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1 is regulated by oxytocin, a highly conserved neurohormone.
2 s as a neurotransmitter, neuromodulator, and neurohormone.
3 ion of serotonin to melatonin, the circadian neurohormone.
4 eactive and appear to release YXFGLamides as neurohormones.
5 hed from spiking to bursting by hypothalamic neurohormones.
6 nts that unload the heart or target systemic neurohormones.
7 of N-linked glycoproteins and peptides, like neurohormones.
8 tion of the peptides that dominate among the neurohormones.
9 and may be released into the blood to act as neurohormones.
10 ation of selective neural circuits by opioid neurohormones.-
11  a neuroactive monoamine that functions as a neurohormone, a neuromodulator, and a neurotransmitter i
12 present study suggests that CRF actions as a neurohormone and as a neurotransmitter in the LC may be
13                                         As a neurohormone and as a neurotransmitter, oxytocin has bee
14  is achieved by a complex array of potential neurohormones and light-sensing molecules.
15 naling molecules, such as neurotransmitters, neurohormones and neuropeptides.
16 ew studies supporting the mediating roles of neurohormones and neurotransmitters (e.g., cortisol, nor
17 nins) are multifunctional peptides acting as neurohormones and neurotransmitters.
18 We examined levels of monoamine metabolites, neurohormones, and neuropeptides in the cerebrospinal fl
19 n protects against pathological responses to neurohormones, and sustained pressure-overload stress.
20                               In addition to neurohormones, another portfolio of biologically active
21 y it has become apparent that in addition to neurohormones, another portfolio of biologically active
22 changes in synthesis and/or release of these neurohormones are central to moult control.
23                                              Neurohormones are considered markers of heart failure pr
24       In the female mosquito, Aedes aegypti, neurohormones are released from the brain in response to
25 ions of a neuron where neurotransmitters and neurohormones are released.
26 ase at neurohypophysial nerve terminals, the neurohormones arginine vasopressin (aVP) and oxytocin (O
27 nce of biologically active molecules such as neurohormones as mediators of disease progression in hea
28 emands on periodically voluminous release of neurohormones at the interface of axon terminals and vas
29              Administration of the pituitary neurohormones B-endorphin or Arg-vasopressin-induced sid
30 ranscription factor; galanin, a hypothalamic neurohormone; BAX, a proapoptotic signaling factor; and
31 m the CNS and appears to be identical to the neurohormone bombyxin, a member of the insulin family of
32 ediately after shedding the old cuticle, the neurohormone bursicon causes the hardening and darkening
33 he mechanisms have remained enigmatic is the neurohormone bursicon, which, after the final molt, coor
34     In an attempt to identify this important neurohormone, bursicon was purified from homogenates of
35           In Aedes aegypti, the antidiuretic neurohormone CAPA inhibits secretion by MTs stimulated b
36  between melatonin--a scotoperiod-responsive neurohormone closely tied to seasonal adaptation--and do
37 reasing putative pulse-time sets for a given neurohormone concentration time series; and then, recurs
38   Here, we determined the role of the stress neurohormone corticotropin-releasing factor (CRF) in str
39  Previous studies have found that the stress neurohormone corticotropin-releasing factor (CRF) inhibi
40 ated by fibers containing the stress-related neurohormone corticotropin-releasing factor (CRF), which
41 locked by antagonists for the stress-related neurohormone corticotropin-releasing factor (CRF).
42 gh a central action of the stress-associated neurohormone corticotropin-releasing factor (CRF).
43  suppression of the expression of the stress neurohormone corticotropin-releasing hormone (CRH) in hy
44                           The stress-related neurohormone, corticotropin-releasing factor (CRF), also
45 Because adrenalectomy also alters release of neurohormone CRF, the present study suggests that CRF ac
46 ogical mediators of cardiac hypertrophy (eg, neurohormones, cytokines, and stretch) have been shown t
47 anosensory neurons in C. elegans release the neurohormone dopamine to promote proteostasis in epithel
48  delivered neurotransmitters and circulating neurohormones elicit a wide range of rhythmic motor outp
49                                  The peptide neurohormone endothelin-1, which elevates diacylglycerol
50 ors and are mimicked by the actions of other neurohormones (endothelin, prostaglandin F(2alpha) angio
51                   Dysregulation of leptin, a neurohormone essential to energy homeostasis, is implica
52 ated peptides are multifunctional regulatory neurohormones found in invertebrates.
53  imply a novel clearance route for drugs and neurohormones from the CSF.
54  systems for probing nonclassical, ancestral neurohormone functions.
55 ion, including cardiovascular diseases, age, neurohormones, genetics, diet, autonomic influences, and
56 riguing consensus that a single hypothalamic neurohormone, gonadotropin-releasing hormone (GnRH), reg
57       Although the circulating level of this neurohormone has been shown to provide independent progn
58 ubject to modulation by neurotransmitters or neurohormones has not been clear.
59 mber of other clinical applications for this neurohormone have emerged.
60                   This review focuses on how neurohormones impact on human skin physiology and pathol
61                 Bursicon, a highly conserved neurohormone implicated in regulation of these processes
62 ortant neurotransmitter, neuromodulator, and neurohormone in insects.
63          Neuropeptide Y (NPY) is an abundant neurohormone in the central and peripheral nervous syste
64 beta-PDHs; Canpr-beta-PDH II appears to be a neurohormone in the SG, whereas Canpr-beta-PDH I may fun
65          Many neuroendocrine neurons release neurohormones in long-duration bursts of secretion.
66 e as neurotransmitters, neuromodulators, and neurohormones in the brain.
67 ance of biologically active molecules (e.g., neurohormones) in disease progression in heart failure.
68 for monogenic amine synthesis and of several neurohormones, including pigment-dispersing factor, vaso
69 rving as the site of release of hypothalamic neurohormones into a plexus of hypophyseal capillaries.
70                               Melatonin is a neurohormone involved in the regulation of circadian rhy
71 ations for how various neuroactive drugs and neurohormones known to modulate extrasynaptic GABA(A) re
72 ncluded changes in exercise capacity, plasma neurohormones, left ventricular function, and overall HF
73       Serum samples, clinical variables, and neurohormone levels from the PRAISE-2 heart failure tria
74              BACKGROUND; Elevated vasoactive neurohormone levels in chronic HF have adverse prognosti
75                                Peak exercise neurohormone levels were unchanged in the training group
76                     Reduction in circulating neurohormones may have a beneficial impact on long-term
77  tumor necrosis factor alpha), much like the neurohormones, may represent another class of biological
78 t suggests that the cytokines, much like the neurohormones, may represent another class of biological
79                          Melatonin, a pineal neurohormone, mediates circadian and seasonal processes
80                              Inasmuch as the neurohormone melatonin is synthetically derived from ser
81 tylserotonin, the precursor of the circadian neurohormone melatonin, is catalyzed by serotonin N-acet
82 ands on exocytotic release; large amounts of neurohormone need to be secreted into the portal capilla
83              Human skin responds to numerous neurohormones, neuropeptides, and neurotransmitters that
84 onadotropin-releasing hormone [GnRH]), a key neurohormone of reproduction.
85 ies designed to reverse the effects of these neurohormones on the kidney have so far had limited succ
86 to Aedes aegypti triggers the release of two neurohormones, ovary ecdysteroidogenic hormone (OEH) and
87 s of heart failure M&M, but changes in these neurohormones over time are associated with correspondin
88                                          The neurohormone oxytocin is a key player in the modulation
89                         Over 20 years ago, a neurohormone, pheromone biosynthesis activating neuropep
90  of heart failure, we examined whether these neurohormones predicted all-cause mortality, cardiovascu
91 okine macrophage migration inhibitory factor neurohormone receptors such as growth hormone- releasing
92 ls in response to forskolin or activation of neurohormone receptors.
93                   These results suggest that neurohormone release from intrapancreatic neurons could
94                         To determine whether neurohormone release within the pancreas might play a ro
95 g four ion channel conductances critical for neurohormone release.
96                        Bursicon is the final neurohormone released at the end of the molting cycle.
97                               Melatonin is a neurohormone released in a circadian manner with peak le
98  understanding of the precise roles of these neurohormones remains rudimentary.
99                     There were no changes in neurohormones, renal function, or troponin I.
100 statistical estimation of unobserved in vivo neurohormone secretion and within-axis, dose-responsive
101                        In separated systems, neurohormone signals act deterministically on target cel
102                                         Many neurohormones stimulate phospholipid hydrolysis and elev
103 ween the 4 anatomic subgroups and any of the neurohormones studied.
104 nd glutamatergic pathways, the expression of neurohormones (such as isotocin) and steroids (e.g. prog
105  induction of oxidative stress transduced by neurohormones, such as angiotensin II and catecholamines
106      Brain (B-type) natriuretic peptide is a neurohormone synthesized predominantly in ventricular my
107 y the coordinated actions of several peptide neurohormones, tachykinin among them.
108      Prolactin (PRL) is a female-predominant neurohormone that is controlled by estrogen and stress.
109 elatonin (N-acetyl-5-methoxytryptamine) is a neurohormone that maintains circadian rhythms(1) by sync
110 he modulatory effects of melatonin, a pineal neurohormone that mediates circadian and seasonal proces
111 veness of gastric vagal afferents to several neurohormones, the aim of the present study was to deter
112 of the Drosophila FMRFamide gene function as neurohormones to modulate the strength of contraction at
113 nse to environmental stressors, whereas, the neurohormone tyramine, which is released during the acut
114 cicotropic hormone and eclosion hormone, two neurohormones under circadian control.
115 fter modification, the cDNA for the putative neurohormone was expressed in a bacterial system, and th
116                                              Neurohormones were measured at study entry and after 16
117 nephrine was superior (P=0.02) and all other neurohormones were similar (P<0.34) during the empaglifl
118 icroorganisms have evolved systems for using neurohormones, which are widely distributed throughout n

 
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