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1                                              Tuberoinfundibular DA neuronal activity was estimated by
2 effect of prolactin on the basal activity of tuberoinfundibular DA neurons in females occurs via a ce
3 es the stimulatory effects of haloperidol on tuberoinfundibular DA neurons, and reveal that delayed i
4 ne the effects of acute hypoprolactinemia on tuberoinfundibular dopamine (DA) neurons using a rabbit
5                                              Tuberoinfundibular dopamine (TIDA) neurons are the centr
6            Tyrosine hydroxylase (TH) mRNA in tuberoinfundibular dopamine (TIDA) neurons is suppressed
7  hormone prolactin is tonically inhibited by tuberoinfundibular dopamine (TIDA) neurons located in th
8 ion of Fos and its related antigens (FRA) in tuberoinfundibular dopamine (TIDA) neurons located in th
9 lly under tonic inhibition by neuroendocrine tuberoinfundibular dopamine (TIDA) neurons of the arcuat
10 s primarily under monoaminergic control, via tuberoinfundibular dopamine (TIDA) neurons projecting to
11 h a central role in puerperal changes is the tuberoinfundibular dopamine (TIDA) neurons that control
12                                              Tuberoinfundibular dopamine (TIDA) neurons, known as neu
13 ishes phasic discharge in rat neuroendocrine tuberoinfundibular dopamine (TIDA) neurons, the main inh
14 lactin secretion, directly or indirectly via tuberoinfundibular dopamine neurons.
15 receptor-mediated activation of hypothalamic tuberoinfundibular dopaminergic (TIDA) neurons occurs vi
16 RL) stimulates release of dopamine (DA) from tuberoinfundibular dopaminergic (TIDA) neurons.
17 oids on regulation of the release of DA from tuberoinfundibular dopaminergic (TIDA), tuberohypophysea
18 d in the labeling of 40% of hypophysiotropic tuberoinfundibular dopaminergic (tyrosine hydroxylase-po
19  and express CRH receptors; most notable are tuberoinfundibular dopaminergic neurons (TIDA).
20 ophyseal dopaminergic neurons, while leaving tuberoinfundibular dopaminergic neurons and the vascular
21 ss may activate the kappa opioid receptor on tuberoinfundibular dopaminergic neurons to increase circ
22 rough direct projections to GnRH neurons and tuberoinfundibular dopaminergic neurons.
23              Similar changes occurred in the tuberoinfundibular GABAergic (TIGA) neurons projecting t
24 ptide, orexins, prolactin-releasing peptide, tuberoinfundibular peptide 39 and neuropeptide B and W)
25                                              Tuberoinfundibular peptide of 39 residues (TIP39) and th
26          Deficiencies in PTH2R or its ligand tuberoinfundibular peptide of 39 residues (TIP39) delaye
27 f the thalamus that contain the neuropeptide tuberoinfundibular peptide of 39 residues (TIP39) densel
28  recently identified natural peptide ligand, tuberoinfundibular peptide of 39 residues (TIP39) for th
29                                              Tuberoinfundibular peptide of 39 residues (TIP39) has be
30                                              Tuberoinfundibular peptide of 39 residues (TIP39) is a l
31                                              Tuberoinfundibular peptide of 39 residues (TIP39) is a s
32                                              Tuberoinfundibular peptide of 39 residues (TIP39) select
33                                              Tuberoinfundibular peptide of 39 residues (TIP39) was id
34  second receptor (PTH2R) and its ligand, the tuberoinfundibular peptide of 39 residues (TIP39), in th
35 oral evidence suggests that the neuropeptide tuberoinfundibular peptide of 39 residues (TIP39), via i
36 crine dopaminergic neurons (NDNs) designated tuberoinfundibular (TIDA), tuberohypophyseal (THDA) and