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1 rons in the ventrolateral subdivision of the ventromedial nucleus.
2 rons of the ventrolateral subdivision of the ventromedial nucleus.
3 detected in leptin-responsive neurons in the ventromedial nucleus.
4 ent of estrogen directly in the hypothalamic ventromedial nucleus.
5 localized to the dorsomedial division of the ventromedial nucleus.
6 nigra and individual nuclei in the thalamus (ventromedial nucleus, 21.3%; central lateral, 18.4%; par
7 Functionally, silencing of ERalpha in the ventromedial nucleus abolished female proceptive and rec
9 stradiol increased GABA and glutamate in the ventromedial nucleus and the vertical diagonal bands.
10 ed a similar pattern of labelling within the ventromedial nucleus and within neurons of the ventrolat
11 ns were found in the dorsomedial area of the ventromedial nucleus, and 76% of them expressed the mRNA
12 nd is detectable in the arcuate nucleus, the ventromedial nucleus, and the dorsomedial nucleus of the
13 containing neurons were most numerous in the ventromedial nucleus, arcuate nucleus, and tuberomamilla
14 s, MCHR mRNA was moderately expressed in the ventromedial nucleus, arcuate nucleus, and zona incerta,
15 ia terminalis; ventrolateral division of the ventromedial nucleus; arcuate nucleus; anterior paravent
16 herefore, COUP-TFII expression levels in the ventromedial nucleus are keys in the ability to resist t
17 lar nucleus, the dorsomedial nucleus and the ventromedial nucleus as well as the region lateral to th
18 rons in the ventrolateral subdivision of the ventromedial nucleus contained both NADPH diaphorase and
19 ed with VGluT2 immunolabeling showed that 1) ventromedial nucleus-derived glutamatergic inputs occur
21 entromedial hypothalamus (VMH) (arcuate plus ventromedial nucleus) glucosensing neurons as potential
22 jection of this vector into the hypothalamic ventromedial nucleus in ovariectomized female mice, expr
23 atively, little astrogliosis was seen in the ventromedial nucleus, lateral hypothalamus, or anterior
24 d prominently by Ucn III fibers included the ventromedial nucleus, medial preoptic nucleus, and ventr
25 riaqueductal gray), the locus coeruleus, the ventromedial nucleus of hypothalamus, the septum and the
26 ween the sexes in the preoptic area (POA) or ventromedial nucleus of the amygdala (AMY), two brain re
28 09 also increased cFOS immunolabeling in the ventromedial nucleus of the hypothalamus (VMH) at the sa
29 d the expression of GABA(B) receptors in the ventromedial nucleus of the hypothalamus (VMH) during em
31 rons was significantly increased only in the ventromedial nucleus of the hypothalamus (VMH) in these
36 females on day 2 of pregnancy; levels in the ventromedial nucleus of the hypothalamus (VMH) were unch
37 is response is modulated by OT action in the ventromedial nucleus of the hypothalamus (VMH), as demon
41 mRNA levels in the ventrolateral part of the ventromedial nucleus of the hypothalamus (VMHVL), an are
42 natomical level, the preoptic area (POA) and ventromedial nucleus of the hypothalamus (VMN) are the f
43 E increased oxytocin receptor binding in the ventromedial nucleus of the hypothalamus (VMN) in the ab
44 htened electrical activity of neurons in the ventromedial nucleus of the hypothalamus (VMN) is necess
46 oestrous rats with bilateral cannulae in the ventromedial nucleus of the hypothalamus (VMN) were infu
47 ar formation, periaqueductal gray (PAG), and ventromedial nucleus of the hypothalamus (VMN) were sequ
48 200 ng per bilateral site) infused into the ventromedial nucleus of the hypothalamus (VMN), inhibite
50 tomized rats, with bilateral implants in the ventromedial nucleus of the hypothalamus (VMN), were hor
51 with bilateral cannulae directed toward the ventromedial nucleus of the hypothalamus (VMN), were hor
52 (CDF-344) with bilateral implants within the ventromedial nucleus of the hypothalamus (VMN), were inj
59 eoptic nucleus, ventrolateral portion of the ventromedial nucleus of the hypothalamus (VMN-VL) in mal
60 sex, had more cells than subordinates in the ventromedial nucleus of the hypothalamus and a larger vo
61 notable exceptions including lateral septum, ventromedial nucleus of the hypothalamus and cingulate g
62 tantia nigra (P < 0.05) and decreased in the ventromedial nucleus of the hypothalamus and the CA1 reg
63 tin receptor-containing regions, such as the ventromedial nucleus of the hypothalamus and the medial
64 ences in the volume of the preoptic area and ventromedial nucleus of the hypothalamus are determined
65 terone-treated females had more pCREB in the ventromedial nucleus of the hypothalamus contrasted to c
66 escent protein (GFP)-positive neurons in the ventromedial nucleus of the hypothalamus express P2X4 su
67 data suggest roles for area X, LMAN, and the ventromedial nucleus of the hypothalamus in female respo
68 eased 5-HTT binding sites temporarily in the ventromedial nucleus of the hypothalamus in the 21-day-o
69 these findings indicate that ERalpha in the ventromedial nucleus of the hypothalamus neurons plays a
70 diaphorase and nitric oxide synthase in the ventromedial nucleus of the hypothalamus of cycling and
71 netic activation of hypothalamic AMPK in the ventromedial nucleus of the hypothalamus reversed nicoti
72 overexpression of GRP78 specifically in the ventromedial nucleus of the hypothalamus was sufficient
73 achieve focused silencing of ERalpha in the ventromedial nucleus of the hypothalamus, a key center o
74 earning and possibly discrimination, and the ventromedial nucleus of the hypothalamus, a region invol
75 ng cells in the medial preoptic area and the ventromedial nucleus of the hypothalamus, but not in the
76 he BST, SCN, PVN, amygdala, anterodorsal and ventromedial nucleus of the hypothalamus, indicating sit
77 old-thioglucose (GTG) induces lesions in the ventromedial nucleus of the hypothalamus, resulting in h
78 ls than females in the medial preoptic area, ventromedial nucleus of the hypothalamus, the arcuate nu
83 icular nucleus, suprachiasmatic nucleus, and ventromedial nucleus of the hypothalamus; the basolatera
84 ases in L-PGDS expression in the arcuate and ventromedial nucleus of the medial basal hypothalamus co
85 or hypothalamus (AH), septal area (SEP), and ventromedial nucleus of the posterior division of the do
86 bstantia nigra pars reticulata (SNr) and the ventromedial nucleus of the thalamus (VMT) in the mediat
87 arcuate nucleus (P < 0.05) and by 75% in the ventromedial nucleus (P < 0.05) of rats fasted 48 h.
89 sis of vibratome sections through the entire ventromedial nucleus showed that NADPH diaphorase cellul
90 the cohort of immature neurons entering the ventromedial nucleus, some appeared to undergo maturatio
91 factor 1 neurons, we generated hypothalamic ventromedial nucleus-specific COUP-TFII KO mice using th
92 he medial preoptic nucleus, median eminence, ventromedial nucleus, suprachiasmatic nucleus, medial se
93 cific thalamocortical neurons located in the ventromedial nucleus, the centrolateral nucleus, and the
94 medial preoptic nucleus (central aspect) and ventromedial nucleus (ventrolateral aspect) of the hypot
95 nucleus, dorsomedial aspect (MPNdm) and the ventromedial nucleus, ventrolateral aspect (VMNvl) in ma
96 IR than females in the medial preoptic area, ventromedial nucleus, ventrolateral portion of the hypot
97 lar nucleus (PVN), dorsomedial nucleus (DM), ventromedial nucleus (VM), medial mammillary nucleus (MM
99 g downregulation of CRF2mRNA in hypothalamic ventromedial nucleus (VMH) after 24 hr of maternal depri
100 amus, DEPTOR was expressed in neurons of the ventromedial nucleus (VMH) and colocalized with proopiom
105 these actions is located in the hypothalamic ventromedial nucleus (VMH), and the activation of AMPK i
106 ve fibers heavily innervate the hypothalamic ventromedial nucleus (VMH), and Ucn 3 injection into the
107 amic paraventricular nucleus (PVN) or in the ventromedial nucleus (VMH), restored plasma glucose.
108 s (PVH), the retrochiasmatic area (RCA), the ventromedial nucleus (VMH), the dorsomedial nucleus (DMH
109 lamic PREP is predominantly expressed in the ventromedial nucleus (VMH), where it regulates glucose-i
111 , 105% and 117% more neurons in hypothalamic ventromedial nucleus (VMN) and parvocellular portion of
112 dopamine receptor mRNAs were detected in the ventromedial nucleus (VMN) by in situ hybridization, ago
113 ited estrogen to neurons in rat hypothalamic ventromedial nucleus (VMN) facilitated lordosis behavior
115 ate the excitatory responses of hypothalamic ventromedial nucleus (VMN) neurons to neurotransmitters.
116 ions aimed at the dorsomedial portion of the ventromedial nucleus (VMN) of the hypothalamus were gene
118 However, the expression of 5HT1A mRNA in the ventromedial nucleus (VMN) was not different between gro
119 nity sites in areas such as the hypothalamic ventromedial nucleus (VMN) where many neurons increase t
121 nucleus (AVPV), medial preoptic area (MPOA), ventromedial nucleus (VMN), and arcuate nucleus (ARC), a
122 that the hypothalamic arcuate nucleus (ARC), ventromedial nucleus (VMN), and lateral hypothalamic are
123 neffective in the arcuate nucleus (ARC), the ventromedial nucleus (VMN), and the preoptic area (POA)
124 changes in men compared to EF women, except ventromedial nucleus (VMN), lateral hypothalamic area (L
125 NST), the medial preoptic nucleus (MPN), the ventromedial nucleus (VMN), the medial amygdala (mAMY),
126 ic nucleus (MPN), arcuate nucleus (ARH), and ventromedial nucleus (VMN), using an unbiased stereologi
129 vations identified the posterior part of the ventromedial nucleus (VMpo) as the major projection targ
130 ated deeper in the parenchyma such as in the ventromedial nucleus were fusiform and showed a bipolar
131 lamus, bed nucleus stria terminalis, and the ventromedial nucleus with no localization apparent elsew
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