ライフサイエンスコーパス: squirrel monkey

1 only been established in New World primates (squirrel monkeys).

2 scle unit contractile characteristics in the squirrel monkey.

3 ry (SI) and primary motor (MI) cortex of the squirrel monkey.

4 transmitter are generated from L-DOPA in the squirrel monkey.

5 p representations of Brodmann area 3b in the squirrel monkey.

6 to NPNFP in the brainstems of 5 cats and one squirrel monkey.

7 ribed in the laboratory rat, owl monkey, and squirrel monkey.

8 els are represented in striate cortex of the squirrel monkey.

9 ns of angioscotomas in striate cortex of the squirrel monkey.

10 ons in New World marmosets, owl monkeys, and squirrel monkeys.

11 duces dyskinesias in normal (ie, unlesioned) squirrel monkeys.

12 ired median and ulnar nerve section in adult squirrel monkeys.

13 ortical area 3b of New World owl monkeys and squirrel monkeys.

14 into localized regions of the caudal GPi in squirrel monkeys.

15 mma-2 herpesvirus saimiri (HVS) of New World squirrel monkeys.

16 body are organized in the cuneate nucleus of squirrel monkeys.

17 DM in owl monkeys and the presumptive DM in squirrel monkeys.

18 gue that DM is a visual area of both owl and squirrel monkeys.

19 1,1'-biphenyl]-3-yl-cyclohexylcarbamate), in squirrel monkeys.

20 nd to inhibit Sidman avoidance responding in squirrel monkeys.

21 ing, and conditioned avoidance responding in squirrel monkeys.

22 ated in the striatum and substantia nigra of squirrel monkeys.

23 ns with transneuronal tracers in four normal squirrel monkeys.

24 y in the adjacent, undamaged cortex of adult squirrel monkeys.

25 -tetrahydrocannabinol (THC) or anandamide in squirrel monkeys.

26 a unilateral lesion of the dorsal column in squirrel monkeys.

27 sory cortex (areas 3b and 1) in anesthetized squirrel monkeys.

28 noise carriers in the auditory core of awake squirrel monkeys.

29 eurochemical effects of nicotine in rats and squirrel monkeys.

30 cending afferents from digit 1 to survive in squirrel monkeys.

31 week after median nerve compression in adult squirrel monkeys.

32 in the cervical spinal cord (C4-C6) in adult squirrel monkeys.

33 PMv) distal forelimb representation (DFL) in squirrel monkeys.

34 gions of the ipsilateral hemisphere in adult squirrel monkeys.

35 l optical imaging of areas 3b and 1 in awake squirrel monkeys.

36 vior when self-administered intravenously by squirrel monkeys.

37 ed hand and normally activated face in adult squirrel monkeys.

38 ll number between young, middle-aged and old squirrel monkeys.

39 during active and passive head movements in squirrel monkeys.

40 ay and compared results from owl monkeys and squirrel monkeys 5-10 weeks after lesions with controls.

41 of hypocretin-1 in the cisternal CSF of the squirrel monkey, a New World primate with a pattern of w

42 of Goodpasture autoantibodies in the GBM of squirrel monkeys, a species susceptible to Goodpasture a

43 These results suggest that in squirrel monkeys activity-dependent mechanisms do normal

44 ns being more numerous in chinchilla than in squirrel monkey, afferent discharge properties are simil

45 ll, 65% of the photocoagulation sites in the squirrel monkey and 37% of sites in macaque monkey elici

46 The three alleles in the squirrel monkey and capuchin have spectral peaks near 56

47 The three alleles in the squirrel monkey and marmoset have been sequenced previou

48 the species that is most divergent from the squirrel monkey and marmoset, suggesting the presence of

49 and tamarin belong to the same family as the squirrel monkey and marmoset, the saki monkey belongs to

50 In one squirrel monkey and one galago we demonstrated that thes

51 In squirrel monkey and owl monkey, receptive fields of magn

52 described in the macaque monkey hold for the squirrel monkey and owl monkey.

53 n various striatal and limbic nuclei in both squirrel monkey and rat.

54 g results for the duct system of humans, the squirrel monkey and the rhesus macaque, making compariso

55 as seeded in the dominant male of a group of squirrel monkeys and an alternative technique in the dom

56 and AMGY genes from humans, orangutans, and squirrel monkeys and estimated that the male-to-female r

57 Indeed, previous experiments on squirrel monkeys and macaque monkeys showed that social

58 ual digit representations of area 3b in four squirrel monkeys and one prosimian galago.

59 Squirrel monkeys and rats were trained to self-administe

60 nd the synthetic cannabinoid WIN 55,212-2 in squirrel monkeys and rats, respectively, and it also pre

61 uR2, on abuse-related effects of nicotine in squirrel monkeys and rats.

62 f primate primary motor cortex (M1) in three squirrel monkeys and two galagos years after the therape

63 of two diurnal primates (macaque monkeys and squirrel monkeys) and one nocturnal primate (owl monkey)

64 g the X-linked pigments of bush baby, human, squirrel monkey, and marmoset, 38 variable positions wer

65 a local area resembled those present in the squirrel monkey, and no evidence was found for column/pa

66 In cats, squirrel monkeys, and macaque monkeys, we found neuroche

67 were placed into DM in galagos, owl monkeys, squirrel monkeys, and macaque monkeys.

68 om two macaque monkeys, two owl monkeys, two squirrel monkeys, and three galagos that were processed

69 the primary somatosensory cortices of adult squirrel monkeys at four postnerve injury survival durat

70 vity within the spinal cords of anesthetized squirrel monkeys at rest and show that the strength of c

71 vements in the distal forelimb zone of M1 of squirrel monkeys, before and after behavioral training o

72 d by magnetic resonance imaging in 31 female squirrel monkeys between the ages of 5 and 17 years.

73 rmine whether brain 5-HT deficits persist in squirrel monkeys beyond the 18-month period studied prev

74 In squirrel monkeys, both blob and interblob regions of V1

75 Preliminary PET/MRI of squirrel monkey brain was conducted along with HPLC asse

76 cular dominance columns are absent in normal squirrel monkeys, but induced to form by strabismus.

77 a1 promoters and (v and vi) in cebid owl and squirrel monkeys by crossovers that fused 5' sequence fr

78 s (FVT) were elicited in 12 maculae of seven squirrel monkeys by laser photocoagulation using optimiz

79 e and THC reinforcement and reinstatement in squirrel monkeys by the CB1-receptor inverse agonist rim

80 and map in somatosensory cortex of our adult squirrel monkeys by transecting the median nerve to one

81 Like the macaque, the squirrel monkey can be considered a useful primate model

82 This study shows that squirrel monkeys can exhibit clear ocular dominance colu

83 HIV-1 did not detectably bind or utilize squirrel monkey CD4 for entry, and marmoset CD4 was also

84 Using human/squirrel monkey chimeras, mutagenesis, and molecular mod

85 enomes of two cytomegalovirus (CMV) species, squirrel monkey CMV (SMCMV) and owl monkey CMV (OMCMV),

86 In squirrel monkeys, connections were also found with corte

87 In owl monkeys and squirrel monkeys, connections were with both the upper a

88 Inferior temporal cortex of squirrel monkeys consists of caudal (ITC), intermediate

89 Brain tissue from the CWD-infected squirrel monkeys contained the abnormal isoform of the p

90 actile adaptation on the optical response of squirrel monkey contralateral SI cortex to vibrotactile

91 The CWD-inoculated squirrel monkeys developed a progressive neurodegenerati

92 cicularis) infected with the same virus, the squirrel monkeys developed more-severe immunosuppression

93 thesis by recording from IN neurons in alert squirrel monkeys during vestibular and proprioceptive st

94 rel monkeys independently of DBP1 binding to Squirrel monkey erythrocytes.

95 Unexpectedly, 76% of the FVT sites in squirrel monkey eyes and 27% of the sites in macaque eye

96 ay structures of human FKBP51, to 2.7 A, and squirrel monkey FKBP51, to 2.8 A, by using multiwaveleng

97 We show here that in squirrel monkeys, focal deprivation by blood vessels lea

98 rat were generally larger than those in the squirrel monkey following injections into the UC or CE.

99 In addition, squirrel monkeys given ICV injections of adenoviral BDNF

100 thing anomalous about the visual capacity of squirrel monkeys has been found to explain their missing

101 In the squirrel monkey, hypocretin-1 works in opposition to the

102 Preliminary squirrel monkey imaging and human serum/liver microsome

103 expressing TRIM5alpha from either tamarin or squirrel monkeys in permissive cell lines resulted in a

104 monkey were significantly slower than in the squirrel monkey, in both species magnocellular neurones

105 show that Salvador (Sal) I P. vivax infects Squirrel monkeys independently of DBP1 binding to Squirr

106 The use of two tracers in squirrel monkeys indicated that terminations from adjace

107 The squirrel monkey is the only primate reported to lack ocu

108 ly follows median nerve transection in adult squirrel monkeys is dependent on normally functioning N-

109 rectly predicted the SCN lesion phenotype in squirrel monkeys: loss of circadian rhythmicity and emer

110 Here we test this hypothesis in adult squirrel monkey males exposed to intermittent social sep

111 ations increased hippocampal neurogenesis in squirrel monkey males.

112 It is known that the squirrel monkey, marmoset, and other related New World (

113 eptors, in the present study we used rat and squirrel monkey models of reward and relapse to examine

114 ) from common marmosets, spider monkeys, and squirrel monkeys, New World monkey (NWM) species that sh

115 Squirrel monkeys normally lack ocular dominance columns

116 ptor subunits in the area 3b cortex of adult squirrel monkeys one and five months after median nerve

117 A comparison of the squirrel monkey opsin sequence with published mammalian

118 acchus herpesvirus is frequently detected in squirrel monkey peripheral blood lymphocytes, indicating

119 n was found in PI(M) of macaques, whereas in squirrel monkeys PI(M) was light.

120 Results suggest that orangutans but not squirrel monkeys possess Stage 6 object permanence capab

121 ded the optical intrinsic signal response of squirrel monkey primary somatosensory cortex (SI) to 25

122 Self-administration of 2-AG by squirrel monkeys provides a valuable procedure for study

123 1R2 residue I67, which corresponds to S67 in squirrel monkey receptor, modulates the higher affinity

124 roviruses such as simian AIDS retrovirus and squirrel monkey retrovirus were also detected in the ass

125 nance imaging (fMRI) studies on anesthetized squirrel monkeys revealed dynamic reorganizations of dig

126 quences of the entire blue opsin gene in the squirrel monkey (Saimiri boliviensis) and the five intro

127 o species of New World monkeys - the diurnal squirrel monkey (Saimiri sciureus) and the nocturnal owl

128 cells outnumber type II hair cells (HCs) in squirrel monkey (Saimiri sciureus) cristae by a nearly 3

129 d 1 hamadryas baboon (Papio hamadryas) and 1 squirrel monkey (Saimiri sciureus) to respond to stimuli

130 zed by two methods in three NWM species, the squirrel monkey (Saimiri sciureus), the tamarin (Saguinu

131 cretin-1 in a wake-consolidating animal, the squirrel monkey (Saimiri sciureus).

132 re of the visual thalamus was re-examined in squirrel monkeys (Saimiri sciureus) and macaques (Macaca

133 Here, we report that infection of squirrel monkeys (Saimiri sciureus) fulfills these requi

134 Three squirrel monkeys (Saimiri sciureus) learned to reach tow

135 thors tested orangutans (Pongo pygmaeus) and squirrel monkeys (Saimiri sciureus) on object permanence

136 Squirrel monkeys (Saimiri sciureus) that had learned to

137 our capuchin monkeys (Cebus apella) and four squirrel monkeys (Saimiri sciureus) were given demonstra

138 s been extensively characterised (humans and squirrel monkeys (Saimiri sciureus)), the aVOR response

139 (MT(C)) in owl monkeys (Aotus trivirgatus), squirrel monkeys (Saimiri sciureus), and macaque monkeys

140 To investigate if squirrel monkeys (Saimiri sciureus), which are reported

141 cellular electrophysiological study employed squirrel monkeys (Saimiri sciureus), which moved freely

142 st established experimental WNV infection of squirrel monkeys (Saimiri sciureus).

143 isual area (DL(C)) were investigated in four squirrel monkeys (Saimiri) following extracellular injec

144 f the nucleus tractus solitarii (NTS) in the squirrel monkey, Saimuri sciureus, was investigated by n

145 The results suggest that the squirrel monkey SI is involved in processing of visceral

146 In anesthetized squirrel monkeys single cell recordings were performed u

147 logical recordings from layer 4C of a normal squirrel monkey, single units were mostly monocular, but

148 Squirrel monkeys solved visible but did not comprehend i

149 One squirrel monkey started to delay gratification in Phase

150 mary cells derived from common marmosets and squirrel monkeys support every phase of HIV-1 replicatio

151 The CXCR4 molecules of both marmosets and squirrel monkeys supported HIV-1 infection, but the CCR5

152 h correspond to residues T40 and E142 in the squirrel monkey Tas1R2, were found to be the critical re

153 otelencephalic terminals showed that, in the squirrel monkey, terminals from CE injections were large

154 ominance columns are less well segregated in squirrel monkeys than macaques, but they are present.

155 Squirrel monkeys that previously self-administered anand

156 tibody Cat-301 differed between macaques and squirrel monkeys, the same subdivisions were displayed.

157 In squirrel monkeys, there was a tendency for caudal DL to

158 y anterograde tracers injected in area MT of squirrel monkeys, to characterize these connections furt

159 hydro-1H-purine-2,6-dione], respectively, in squirrel monkeys trained to intravenously self-administe

160 ylogenetically with those of the opossum and squirrel monkey, two of its preferred mammalian hosts in

161 Male squirrel monkeys underwent quantitative PET studies of c

162 In three other squirrel monkeys, unilateral dorsal column lesions were

163 Results indicate that squirrel monkeys vaccinated with SEL-068 failed to acqui

164 olgi cells and recorded these neurons in the squirrel monkey ventral paraflocculus during oculomotor

165 The area 3b hand cortex of adult squirrel monkeys was mapped during the first minutes to

166 apparent lack of ocular dominance columns in squirrel monkeys, we made eye injections with transneuro

167 (SAM) tones in the auditory cortex of awake squirrel monkeys, we show that the prior presentation of

168 ddle temporal (MT) areas of visual cortex in squirrel monkeys were compared with PI subdivisions reve

169 ps from four hemispheres of two normal adult squirrel monkeys were created and used to derive express

170 avior and vocalizations of four group-housed squirrel monkeys were examined following administration

171 ceptibility of nonhuman primates to CWD, two squirrel monkeys were inoculated with brain tissue from

172 Twenty squirrel monkeys were randomized to intermittent stress

173 butal, or halothane (in N2O/O2) anesthetized squirrel monkeys were tested for responses to distention

174 In Experiment 3, squirrel monkeys were tested using the procedure of Expe

175 he present study compared visual learning in squirrel monkeys with ablations of ITC; ITI and ITR (gro

176 aural frequency map changes is chronicled in squirrel monkeys with asymmetric hearing loss induced by

177 In two squirrel monkeys with forelimb amputation, physiological