ライフサイエンスコーパス: multiparous

1 being older than 25 years of age, and being multiparous.

2 y in those who are minority, low income, and multiparous.

3 reganglionic neurons in both nulliparous and multiparous aged rats compared to the young adult group.

4 Data from 822 primiparous and 2055 multiparous American women who participated in the Infan

5 pocampal-specific neurotoxic insult in adult multiparous and virgin Long-Evans rats.

6 1-expressing subline, G4, 38% (12/31) of the multiparous animals aged 12-20 months developed hyperpla

7 exhibit accelerated mammary tumorigenesis in multiparous animals.

8 ersion of a lactation-deficient phenotype in multiparous animals.

9 The multiparous brain exhibited features of immune suppressi

10 Multiparous but not virgin females exhibited a greatly e

11 ibe the pattern of litter size variation for multiparous carnivores.

12 tional water reservoir in the postpartum and multiparous cohorts pointing to redistribution of water

13 ttermilk was generated from three individual multiparous cows at 13 time points over the first three

14 In contrast, in multiparous dams, Vhl(-/-) mammary glands exhibited a pr

15 Furthermore, recent studies using multiparous, ErbB2/Neu-overexpressing mouse mammary tumo

16 Multiparous ewes were assigned to a control (CON) diet [

17 n, more than half (15 of 29) of the WAP-CR-1 multiparous female mice developed multifocal mammary tum

18 nd the development of mammary hyperplasia in multiparous female mice.

19 wer urogenital tract in aged nulliparous and multiparous female rats.

20 Case Report: Our case is of a middle-aged multiparous female who presented with amenorrhea for thr

21 te infarction that occurred in a 32-year-old multiparous female.

22 Resultant bitransgenic, multiparous, female progeny expressing both S100A4 and N

23 neic stem cell transplantation is the use of multiparous females as donors.

24 avioral recovery was significantly better in multiparous females compared with nulliparous mice 1 mo

25 This phenotype was exaggerated in multiparous females expressing ErbB2deltaIC.

26 Multiparous females had significantly lower concentratio

27 In contrast to naive females, multiparous females have measurable levels of circulatin

28 was examined in primiparous and age-matched multiparous females on postpartum days 5 (PPD5) and PPD1

29 The adaptations observed in multiparous females provide an innate model for the stud

30 ld, and (iii) the existence of a fraction of multiparous females that remain uninfected in spite of m

31 rannual differences in POP concentrations in multiparous females' milk from five breeding seasons bet

32 of multiparous WAP-CR-1 mice as compared to multiparous FVB/N mice suggesting increased cell prolife

33 S model included: parity (nulliparous versus multiparous); gestational age on admission; headache/vis

34 nk carcinomas is accompanied by a failure of multiparous glands to undergo postlactational involution

35 f Plk2 increased the formation of lesions in multiparous glands.

36 Milk polar lipids from 144 multiparous Holstein-Friesian dairy cows fed different d

37 Mammary tissue from multiparous matrilysin-expressing mice showed decreased

38 mined the peripheral lymphoid populations of multiparous mice and humans for evidence of priming of C

39 Emv1 was expressed in the spleens of multiparous mice but not in those of virgin mice, and Bx

40 ry gland epithelial proliferation and 24% of multiparous mice develop mammary gland cancer.

41 ison of normal and SCID mice, and testing of multiparous mice for CTL against fetal Ags, we found tha

42 Multiparous mice had higher levels of VEGF, both at base

43 After acute stroke, multiparous mice had smaller infarcts, less glial activa

44 Multiparous mice presented with mammary carcinomas after

45 Female multiparous mice that carry the MMTV-DeltaN-beta-catenin

46 Age-matched virgin (i.e., nulliparous) and multiparous mice were subjected to 60 min of reversible

47 ras virgin mice with natural estrous cycles, multiparous mice with cyclically elevated reproductive h

48 However, multiparous mice, in which the involuting mammary epithe

49 pment and to production of mammary tumors in multiparous mice.

50 more common in the highly consanguineous and multiparous Middle Eastern populations, and our Cairo fi

51 Examination of mammary glands from multiparous MMTV-MAT animals revealed the development of

52 We now report that multiparous MMTV-MUC1 transgenic mice stochastically dev

53 genesis, the pattern of tumor development in multiparous MMTV-Neu mice remains stochastic, suggesting

54 ubtype reduces the onset of tumorigenesis in multiparous MMTV-neu transgenics.

55 In aged multiparous MMTV/CR-1 mice, the hyperplastic phenotype w

56 ith decreased odds of delayed OL but only in multiparous mothers (OR: 0.79; 95% CI: 0.67, 0.94).

57 s of 173,205 singleton infants born alive to multiparous mothers in Utah from 1989 to 1996.

58 a separate multiple linear regression model, multiparous NLPP women who did not use multivitamin and

59 ty (nulliparous OR, 1.60; 95% CI, 1.07-2.38; multiparous OR, 3.42; 95% CI, 2.23-5.24).

60 irth data, women with P-SCAD were more often multiparous (p = 0.0167), had a history of infertility t

61 rt that mammary gland stroma from mature and multiparous rats prevents neoplastic development and enc

62 l responses of nulliparous, primiparous, and multiparous rats were assessed using a dry land maze (DL

63 ns of young adult, aged nulliparous and aged multiparous rats were identified by retrograde tracing w

64 change in the density of collagen fibers in multiparous rats.

65 In addition, multiparous TGFalpha-expressing female transgenics frequ

66 at lower gestational weight gain (GWG) among multiparous than among primiparous women.

67 end the concept of a lower optimal GWG among multiparous than primiparous women to American women.

68 Multiparous transgenic female offspring from c-erbB-2-ex

69 ysplasia or neoplasia during the lifespan of multiparous transgenic mice.

70 rats were investigated that included virgin, multiparous, two- and fourteen-day postpartum primiparou

71 and MAPK were detected in mammary glands of multiparous WAP-CR-1 mice as compared to multiparous FVB

72 Nonlactating, multiparous WAP-DES mice exhibited hyperplastic lesions

73 We previously reported that multiparous WAP-TGFalpha transgenic mice develop mammary

74 imately twofold higher in primiparous versus multiparous women (21% versus 13%; P < 0.01).

75 rnal peripheral blood in primiparous than in multiparous women (35%; P < 0.001), with a >12-fold diff

76 gained more weight during pregnancy than did multiparous women (mean +/- SD: 15.9 +/- 6.9 compared wi

77 his was more than 8 times greater than other multiparous women (OR, 8.5; 95% CI, 3.2-22.3) and nullip

78 ination practices among the poorest, single, multiparous women and among mothers who do not deliver a

79 CI, 1.3-3.5) the risk associated with other multiparous women in labor (n = 151 549), and similar to

80 he caesarean section rate after induction in multiparous women increased significantly across all HDI

81 CT pelvimetry in a relatively large group of multiparous women who passed a trial of labor successful

82 non-obstetrical indications in non-pregnant multiparous women with a successful vaginal delivery.

83 d from 100 uncomplicated term pregnancies of multiparous women with one or more typically developing

84 ough pelvic diameters were somewhat lower in multiparous women with short stature.

85 s-match assays may need to be implemented in multiparous women, given our results.

86 Among multiparous women, multiple linear regression showed tha

87 Compared with multiparous women, primiparous mothers experienced a del

88 women with higher exhaustion scores, and, in multiparous women, those who breast-fed less frequently

89 n, and no group differences were found among multiparous women.

90 nts increased with increasing GWG only among multiparous women.

91 fect seems to be most important in older and multiparous women.

92 th increasing GWG among both primiparous and multiparous women.

93 ss methylation was observed in lean or older multiparous women.

94 influence mammary carcinoma pathogenesis in multiparous women.

95 ies of sphincter function in nulliparous and multiparous women.

96 is likely to be different in primiparous and multiparous women.