ライフサイエンスコーパス: medial preoptic nucleus

1 ced correlated positively with pTH-ir in the medial preoptic nucleus.

2 pulation of POMC neurons that project to the medial preoptic nucleus.

3 bed nucleus of the stria terminalis and the medial preoptic nucleus.

4 ical signature of estrogen activation of the medial preoptic nucleus.

5 Neurons in these areas project to the medial preoptic nucleus.

6 ing pDARPP-32 immunoreactivity by 92% in the medial preoptic nucleus, 134% in the caudal ventromedial

7 opioid receptor (MOR) internalization in the medial preoptic nucleus, an important step for full expr

8 RNA expression in the central portion of the medial preoptic nucleus and posterodorsal medial amygdal

9 to regulate motivation and reward (i.e., the medial preoptic nucleus and ventral tegmental area) rela

10 Steroid regulation of OFQ/N and NOP in the medial preoptic nucleus and VMH is consistent with emerg

11 II fibers included the ventromedial nucleus, medial preoptic nucleus, and ventral premammillary nucle

12 Castration reduced PRir in males' medial preoptic nucleus, anteroventral periventricular n

13 ng sympathetic pathway appears to target the medial preoptic nucleus as its key nodal point, receivin

14 nkephalin (DAMGO) or endomorphin-1, into the medial preoptic nucleus attenuated lordosis, and their e

15 containing neurons were most abundant in the medial preoptic nucleus, bed nucleus of the stria termin

16 In the medial preoptic nucleus (central aspect) and ventromedia

17 raventricular nucleus; reproductive: lateral medial preoptic nucleus; defensive: anterior hypothalami

18 r predominantly in the posterior PVN; and 3) medial preoptic nucleus-derived inputs to the PVN are no

19 nalis, medial and lateral preoptic areas and medial preoptic nucleus), diencephalon (viz., subincerta

20 tria terminalis, ventral aspect (INSTv), the medial preoptic nucleus, dorsomedial aspect (MPNdm) and

21 increase, whereas, in the medial part of the medial preoptic nucleus, estrogen and progesterone were

22 d estradiol-induced activation of MOR in the medial preoptic nucleus, leading to female sexual recept

23 ed during maternal aggression, including the medial preoptic nucleus (likely to represent an importan

24 f time of day or day of estrous cycle in the medial preoptic nucleus, median eminence, ventromedial n

25 eling was found in the medial preoptic area, medial preoptic nucleus, median preoptic nucleus, and la

26 vasculosum of the lamina terminalis (OVLT), medial preoptic nucleus (MNPO), subfornical organ (SFO),

27 The magnocellular division of the medial Preoptic nucleus (MPN mag) plays a critical role

28 c area, the magnocellular subdivision of the medial preoptic nucleus (MPN mag).

29 phosphorylated PAK1 immunoreactivity in the medial preoptic nucleus (MPN) but not the arcuate nucleu

30 The medial preoptic nucleus (MPN) of the medial preoptic are

31 gestin receptor (PR) immunoreactivity in the medial preoptic nucleus (MPN) of the rat brain is due to

32 nteroventral periventricular nucleus (AVPV), medial preoptic nucleus (MPN), arcuate nucleus (ARH), an

33 here that a select subset of neurons in the medial preoptic nucleus (MPN), lateral hypothalamic area

34 re lower levels of V(1a)R binding within the medial preoptic nucleus (MPN), medial preoptic area (MPO

35 and AR-ir were colocalized in neurons of the medial preoptic nucleus (MPN), the dorsal medial amygdal

36 nucleus of the stria terminalis (BNST), the medial preoptic nucleus (MPN), the ventromedial nucleus

37 zation of mu-opioid receptors (MORs), in the medial preoptic nucleus (MPN).

38 hase immunoreactive (bNOS-ir) neurons in the medial preoptic nucleus (MPN).

39 eus [AVPV], median preoptic area [MePO], and medial preoptic nucleus [MPN]), at young (3 months), mid

40 nt oSDN occupies the central division of the medial preoptic nucleus (MPNc) and consists of a cluster

41 of the SDN-POA, the central division of the medial preoptic nucleus (MPNc), over the first 13 days p

42 and the central and medial divisions of the medial preoptic nucleus (MPNc, MPNm, respectively) revea

43 os co-localization in the medial part of the medial preoptic nucleus (MPNm), where half of the neuron

44 stimulate the magnocellular division of the medial preoptic nucleus of castrates.

45 Stimulation of the medial preoptic nucleus of the hypothalamus (MPO) has be

46 ustrum, bed nucleus of the stria terminalis, medial preoptic nucleus, paraventricular nucleus, medial

47 leus, anteroventral periventricular nucleus, medial preoptic nucleus, paraventricular nucleus, suprac

48 iors occur in a variety of mammals, with the medial preoptic nucleus (POM) and the ventromedial hypot

49 abeling for the opioid met-enkephalin in the medial preoptic nucleus (POM) correlates positively with

50 The sexually dimorphic medial preoptic nucleus (POM) in Japanese quail has for

51 ere denser in several regions, including the medial preoptic nucleus (POM) in low singing males.

52 We show here that T implants in the medial preoptic nucleus (POM) of castrated male canaries

53 The medial preoptic nucleus (POM) regulates male sexual beha

54 n of sexual behavior, including in quail the medial preoptic nucleus (POM).

55 d for >24 hr after estrogen treatment in the medial preoptic nucleus, the principal part of the bed n

56 rulline-positive cells was identified in the medial preoptic nucleus, the suprachiasmatic nucleus, an

57 iveness of the magnocellular division of the medial preoptic nucleus to pheromones.

58 (MeA), bed nucleus of the stria terminalis, medial preoptic nucleus, ventrolateral portion of the ve

59 A projection from the BSTp to the medial preoptic nucleus was also weaker in females but w

60 us of the stria terminalis (BNST) and to the medial preoptic nucleus, whereas MeA projects to adjacen