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1 eptides derived from a proteolytic digest of follicle stimulating hormone.
2 cycle patterns or on elevated (>20 IU/liter) follicle-stimulating hormone.
3 but had no effect on luteinizing hormone or follicle-stimulating hormone.
4 volved in the response of gonadal tissues to follicle-stimulating hormone.
5 ), androstenedione, luteinizing hormone, and follicle-stimulating hormone.
6 iandrosterone sulfate, insulin, glucagon, or follicle-stimulating hormone after baseline hormone valu
7 Following superovulation with recombinant follicle-stimulating hormone and administration of gonad
9 mice and was associated with decreased serum follicle-stimulating hormone and higher claudin-11 expre
11 male mice do not feminize, and the levels of follicle-stimulating hormone and IL-6 are inhibited.
12 ted with a decrease in the concentrations of follicle-stimulating hormone and luteinising hormone, an
13 ll explore in detail effects on secretion of follicle-stimulating hormone and luteinising hormone.
14 higher body mass index (P = .05), and lower follicle-stimulating hormone and luteinizing hormone (ea
17 acterized by increasing dyssynchrony between follicle-stimulating hormone and luteinizing hormone in
18 fetime history of depression also had higher follicle-stimulating hormone and luteinizing hormone lev
20 ge in menopausal status, increased levels of follicle-stimulating hormone and luteinizing hormone, an
21 levels were elevated, as were the levels of follicle-stimulating hormone and luteinizing hormone.
23 hormone secretion and on pituitary hormone (follicle-stimulating hormone and prolactin), CgA, and Cg
24 iation into spermatozoa, whereas recombinant follicle-stimulating hormone and steroid hormones are in
25 imulatory actions of luteinizing hormone and follicle-stimulating hormone and to 17beta-estradiol and
27 tosterone or estradiol, leutinizing hormone, follicle stimulating hormone, and prolactin were determi
28 Activin acts in the pituitary to stimulate follicle-stimulating hormone, and is antagonized by endo
29 one, and increased variability of estradiol, follicle-stimulating hormone, and luteinizing hormone ar
30 ned 12-month analysis evaluated E2, E1, E1S, follicle-stimulating hormone, and luteinizing hormone le
31 ns, gonadotropin-releasing hormone agonists, follicle-stimulating hormone, and luteinizing hormone.
32 the urinary forms of estrogen, progesterone, follicle-stimulating hormone, and luteinizing hormone.
34 estosterone, dehydroepiandrosterone sulfate, follicle-stimulating hormone, and sex hormone-binding gl
35 ome reaction as well as luteinizing hormone, follicle-stimulating hormone, and testosterone serum lev
36 ologic surgery, hormone replacement therapy, follicle-stimulating hormone, and vasomotor symptoms.
38 1p14.1 SNP, rs11031006, in the region of the follicle-stimulating hormone B polypeptide (FSHB) gene s
41 localizes to alpha-glycoprotein subunit- and follicle-stimulating hormone beta-positive cells of the
42 f pulses from the hypothalamus and regulates follicle-stimulating hormone beta-subunit (FSHbeta) gene
44 ations with sex hormone-binding globulin and follicle-stimulating hormone (beta = -0.04, 95% confiden
46 and the gene was localized to within 3 cM of follicle-stimulating hormone, beta polypeptide in the mi
47 we report that exoloop 3 of FSH-R constrains follicle-stimulating hormone binding to the exodomain.
48 Activin stimulates whereas inhibin blocks follicle-stimulating hormone biosynthesis and secretion
49 irculating levels of luteinizing hormone and follicle-stimulating hormone but apparently normal respo
50 d in granulosa cells of growing follicles by follicle-stimulating hormone, but the highest levels of
51 gonadotropin, human luteinizing hormone, and follicle stimulating hormone by surface plasmon resonanc
52 ostic variables: age, body-mass index, basal follicle-stimulating hormone concentration, and the numb
56 glycopeptides of equine and human pituitary follicle stimulating hormone (eFSH and hFSH) have been c
57 amples were assayed for luteinizing hormone, follicle-stimulating hormone, estradiol, and progesteron
58 t flashes, night sweats) and serum levels of follicle-stimulating hormone, estradiol, and sex hormone
59 corresponding serum luteinizing hormone and follicle-stimulating hormone fell progressively during t
60 mones from the hypothalamus, luteinizing and follicle stimulating hormones from the pituitary, and go
63 a have implicated the pituitary gonadotropin follicle stimulating hormone (FSH) as both a risk factor
68 Treatment of cultured Sertoli cells with follicle stimulating hormone (FSH) significantly increas
73 lower estradiol, bioavailable estradiol, and follicle-stimulating hormone (FSH) (all p < 0.05) than w
75 ic protein-15 (BMP-15) can directly modulate follicle-stimulating hormone (FSH) action in rat granulo
78 esumption of menses and serial monitoring of follicle-stimulating hormone (FSH) and inhibin A and B l
82 ght have an acute effect on the secretion of follicle-stimulating hormone (FSH) and luteinizing hormo
83 Leptin produced a dose-related increase in follicle-stimulating hormone (FSH) and luteinizing hormo
84 ole in reproductive physiology by regulating follicle-stimulating hormone (FSH) and luteinizing hormo
85 an inhibitor of prostaglandin signaling and follicle-stimulating hormone (FSH) and luteinizing hormo
86 ols the release of the gonadotropic hormones follicle-stimulating hormone (FSH) and luteinizing hormo
87 GnRH regulates the pituitary gonadotropin's follicle-stimulating hormone (FSH) and luteinizing hormo
88 ynthesis and secretion of the gonadotropins, follicle-stimulating hormone (FSH) and luteinizing hormo
89 one, testosterone, luteinizing hormone (LH), follicle-stimulating hormone (FSH) and sex hormone-bindi
91 is Review, we briefly outline the roles that follicle-stimulating hormone (FSH) and testosterone play
93 Multiple interactions exist between human follicle-stimulating hormone (FSH) and the N-terminal ho
97 teinizing hormone (LH) secretion and that of follicle-stimulating hormone (FSH) could be valuable in
99 nses in the preceding 6 months and levels of follicle-stimulating hormone (FSH) in the postmenopausal
100 ts the beta-subunit of the pituitary hormone follicle-stimulating hormone (Fsh) increases bone mass i
106 ed whether all-trans-retinoic acid (tRA) and follicle-stimulating hormone (FSH) modulate RARalpha rec
107 mvent this problem, a genetically engineered follicle-stimulating hormone (FSH) mutant protein was pr
108 stis by conjugating Adjudin to a recombinant follicle-stimulating hormone (FSH) mutant, which serves
109 Studies-Depression Scale [CES-D Scale]) and follicle-stimulating hormone (FSH) plasma levels of depr
110 way, based on evidence that the GPCR agonist follicle-stimulating hormone (FSH) promotes the protein
111 lenge experiments to identify regions in the follicle-stimulating hormone (FSH) receptor (FSHR) ECD t
113 ceptors are highly conserved, we mutated the follicle-stimulating hormone (FSH) receptor at the corre
115 mely, BMP-15 promotes GC mitosis, suppresses follicle-stimulating hormone (FSH) receptor expression,
116 ependent of transcription, androgens enhance follicle-stimulating hormone (FSH) receptor expression,
118 ught to elucidate the mechanism by which the follicle-stimulating hormone (FSH) receptor signals to p
119 hormone (LH)/chorionic gonadotropin (CG) or follicle-stimulating hormone (FSH) receptor, that at lea
121 there is a separate hypothalamic control of follicle-stimulating hormone (FSH) release distinct from
125 ycoprotein hormones, luteinizing hormone and follicle-stimulating hormone (FSH), act through their co
126 The gonadotropins, luteinizing hormone (LH), follicle-stimulating hormone (FSH), and chorionic gonado
128 serum level of antimullerian hormone (AMH), follicle-stimulating hormone (FSH), and inhibin B and ur
129 o direct the synthesis of the gonadotropins, follicle-stimulating hormone (FSH), and luteinizing horm
131 es undergo exponential growth in response to follicle-stimulating hormone (FSH), largely as a result
132 Fos family members in response to hormones (follicle-stimulating hormone (FSH), luteinizing hormone
133 tary, this innervation was observed close to follicle-stimulating hormone (FSH), luteinizing hormone
134 e sulfate (DHEAS), luteinizing hormone (LH), follicle-stimulating hormone (FSH), prolactin, fasting p
135 s 6-12 h after stimulation with forskolin or follicle-stimulating hormone (FSH), the major physiologi
136 iometry, and measurements of BNP, NT-proBNP, follicle-stimulating hormone (FSH), total testosterone,
137 cells to proliferate normally in response to follicle-stimulating hormone (FSH), whereas mutant males
138 vels of estradiol in women are controlled by follicle-stimulating hormone (FSH), which regulates tran
139 progesterone, luteinizing hormone (LH), and follicle-stimulating hormone (FSH), which were measured
140 phosphorylation, and thus, the expression of follicle-stimulating hormone (FSH)- and testosterone-ind
141 lial ovarian cancer nor its interaction with follicle-stimulating hormone (FSH)-driven proliferation
143 ells (GCs) and produces a marked decrease in follicle-stimulating hormone (FSH)-induced progesterone
144 We sought to elucidate the role of AKT in follicle-stimulating hormone (FSH)-mediated granulosa ce
150 lls [expressing luteinizing hormone (LH) and follicle-stimulating hormone (FSH)], with adrenocorticom
151 as the premature ovarian failure (POF) rate (follicle-stimulating hormone [FSH] >/= 40 IU/L) after 1
153 d that mice deficient in the beta-subunit of follicle-stimulating hormone (FSHbeta) are protected fro
154 pressing a glycoprotein hormone receptor for follicle-stimulating hormone (FSHR), CXC- (CXCR-2), and
155 , greater than 3 months of amenorrhea, and a follicle-stimulating hormone > or = 30 MIU/mL at the 12-
156 enstrual periods and serum concentrations of follicle-stimulating hormone >25 IU/L), meeting criteria
157 human chorionic gonadotropin (hCG) and human follicle-stimulating hormone had shown that it was possi
159 een human choriogonadotropin (hCG) and human follicle-stimulating hormone (hFSH), but determinants of
161 sary for embryonic development and pituitary follicle-stimulating hormone homeostasis, mice deficient
162 pausal status and in levels of estradiol and follicle-stimulating hormone in 2,659 women followed in
163 5+/-4.6 IU per liter (P<0.001), the level of follicle-stimulating hormone increased from 2.5+/-1.7 to
164 effects of recombinant BMP-4 and -7 on FSH (follicle-stimulating hormone)-induced rat granulosa cyto
165 family of small G-proteins is essential for follicle stimulating hormone-induced signaling events an
166 Body and testicular weight, testosterone, follicle-stimulating hormone level, and luteinizing horm
167 vaginal dryness (LR+ range, 1.48-3.79), high follicle-stimulating hormone levels (LR+ 3.06; 95% CI, 2
169 with heavier menstrual bleeding, and higher follicle-stimulating hormone levels were associated with
170 tography and tandem mass spectrometry assay; follicle-stimulating hormone levels were measured at bas
171 , evaluated using anti-Mullerian hormone and follicle-stimulating hormone levels, was similar in both
172 tory findings (insulin-like growth factor 1, follicle-stimulating hormone, luteinizing hormone, and t
173 mong pituitary tumors, 30% (7/23), mainly in follicle-stimulating hormone/luteinizing hormone-produci
174 he transplantation in both patients by serum follicle-stimulating hormone measurements (patient A, 47
175 ment led to significant increases in CgB and follicle-stimulating hormone mRNAs in gonadotroph adenom
176 l Interview for DSM-IV, and plasma levels of follicle-stimulating hormone obtained at 3-6-month inter
177 sociated with a lower likelihood of elevated follicle-stimulating hormone (odds ratio (OR)=0.6, 95% c
178 before the FMP in the log rate of change of follicle-stimulating hormone (odds ratio, 0.65; 95% CI,
179 le development by attenuating the effects of follicle stimulating hormone on follicle growth and inhi
183 adenomas, a gonadotroph luteinizing hormone/follicle-stimulating hormone-positive adenoma, exhibited
184 ed for individuals with a rapidly increasing follicle-stimulating hormone profile (P< or =.001) and a
185 icles, treatment with R-spondin2, similar to follicle stimulating hormone, promoted the development o
186 r ovarian stimulation with the letrozole and follicle-stimulating hormone protocol preserves fertilit
187 elical loops of luteinizing hormone receptor/follicle stimulating hormone receptor/thyroid stimulatin
189 in reaction techniques for the evaluation of follicle-stimulating hormone receptor (FSHR) expression
191 The luteinizing hormone receptor (LHR) and follicle-stimulating hormone receptor (FSHR) have an app
195 had a Sertoli cell appearance and expressed follicle-stimulating hormone receptor within the seminif
196 d the conserved serine in the LH (S277I) and follicle-stimulating hormone receptors (S273I) and obser
197 ot only are observed in regions that control follicle-stimulating hormone release but also are coloca
200 er this peptide, known to selectively induce follicle-stimulating hormone release, is coexpressed in
201 e to TGF-beta with significant inhibition of follicle-stimulating hormone secretion at higher concent
202 entrations (10(-9) mol/L) and stimulation of follicle-stimulating hormone secretion at lower concentr
203 anscriptional activity and by suppression of follicle-stimulating hormone secretion by cultured anter
204 ding, activin transcriptional responses, and follicle-stimulating hormone secretion substantiates the
205 Increased luteinizing hormone relative to follicle-stimulating hormone secretion, insulin resistan
206 stradiol, progesterone, luteinizing hormone, follicle-stimulating hormone, sex hormone-binding globul
207 Although follicles responded to initial follicle-stimulating hormone stimulation and developed n
208 onized the inhibitory effects of BMP4 on the follicle-stimulating hormone stimulation of progesterone
209 ta superfamily, is an important modulator of follicle-stimulating hormone synthesis and secretion in
210 ne (Tam-IVF) or in combination with low-dose follicle-stimulating hormone (TamFSH-IVF) or letrozole 5
211 amples were assayed for levels of estradiol, follicle-stimulating hormone, testosterone, and dehydroe
212 s do not support the use of urinary or blood follicle-stimulating hormone tests or antimullerian horm
214 combinant JY-1 protein regulates function of follicle-stimulating hormone-treated ovarian granulosa c
215 y end point was POF, defined as at least one follicle-stimulating hormone value of > 40 IU/L after 2
216 onths, and/or oophorectomy, and/or increased follicle-stimulating hormone values for reproductive-age
217 ng for the aromatase and the receptor of the follicle stimulating hormone were higher in contaminated
218 eir plasma levels of luteinizing hormone and follicle stimulating hormone were inappropriately low.
219 diol, progesterone, luteinizing hormone, and follicle-stimulating hormone were measured in serum up t
220 diol, progesterone, luteinizing hormone, and follicle-stimulating hormone were measured up to 8 times
221 sing hormone (GnRH) agonists and recombinant follicle-stimulating hormone were studied prospectively.
222 (human leutinizing hormone) and hFSH (human follicle stimulating hormone) were > 1 microM and approx
223 ost of patients (93%) had abnormal values of follicle-stimulating hormone, whereas the number of pati
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