ライフサイエンスコーパス: olfactory tubercle

1 ctory-auditory convergence upstream from the olfactory tubercle.

2 bnuclei examined within the hypothalamus and olfactory tubercle.

3 ared in the striatum, nucleus accumbens, and olfactory tubercle.

4 perirhinal projections were primarily to the olfactory tubercle.

5 bens, along with light label in the adjacent olfactory tubercle.

6 eral caudate putamen, nucleus accumbens, and olfactory tubercle.

7 ateral and paraventricular hypothalamus, and olfactory tubercle.

8 ceral stimuli in the striatal compartment of olfactory tubercle.

9 teral shell of the nucleus accumbens and the olfactory tubercle.

10 and terminated lightly within layer 3 of the olfactory tubercle.

11 eral shell of the nucleus accumbens, and the olfactory tubercle.

12 integrated into limbic-motor circuits by the olfactory tubercle.

13 leus as well as in the nucleus accumbens and olfactory tubercle.

14 l ventral pallidum and pallidal parts of the olfactory tubercle.

15 arily to the striatum, nucleus accumbens and olfactory tubercles.

16 In vivo extracellular recordings from the olfactory tubercle, a trilaminar structure within the ba

17 ria terminalis, the claustrum (alpha1G), the olfactory tubercles (alpha1H and alpha1I), and the subth

18 accumbens among females (p<0.01) and in the olfactory tubercle among both females (p<0.05) and males

19 ar cortex, ventral tenia tecta, and anterior olfactory tubercle and piriform cortex) have cells that

20 ar levels of gene expression remained in the olfactory tubercle and the inferior colliculus, with som

21 m the nucleus tractus solitarii (NTS) to the olfactory tubercle and the midline/intralaminar thalamus

22 Subsequently, NiV disseminated to the olfactory tubercle and throughout the ventral cortex.

23 accumbens, caudate putamen, frontal cortex, olfactory tubercle and VTA.

24 d DA release from the rat striatum (STR) and olfactory tubercles and NE release from hippocampus, tha

25 microM) evoked [3H]DA release from striatum, olfactory tubercles and prefrontal cortex (PFC), and [3H

26 vel of the ventral caudate, ventral putamen, olfactory tubercle, and accumbens core and shell.

27 operties of the striatum, nucleus accumbens, olfactory tubercle, and central nucleus of the amygdala.

28 n staining were seen in the dorsal striatum, olfactory tubercle, and cerebellar vermis.

29 Gsh2 have severe hypoplasia of the striatum, olfactory tubercle, and interneurons that migrate from t

30 The perirhinal cortex, olfactory tubercle, and most subdivisions of the hippoca

31 Line differences in ENK expression in the olfactory tubercle, and possibly the nucleus accumbens,

32 the CNS, which was strongest in neostriatum, olfactory tubercle, and supraoptic nucleus.

33 brain, structures such as the accumbens, the olfactory tubercle, and the amygdala have lost legitimac

34 urons in the striatum, nucleus accumbens and olfactory tubercle, and to granule and periglomerular ce

35 re and shell), cell bridges of the striatum, olfactory tubercles, and areas of extended amygdala with

36 plexus, striatum, hippocampus, hypothalamus, olfactory tubercles, and spinal cord.

37 r rates of glucose utilization in the medial olfactory tubercle, anterior nucleus accumbens and dorso

38 the caudate-putamen, nucleus accumbens, and olfactory tubercle, as well as structures that receive o

39 triatum, nucleus accumbens (core and shell), olfactory tubercle, bed nucleus of stria terminalis (BST

40 y depleted in striatum and nucleus accumbens/olfactory tubercle, but not septum, hypothalamus, or ven

41 was also decreased in the nucleus accumbens/ olfactory tubercle, but this effect was observed after 1

42 e receptor D2 mRNA was also increased in the olfactory tubercle, caudate putamen, and the nucleus acc

43 lactosidase gene expression was found in the olfactory tubercle, caudate, hippocampus, piriform corte

44 ygdala, lateral nucleus of the hypothalamus, olfactory tubercle, caudate-putamen, nucleus accumbens a

45 limbic and basal forebrain regions including olfactory tubercle, central nucleus of the amygdala, and

46 ical targets of MO were the medial striatum, olfactory tubercle, claustrum, nucleus accumbens, septum

47 In the nucleus accumbens and olfactory tubercle, CRF1 binding was initially the same

48 Similar results were obtained for olfactory tubercle determinations, with the exception th

49 um into the accumbens core and shell and the olfactory tubercle does not reflect the functional organ

50 Corpus striatal and olfactory tubercle dopamine.

51 nding was found in the nucleus accumbens and olfactory tubercle following twice daily cocaine injecti

52 ntly depleted in striatum, nucleus accumbens/olfactory tubercle, hippocampus, somatosensory cortex, b

53 on analyses placed the nucleus accumbens and olfactory tubercle in the striatal system, functional li

54 he induseum griseum and taenia tecta; in the olfactory tubercle; in CA1-CA3, the hilus of the dentate

55 triatal complex (caudate n, n. accumbens and olfactory tubercle), indicating that PDE10A is expressed

56 CB2 immunoreactivity was also observed in olfactory tubercle, islands of Calleja, cerebral cortex,

57 caudate and 33% in the ventral striatum and olfactory tubercle labeled by the aFGF cRNA.

58 Light projections end in the olfactory tubercle, lateral septal nucleus, posterior ba

59 s that the medial accumbens shell and medial olfactory tubercle mediate the rewarding effects of coca

60 Our findings are novel in showing that olfactory tubercle neurons participate in such coding sc

61 protein and mRNA were observed in striatum, olfactory tubercle, nucleus accumbens, amygdala, and neo

62 84 binding sites in SHR were observed in the olfactory tubercle, nucleus accumbens, basolateral amygd

63 pamine receptor D1 mRNA was increased in the olfactory tubercle, nucleus accumbens, caudate putamen,

64 e in seizure circuitry: the piriform cortex, olfactory tubercle, nucleus accumbens, caudate-putamen,

65 , hippocampus, hypothalamus, cerebellum, and olfactory tubercle of naive rats.

66 er binding were observed in the striatum and olfactory tubercle of rats and control and alpha2A KO mi

67 nments, and the accompanying changes in both olfactory tubercle (OT) and hypothalamic (HYPOTH), norep

68 and nucleus accumbens (NAC), and within the olfactory tubercle (OT) and orbital cortex.

69 P and the polymorph (pallidal) region of the olfactory tubercle (OT) and transynaptic infection of a

70 c connections to nucleus accumbens (NAc) and olfactory tubercle (OT) neurons.

71 on of the preproenkephalin (ENK) gene in the olfactory tubercle (OT) portion of the ventral striatum

72 the ventral striatum's nucleus accumbens and olfactory tubercle (OT) suggests the distributed involve

73 The olfactory tubercle (OT), a ventral striatum structure th

74 es of rat striatum, nucleus accumbens (NAc), olfactory tubercles (OT) and prefrontal cortices (PFC) i

75 the anterior piriform cortex (APCx) and the olfactory tubercle (OTu) are activated during nursing-as

76 to the caudate putamen and nucleus accumbens/olfactory tubercle, respectively, constituting mesostria

77 ising frontal piriform cortex (PirF) and the olfactory tubercle responded preferentially to attended

78 Remarkably, 19% of olfactory tubercle single units also showed robust respo

79 orebrain, of anesthetized mice revealed that olfactory tubercle single units selectively respond to o

80 ferent CIN responses, we recorded from adult olfactory tubercle slices in the mouse ventral striatum.

81 unoreactive (-ir) perikarya were seen in the olfactory tubercle, striatum, medial septal nucleus, ver

82 Here we show that neurons in the olfactory tubercle subregion of the ventral striatum rob

83 ower amounts in striatum, nucleus accumbens, olfactory tubercle, thalamus, and substantia nigra.

84 ed substantially stronger projections to the olfactory tubercle than did the early-generated cells.

85 rhinal cortex, the endopiriform nucleus, the olfactory tubercle, the anterior olfactory nucleus and t

86 usion) is readily self-administered into the olfactory tubercle, the most ventral portion of the vent

87 binding were significantly higher within the olfactory tubercle, ventral tegmental area, and NAc core

88 ce, (11)C tracer binding in the striatum and olfactory tubercle was low, similar to that of the front

89 nucleus accumbens, which, together with the olfactory tubercle, was noted to be part of the ventral

90 s in caudate-putamen, nucleus accumbens, and olfactory tubercle were evaluated.

91 ion exhibiting DCL expression is part of the olfactory tubercle where DCL is found in the neuropil of

92 between the medial nucleus accumbens and the olfactory tubercle, whereas the perirhinal projections w

93 t projects throughout layer IA of the entire olfactory tubercle, with apparently more fibres in the l