ライフサイエンスコーパス: endometrial biopsy

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1 ay help determine which women should undergo endometrial biopsy.

2 tologic risk (based on subtype and grade) in endometrial biopsies.

3 omen taking estrogen plus progestin required endometrial biopsies (33% vs 6%; P<.001).

4 Endometrial biopsies also were obtained from 4 healthy c

5 to 11% and 16% over pathways initiated with endometrial biopsy are predicted.

6 tween DNA methylation and gene expression in endometrial biopsies collected from 17 healthy fertile-a

7 microarray experiments on 31 postmenopausal endometrial biopsies, comprising 11 benign and 20 malign

8 PTEN expression via immunohistochemistry in endometrial biopsies diagnosed as EH in 138 cases, who w

9 In this study, office endometrial biopsies (EMBs) were obtained during the ini

10 archers advocate routine ultrasonography and endometrial biopsy for screening asymptomatic women rece

11 cificity of transvaginal ultrasonography and endometrial biopsy for the detection of endometrial dise

12 Lower genital tract specimens and endometrial biopsies from 147 women with pelvic inflamma

13 Pathological changes seen in the endometrial biopsies included acute rejection and acute

14 ne expression profiles from mid-luteal phase endometrial biopsies (n = 115) from women experiencing R

15 The increased burden of endometrial biopsies required to assess vaginal bleeding

16 e absence of abnormality at HSG and a normal endometrial biopsy result may eliminate the need for fur

17 Analysis of 70 midluteal endometrial biopsies revealed an inverse correlation bet

18 r-derived endometrial cells were detected in endometrial biopsy samples from all bone marrow recipien

19 the target population by using office-based endometrial biopsy versus transvaginal US as starting po

20 Loss of PTEN expression in endometrial biopsies was neither associated with nor a s

21 Endometrial biopsies were taken and total RNA extraction

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