ライフサイエンスコーパス: uteri

1 hylstilbestrol (DES) treatment in the mature uteri.

2 isolated longitudinal smooth muscle from rat uteri.

3 ing tumor development in Cdh1(d/d)Trp53(d/d) uteri.

4 ic analyses of isolated GE and Foxa2-deleted uteri.

5 phosphatidylethanolamine levels in pregnant uteri.

6 reased both the level and function of LIF in uteri.

7 ration and differentiation in C/EBPbeta-null uteri.

8 tion patterns were counted in glands from 30 uteri.

9 n the luminal epithelium of PUGKO but not WT uteri.

10 sected from ethanol-fixed, paraffin-embedded uteri.

11 g those of the bladder, pancreas, and cervix uteri.

12 eudohermaphrodites that possess oviducts and uteri.

13 of these genes in wild-type and ERalpha(-/-) uteri.

14 parison to the same compartments in WT mouse uteri.

15 played underdeveloped external genitalia and uteri.

16 two that consisted of neonatally DES-exposed uteri.

17 ), breast (31%; 95% CI, 11%-51%), and corpus uteri (27%; 95% CI, 11%-43%).

18 and HB-EGF appears unaffected in the mutant uteri, a decrease is observed in the intensity and numbe

19 ncluding infertility, relatively hypoplastic uteri, abnormal ovaries, stunted mammary gland ductal de

20 c mediators were sustained in UtEpialphaERKO uteri after E(2) treatment.

21 ations among the cPten(f/f)Grp78(f/f) murine uteri also corresponded to abrogation of AKT activation

22 We also show that APC(cKO) mutant uteri and human endometrial cancer have decreased stroma

23 Participants, aged 25-42 years, had intact uteri and no history of cancer or fibroids at enrollment

24 lowed 22,895 premenopausal women with intact uteri and no prior self-reported diagnosis of uterine le

25 xamination showed severe inflammation in the uteri and vaginae of progesterone-treated animals, where

26 Rudimentary uteri are common in patients with MRKH syndrome.

27 h is expressed in gestation day 8.5 pregnant uteri, as well as in uterine stromal cells and endotheli

28 istributions of uNK cells in WT and NOS-2-/- uteri at any stage of gestation.

29 The risk of corpus uteri cancer was significantly increased at ages 15-44 y

30 ossibly bladder cancer, melanoma, and corpus uteri cancer, but are at a decreased risk for breast can

31 Two uteri contained intraluminal blood, and two showed signs

32 oluble extracts prepared from day 7 pregnant uteri containing implanted embryos.

33 Uteri deprived of Notch1 signaling demonstrated decrease

34 in the presence of males, their ovaries and uteri develop normally and they are fertile.

35 myomatous, Med12 c.131G>A variant-expressing uteri developed chromosomal rearrangements.

36 ype blastocysts were transferred into mutant uteri distal to the transformed region on day 2.5 of pse

37 Additionally, Wnt-7a mutant uteri do not form glands.

38 K) cells were the predominant populations in uteri during early to midgestation, whereas T and B cell

39 (COX2), was downregulated in LPA3-deficient uteri during pre-implantation.

40 In mouse uteri, early- and late-phase estrogen-regulated gene res

41 In addition, mutant uteri exhibited decreased decidualization in response to

42 netic protein activities and that the mutant uteri failed to respond to exogenous estradiol stimulati

43 ther probe the mechanism of this phenomenon, uteri from 7-day-old control or DES-exposed donors were

44 etrial tissues from women were compared with uteri from a mouse model (tissue recovered 0, 4, 8, 24 a

45 us indirectly via ER-positive stromal cells, uteri from adult ER-deficient ER knockout (ko) mice and

46 Uteri from Chst10(-/-) females at the pro-estrus stage w

47 Histologic examination of uteri from cPten(f/f)Grp78(f/f) mice also revealed no co

48 activated in vivo by 17 beta-estradiol (E2), uteri from ovariectomized mice were examined for enhance

49 and epithelial cells were then cultured from uteri from such animals and provided with retinol or wit

50 Examination of uteri from time pregnant mutant females revealed defects

51 Uteri from wild-type (WT) and NOS-2-/- mice were collect

52 lume was 6.4 mL (range, 0.4-80.2 mL), and 18 uteri had a volume greater than 10 mL.

53 report that, after PMSG treatment, collected uteri had markedly higher levels of retinoic acid than d

54 eir blood and tissues, including ovaries and uteri harvested.

55 Uteri have a constant caudal relationship to ovaries.

56 aginas have stratified epithelium and normal uteri have simple columnar epithelium, however, mutant u

57 simple columnar epithelium, however, mutant uteri have stratified epithelium.

58 ian ducts leads to retention of oviducts and uteri in males.

59 uction, the diminished endometrial growth in uteri in response to exogenous gonadotropins indicates t

60 of 24 surgical specimens of ovary and adnexa uteri in the fresh state from 15 patients was performed

61 radiol (E(2)), but not in KIKO or alpha ERKO uteri, indicating ER alpha- and ERE-dependent regulation

62 uces proliferation in wild type but not KIKO uteri, indicating that IGF1 replacement does not rescue

63 cancer, the malignant neoplasm of the cervix uteri is the second most common cancer among women world

64 pe II carcinomas, we hypothesized that mouse uteri lacking both Trp53 and Cdh1 would exhibit a phenot

65 In mouse uteri lacking Hand2, continued induction of these FGFs i

66 y compared for efficacy and potency in hone, uteri, lipids, and adipose tissues in an ovariectomized

67 uded 102,164 premenopausal women with intact uteri, no prior history of UL or cancer, and prenatal DE

68 eosinophils and BM8+, Ia+, and CD4+ cells in uteri obtained from adult Ovx control and E2-treated C57

69 Cytosolic proteins from uteri of 19-day-old rats were analyzed by an electrophor

70 The uteri of adult conditional beta-catenin mutants are gros

71 The uteri of adult FOXA2-deleted mice were morphologically n

72 LIF initiated blastocyst implantation in the uteri of both gland-containing and glandless adult FOXA2

73 Among the major products secreted by the uteri of cattle, sheep, and pigs during pregnancy are gl

74 of the genes differentially regulated in the uteri of Cdh1(d/d)Trp53(d/d) mice were involved in infla

75 ges, were also detected and increased in the uteri of Cdh1(d/d)Trp53(d/d) mice, suggesting that an in

76 roliferation and complex angiogenesis in the uteri of Cdh1(d/d)Trp53(d/d) mice.

77 enes, Hoxa10 and cyclin D3, was decreased in uteri of early pregnant Bteb1-null mutants, whereas that

78 vivo system, EGF effects were studied in the uteri of ER knockout (ERKO) mice, which lack functional

79 egulation of several P(4)-regulated genes in uteri of Fkbp52(-/-) mice, establishes this cochaperone

80 REA mRNA and protein levels in uteri of heterozygous animals were half that of the wild

81 s, we compared E2's mitogenic effects on the uteri of Igf1-targeted gene deletion (null) and wild-typ

82 f lactoferrin promoter was determined in the uteri of immature (17-day-old) and mature (21- and 30-da

83 We also show that the adipocytes in the uteri of mice conditionally deleted for beta-catenin are

84 lly normal and contained glands, whereas the uteri of neonatal FOXA2-deleted mice were completely agl

85 fat depots to produce estrogenic effects in uteri of ovariectomized mice.

86 o gene was significantly increased in normal uteri of p53(wt/wt) mice but not in either normal uterus

87 Lower LIF levels were observed in the uteri of p53-/- mice than in those of p53+/+ mice, parti

88 hesis that endometrial precancers persist in uteri of patients with endometrial carcinoma and are mon

89 0 is seen in response to progesterone in the uteri of Pgr(-/-) mutant mice lacking progesterone nucle

90 Uteri of PR knockout mice failed to express this mRNA, e

91 dition to altered stromal cell function, the uteri of PR(cre/+)Wnt4(f/f) (Wnt4(d/d)) mice displayed a

92 s observed for the epithelial cells from the uteri of prepubertal animals treated with PMSG, cells pr

93 y smooth muscle and stromal cells taken from uteri of prepubertal or PMSG-treated rats (shown previou

94 higher levels of retinoic acid than did the uteri of prepubertal rats treated with the control vehic

95 of blastocysts, which, after transfer to the uteri of pseudo-pregnant foster mothers, can produce via

96 Furthermore, uteri of Stat3(d/d) mice were unable to undergo a well-c

97 Shortly after birth, the uteri of the conditional mutants appear smaller and less

98 d steroid-hormone-dependent responses in the uteri of these mice.

99 compared global gene expression profiles in uteri of wild-type and Hoxa-10(-/-) mice after inducing

100 terone response element of Gpr64 gene in the uteri of wild-type mice treated with P4.

101 tion fromMsx1(d/d)/Msx2(d/d)and floxed mouse uteri on d 4 of pseudopregnancy.

102 aling in vivo by using tissues isolated from uteri on different days over the implantation period.

103 rating cell nuclear antigen expression in WT uteri only.

104 Corpus uteri, postmenopausal breast, and colon cancers accounte

105 In neonatal uteri, prenatal arsenic increased ER-alpha expression an

106 ltured epithelial cells from the prepubertal uteri [shown previously to be negative for CRABP(II)] or

107 icular stromal tumors and large fluid-filled uteri that were identical in phenotype to MIS ligand/alp

108 In rat uteri they are estrogen antagonists/weak agonists and de

109 lack of response of the C/EBPbeta-deficient uteri to an artificial deciduogenic stimulus, indicating

110 also evident upon in vivo exposure of mouse uteri to culture medium conditioned by low-quality human

111 The virtual absence of lesions in control uteri transplanted to DES hosts eliminated host systemic

112 orphological orientation of crypts in rodent uteri was recognized more than a century ago, but the me

113 target genes in uterine sarcomas and normal uteri, we found that expression of the Reprimo gene was

114 ation was experimentally delayed, homozygous uteri were able to support survival of blastocysts compa

115 Rudimentary uteri were found in 61 patients (92%); 54 were bilateral

116 Dissections of embryonic day-8.5 uteri yielded no homozygous embryos; thus, the mice die