戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ay help determine which women should undergo endometrial biopsy.
2 pithelial organoid (EEO) cultures from human endometrial biopsies.
3 tologic risk (based on subtype and grade) in endometrial biopsies.
4 omen taking estrogen plus progestin required endometrial biopsies (33% vs 6%; P<.001).
5                                              Endometrial biopsies also were obtained from 4 healthy c
6 luding the identification of plasma cells in endometrial biopsies and the detection of colorectal can
7 ined an average of > 9000 sequence reads per endometrial biopsy, and found the endometrial microbiota
8  to 11% and 16% over pathways initiated with endometrial biopsy are predicted.
9 tween DNA methylation and gene expression in endometrial biopsies collected from 17 healthy fertile-a
10 lied to obtain the transcriptomic profile of endometrial biopsies collected from nonpregnant women wh
11 rofile of isolated SSEA-1(+) EECs from eight endometrial biopsies compared to SSEA-1(-) EECs.
12  microarray experiments on 31 postmenopausal endometrial biopsies, comprising 11 benign and 20 malign
13  PTEN expression via immunohistochemistry in endometrial biopsies diagnosed as EH in 138 cases, who w
14                        In this study, office endometrial biopsies (EMBs) were obtained during the ini
15 archers advocate routine ultrasonography and endometrial biopsy for screening asymptomatic women rece
16 cificity of transvaginal ultrasonography and endometrial biopsy for the detection of endometrial dise
17            Lower genital tract specimens and endometrial biopsies from 147 women with pelvic inflamma
18                               Examination of endometrial biopsies from 924 women revealed that the re
19             Pathological changes seen in the endometrial biopsies included acute rejection and acute
20 ne expression profiles from mid-luteal phase endometrial biopsies (n = 115) from women experiencing R
21 isation in quantitative RT-PCR studies using endometrial biopsies obtained from women with endometria
22                      The increased burden of endometrial biopsies required to assess vaginal bleeding
23 e absence of abnormality at HSG and a normal endometrial biopsy result may eliminate the need for fur
24                     Analysis of 70 midluteal endometrial biopsies revealed an inverse correlation bet
25 r-derived endometrial cells were detected in endometrial biopsy samples from all bone marrow recipien
26  the target population by using office-based endometrial biopsy versus transvaginal US as starting po
27                   Loss of PTEN expression in endometrial biopsies was neither associated with nor a s
28                                              Endometrial biopsies were taken and total RNA extraction