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1 wer endometrial expression of FST during the luteal phase.
2 id-follicular phase to the symptomatic, late luteal phase.
3 ncreased from the mid-follicular to the late luteal phase.
4 r for half of the menstrual cycle during the luteal phase.
5 teins (P = 5.62E-4) were elevated during the luteal phase.
6 e of 18 proteins that best distinguished the luteal phase.
7 n </= 5 ng/mL and no LH peak in the mid/late luteal phase.
8 rgery during the follicular phase versus the luteal phase.
9 its precursors) were associated with shorter luteal phase.
10 eft fronto-polar cortex more than during the luteal phase.
11 ating hormone and luteinizing hormone in the luteal phase.
12 d a 0.06-log(PdG) decrease (p = 0.03) in the luteal phase.
13 ficantly associated with length of the prior luteal phase.
14 icular phase and then decreased again in the luteal phase.
15 ls the entire night in the luteal and pseudo luteal phase.
16 se, and 0.76 +/- 0.07 kJ/min during the late luteal phase.
17 ity (P = 0.09) during menses than during the luteal phase.
18 -cycle compared with both the follicular and luteal phases.
19 E1 were determined during the follicular and luteal phases.
20  follicular phase to the mid luteal and late luteal phases.
21 levels during the follicular, ovulatory, and luteal phases.
22 easured in the early and late follicular and luteal phases.
23 sion showed that decreases in follicular and luteal phase 17beta-estradiol levels were positively ass
24 hthalate (MCOP) were associated with shorter luteal phase [2nd tertile vs. 1st tertile: -0.5 days (95
25         BPA was also associated with shorter luteal phase [2nd vs. 1st: -0.8 days (95% CI: -1.2, -0.4
26 men comprised the study cohort: 230 (28%) in luteal phase; 363 (44%) in follicular phase; and 241 gro
27 ase (59 [17]) compared with women during the luteal phase (53 [14]) and compared with men (46 [16]; P
28 tal cortex and amygdala more than during the luteal phase (6-10 days after luteinizing hormone surge)
29 ic the decidualizing steroidal milieu of the luteal phase and early pregnancy.
30 ition of uILCs in the endometrium during the luteal phase and in the decidua during early pregnancy.
31 traception could mimic the high-progesterone luteal phase and predispose women to human immunodeficie
32 cular phase, 0.70 +/- 0.10 kJ/min during the luteal phase, and 0.76 +/- 0.07 kJ/min during the late l
33 e onset of melatonin levels for women in the luteal phase, but it had little effect on melatonin leve
34  not meet criteria for either follicular- or luteal-phase categories.
35 ins indicates that AR(-/-) females exhibit a luteal phase defect.
36 poradic anovulation, irregular cycle length, luteal phase deficiency, long menses, and heavy blood lo
37 mones measured either midcycle or during the luteal phase, despite good statistical power to detect m
38 tinuous (full-cycle dosing) or intermittent (luteal-phase dosing) sertraline.
39 e anxiety and dysphoria associated with late luteal phase dysphoria disorder and major unipolar depre
40 lection of gene expression profiles from mid-luteal phase endometrial biopsies (n = 115) from women e
41 o [OR] 1.11, 95% CI 1.03-1.20; p=0.0063) and luteal phase endometrial thickness lower (0.90, 0.83-0.9
42 g was associated with decreased midcycle and luteal-phase estradiol levels.
43 5-1988) of a prospective study, midcycle and luteal-phase estrogens and progestins were measured in 1
44                                              Luteal-phase females showed diminished subjective drug e
45 lar phase was more irregular than during the luteal phase for both FSH and LH (P < 0.01).
46  of the menstrual cycle (n=30) or the pseudo luteal phase for oral contraceptive users (n=32).
47 in the vaginal lumen and increase during the luteal phase (high progesterone).
48 articular susceptibility observed during the luteal phase in nonhuman primate models and ex vivo huma
49 th, 16.0 (standard deviation, 4.4) days; and luteal phase length, 12.9 (standard deviation, 1.7) days
50 w or a window determined by assuming a fixed luteal phase length, would be simpler.
51 and increased follicular phase and decreased luteal phase lengths; Hispanic ethnicity with anovulatio
52 sing linear mixed models for follicular- and luteal-phase lengths, discrete-time fecundability models
53 ese chemicals in relation to follicular- and luteal-phase lengths, time to pregnancy, and early pregn
54 ated from sputum during exacerbations in the luteal phase (low estradiol).
55  any of the following cycle endpoints: short luteal phase (&lt; or = 10 days), long follicular phase (>
56  to an increased risk for anovulation, short luteal phase (&lt; or =10 days), long follicular phase (> o
57 en during the early follicular (EFP) and mid-luteal phase (MLP) of the menstrual cycle.
58             Sodium cravings increased in the luteal phase of all cycles but were not accompanied by i
59 ons comparable to levels observed during the luteal phase of premenopausal women and were significant
60 myomata than myometrium, but only during the luteal phase of the cycle.
61 ats mimics the progesterone component of the luteal phase of the human menstrual cycle, these finding
62 ature levels in women were tested during the luteal phase of the menstrual cycle (n=30) or the pseudo
63 omen using no long-term contraceptive in the luteal phase of the menstrual cycle also had a 3.25 time
64 h levels comparable to those observed in the luteal phase of the menstrual cycle and modestly increas
65                 The results for women in the luteal phase of the menstrual cycle are consistent with
66 egnanolone levels from the follicular to the luteal phase of the menstrual cycle by blocking the conv
67 s were significantly (P=0.0078) lower in the luteal phase of the menstrual cycle compared to the foll
68    Changes in neurosteroid levels during the luteal phase of the menstrual cycle may precipitate affe
69 onadotropin secretion was blocked during the luteal phase of the menstrual cycle with a gonadotropin-
70 istered to female rhesus macaques during the luteal phase of the menstrual cycle, 40 min before admin
71  T cell populations were detected during the luteal phase of the menstrual cycle, and longitudinal an
72      In conclusion, TEF decreased during the luteal phase of the menstrual cycle, possibly as a resul
73  often occur during pregnancy and during the luteal phase of the menstrual cycle, when levels of prog
74 with plasma estradiol and estrone during the luteal phase of the menstrual cycle.
75  did not result from sodium retention in the luteal phase of the menstrual cycle.
76 V infection during the progesterone-dominant luteal phase of the menstrual cycle.
77 vulation phase and with urine PdG during the luteal phase of the menstrual cycle.
78 rder and 11 healthy female volunteers in the luteal phase of the menstrual cycle.
79                                   During the luteal phase of the sodium restriction cycle, significan
80 rovided) were measured in the follicular and luteal phases of 2 menstrual cycles before a single inje
81  of the first menstrual cycle and during the luteal phases of both the first and third menstrual cycl
82 valuated in clinic during the follicular and luteal phases of each menstrual cycle.
83 l females, and females in the follicular and luteal phases of the menstrual cycle (FDR-adjusted p-val
84  in the younger women (in the follicular and luteal phases of the menstrual cycle).
85 e glucuronide (E1G) in the periovulatory and luteal phases of the menstrual cycle, and to assess the
86 women during the the mid-follicular and late luteal phases of the menstrual cycle.
87 wice, at the (1) late follicular and (2) mid luteal phases of the menstrual cycle.
88 ding with the follicular, periovulatory, and luteal phases of their menstrual cycle were studied.
89 lab during the follicular, ovulatory and mid-luteal phases of their menstrual cycles.
90  fertility (n = 5) during the follicular and luteal phases of their reproductive cycles.
91                Shedding increased during the luteal phase only among women with CD4 counts of <350 ce
92 bitors, taken throughout the cycle or during luteal phases only, is also well established.
93 s increased sixfold to eightfold in the late luteal phase (P < 0.001) and those of swelling or bloati
94  and neutrophil gene set signatures with the luteal phase (P < 0.05).
95 re higher in the late follicular than in the luteal phase (P = 0.02 and P = 0.04, respectively).
96 re higher in the late follicular than in the luteal phase (P = 0.03 and P = 0.02, respectively).
97 nsive pregnancies were tested during the mid-luteal phase (PRE) and early pregnancy (EARLY; 6.2 +/- 1
98 previously, we showed more inhibition in the luteal phase relative to the midfollicular menstrual pha
99 es during the follicular, periovulatory, and luteal phases, respectively (P = .01).
100 ases, and directly with the probability of a luteal-phase rise in progesterone.
101 pooled to create follicular-, midcycle-, and luteal-phase samples, respectively, for analysis.
102 inary sodium loss, not retention, during the luteal phase; severity of menstrual symptoms was unchang
103                                  Compared to luteal phase sheep, both ERalpha and ERbeta levels in UA
104 ed in women with PMDD from follicular to the luteal phases, suggesting the absence of effect of the l
105 ore energy at rest (4.3%; P = 0.0002) in the luteal phase than in the follicular phase.
106 t is greater during the early follicular and luteal phases than in the late follicular (periovulatory
107                       Conversely, during the luteal phase there were factors overexpressed (including
108                                       Median luteal phase titres of progesterone were 121% higher (p=
109 re collected, characterized as follicular or luteal phase using days since last menstrual period, and
110 ng postovulation (average of luteal and late luteal phases), when it was 0.73 +/- 0.07 kJ/min, compar
111 antly higher than those measured in the late luteal phase, whereas aging and cigarette smoking reduce
112 mmunocytochemically detectable GAL-R1 in the luteal phase, whereas only a twentieth expressed GAL-R1
113 offer candidate mechanisms through which the luteal phase, wherein progesterone is dominant relative
114 modeling and leukocyte infiltration with the luteal phase, which may represent potential hormone-asso

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