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1 es on the day of induction of ovulation with human chorionic gonadotropin.
2 diated by high circulating concentrations of human chorionic gonadotropin.
3 ty associated with the beta-core fraction of human chorionic gonadotropin.
4 or estrogen and progesterone metabolites and human chorionic gonadotropin.
5 h weekly levels of estrone-3-glucuronide and human chorionic gonadotropin.
7 pregnant mare serum gonadotropin followed by human chorionic gonadotropin also stimulated cumulus exp
8 administration of exogenous testosterone or human chorionic gonadotropin (an LH receptor agonist), r
9 ased on an increased blood level of the beta human chorionic gonadotropin and a histopathological exa
10 mg per day on days 1, 8, and 15]), patients' human chorionic gonadotropin and alfa-fetoprotein concen
12 ght to be induced by two placental hormones: human chorionic gonadotropin and human chorionic somatot
13 were significantly, directly associated with human chorionic gonadotropin and inversely with estrone-
15 nt of two maternal serum hormones, free beta-human chorionic gonadotropin and pregnancy-associated pl
16 n maternal age, maternal levels of free beta human chorionic gonadotropin and pregnancy-associated pl
17 f maternal age, maternal levels of free beta human chorionic gonadotropin and pregnancy-associated pl
18 gically, biochemically (by the production of human chorionic gonadotropin and progesterone), and immu
23 edent pregnancy, serum concentration of beta-human chorionic gonadotropin, and stage of disease, with
24 cosylated protein domains (F(c)) of two anti-human chorionic gonadotropin antibodies were proteolytic
25 elopment of effective treatments, the use of human chorionic gonadotropin as a biomarker, and central
26 ot confirm the primary site and the level of human chorionic gonadotropin as independent factors.
27 ein A [PAPP-A], and the free beta subunit of human chorionic gonadotropin at 10 weeks 3 days through
29 recognizes the GVL peptide (GVLPALPQV) from human chorionic gonadotropin beta presented by the pepti
32 intracellular kinetic folding pathway of the human chorionic gonadotropin beta-subunit (hCG-beta) rev
33 g ability to secretion and assembly with the human chorionic gonadotropin beta-subunit (hCG-beta).
34 n choriocarcinoma that was confirmed by beta human chorionic gonadotropin (beta-HCG) levels and histo
35 e assessed for four mRNA tumor markers: beta-human chorionic gonadotropin (beta-hCG), oncogene recept
36 ative serum alpha-fetoprotein (AFP) and beta-human chorionic gonadotropin (betaHCG) levels were 483 n
37 ligand signaling despite moderate levels of human chorionic gonadotropin binding in transfected cell
38 vivo, treatment with a desensitizing dose of human chorionic gonadotropin caused transcriptional down
39 odimers, which include the placental hormone human chorionic gonadotropin (CG) and the anterior pitui
41 chimeric glycoprotein substrates by agalacto human chorionic gonadotropin, comprising 29 nM for beta4
42 of mutant receptors and is dependent on the human chorionic gonadotropin dose, the surface concentra
43 leptin, cortisol, and reproductive hormones (human chorionic gonadotropin, estradiol, progesterone, h
44 rning urine samples were collected to assess human chorionic gonadotropin, estrone-3-glucuronide, and
45 ciated pre-mRNA encoding the beta-subunit of human chorionic gonadotropin gene 6 and pre-trans-splici
46 lines of prior therapy (P < .001), baseline human chorionic gonadotropin > or = 1,000 U/L (P = .01),
47 sk disease at the time of GCT diagnosis, and human chorionic gonadotropin >/= 1,000 mIU/mL at initiat
48 ultrasonography and sensitive tests for beta-human chorionic gonadotropin have evolved, the presentat
49 kers were alpha-fetoprotein (AFP) 2.0 ng/mL, human chorionic gonadotropin (hCG) 151,111 IU/L, and lac
50 multiple preovulatory follicles, followed by human chorionic gonadotropin (hCG) administration (day 0
52 cribe chimeras of two glycoprotein hormones, human chorionic gonadotropin (hCG) and human follitropin
53 nesis by adrenocorticotropic hormone (ACTH), human chorionic gonadotropin (hCG) and oestrogen, and in
55 e immunoassays for two model cancer markers, human chorionic gonadotropin (hCG) and prostate specific
62 ational trophoblastic disease include raised human chorionic gonadotropin (hCG) concentrations 6 mont
63 ntly, we proposed that the pregnancy hormone human chorionic gonadotropin (hCG) efficiently attracts
65 examined by univariate analysis; only serum human chorionic gonadotropin (HCG) had an impact on surv
68 onadotropin-releasing hormone (GnRH) gene by human chorionic gonadotropin (hCG) in GT1-7 neurons.
71 omas in immune-compromised mice that secrete human chorionic gonadotropin (hCG) into the host mouse a
77 obably down-regulated at about the time that human chorionic gonadotropin (hCG) is first expressed in
79 ting studies do not establish a single serum human chorionic gonadotropin (hCG) level that is diagnos
80 ects of clinical grade crude preparations of human chorionic gonadotropin (hCG) on Kaposi's sarcoma,
90 cinoma on the basis of persistently positive human chorionic gonadotropin (hCG) test results in the a
92 GRTH gene transcription is stimulated by human chorionic gonadotropin (hCG) via cyclic AMP-induce
93 t drug resistance to EMA/CO, and because the human chorionic gonadotropin (hCG) was near normal, they
95 s on a rat breast cancer model indicate that human chorionic gonadotropin (hCG), a hormone that is pr
98 hich recognizes both luteinizing hormone and human chorionic gonadotropin (hCG), as the tissue-specif
99 markers, human C-reactive protein (CRP) and human chorionic gonadotropin (hCG), by using fluorescent
100 various pregnancy-related hormones including human chorionic gonadotropin (hCG), estrogen, progestero
101 ococci express a surface feature that mimics human chorionic gonadotropin (hCG), the cognate ligand f
102 rum alpha-fetoprotein, unconjugated estriol, human chorionic gonadotropin (hCG), the free beta subuni
103 Furthermore, using the mediator molecule human chorionic gonadotropin (hCG), we interface the int
110 ring three markers (alpha-fetoprotein [AFP], human chorionic gonadotropin [hCG], and lactate dehydrog
111 EREG, and the intracellular beta subunit of human chorionic gonadotropin (hCGbeta) and peroxisome pr
112 scent detection of three markers: beta-chain human chorionic gonadotropin, hepatocyte growth factor r
113 samples and real immunorecognition assays of human chorionic gonadotropin hormone are well below the
114 ection of a set of three fertility hormones: human chorionic gonadotropin, human luteinizing hormone,
115 irole and stimulation of cAMP synthesis with human chorionic gonadotropin in cells transfected with e
116 n alone in three, alpha-fetoprotein and beta human chorionic gonadotropin in one) suffered a relapse,
117 h the chimeric receptor could not respond to human chorionic gonadotropin in producing cAMP, co-expre
119 an be pharmacologically rescued by exogenous human chorionic gonadotropin, indicating that LH-respons
121 dicated that age, preceding pregnancy event, human chorionic gonadotropin level, World Health Organiz
124 Point mutations in the luteinizing hormone/human chorionic gonadotropin (LH/hCG) receptor have been
125 d with the regulation of luteinizing hormone/human chorionic gonadotropin (LH/hCG) receptor mRNA stab
129 ts had increased alpha fetoprotein (n = 18), human chorionic gonadotropin (n = 5), or both (n = 2); n
130 engineered hCG-SNAP fusion reporter protein (human chorionic gonadotropin-O(6) -alkylguanine-DNA alky
131 ha-fetoprotein of 100 ng/mL or greater or of human chorionic gonadotropin of 5,000 U/L or greater (gr
132 clinical evidence and highly elevated serum human chorionic gonadotropin or alfa-fetoprotein concent
133 4 of them either after the administration of human chorionic gonadotropin or during the physiologic r
135 were used to bind the glycoprotein hormone, human chorionic gonadotropin, produced during normal pre
136 and, over time, produce extensive amounts of human chorionic gonadotropin, progesterone, placental gr
138 alpha-helix (TM3) of the luteinizing hormone/human chorionic gonadotropin receptor (LH/hCGR) in regul
140 metry assay) was inhibited by 57 %, and both human chorionic gonadotropin secretion and L-leucine inf
141 -derived CTBs in low oxygen leads to reduced human chorionic gonadotropin secretion and STB-associate
144 failure was defined as a negative serum beta-human chorionic gonadotropin test (beta-hCG < 6 IU/L) 17
145 rual period, and a combination of a positive human chorionic gonadotropin test and an outpatient obst
146 ictive of a pregnancy outcome was a positive human chorionic gonadotropin test; least predictive was
148 ased on a modified commercial strip test for human chorionic gonadotropin, the hormone used to detect
149 nsulin acts independently or additively with human chorionic gonadotropin to enhance androstenedione
150 ing (measurement of alpha-fetoprotein, total human chorionic gonadotropin, unconjugated estriol, and
151 and apply this platform to the detection of human chorionic gonadotropin using surface plasmon reson
152 rine specimens for up to 1 year, and urinary human chorionic gonadotropin was assayed to detect conce
156 Histologic subtype and increase of beta-human chorionic gonadotropin were not significantly corr
157 ved at low micromolar concentrations of hCG (human chorionic gonadotropin), while measured Kd values
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