ライフサイエンスコーパス: luminal epithelium

1 ole as a lineage survival factor in prostate luminal epithelium.

2 -negative (ER(-)) progenitors in the mammary luminal epithelium.

3 e subsequent persistent proliferation of the luminal epithelium.

4 decrease in the proliferation of the mammary luminal epithelium.

5 increase in Ang-2 expression occurred in the luminal epithelium.

6 -SIGN(+) DCs were localized just beneath the luminal epithelium.

7 minent in most of the oviduct but not in the luminal epithelium.

8 inal bleeding and delayed restoration of the luminal epithelium.

9 phases of the cycle and is restricted to the luminal epithelium.

10 eraction between LIF and its receptor at the luminal epithelium.

11 ly impacts involution of the endometrium and luminal epithelium.

12 d for embryo attachment and adherence to the luminal epithelium.

13 endometrial regions between FC and RIF (685 luminal epithelium, 293 glandular epithelium, 419 sublum

14 ponents, was located immediately beneath the luminal epithelium and along the glandular epithelium pr

15 nd cellular interactions between the uterine luminal epithelium and blastocyst trophectoderm.

16 s of human breast tumors, both normal breast luminal epithelium and estrogen receptor (ESR1)-positive

17 ription of Ihh increases dramatically in the luminal epithelium and glands from day 3, reaching very

18 vealed high expression of enJSRV mRNA in the luminal epithelium and glandular epithelium of the uteru

19 Reelin was expressed in the luminal epithelium and myoepithelium of the normal human

20 Cox2 is normally expressed in the luminal epithelium and stroma at the site of blastocyst

21 of proteins associated with implantation in luminal epithelium and stroma.

22 iated when an embryo attaches to the uterine luminal epithelium and subsequently penetrates into the

23 ports the development and maintenance of the luminal epithelium and that a subset of prostate cancer

24 ed invasion of trophoblast cells through the luminal epithelium and the basement membrane, transforma

25 exquisitely restricted to the mouse uterine luminal epithelium and underlying stroma adjacent to the

26 nct localization and kinetics in the uterine luminal epithelium and underlying stromal cells, suggest

27 in different prostatic cell types: stromal, luminal epithelium, and macrophages, respectively.

28 the blastocyst trophectoderm and the uterine luminal epithelium are essential for implantation.

29 hat embryo attachment and the removal of the luminal epithelium are not altered in uterine Parp1, Par

30 TM, which is synthesized exclusively in the luminal epithelium at the site of blastocyst apposition,

31 Uterine SLA and beta(2)m increased in luminal epithelium between days 5 and 9, then decreased

32 as expressed specifically in the endometrial luminal epithelium but not in the conceptus.

33 plained infertility, most prominently in the luminal epithelium, but downregulated in the endometrium

34 noviral-Cre-mediated SmoM2 expression in the luminal epithelium, but not in the myoepithelium, was re

35 um (BE) occurred upon ErbB3 targeting in the luminal epithelium, but not upon its targeting in the BE

36 ukin 6, were induced upon ErbB3 depletion in luminal epithelium cells, which increased growth of BE c

37 However, the AR is a key factor in luminal epithelium differentiation and was shown to have

38 In Fst-cKO mice, the uterine luminal epithelium does not respond properly to estrogen

39 ated when the embryo attaches to the uterine luminal epithelium during early pregnancy.

40 ribute to the rapid restoration of an intact luminal epithelium during endometrial repair.

41 ithelial cells lack tight junctions, and the luminal epithelium exhibits profound disruptions to cell

42 These findings indicate that the SRC-2(d/d) luminal epithelium fails to exhibit a plasma membrane tr

43 The uterine luminal epithelium folds characteristically in mammals,

44 CP1 expression and suggest that mammary duct luminal epithelium has an important role in controlling

45 e either basal or luminal cells, whereas the luminal epithelium has not been demonstrated to contribu

46 at become incorporated into the newly formed luminal epithelium have their origins in one or more of

47 3p expression only in mouse uterine surface (luminal) epithelium impaired receptivity and led to impl

48 smembrane form detected HB-EGF TM in uterine luminal epithelium in a spatial manner similar to that o

49 phoblasts bound to ligand-expressing uterine luminal epithelium in tissue sections.

50 between the trophectoderm epithelium and the luminal epithelium is essential for implantation, we inv

51 (PC) populations, and defined glandular and luminal epithelium (LE) cell differentiation trajectorie

52 Stat3 is phosphorylated in the luminal epithelium (LE) in response to LIF, and this pho

53 is expressed specifically by the endometrial luminal epithelium (LE) of the ovine uterus in concert w

54 receptors are expressed predominantly in the luminal epithelium (LE) of the uterus.

55 nd exchangers have been identified in the ES luminal epithelium, mainly in animal studies, but there

56 ducts, the early neoplastic cells coexpress luminal epithelium markers cytokeratin 8, androgen recep

57 epithelial cells) and two lines derived from luminal epithelium (MCF-7 and ZR-75-1) with chemotherape

58 m 0.34 to 0.90 compared with adjacent normal luminal epithelium (mean of all samples, 0.68; 95% confi

59 in clinical samples show its location in the luminal epithelium of normal prostate, benign prostatic

60 1 protein and microvilli were present on the luminal epithelium of PUGKO but not WT uteri.

61 ction of a carrier-mediated system in mature luminal epithelium of small intestine.

62 acenta is the embryonal trophotaenia/ovarian luminal epithelium of the goodeid fishes.

63 The luminal epithelium of the mammary gland is organized int

64 d a constitutively active SGK1 mutant in the luminal epithelium of the mouse uterus.

65 esized by nonciliated secretory cells in the luminal epithelium of the oviduct, is displayed on the c

66 luminal syringeal tissues, especially in the luminal epithelium of the trachea and pessulus.

67 was found to be transiently expressed in the luminal epithelium on late day 4 and then in the stroma

68 s and cytokines, which are key regulators in luminal epithelium proliferation, trophoblast developmen

69 lateral adherens junctions of the SRC-2(d/d) luminal epithelium, respectively.

70 We term these luminal epithelium secretory factors 'mammokines'.

71 e growth factor (HB-EGF) is expressed in the luminal epithelium solely at the site of blastocyst appo

72 owth factor (HB-EGF) is induced in the mouse luminal epithelium solely at the site of blastocyst appo

73 gle-cell RNA sequencing shows that glandular luminal epithelium subtypes express transcripts that enc

74 Hegfl is expressed solely in the uterine luminal epithelium surrounding the blastocyst prior to a

75 GF) mRNA is synthesized in the mouse uterine luminal epithelium temporally, just prior to implantatio

76 een the blastocyst trophectoderm and uterine luminal epithelium that occurs at 2200-2300 h on day 4 (

77 -Flp is expressed in a mosaic pattern in the luminal epithelium, the Flp-mediated activation of a mut

78 le transcription factor, NFATc1 in prostatic luminal epithelium to PCa can affect expression of diver

79 ostate cancer, lower Sirt1 expression in the luminal epithelium was associated with poor prognosis.

80 Within the luminal epithelium, we noted a further restriction.

81 e undifferentiated epithelium and determined luminal epithelium were heterogeneous and contained seve

82 corpora lutea, increased SLA and beta(2)m in luminal epithelium, whereas a progesterone receptor anta

83 stly inhibited early Cox-2 expression in the luminal epithelium, while dramatically diminishing late