ライフサイエンスコーパス: basalis

1 orizontal diagonal band, but not the nucleus 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 samples were spatially restricted to decidua basalis.

6 r expression was observed within the stratum basalis.

7 cal cortical projections back to the nucleus basalis.

8 ation of cholinergic inputs from the nucleus basalis.

9 ation of cholinergic inputs from the nucleus basalis.

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

11 luminal narrowing and a hypocellular decidua basalis.

12 predilection for replication in the decidua basalis.

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

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

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

16 of the acoustic stimulus paired with nucleus basalis activation.

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

18 cholinergic neurons in the anterior nucleus basalis (aNB) of the basal forebrain are increasingly ac

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

20 study, dNK from human term pregnancy decidua basalis and decidua parietalis tissues were compared wit

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

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

23 Neurons of the basal forebrain nucleus basalis and posterior substantia innominata (NBM/SI(p))

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

51 l atrophy and degeneration following nucleus basalis lesions.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

87 teral quisqualic acid lesions of the nucleus basalis magnocellularis.

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

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

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

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

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

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

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

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

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

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

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

99 choline following stimulation of the nucleus basalis (NB) of Meynert have been recently examined in t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

114 nse cholinergic projections from the nucleus basalis of Meynert (NBM) and the horizontal limb of the

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

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

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

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

119 Dysfunction of the nucleus basalis of Meynert (NBM), a basal forebrain structure th

120 kers of neurodegeneration within the nucleus basalis of Meynert (NbM), a subregion of the basal foreb

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

122 tex (IC), central amygdala (CE), and nucleus basalis of Meynert (NBM), which decomposes the affective

123 The nucleus basalis of Meynert (NbM), which serves as the primary so

124 ns in the substantia innominate (SI)/nucleus basalis of Meynert (nBM)-medial prefrontal cortex (mPFC)

125 rtex from cholinergic neurons in the nucleus basalis of Meynert (NBM).

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

127 ergic basal forebrain nuclei CH4/4p (nucleus basalis of Meynert [NBM]) and CH1/2/3.

128 ved cholinergic axonal health in the nucleus basalis of Meynert akin to wildtype mice.

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

130 dies have shown that the cholinergic nucleus basalis of Meynert and its white matter projections are

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

132 white matter projections between the nucleus basalis of Meynert and the cortex are altered in neurode

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

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

135 that degeneration of the cholinergic nucleus basalis of Meynert in Alzheimer's disease and dementia w

136 and attention than the volume of the nucleus basalis of Meynert itself and might be an early indicato

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

138 mpairment, loss of integrity of both nucleus basalis of Meynert pathways was associated with increase

139 Nucleus basalis of Meynert volume was reduced in all clinical gr

140 requency was associated with smaller nucleus basalis of Meynert volumes (beta = 0.22, P = 0.02) and i

141 matter pathways originating from the nucleus basalis of Meynert was performed using diffusion-weighte

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

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

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

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

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

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

148 ly in subregions associated with the nucleus basalis of Meynert, suggesting that it is the cholinergi

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

150 lumetric measures of hippocampus and nucleus basalis of Meynert, using a receiver operating character

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

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

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

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

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

156 cholinergic axonal swellings in the nucleus basalis of Meynert.

157 substantia nigra, and the forebrain nucleus basalis of Meynert.

158 ts, with the lowest tethering in the nucleus basalis of Meynert.

159 arly degeneration of the cholinergic nucleus basalis of Meynert.

160 mpal volume or volume of cholinergic nucleus basalis of Meynert.

161 edial and a lateral pathway from the nucleus basalis of Meynert.

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

163 as the pedunculopontine nucleus and nucleus basalis of Meynert.

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

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

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

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

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

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

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

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

172 6-NGF conjugate restored the size of nucleus basalis perikarya to within normal limits relative to th

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

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

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

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

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

178 Decidua basalis sections from term (n = 10), idiopathic preterm

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

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

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

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

183 Nucleus basalis stimulation produced electroencephalogram desync

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

185 ed primarily outside the cholinergic nucleus basalis subfields.

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

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

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

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

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

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

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

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

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

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

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

197 In the basalis, we define signaling between fibroblasts and an

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

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

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

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

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