ライフサイエンスコーパス: basalis

1 samples were spatially restricted to decidua basalis.

2 otoxin, anti-p75NTR-saporin into the nucleus basalis.

3 s (CA 2/3), and neuronal loss in the nucleus basalis.

4 nucleus, the diagonal band, and the nucleus basalis.

5 cal cortical projections back to the nucleus basalis.

6 ation of cholinergic inputs from the nucleus basalis.

7 ation of cholinergic inputs from the nucleus basalis.

8 riatum, globus pallidus, septum, and nucleus basalis.

9 luminal narrowing and a hypocellular decidua basalis.

10 predilection for replication in the decidua basalis.

11 Lhx8 mutants lack the nucleus basalis, a major source of the cholinergic input to the

12 However, the effect of nucleus basalis activation on sensory processing remains poorly

13 Pairing sensory stimulation with nucleus basalis activation shifted the preferred stimuli of cort

14 of the acoustic stimulus paired with nucleus basalis activation.

15 in the neocortex, limbic system, and nucleus basalis, among others.

16 ng the hippocampus, caudate nucleus, nucleus basalis and cortex.

17 cytes which have moved away from the stratum basalis and from their natural substrate.

18 ead is found in stromal cells of the decidua basalis and metrial gland and following infection, in en

19 s received unilateral lesions of the nucleus basalis and were infused intracerebroventricularly (i.c.

20 s were detected in the contralateral nucleus basalis, and in the ipsilateral and contralateral medial

21 e site of listerial infection in the decidua basalis, and infection by Listeria remained unrestrained

22 ly identified as an extension of the nucleus basalis, as well as ChAT(-) cells, release the inhibitor

23 glands at g.d. 8, 10, and 12 and in decidua basalis at g.d. 12 (p < 0.05).

24 Within the nucleus basalis, choline acetyltransferase was found in 35% of t

25 arietal cholinergic fiber density or nucleus basalis cholinergic neuron number or volume were found a

26 m2-immunoreactive neurons within the nucleus basalis complex from aged controls and AD patients revea

27 airing a tone with activation of the nucleus basalis could induce RF plasticity in the waking guinea

28 erase (ChAT)-containing cells in the nucleus basalis following a unilateral injection of ibotenic aci

29 Analysis of the decidua basalis from early pregnancy demonstrated expression of

30 gic neurons in the medial septum and nucleus basalis from the effects of excitotoxic or mechanical in

31 sults strengthen the hypothesis that nucleus basalis gates neural plasticity necessary for instrument

32 injection of ibotenic acid into the nucleus basalis; however, these effects were not related to horm

33 also be found in the locus ceruleus, nucleus basalis, hypothalamus, cerebral cortex, cranial nerve mo

34 affiliation explains the role of the nucleus basalis in modulating the impact and memorability of inc

35 ted neural circuits, as evidenced by nucleus basalis-induced changes in thalamic responses.

36 of GABAergic transmission by bilateral intra-basalis infusion of the benzodiazepine receptor agonist

37 ory systems, such as the cholinergic nucleus basalis, interact with and refine cortical circuits.

38 lateral ibotenic acid lesions of the nucleus basalis interfered with passive avoidance and spatial me

39 od, the cholinergic circuitry of the nucleus basalis is emerging as one of the most strategically pos

40 The nucleus basalis is located at the confluence of the limbic and r

41 holinergic projection neurons in the nucleus basalis is observed and is ascribed to an early and pers

42 Thus paired activation of the nucleus basalis is sufficient to induce receptive field plastici

43 ogenous endometrial stem cells reside in the basalis layer and serve as a source of cells that differ

44 ine-sensitive manners in bilaterally nucleus basalis lesioned rats; and (3) elevate high-affinity [3H

45 New results indicate that nucleus basalis lesions prevent motor cortex map plasticity and

46 l atrophy and degeneration following nucleus basalis lesions.

47 Freshly isolated decidua basalis macrophages expressed lower levels of ILT2 than

48 ed in the striatum (4.2%) and in the nucleus basalis magnocellularis (19.2%) 3-12 h following adminis

49 Since the Nucleus Basalis Magnocellularis (Meynert in humans and primates)

50 idence have supported a role for the nucleus basalis magnocellularis (NB) in attentional mechanisms;

51 with quisqualic acid lesions of the nucleus basalis magnocellularis (nBM) and control rats were comp

52 with 192 IgG-saporin lesions of the nucleus basalis magnocellularis (NBM) and sham-operated rats wer

53 vious research has demonstrated that nucleus basalis magnocellularis (nbm) corticopetal cholinergic n

54 if a selective cholinergic lesion of nucleus basalis magnocellularis (Nbm) could affect the number an

55 the hypothesis that the cholinergic nucleus basalis magnocellularis (NBM) is involved in solving pro

56 ns of the medial septum area (MS) or nucleus basalis magnocellularis (NBM) on amplitude and phase cha

57 ing rats: cholinergic lesions of the nucleus basalis magnocellularis (NBM) produce larger declines in

58 als were lesioned bilaterally in the nucleus basalis magnocellularis (nBM) using either quisqualic ac

59 diagonal band of Broca (HDB) and the nucleus basalis magnocellularis (NBM) were counted.

60 Fluctuations in the nucleus basalis magnocellularis (NBM) were highly variable, with

61 teral 192 IgG-saporin lesions to the nucleus basalis magnocellularis (nBM) were tested on olfactory d

62 toxic- or sham-lesion surgery of the nucleus basalis magnocellularis (NBM), the basal forebrain nucle

63 or immunoreactive neurons within the nucleus basalis magnocellularis (NBM), the horizontal limb of th

64 The BLA projects to the nucleus basalis magnocellularis (NBM), which sends broad choline

65 week-old right-sided ablation of the nucleus basalis magnocellularis (NBM).

66 and its release is regulated by the nucleus basalis magnocellularis (NBM).

67 he cholinergic substantia innominata/nucleus basalis magnocellularis (SI/nBM) is important for both s

68 he cholinergic substantia innominata/nucleus basalis magnocellularis (SI/nBM) on performance are exam

69 sublenticular substantia innominata/nucleus basalis magnocellularis (SI/nBM), as well as certain cor

70 d loss of cholinergic neurons in the nucleus basalis magnocellularis after intracerebroventricular in

71 lts demonstrated that lesions of the nucleus basalis magnocellularis and frontal cortex selectively r

72 l cholinergic lesions applied to the nucleus basalis magnocellularis and substantia innominata (NBM/S

73 sted that cholinergic neurons in the nucleus basalis magnocellularis and substantia innominata (NBM/S

74 Injection of lidocaine into the nucleus basalis magnocellularis produced a profile of behavioral

75 Lesions of the nucleus basalis magnocellularis were without effect on the patte

76 es in trkA mRNA were detected in the nucleus basalis magnocellularis, and no significant changes in N

77 limb of the diagonal band of Broca, nucleus basalis magnocellularis, and striatum of gonadectomized

78 dial septum, diagonal band of Broca, nucleus basalis magnocellularis, and striatum were processed for

79 injection of ibotenic acid into the nucleus basalis magnocellularis, or unilateral transection of th

80 es in the medial septal area and the nucleus basalis magnocellularis, radiofrequency lesions of the f

81 of colchicine or vehicle in the rat nucleus basalis magnocellularis, the time course of changes in s

82 teral quisqualic acid lesions of the nucleus basalis magnocellularis.

83 ity p75 neurotrophin receptor in the nucleus basalis Meynert failed to reveal differences between veh

84 nucleus accumbens; ventral pallium; nucleus basalis Meynert; bed nucleus of the stria terminalis; pr

85 d with electrical stimulation of the nucleus basalis (NB) 300 to 400 times per day for 20-25 days.

86 d with electrical stimulation of the nucleus basalis (NB) at tone offset.

87 P (SP) excites large neurons of the nucleus basalis (NB) by inhibiting an inward rectifier K(+) chan

88 Degeneration of cholinergic nucleus basalis (NB) cortical projection neurons is associated w

89 The nucleus basalis (NB) has been implicated in memory formation ind

90 The nucleus basalis (NB) in the basal forebrain provides most of the

91 gic innervation of the cortex by the nucleus basalis (NB) is known to modulate cortical neuronal resp

92 The nucleus basalis (NB) mediates cortical electroencephalograph (EE

93 Cholinergic basal forebrain (CBF) nucleus basalis (NB) neurons display neurofibrillary tangles (NF

94 Electrical activation of the nucleus basalis (NB) of Meynert, the source of neocortical acety

95 Pairing pulsed noises with nucleus basalis (NB) stimulation in awake rats for 4 weeks broad

96 lution within the CBF neurons of the nucleus basalis (NB) using tissue from subjects with no cognitiv

97 ustic stimuli with activation of the nucleus basalis neuromodulatory system.

98 h release from cortical afferents of nucleus basalis neurones in vivo.

99 h markers were expressed robustly in nucleus basalis neurons and across all three groups.

100 te that alterations in the number of nucleus basalis neurons containing trkA immunoreactivity occurs

101 lz-50) immunostaining in cholinergic nucleus basalis neurons existed even in the cognitively normal s

102 marked reduction in trkA-containing nucleus basalis neurons in end-stage Alzheimer's disease (AD).

103 e percentage of tauopathy-containing nucleus basalis neurons was greater in the cognitively impaired

104 he number of p75(NTR)-immunoreactive nucleus basalis neurons was significantly correlated with perfor

105 Seventy-five days later, cholinergic nucleus basalis neurons were atrophic ipsilateral to the lesion

106 s of the diagonal band (DB), and the nucleus basalis of Meynert (NB).

107 ial septal/diagonal band (MS/DB) and nucleus basalis of Meynert (NBM) also reveal a selective choline

108 in ChAT and trkA are observed in the nucleus basalis of Meynert (nBM) of both age groups.

109 In the nucleus basalis of Meynert (NBM) of middle-aged monkeys, the num

110 f these receptor subunits within the nucleus basalis of Meynert (NBM) of non-demented elderly humans.

111 Acetylcholine neurons in nucleus basalis of Meynert (NBM) were selectively lesioned with

112 al cholinergic neuron numbers in the nucleus basalis of Meynert (nbM), stereologic methods were appli

113 a (MS) and the substantia innominata/nucleus basalis of Meynert (SI).

114 igra, raphe nuclei, locus coeruleus, nucleus basalis of Meynert and dorsal motor nucleus of vagus.

115 (ERT) on cholinergic neurons in the nucleus basalis of Meynert and on cholinergic fibers in the pref

116 Although cholinergic neurons in the nucleus basalis of Meynert are a major source of cholinergic pro

117 part in budgerigars of the mammalian nucleus basalis of Meynert consists of a field of cholinergic ne

118 ence in orexinergic fiber density in nucleus basalis of Meynert or locus ceruleus compared to control

119 cus coeruleus, ventral tegmentum and nucleus basalis of Meynert, and efferent projections to the puta

120 b of the diagonal band of Broca, the nucleus basalis of Meynert, and the inferior olivary nucleus.

121 dial septum, diagonal band of Broca, nucleus basalis of Meynert, bed nucleus of stria terminalis, amy

122 the diagonal band of Broca, and the nucleus basalis of Meynert, medial habenular nucleus, zona incer

123 differences in ChAT activity in the nucleus basalis of Meynert, nor any of several neocortical areas

124 nucleus of the vagus, but not in the nucleus basalis of Meynert, raphe nucleus, or other brain region

125 nculopontine/laterodorsal tegmentum, nucleus basalis of Meynert, thalamus, and locus ceruleus) of aff

126 pronounced in posterior parts of the nucleus basalis of Meynert, whereas in AD, atrophy was more exte

127 located in the Ch4 cell group of the nucleus basalis of Meynert.

128 s that originate from neurons in the nucleus basalis of Meynert.

129 f the diagonal band of Broca and the nucleus basalis of Meynert.

130 magnocellular preoptic area, and the nucleus basalis of Meynert.

131 nucleus of the X cranial nerve, and nucleus basalis of Meynert.

132 as the pedunculopontine nucleus and nucleus basalis of Meynert.

133 motor nucleus of the vagus, and the nucleus basalis of Meynert.

134 The nucleus basalis of the basal forebrain is an essential component

135 For example, the nucleus basalis of the forebrain plays a critical role in enhanc

136 band, but not in the medial septum, nucleus basalis, or striatum of females vs. males.

137 d similar reduction in the number of nucleus basalis p75(NTR)-immunoreactive neurons was seen in indi

138 isodic electrical stimulation of the nucleus basalis, paired with an auditory stimulus, results in a

139 cal acetylcholine by examining whether intra-basalis perfusion of dopamine antagonists attenuates thi

140 amine administration was unaffected by intra-basalis perfusions of high concentrations of D1- (100 mi

141 6-NGF conjugate restored the size of nucleus basalis perikarya to within normal limits relative to th

142 the nucleus posterioris amygdalopallii pars basalis (PoAb) and pars compacta (PoAc), the nucleus tae

143 area 46, and in the component of the nucleus basalis projecting to this region.

144 ong-range connections from thalamus, nucleus basalis, raphe, and distant cortical areas, including ip

145 neurons of the substantia innominata/nucleus basalis region, and their innervation of the posterior p

146 Decidua basalis samples (8 to 12 weeks gestation) were examined

147 band (HDB) and substantia innominata/nucleus basalis (SI/NB) following ovariectomy.

148 contralateral substantia innominata/nucleus basalis (SI/nBM) failed to show the enhanced attentional

149 EHD2-scTNFR2 into the magnocellular nucleus basalis significantly protected cholinergic neurons and

150 in rat visual cortex, we found that nucleus basalis stimulation caused prominent decorrelation betwe

151 Nucleus basalis stimulation produced electroencephalogram desync

152 Paired tone/nucleus basalis stimulation, but not unpaired stimulation, induc

153 ed primarily outside the cholinergic nucleus basalis subfields.

154 cle was infused into the area of the nucleus basalis/substantia innominata of the basal forebrain.

155 aired a tone with stimulation of the nucleus basalis, the main subcortical source of cortical acetylc

156 tify pre-tangle cytopathology in the nucleus basalis, the source of cortical cholinergic innervation.

157 with stimulation of the cholinergic nucleus basalis to induce auditory cortex map plasticity outside

158 cholinergic fibres extended from the nucleus basalis to the cerebral cortex and amygdala and were des

159 link the cholinergic neurons of the nucleus basalis to the human cerebral cortex.

160 Large neurons of the cholinergic nucleus basalis together with CA1 and CA3 pyramidal neurons were

161 olfactory bulbs, frontal cortex, or nucleus basalis/ventral pallidum following hormone treatment; ho

162 cortex, olfactory bulbs, septum, and nucleus basalis/ventral pallidum were dissected.

163 ng to this region of cortex from the nucleus basalis was also reduced by 50 +/- 6%.

164 Although nucleus basalis was stimulated only for a few minutes, reorganiz

165 gic neurons in the medial septum and nucleus basalis were detected and quantified using immunohistoch

166 eus basorostralis (previously called nucleus basalis), whereas input from the rest of the body follow

167 and and in the posterior half of the nucleus basalis, which is where there was the greatest overlap b

168 The anatomical continuity of the nucleus basalis with other basomedial limbic structures may unde

169 g evidence from a second species, Rhombodera basalis, with particular focus on the lobula complex (LO