ライフサイエンスコーパス: reticulata

1 obus pallidus and the substantia nigra (pars reticulata).

2 tructure using Trinidadian guppies (Poecilia reticulata).

3 rates in wild Trinidadian guppies (Poecilia reticulata).

4 pulations of the Trinidadian guppy (Poecilia reticulata).

5 he colour patterns of male guppies (Poecilia reticulata).

6 entopeduncular nucleus and substantia nigra reticulata.

7 ainstem, including the substantia nigra pars reticulata.

8 ng female mate choice in the guppy, Poecilia reticulata.

9 nd caudal parts of the substantia nigra pars reticulata.

10 ositus nucleus and the substantia nigra pars reticulata.

11 tral pallidum and the substantia nigra, pars reticulata.

12 ticular formation, and substantia nigra pars reticulata.

13 , globus pallidus, and substantia nigra pars reticulata.

14 he globus pallidus and substantia nigra pars reticulata.

15 s did the striatum and substantia nigra pars reticulata.

16 on of D-amphetamine in substantia nigra pars reticulata.

17 ic acid lesions of the substantia nigra pars reticulata.

18 microdialysis probe in substantia nigra pars reticulata.

19 BAergic neurons in the substantia nigra pars reticulata.

20 a into the ancestral mandarin species Citrus reticulata.

21 rs compacta ventralis and dorsalis from pars reticulata.

22 to the homolog of the substantia nigra pars reticulata.

23 ubthalamic nucleus and substantia nigra pars reticulata.

24 lia output neurons in substantia nigra, pars reticulata.

25 rom globus pallidus or substantia nigra pars reticulata.

26 pars compacta (SNC) or substantia nigra pars reticulata.

27 ices from rat or mouse substantia nigra pars reticulata.

28 neurons of the VTA and substantia nigra pars reticulata.

29 HC) in wild and ornamental guppies, Poecilia reticulata.

30 xylase (TH) positive cell bodies in the pars reticulata.

31 the entopeduncular nucleus, and the SN pars reticulata.

32 antly increased in the substantia nigra pars reticulata (13.5+/-4.1 and 26.3+/-2.9%, respectively) an

33 the SN of the non-lesioned hemisphere (pars reticulata: 14.8+/-1.19 O.D. control vs. 36+/-2.6 O.D. B

34 d that activity in the substantia nigra pars reticulata, a basal ganglia output, predictably differed

35 marily extrasynaptic in the substantia nigra reticulata, a terminal region with identified synaptic c

36 e show that interacting guppy fish (Poecilia reticulata) achieve a superior level of numerosity discr

37 y transplanted Trinidadian guppies (Poecilia reticulata) adapted to living with cichlid predators to

38 BAergic neurons in the substantia nigra pars reticulata also were recorded and filled with biotinamid

39 Dried citrus peel derived from Citrus reticulata, also called "chenpi", possesses a complex mi

40 s (D1+) project to the substantia nigra pars reticulata and are thought to facilitate movement.

41 cial varieties of mandarin, including Citrus reticulata and Citrus unshiu species and a mandarin x ta

42 ic transmission in the substantia nigra pars reticulata and entopeduncular nucleus, two major targets

43 d moderate staining in substantia nigra pars reticulata and entopeduncular nucleus.

44 atibility complex (MHC) in guppies (Poecilia reticulata and P. obscura) and swamp guppies (Micropoeci

45 m 684 globus pallidus, substantia nigra pars reticulata and subthalamic neurons recorded in intact, s

46 e anaesthesia from the substantia nigra pars reticulata and subthalamic nucleus along with cortical e

47 opposes DOP transmission in substantia nigra reticulata and that NOP receptor antagonists might be us

48 BG), especially in the substantia nigra (SN) reticulata and the globus pallidus (GP), have a high den

49 eactive nuclei were concentrated in the pars reticulata and the majority of labeled nigral neurons di

50 ogous to the mammalian substantia nigra pars reticulata and was also renamed accordingly.

51 rminal was estimated in the substantia nigra reticulata and was considerably less than the number of

52 ch ramified within the substantia nigra pars reticulata and/or pars compacta.

53 ivulus hartii), omnivorous guppies (Poecilia reticulata) and omnivorous crabs (Eudaniela garmani).

54 lobus pallidus interna/substantia nigra pars reticulata, and infusion of recombinant glial derived ne

55 in the substantia nigra pars compacta, pars reticulata, and pars lateralis), and 51% in nucleus A10

56 output is initiated in substantia nigra pars reticulata, and this influence contributes to the effect

57 m, globus pallidus and substantia nigra pars reticulata, and was not detectable in the subthalamic nu

58 s that D1 receptors in substantia nigra pars reticulata are involved in the excitatory component of d

59 eduncular nucleus, and substantia nigra pars reticulata, areas of the basal ganglia receiving striata

60 pment of decay in harvested mandarin (Citrus reticulata Blanco cv. Shatang.) fruit in vivo.

61 ampal CA3 region and in the substantia nigra-reticulata but increases in serotonin transporters in th

62 he dorsal striatum and substantia nigra pars reticulata by activating TRPM2 channels.

63 Neurons of the substantia nigra pars reticulata can be readily and fully inhibited by endogen

64 BAergic neurons of the substantia nigra pars reticulata cannot be differentiated on the basis of thei

65 al-lateral part of the substantia nigra pars reticulata (cdlSNr), directly or indirectly through the

66 populations of Trinidadian guppies (Poecilia reticulata), characterized by differences in phenotypic

67 a critical zone in the substantia nigra pars reticulata contralateral to a cortical lesion.

68 ion neurons target the substantia nigra pars reticulata (direct pathway) or the lateral globus pallid

69 area, caudate putamen, substantia nigra pars reticulata, entorhinal cortex, central amygdala, lateral

70 he globus pallidus and substantia nigra pars reticulata following lesions of the nigrostriatal tract.

71 kworm), Hyalella azteca (scud), and Poecilia reticulata (guppy), which yielded a high-quality databas

72 ents from striatum, globus pallidus, or pars reticulata have been shown to be mediated predominantly

73 he globus pallidus and substantia nigra pars reticulata, however, mGluR1a-ir was tightly clustered al

74 In the SN pars reticulata, ibotenic acid reduced the number of neurons

75 gs from neurons in the substantia nigra pars reticulata in rat brain slices and labeled them with bio

76 Trinidadian guppies (Poecilia reticulata) inhabiting stream reaches with different pre

77 ex blinking is (1) the substantia nigra pars reticulata inhibits SC neurons, (2) the SC excites tonic

78 ubthalamic nucleus and substantia nigra pars reticulata ipsilateral to the lesion.

79 he globus pallidus and substantia nigra pars reticulata is caused by abnormal striatal activity.

80 In guppies (Poecilia reticulata), male colour pattern is both diverse and her

81 nigral D2 receptors, perhaps located on pars reticulata neurons themselves, to regulate basal ganglia

82 of quinpirole to attenuate responses of pars reticulata neurons to GABA.

83 is mediated by D2 receptors located on pars reticulata neurons.

84 noid agonists, applied locally into the pars reticulata of substantia nigra (SNpr), could modulate st

85 Likewise, D-amphetamine applied into pars reticulata of substantia nigra by reverse dialysis produ

86 7,8-diol (SKF 38393) hydrochloride into pars reticulata of substantia nigra elicited a significant in

87 iles of neurons in the substantia nigra pars reticulata of the basal ganglia and in the superior coll

88 lgaris-leucoagglutinin (PHA-L) into the pars reticulata of the substantia nigra (SNR).

89 output neurons (the globus pallidus and pars reticulata of the substantia nigra).

90 s area, cerebellar molecular layer, and pars reticulata of the substantia nigra.

91 on of the hippocampus, substantia nigra pars reticulata, pallidum, and deep cerebellar nuclei.

92 nge is an F1 hybrid of pure C. maxima and C. reticulata parents, thus implying that wild mandarins we

93 d this in the context of two guppy (Poecilia reticulata) populations that have been subject to an int

94 the basal ganglia, the substantia nigra pars reticulata, projects via the thalamus to TE.

95 average firing rate of substantia nigra pars reticulata reduces the incidence of seizures.

96 af reticulation, we analyzed the Arabidopsis RETICULATA-RELATED (RER) gene family, several members of

97 ation was identical in substantia nigra pars reticulata slices prepared from TKO and wild-type mice.

98 nhibit output from the substantia nigra pars reticulata (SNpr) and internal pallidal segment (GPi).

99 n LFPs recorded in the substantia nigra pars reticulata (SNpr) and motor cortex (MCx) in the hemipark

100 reases in motor cortex-substantia nigra pars reticulata (SNpr) coherence emerged in the 8-25 Hz range

101 colliculus (SC) or the substantia nigra pars reticulata (SNpr) contralateral to the cortical lesion.

102 voked by inhibition of substantia nigra pars reticulata (SNpr) in the nonhuman primate.

103 of APP domains in rat substantia nigra pars reticulata (SNpR) neurons targeted for delayed degenerat

104 nucleus (EPN) and the substantia nigra pars reticulata (SNpr) on the intact side of the brain, but r

105 of the basal ganglia, substantia nigra pars reticulata (SNpr), and entopeduncular nucleus.

106 pontine nucleus to the substantia nigra pars reticulata (SNr) act on muscarinic acetylcholine recepto

107 nkey, but not the rat, substantia nigra pars reticulata (SNr) also harbored a significant level of ne

108 e demonstrate that the substantia nigra pars reticulata (SNr) also provides a massive input to Pf in

109 rominent involvement of the substantia nigra reticulata (SNR) among other structures in the hypoglyce

110 St projects to the GP, substantia nigra pars reticulata (SNr) and pars compacta (SNc), but not the th

111 ssed GFRalpha-1 in the substantia nigra pars reticulata (SNR) and the ventral tegmental area (VTA).

112 the involvement of the substantia nigra pars reticulata (SNr) and the ventromedial nucleus of the tha

113 BAergic neurons in the substantia nigra pars reticulata (SNr) and with distal dendrites (in SNr) of D

114 jection neurons in the substantia nigra pars reticulata (SNr) are key basal ganglia output neurons.

115 pmental changes in the substantia nigra pars reticulata (SNr) associated with the expression of group

116 ergic neurons in mouse substantia nigra pars reticulata (SNr) brain slices.

117 al ganglia through the substantia nigra pars reticulata (SNr) controls active avoidance.

118 ght microscope level, neurons of the SN pars reticulata (SNr) displayed moderate to strong immunoreac

119 glutamatergic input to substantia nigra pars reticulata (SNr) from the subthalamic nucleus (STN) is b

120 Substantia nigra pars reticulata (SNr) GABAergic neurons are projection neuron

121 s of the striatum, the substantia nigra pars reticulata (SNr) has been hypothesized to play a role in

122 red BG output from the substantia nigra pars reticulata (SNr) in mice while monitoring their movement

123 ganglia output nucleus substantia nigra pars reticulata (SNr) in mice.

124 posterior area of the substantia nigra pars reticulata (SNR) in rats.

125 idence that the monkey substantia nigra pars reticulata (SNr) in the basal ganglia represents stable,

126 Substantia nigra pars reticulata (SNr) is a key basal ganglia output nucleus c

127 The substantia nigra pars reticulata (SNr) is the primary output nucleus for the b

128 directly projecting to the substantia nigra reticulata (SNr) lose tonic presynaptic inhibition by GA

129 GABA agonist, into the substantia nigra pars reticulata (SNr) markedly reduced blink amplitude.

130 ordings were made from substantia nigra pars reticulata (SNr) neurones in rat midbrain slices.

131 under voltage clamp in substantia nigra zona reticulata (SNR) neurones in the rat midbrain slice.

132 with non-dopaminergic substantia nigra pars reticulata (SNr) neurons and proximal dendrites of dopam

133 ltered the activity of substantia nigra pars reticulata (SNr) neurons of the basal ganglia (BG) and h

134 ivity and responses of substantia nigra pars reticulata (SNr) neurons to GABA, glutamate (GLU), and d

135 effects of DBS of the substantia nigra pars reticulata (SNr) on amygdala-kindled seizures.

136 rons downstream in the substantia nigra pars reticulata (SNr) only responded to Stop cues in trials w

137 output neurons in the substantia nigra pars reticulata (SNr) receive strong CARTir input from the ac

138 Substantia nigra pars reticulata (SNr) receives both GABAergic and glutamaterg

139 pallidus externa (GPe) and substantia nigra reticulata (SNr) revealed that high-frequency DBS, but n

140 ndrites located in the substantia nigra pars reticulata (SNr) than on those located in SNc, revealing

141 ochemistry, in the rat substantia nigra pars reticulata (SNr) through an acute and persistent augment

142 BAergic input from the substantia nigra pars reticulata (SNr) to the deep SC/Me.

143 BAergic neurons of the substantia nigra pars reticulata (SNr) tonically inhibit the target nuclei of

144 erlying brain, and the substantia nigra pars reticulata (SNr) were compared with contralateral brain

145 jection neurons of the substantia nigra pars reticulata (SNr), a key basal ganglia output nucleus, is

146 rn is expressed in the substantia nigra pars reticulata (SNr), a main target of striatal efferents an

147 BAergic neurons of the substantia nigra pars reticulata (SNr), a major output of the basal ganglia, p

148 atory influence on the substantia nigra pars reticulata (SNR), a major output structure of the basal

149 al-output nucleus, the substantia nigra pars reticulata (SNr), and the presence of modulatory input f

150 cular nucleus (EP) and substantia nigra pars reticulata (SNr), as does the acute injection of levodop

151 r midbrain target, the substantia nigra pars reticulata (SNr), at E14 in the mouse with a robust conn

152 BAergic neurons of the substantia nigra pars reticulata (SNr), but not in DA neurons of the substanti

153 bers were identified in the substantia nigra reticulata (SNr), NAC, OT, septum and orbital cortex.

154 und strain mice in the substantia nigra pars reticulata (SNr), subthalamic nucleus (STN), rostromedia

155 We recorded from the substantia nigra pars reticulata (SNR), the major basal ganglia output nucleus

156 obus pallidus (GP) and substantia nigra pars reticulata (SNr), together with the ipsilateral frontal

157 Meriones unguiculatus) substantia nigra pars reticulata (SNr), whose "neuronal" phenotype was confirm

158 and the contralateral substantia nigra pars reticulata (SNr).

159 bus pallidus (GP), and substantia nigra pars reticulata (SNr).

160 neurons in the ipsilateral substantia nigra reticulata (SNR).

161 amic nucleus (STN) and substantia nigra zona reticulata (SNR).

162 n GABA release in the substantia nigra, pars reticulata (SNr).

163 GABA concentrations in substantia nigra pars reticulata (SNr).

164 NS cell bodies in the pars compacta and pars reticulata (TH immunohistochemistry and Cresyl violet hi

165 N) consists of GABAergic neurons of the pars reticulata that inhibit thalamic neurons and provide the

166 tivity in both STN and substantia nigra pars reticulata, the main output structure of basal ganglia i

167 ld 'mandarin' diverges substantially from C. reticulata, thus suggesting the possibility of other unr

168 t projections from the substantia nigra pars reticulata to the deep layers of the superior colliculus

169 atibility Complex (MHC) of guppies (Poecilia reticulata) to study the turnover rate of alleles (tempo

170 nd 5-HT release in the substantia nigra pars reticulata, using a common stimulation in a single rat.

171 n, subthalamic nucleus, and substantia nigra reticulata), ventral thalamus, geniculate nuclei, and te

172 ected in striatum than substantia nigra (SN) reticulata, whereas N/OFQ receptor antagonists were inef

173 a lesser extent in the substantia nigra pars reticulata, while no hybridization signal was detectable

174 evels of both the pars compacta and the pars reticulata, with little labeling rostrally.