ライフサイエンスコーパス: uterine horn

1 myometrium to develop extrusion outside the uterine horn.

2 ellular and molecular characteristics of the uterine horn.

3 is (mouse pneumonitis strain MoPn) into each uterine horn.

4 histiocytic inflammation was observed in the uterine horns.

5 ith mini-osmotic pumps that delivered CSP to uterine horns.

6 elopment of cystic tumors in the ovaries and uterine horns.

7 vaccinated with MOMP carried embryos in both uterine horns.

8 ed lengthening of the small bowel and of the uterine horns.

9 medium or U. parvum was inoculated into each uterine horn and animals were evaluated for intra-amniot

10 y weight, increased adipose tissue, enlarged uterine horns, and increased inflammation in the HFD gro

11 number of implantation sites in the treated uterine horns as compared to control horns.

12 ually severe dilatation and pathology in the uterine horns but normal oviduct pathology after infecti

13 Briefly, for the ER group, a uterine horn containing 1-2 embryos was translocated to

14 n in myeloid cells in the vagina (day 3) and uterine horns (day 7), followed by a marked rise in the

15 The uterine horns decreased in size postpartum, ultimately r

16 We now report that the uterine horn dilation correlates with glandular duct dil

17 Screening 12 strains of mice for uterine horn dilation following C. muridarum infection r

18 The severity scores of uterine horn dilation observed macroscopically correlate

19 l relevance of nontubal pathologies, such as uterine horn dilation, developed in mice following chlam

20 ficantly alter the C. muridarum induction of uterine horn dilation.

21 mical alterations of the vagina, cervix, and uterine horns during pregnancy and postpartum using the

22 During infection, Il1a(-/-) oviducts and uterine horns exhibited reduced neutrophil infiltration,

23 ue anatomical features, including long, thin uterine horns, fragile salpinges, short ovarian suspenso

24 nflammatory cells were significantly less in uterine horns from IRF3 KO mice than in those from contr

25 ridarum into the mouse uterus increased both uterine horn/glandular duct dilation and hydrosalpinx.

26 Nevertheless, the chlamydial induction of uterine horn/glandular duct dilation may be used to eval

27 lpinx, was not required for the induction of uterine horn/glandular duct dilation.

28 ked fluid accumulation and distension of the uterine horns in the vast majority of those animals.

29 uid (ULF) in the most cranial portion of the uterine horn ipsilateral to the corpus luteum.

30 determine whether nerve fiber density of the uterine horn is altered during the estrous cycle and, if

31 cally reducing placental blood supply in one uterine horn, leaving the contralateral horn as internal

32 The dilated glandular ducts pushed the uterine horn lumen to closure or dilation and even broke

33 ome composition of the uterine body (UB) and uterine horn mucosa (UH) samples using 16S rRNA sequenci

34 lue) was injected in the cervical end of the uterine horn of virgin rats.

35 lammation was significantly increased in the uterine horns of C57 mice compared to that of C3H mice.

36 bryo (P-, n = 7) in pregnant mares, and both uterine horns of nonbred mares (NB, n = 6).

37 ially recruited to the upper GT (oviduct and uterine horn) over the lower GT (cervical-vaginal region

38 ase that ascended from the endocervix to the uterine horns, oviducts, and ovaries in a temporal fashi

39 e Chlamydia, 81% (17/21) had embryos in both uterine horns (P > 0.05).

40 immunized with ovalbumin had embryos in both uterine horns (P < 0.05).

41 gest that IRF3 has a role in protection from uterine horn pathology that is independent of its functi

42 In all cases, one of the uterine horns revealed collection due to a hemivaginal s

43 Anterogradely labeled axons innervated each uterine horn, these projected rostrally or caudally from

44 s, likely due to the leakage of LPS from the uterine horns through the cervix.

45 of preimplantation embryos from mutant Hmx3 uterine horns to wild-type pseudopregnant females result

46 al (in the vaginal lumen) and distal (in the uterine horns) to the site of topical delivery.

47 In contrast, severe distention of the uterine horns was observed in all infected C57 mice comp

48 ion day 22 SD rats were anesthetized and the uterine horns were exteriorized and placed in a water ba

49 FPUs in the left and right uterine horns were IUGR cases and controls, respectively

50 After 7-9 days, uterine horns were stained to visualize traced nerve axo

51 Measurements of the vagina, cervix, and uterine horns were taken by analyzing MRI segmentations

52 s injected to the amniotic fluid sacs in one uterine horn, whereas the contralateral amniotic sacs we

53 ranscripts were compared among three groups: uterine horn with an embryo (P+, n = 7), without an embr