ライフサイエンスコーパス: nulliparous

1 study (mean age, 28.1 [SD, 6.0] years; 41.4% nulliparous).

2 Nine of the 35 women were nulliparous.

3 cancer (relative risk (RR) for parous versus nulliparous: 0.69, 95% confidence interval (CI) 0.65-0.7

4 pective studies (1979-2006) including 32,641 nulliparous (1,612 breast cancers) and 204,270 parous (8

5 and when the recipient was parous (31%) than nulliparous (7%) or male (13%; P =.02).

6 requent when the donor was parous (32%) than nulliparous (9%) or male (13%; P =.03) and when the reci

7 Data from 10 nulliparous, age-matched women were used as the control.

8 actating, four nonlactating postpartum, four nulliparous) aged 28-32 y were given protein intakes of

9 Eligible participants were nulliparous and aged 19 years or younger, and were recru

10 parasympathetic neurons of young adult, aged nulliparous and aged multiparous rats were identified by

11 Women were nulliparous and free of the metabolic syndrome at baseli

12 of sympathetic preganglionic neurons in both nulliparous and multiparous aged rats compared to the yo

13 ontrol of the lower urogenital tract in aged nulliparous and multiparous female rats.

14 , long-term studies of sphincter function in nulliparous and multiparous women.

15 iple cell types from normal breast tissue of nulliparous and parous women and carriers of BRCA1 or BR

16 y outcomes were unrelated to walking in both nulliparous and parous women.

17 d whether extracellular matrix isolated from nulliparous and postlactating (involuting) rat mammary g

18 en Snail; whereas, BMP-5 levels were high in nulliparous and regressing glands.

19 Here we report that aged nulliparous and uniparous female WAP-EPM transgenic mice

20 Age-matched virgin (i.e., nulliparous) and multiparous mice were subjected to 60 m

21 Three quarters of the women were nulliparous, and 5 had twin pregnancies; the median gest

22 was 61 kg (IQR 55-68), 58% of the women were nulliparous, and median daily caloric intake was 1,840 c

23 had planned the pregnancy or those who were nulliparous before the cohort pregnancy.

24 We demonstrate that mammary glands of nulliparous Brca1/p53-deficient mice accumulate lateral

25 tages in the first month postpartum than did nulliparous control women.

26 rtal saline-treated females when compared to nulliparous controls.

27 within the MBH in diestrus, never pregnant (nulliparous) controls, postpartum day 5 (PPD5), PPD10, P

28 ified that parity number of 1, 2 or 3 versus nulliparous demonstrated significant negative associatio

29 e CA1 region of hippocampal slices from both nulliparous female and male rats through a previously un

30 A proportion of nulliparous females also exhibited maternal responsivene

31 ve decline were compared to three-month old, nulliparous females that had regular (4-5 days) or irreg

32 Nulliparous females were at higher odds to develop perio

33 Although in adult nulliparous females, a single ThrbPV allele did not cont

34 of chemical associations with ANA in males, nulliparous females, and parous females; these estimates

35 The nulliparous females, however, outperformed parous rats d

36 ces between the mammary glands of parous and nulliparous females.

37 sed with age, with the exception of presumed nulliparous females.

38 he EPM and a novel stimulus test relative to nulliparous females.

39 Subjects were nulliparous, had one prior pregnancy or less, delivered

40 ion in a prospective cohort of normotensive, nulliparous Hispanic (n = 863) and non-Hispanic Caucasia

41 of single cell (1 x 10(5)) suspensions into nulliparous hosts and testing for hyperplastic outgrowth

42 ral analgesia complicates up to one-third of nulliparous labors.

43 number during involution, which returned to nulliparous levels with full regression.

44 as chemotactic for macrophages compared with nulliparous mammary ECM.

45 and low matrix metalloproteinase activity in nulliparous mammary matrix and fragmented FN and high ma

46 hamber and three-dimensional culture assays, nulliparous mammary matrix was found to suppress motilit

47 icroarray expression profiling of parous and nulliparous mammary tissue from these four strains yield

48 Using these matrices as substratum, nulliparous matrix was found to promote ductal organizat

49 o, MDA-MB-231 cells, premixed with Matrigel, nulliparous matrix, or involution matrix, were injected

50 better in multiparous females compared with nulliparous mice 1 mo after stroke.

51 ithelium, and overexpression of MRG in young nulliparous mice can induce differentiation.

52 Mammary glands from nulliparous mice expressing Sim2s driven by the mouse ma

53 ibited dramatic morphological alterations in nulliparous mice mammary glands.

54 Expression studies in nulliparous mice that carry a NLS-lacZ transgene downstr

55 frequent in involuted mice or in age-matched nulliparous mice.

56 ar to the metastasis frequencies observed in nulliparous mice.

57 le of MECs across four developmental stages; nulliparous, mid gestation, lactation and post involutio

58 CITED1 was strongly expressed in nulliparous mouse mammary epithelial cells and, when exp

59 motes precocious alveolar differentiation in nulliparous mouse mammary glands, suggesting that SIM2s

60 port an increased risk of preeclampsia among nulliparous Norwegian women with background levels of PF

61 at significantly increased risk if they were nulliparous or had a late age at first live birth and ha

62 breast cancer risk in women who were either nulliparous or had their first live birth after age 30 (

63 eans stratified by race and baseline parity (nulliparous or parous) were fully adjusted for study cen

64 ition in 110 women aged 20-40 y who had been nulliparous or primiparous.

65 rs OR, 6.07; 95% CI, 2.81-13.10) and parity (nulliparous OR, 1.60; 95% CI, 1.07-2.38; multiparous OR,

66 with double opacification in 123 consecutive nulliparous patients (mean age, 32.13 years; age range,

67 nfants are complications in about 15% of all nulliparous pregnancies.

68 tute of Child Health and Human Development's Nulliparous Pregnancy Outcomes Study-Monitoring Mothers-

69 A total of 18,775 nulliparous pregnant women enrolled between 2006 and 200

70 of Public Health, we carried out a study of nulliparous pregnant women enrolled in 2003-2007 (466 ca

71 We studied 209 healthy nulliparous pregnant women referred to an inner-city dis

72 of age, cognitive and emotional responses of nulliparous, primiparous, and multiparous rats were asse

73 ffects of pregnancy against breast cancer in nulliparous rats by short term specific hormonal interve

74 r matrix was isolated from mammary glands of nulliparous rats or rats with mammary glands undergoing

75 Here, we show that short term treatment of nulliparous rats with pregnancy levels of estradiol 17be

76 For HL patients, nulliparous status and "B" symptoms predicted inferior P

77 Among nulliparous, subfertile women, neither any fertility dru

78 Older nulliparous transgenic mice (9-17 months) showed a marke

79 one v < one drink per week; P =.16), parity (nulliparous v parous; P =.45), history of benign breast

80 The aggregated hazard ratio for nulliparous versus all parous women = 1.27 (95% confiden

81 The final miniPIERS model included: parity (nulliparous versus multiparous); gestational age on admi

82 ring the responses of mammary epithelia from nulliparous versus parous females to hormonal stimulatio

83 nfidence interval: 1.21, 1.34), and that for nulliparous versus women <25 years of age at first birth

84 ed USVs, mothers of 6- to 8-day-old pups and nulliparous virgin females exhibited equivalent levels o

85 A 24-year-old nulliparous woman developed mildly elevated blood pressu

86 parous women compared with 14.4% (n = 40) of nulliparous women (incidence rate per 100 person-years,

87 All five patients were nulliparous women (mean age, 34.4 years; age range, 28-4

88 Twenty-eight nulliparous women (not taking any hormones) received int

89 ous women were at reduced risk compared with nulliparous women (OR = 0.2; 95% CI: 0.1, 0.3).

90 parous women (OR, 8.5; 95% CI, 3.2-22.3) and nulliparous women (OR, 8.8; 95% CI, 3.2-24.2).

91 for those >15 years, RR 0.76), compared with nulliparous women (P for trend = 0.007).

92 n of 41-42 weeks to 40 weeks of gestation in nulliparous women aged >/=35 years may reduce overall ra

93 ks and the risk of perinatal mortality among nulliparous women aged >/=35 years.

94 adverse effect on the mother or infant among nulliparous women aged >/=35 years.

95 Among the cohort of 77,327 nulliparous women aged 35 to 50 years delivering a singl

96 We conducted a randomized trial of 750 nulliparous women at term who were in spontaneous labor

97 tating than in nonlactatating postpartum and nulliparous women because of the relatively greater redu

98 583,340 live-born singleton infants born to nulliparous women between 1992 and 1994 and weighing bet

99 Although the baseline risk is higher for nulliparous women compared with parous women, these resu

100 psia Prevention trial, a randomized study of nulliparous women conducted in five US medical centers f

101 (n = 151 549), and similar to the risk among nulliparous women in labor (n = 137 160; OR, 1.3; 95% CI

102 Analysis of data for abortions among nulliparous women in Scotland 1992-2008 demonstrated tha

103 and September 1996, we randomly assigned 761 nulliparous women in spontaneous labor at term who reque

104 was not associated with ovarian cancer among nulliparous women or among ever-pregnant women either be

105 5 years postpartum have worse prognosis than nulliparous women or women diagnosed during pregnancy.

106 ning to predict spontaneous preterm birth in nulliparous women using serial measurements of vaginal f

107 rtum and at 52 wk postpartum, and that of 10 nulliparous women was examined at equivalent intervals,

108 t underrepresentation of parous women versus nulliparous women was observed (P = 0.02).

109 -2 wk and 1, 2, 4, or 8 mo postpartum and 13 nulliparous women were studied.

110 tudy support the hypothesis that a subset of nulliparous women who experience infertility may be at i

111 We randomly assigned 4589 healthy nulliparous women who were 13 to 21 weeks pregnant to re

112 er, randomized, double-blind trial involving nulliparous women who were at low risk for preeclampsia.

113 We randomly assigned 5341 nulliparous women who were at term and in early labor to

114 The association was present primarily among nulliparous women whose abortions occurred prior to 9 we

115 revention Trial, 1992-1995) examines whether nulliparous women with a prior abortion who change partn

116 We conducted a prospective cohort study of nulliparous women with a singleton pregnancy in Cambridg

117 POP) study was a prospective cohort study of nulliparous women with a viable singleton pregnancy at t

118 ed when these findings are present in young, nulliparous women with abdominal or pelvic pain.

119 ], 3%-81%) lower incidence of breast cancer; nulliparous women with anorexia nervosa had a 23% (95% C

120 A prospective observational cohort study of nulliparous women with singleton pregnancies, from 8 cli

121 Among nulliparous women with singleton pregnancies, quantitati

122 Screening of nulliparous women with universal third trimester fetal b

123 ormed a nested case-control study of healthy nulliparous women within the Calcium for Preeclampsia Pr

124 e Journal, Parker et al. examine whether, in nulliparous women, a history of induced abortion is asso

125 For nulliparous women, adjusted PMD was higher by 8.6% per m

126 ated with a lower risk of preeclampsia among nulliparous women, but it remains unclear whether this a

127 ter adjustment for relevant confounders (for nulliparous women, odds ratio (OR) = 1.12, 95% confidenc

128 Among nulliparous women, risk was increased among women with a

129 Among nulliparous women, the hazard ratios for current menopau

130 Among nulliparous women, there appears to be an association be

131 Relative to nulliparous women, those with 1 or 2 children had a 30%

132 Parous women had heavier fetuses than nulliparous women, with the disparity being greater in t

133 Compared with nulliparous women, women who had four or more pregnancie

134 ion does not prevent preeclampsia in healthy nulliparous women.

135 no risk reduction due to calcium in healthy nulliparous women.

136 ed with serum hormone levels among 83 young, nulliparous women.

137 on, or adverse perinatal outcomes in healthy nulliparous women.

138 I: -54 to -23%) concentrations compared with nulliparous women.

139 rtum breast tissue compared with tissue from nulliparous women.

140 g by parity, this association was limited to nulliparous women.

141 predicts breast cancer risk, particularly in nulliparous women.

142 ciated with adjusted PMD (P(ACT) < 0.05) for nulliparous women.

143 ard processing and appetitive motivation, in nulliparous women.

144 s well recognized among parous compared with nulliparous women.

145 sia Prevention trial, which involved healthy nulliparous women.

146 ease with each child born when compared with nulliparous women.