice were morphologically n
102 LIF initiated blastocyst implantation in the uteri of both gland-containing and glandless adult FOXA2
103     Among the major products secreted by the uteri of cattle, sheep, and pigs during pregnancy are gl
104 of the genes differentially regulated in the uteri of Cdh1(d/d)Trp53(d/d) mice were involved in infla
105 ges, were also detected and increased in the uteri of Cdh1(d/d)Trp53(d/d) mice, suggesting that an in
106 roliferation and complex angiogenesis in the uteri of Cdh1(d/d)Trp53(d/d) mice.
107 enes, Hoxa10 and cyclin D3, was decreased in uteri of early pregnant Bteb1-null mutants, whereas that
108 vivo system, EGF effects were studied in the uteri of ER knockout (ERKO) mice, which lack functional
109 egulation of several P(4)-regulated genes in uteri of Fkbp52(-/-) mice, establishes this cochaperone
110               REA mRNA and protein levels in uteri of heterozygous animals were half that of the wild
111 f different length, or (iv) developed in the uteri of high- or subfertile heifers.
112 s, we compared E2's mitogenic effects on the uteri of Igf1-targeted gene deletion (null) and wild-typ
113 f lactoferrin promoter was determined in the uteri of immature (17-day-old) and mature (21- and 30-da
114      We also show that the adipocytes in the uteri of mice conditionally deleted for beta-catenin are
115 lly normal and contained glands, whereas the uteri of neonatal FOXA2-deleted mice were completely agl
116  fat depots to produce estrogenic effects in uteri of ovariectomized mice.
117 o gene was significantly increased in normal uteri of p53(wt/wt) mice but not in either normal uterus
118        Lower LIF levels were observed in the uteri of p53-/- mice than in those of p53+/+ mice, parti
119 hesis that endometrial precancers persist in uteri of patients with endometrial carcinoma and are mon
120 0 is seen in response to progesterone in the uteri of Pgr(-/-) mutant mice lacking progesterone nucle
121                                              Uteri of PR knockout mice failed to express this mRNA, e
122 dition to altered stromal cell function, the uteri of PR(cre/+)Wnt4(f/f) (Wnt4(d/d)) mice displayed a
123 s observed for the epithelial cells from the uteri of prepubertal animals treated with PMSG, cells pr
124 y smooth muscle and stromal cells taken from uteri of prepubertal or PMSG-treated rats (shown previou
125  higher levels of retinoic acid than did the uteri of prepubertal rats treated with the control vehic
126 of blastocysts, which, after transfer to the uteri of pseudo-pregnant foster mothers, can produce via
127                                 Furthermore, uteri of Stat3(d/d) mice were unable to undergo a well-c
128                     Shortly after birth, the uteri of the conditional mutants appear smaller and less
129                                          The uteri of these mice were hypoplastic with reduced estrog
130 d steroid-hormone-dependent responses in the uteri of these mice.
131  compared global gene expression profiles in uteri of wild-type and Hoxa-10(-/-) mice after inducing
132 terone response element of Gpr64 gene in the uteri of wild-type mice treated with P4.
133 tion fromMsx1(d/d)/Msx2(d/d)and floxed mouse uteri on d 4 of pseudopregnancy.
134 aling in vivo by using tissues isolated from uteri on different days over the implantation period.
135 rating cell nuclear antigen expression in WT uteri only.
136    Transcriptomic analyses of DICER1 deleted uteri or Ishikawa cells revealed unique transcriptomic p
137                                       Corpus uteri, postmenopausal breast, and colon cancers accounte
138                                  In neonatal uteri, prenatal arsenic increased ER-alpha expression an
139 tocin receptor (Oxtr) expression at 18.25 in uteri resulting in PTB.
140       Transcriptome analyses of estrus stage uteri revealed a set of 710 genes shared only between th
141 and spatial transcriptomics of adult control uteri revealed novel markers of uterine epithelial stem
142 ltured epithelial cells from the prepubertal uteri [shown previously to be negative for CRABP(II)] or
143 icular stromal tumors and large fluid-filled uteri that were identical in phenotype to MIS ligand/alp
144                                       In rat uteri they are estrogen antagonists/weak agonists and de
145     Postnatally, Osr1 was expressed in mouse uteri throughout their lifespan, peaking at postnatal da
146  lack of response of the C/EBPbeta-deficient uteri to an artificial deciduogenic stimulus, indicating
147  also evident upon in vivo exposure of mouse uteri to culture medium conditioned by low-quality human
148    The virtual absence of lesions in control uteri transplanted to DES hosts eliminated host systemic
149 orphological orientation of crypts in rodent uteri was recognized more than a century ago, but the me
150  target genes in uterine sarcomas and normal uteri, we found that expression of the Reprimo gene was
151 ation was experimentally delayed, homozygous uteri were able to support survival of blastocysts compa
152 weight, and histopathology end points of the uteri were analyzed at postnatal (PND) day 21, 90, and 3
153      Transcriptomic analyses of estrus stage uteri were conducted on PND365 rats.
154             The gene profiles of adenomyotic uteri were examined at postnatal day 42.
155                                  Rudimentary uteri were found in 61 patients (92%); 54 were bilateral
156                      Post-pubertal Ctcf(d/d) uteri were hypoplastic with significant reduction in bot
157             Dissections of embryonic day-8.5 uteri yielded no homozygous embryos; thus, the mice die

 
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