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1 g orexin, melanin-concentrating hormone, and luteinizing hormone-releasing hormone.
2 steroid ablation using leuprolide acetate, a luteinizing hormone-releasing hormone agonist (LHRHa), i
3 d) (PLGA) microspheres encapsulating a model luteinizing hormone-releasing hormone agonist (LHRHa)-ba
5 AST, which was defined as 6 months of both a luteinizing hormone-releasing hormone agonist and an ant
6 ts receiving combined androgen blockade with luteinizing hormone-releasing hormone agonist and bicalu
7 t/aromatase inhibitor per local guidelines (+luteinizing hormone-releasing hormone agonist in pre-/pe
9 les, followed by total androgen suppression (luteinizing hormone-releasing hormone agonist plus bical
10 raterone 1 g daily plus prednisone 10 mg and luteinizing hormone-releasing hormone agonist until prog
11 tients were randomized soon after initiating luteinizing hormone-releasing hormone agonist with antia
12 n deprivation (AD) to cixutumumab added to a luteinizing hormone-releasing hormone agonist with bical
13 S; two injections of every-3-months depot of luteinizing hormone-releasing hormone agonist) to primar
14 Patients were randomly assigned 2:1 to a luteinizing hormone-releasing hormone agonist, bicalutam
15 (arm 1) or RT plus TAS (arm 2) consisting of luteinizing hormone-releasing hormone agonist/antagonist
21 ; and three, when chemical suppression using luteinizing hormone-releasing hormone agonists is the ch
23 ombesin (AN-215), somatostatin (AN-238), and luteinizing hormone-releasing hormone (AN-207) consisted
25 state cancer were performed before and after luteinizing hormone-releasing hormone analog treatment.
26 of 5 ng per milliliter or higher received a luteinizing hormone-releasing hormone analogue and an an
28 All patients underwent administration of the luteinizing hormone-releasing hormone antagonist degarel
30 the delivery of targeted therapeutic agents [Luteinizing Hormone-Releasing Hormone conjugated paclita
31 Hormone conjugated paclitaxel (PTX-LHRH) and Luteinizing Hormone-Releasing Hormone conjugated prodigi
32 in, corticotropin-releasing factor, galanin, luteinizing hormone-releasing hormone, enkephalin, subst
34 rporation into targeted cytotoxic analogs of luteinizing hormone-releasing hormone intended for cance
35 odoxorubicin (AN-201) conjugated to [D-Lys6] luteinizing hormone-releasing hormone (LH-RH) (AN-207),
36 ound that the t(1/2) of AN-152, an analog of luteinizing hormone-releasing hormone (LH-RH) containing
38 bit nitric oxidergic (NOergic) activation of luteinizing hormone-releasing hormone (LH-RH) release fr
39 eloped a targeted cytotoxic analog AN-207 of luteinizing hormone-releasing hormone (LH-RH), consistin
40 152, a conjugate of doxorubicin and [D-Lys6]-luteinizing hormone-releasing hormone (LH-RH), is more p
43 synthesis, is involved in the suppression of luteinizing hormone releasing hormone (LHRH) before pube
44 favorable for the release of a neuropeptide, luteinizing hormone releasing hormone (LHRH) from these
46 n of prostaglandin E2, which then stimulates luteinizing hormone releasing hormone (LHRH) neurons to
47 dy single-chain variable fragment (scFv) and luteinizing hormone releasing hormone (LHRH) peptide, re
51 n releasing hormone-1 [GnRH-1, also known as luteinizing hormone releasing hormone (LHRH)] neurons ca
52 Previously, we have shown that two types of luteinizing hormone-releasing hormone (LHRH) -like neuro
53 The effects of depot formulations of the luteinizing hormone-releasing hormone (LHRH) agonist Dec
55 orticotropic hormone (ACTH) and hypothalamic luteinizing hormone-releasing hormone (LHRH) agonist, [D
57 the recent developments on BPH therapy with luteinizing hormone-releasing hormone (LHRH) antagonist
58 tance and (5) a modified synthetic analog of luteinizing hormone-releasing hormone (LHRH) as a target
59 gs (prodigiosin or paclitaxel) conjugated to Luteinizing Hormone-Releasing Hormone (LHRH) for the spe
62 ergic expression coincides with migration of luteinizing hormone-releasing hormone (LHRH) neurons fro
63 id (GABAergic) synaptic input onto embryonic luteinizing hormone-releasing hormone (LHRH) neurons mai
68 uropeptide Y (NPY) potentiates the effect of luteinizing hormone-releasing hormone (LHRH) on luteiniz
70 To investigate the possibility that a second luteinizing hormone-releasing hormone (LHRH) population
72 To understand the mechanism of pulsatile luteinizing hormone-releasing hormone (LHRH) release, we
73 low doses (5-30 nM) induced large amounts of luteinizing hormone-releasing hormone (LHRH) release, wh
74 implicated in the neuroendocrine control of luteinizing hormone-releasing hormone (LHRH) secretion a
75 estigate the mechanism by which Mn2+ induces luteinizing hormone-releasing hormone (LHRH) secretion f
76 s by which the neuroendocrine brain controls luteinizing hormone-releasing hormone (LHRH) secretion.
78 large doses of Cetrorelix, an antagonist of luteinizing hormone-releasing hormone (LHRH), reduces le
79 naling pathway that prompts the secretion of luteinizing hormone-releasing hormone (LHRH), the neurop
80 osecretory neurons to stimulate secretion of luteinizing hormone-releasing hormone (LHRH), the neurop
81 ure activation of those neurons that produce luteinizing hormone-releasing hormone (LHRH), the neurop
82 t of norepinephrine (NE) on the secretion of luteinizing hormone-releasing hormone (LHRH), the neurop
85 ng afferent pathways to neurons synthesizing luteinizing hormone-releasing hormone (LHRH, also known
86 (68)Ga-PSMA-11 PET imaging in hormone-naive (luteinizing hormone-releasing hormone [LHRH] +/- bicalut
87 itive tumors also received letrozole (plus a luteinizing hormone-releasing hormone [LHRH] agonist if
88 diation plus immediate androgen suppression (luteinizing hormone-releasing hormone [LHRH] agonist), w
89 that FSHRF might be an analogue of mammalian luteinizing hormone-releasing hormone (m-LHRH) and evalu
91 k suggests that cytotoxic peptide analogs of luteinizing hormone-releasing hormone, somatostatin, and
92 s monotherapy or with adjuvant castration or luteinizing hormone-releasing hormone superagonists to b