ライフサイエンスコーパス: Macaca mulatta

1 come of Mtb challenge in non-human primates (Macaca mulatta).

2 cue-primed reinstatement in rhesus macaques (Macaca mulatta).

3 itron emission tomography in rhesus monkeys (Macaca mulatta).

4 nds recorded in auditory cortex of primates (Macaca mulatta).

5 rly visual cortices of anesthetized monkeys (Macaca mulatta).

6 e vestibular loss in alert behaving monkeys (Macaca mulatta).

7 mental health in a sample of rhesus monkeys (Macaca mulatta).

8 d CD8 T-lymphocyte-depleted rhesus macaques (Macaca mulatta).

9 us (i.v.) exposure route in rhesus macaques (Macaca mulatta).

10 attentional processes in the primate brain (Macaca mulatta).

11 eral cortical areas in adult Rhesus monkeys (Macaca mulatta).

12 of signals in the visual cortex of macaques (Macaca mulatta).

13 visual selection process in rhesus macaques (Macaca mulatta).

14 ogically and behaviorally in rhesus monkeys (Macaca mulatta).

15 and unrelated adult female rhesus macaques (Macaca mulatta).

16 nar (PI) to cortical area MT in the primate (Macaca mulatta).

17 alth and periodontitis in nonhuman primates (Macaca mulatta).

18 as a candidate priority map in the macaque (Macaca mulatta).

19 young, middle aged, and old rhesus monkeys (Macaca mulatta).

20 ual cortex of anaesthetized macaque monkeys (Macaca mulatta).

21 on executive function in the rhesus monkey (Macaca mulatta).

22 baboon (Papio hamadryas) and rhesus monkeys (Macaca mulatta).

23 tical visual processing (area V1) in monkey (Macaca mulatta).

24 n monkeys (Cebus apella) and rhesus monkeys (Macaca mulatta).

25 levels were inoculated into rhesus monkeys (Macaca mulatta).

26 s vaccines in SIV(mac251)-infected macaques (Macaca mulatta).

27 d the perceptual strategies of two macaques (Macaca mulatta).

28 a) previously identified in rhesus macaques (Macaca mulatta).

29 e fore brain of three female rhesus monkeys (Macaca mulatta).

30 nsmission of infant abuse in rhesus monkeys (Macaca mulatta).

31 ling SIVmac251 infection in rhesus macaques (Macaca mulatta).

32 an Plasmodium vivax malaria (P. cynomolgi in Macaca mulatta).

33 c T lymphocyte responses in rhesus macaques (Macaca mulatta).

34 ntrol subjects and in 17 eyes of 13 monkeys (Macaca mulatta).

35 dity in colonies of captive rhesus macaques (Macaca mulatta).

36 pha(2)) in PFC area 46 of 38 rhesus monkeys (Macaca mulatta).

37 and tested this capacity in rhesus macaques (Macaca mulatta).

38 nously inoculated into four rhesus macaques (Macaca mulatta).

39 to (inputs) the ACC of adult rhesus monkeys (Macaca mulatta).

40 visual cortex (V1; N = 15) of male monkeys (Macaca mulatta).

41 in a group of free-ranging rhesus macaques (Macaca mulatta).

42 processing system [8-10]: the rhesus monkey (Macaca mulatta).

43 ajectories observed in five rhesus macaques (Macaca mulatta).

44 bject-processing pathway, in rhesus monkeys (Macaca mulatta).

45 rus (SIV)-infected juvenile rhesus macaques (Macaca mulatta).

46 ted visual exploration in nonhuman primates (Macaca mulatta).

47 ng electrical stimulation in rhesus monkeys (Macaca mulatta).

48 urbation in pathogenesis in rhesus macaques (Macaca mulatta).

49 small nonhuman primate, the rhesus macaque (Macaca mulatta).

50 ed by stimulation artifact in awake monkeys (Macaca mulatta).

51 orhinal cortex in 2-week-old rhesus monkeys (Macaca mulatta).

52 crophage turnover in Indian rhesus macaques (Macaca mulatta).

53 normal and MPTP-lesioned nonhuman primates (Macaca mulatta).

54 d nicotine-experienced adult rhesus monkeys (Macaca mulatta).

55 d IGF-1 treatment on normal binocular infant Macaca mulatta.

56 the parental wild-type MV in a natural host, Macaca mulatta.

57 ion converge in single neurons of area V2 in Macaca mulatta.

58 y of friendships in juvenile rhesus monkeys (Macaca mulatta): (1) individual characteristics includin

59 (1-85 years old) and two nonhuman primates (Macaca mulatta, 15 and 17 years old) were immunohistoche

60 es from 5 of 16 asymptomatic rhesus monkeys (Macaca mulatta) (31%) were positive for a curved gram-ne

61 Captive-bred adolescent male rhesus monkeys (Macaca mulatta) (4-10 kg) were used as recipients and do

62 In the rhesus monkey (Macaca mulatta) a nonclassical MHC class I molecule, Mam

63 s of natal dispersal age in rhesus macaques (Macaca mulatta), a species with male dispersal.

64 wo conditions: while rhesus macaque monkeys (Macaca mulatta) actively performed a threshold amplitude

65 Subjects Twenty-eight rhesus monkeys (Macaca mulatta) aged 24 to 30 months were used for the s

66 with the trigeminal blink reflex in monkeys (Macaca mulatta) alters the effective balance between fix

67 from multiple locations within the primate (Macaca mulatta) amygdala spatially defined and statistic

68 arch biases in 2 species of macaque monkeys (Macaca mulatta and Macaca arctoides) were explored over

69 ental glaucoma was induced in adult monkeys (Macaca mulatta and Macaca fascicularis) by laser applica

70 een behavioral inhibition in rhesus monkeys (Macaca mulatta) and airway hyperresponsiveness, but not

71 e, we infected a small group of male rhesus (Macaca mulatta) and cynomolgus (Macaca fascicularis) mac

72 vets (Chlorocebus aethiops), rhesus macaque (Macaca mulatta) and cynomolgus macaque (Macaca fascicula

73 the demographic history of rhesus macaques (Macaca mulatta) and document the extent of linkage diseq

74 ctivity in humans, chimpanzees and macaques (Macaca mulatta) and found a prominent temporal lobe proj

75 culomotor vermis of behaving rhesus monkeys (Macaca mulatta) and found neurons that increased or decr

76 yes of 10 anesthetized adult rhesus monkeys (Macaca mulatta) and from 4 normal humans.

77 In Experiment 1, we trained rhesus monkeys (Macaca mulatta) and humans (Homo sapiens) on adjacent pa

78 with aging and menopause in rhesus monkeys (Macaca mulatta) and that these metrics correlate with de

79 p (i.e., Old World monkeys: rhesus macaques, Macaca mulatta), and (3), the presentation of artificial

80 primary visual cortex of the rhesus macaque (Macaca mulatta), and also show that, like in rodents, ST

81 for humans (Homo sapiens), rhesus macaques (Macaca mulatta), and several other nonhuman primate spec

82 her primate species (Cercopithecus tantalus, Macaca mulatta, and Aotus trivirgatus) was not increased

83 ids metabolism in the brain of MPTP-lesioned Macaca mulatta, and in the serum and cerebrospinal fluid

84 tently across 4 monkeys (1 female and 1 male Macaca mulatta; and 2 male Macaca fascicularis).

85 rimate (NHP) model of Lyme disease, 16 adult Macaca mulatta animals inoculated with strain N40 of B.

86 Rhesus macaques (Macaca mulatta) appear to be robustly risk-seeking in co

87 SIV-infected Indian rhesus macaques (Macaca mulatta) are an important animal model for humans

88 Rhesus macaques (Macaca mulatta) are key for modeling human immune respon

89 Indian rhesus macaques (Macaca mulatta) are routinely used in preclinical studie

90 find that most MT neurons in rhesus monkeys (Macaca Mulatta) are selective for depth sign based on bo

91 Infant rhesus macaques (Macaca mulatta) are susceptible to diarrhea making them

92 Rhesus macaques (Macaca mulatta) are the most widely used nonhuman primat

93 Rhesus macaques (Macaca mulatta) are the most widely used nonhuman primat

94 Rhesus macaques (Macaca mulatta) are the primate most used for biomedical

95 We recorded single neuron responses from Macaca mulatta area V2 to a display of two bright and tw

96 orearm muscular activity of rhesus macaques (Macaca mulatta) as they reached, grasped, and carried ob

97 s in the OFC encode the values that monkeys (Macaca mulatta) assign to different goods when they choo

98 ution of periodontitis in nonhuman primates (Macaca mulatta) at different ages.

99 encoding of naturalistic sounds in primate (Macaca mulatta) auditory cortex we here investigate pote

100 thymus from normal neonatal rhesus macaques (Macaca mulatta) between 0 and 21 days of age.

101 abey [Lophocebus albigena], rhesus macaques [Macaca mulatta], bonnet macaque [Macaca radiate], and ol

102 tion transcriptional atlas of rhesus monkey (Macaca mulatta) brain development that combines dense te

103 ivity of GnIH neurons in the rhesus macaque (Macaca mulatta) brain.

104 rresponding sites within the macaque monkey (Macaca mulatta) brain.

105 the myenteric plexus, of the rhesus monkey (Macaca mulatta) by immunohistochemistry and directly com

106 eplaced in mature non-human primate oocytes (Macaca mulatta) by spindle-chromosomal complex transfer

107 in 55 young, healthy, adult rhesus monkeys (Macaca mulatta) by tying 2.0 silk ligatures at the gingi

108 tained in humans (A118G) and rhesus macaques Macaca mulatta (C77G).

109 lamic nuclei in the embryonic rhesus monkey (Macaca mulatta) can be defined by combinatorial expressi

110 eractions to examine whether rhesus monkeys (Macaca mulatta) can learn dominance relationships betwee

111 Here we address whether rhesus monkeys (Macaca mulatta) can learn the abstract concept of "middl

112 of neurons in area V4 of the rhesus monkey (Macaca mulatta) can reliably predict large changes in an

113 sted with a meta-analysis of rhesus monkeys (Macaca mulatta), capuchin monkeys (Cebus apella), and pi

114 Rhesus monkeys (Macaca mulatta) chronically administered opioids were mo

115 o-random manual tracking task in the monkey (Macaca mulatta), climbing fiber discharge dynamically co

116 nzees (Pan troglodytes), and rhesus monkeys (Macaca mulatta) completed the same relational matching-t

117 In SIV-infected Indian rhesus macaques (Macaca mulatta), comprehensive CD8+ T cell epitope ident

118 Primate (Macaca mulatta) cone pedicles, labeled with an antibody

119 learning paradigm in which Rhesus macaques (Macaca mulatta) controlled a computer cursor by modulati

120 s indicates that adult female rhesus monkey (Macaca mulatta) coos are individually distinctive but th

121 dy was to determine whether rhesus macaques (Macaca mulatta) could generalize successful performance

122 Rhesus monkeys (Macaca mulatta) develop strategies to acquire and execut

123 al pattern, responses of neurons in macaque (Macaca mulatta) dorsal anterior cingulate cortex (dACC)

124 We found that neurons in primate (Macaca mulatta) dorsal anterior cingulate cortex, an are

125 the activity of dopamine neurons in monkeys (Macaca mulatta) during a Pavlovian procedure with appeti

126 e substantia nigra pars compacta of monkeys (Macaca mulatta) during a reaching task in which the ener

127 local field potentials in MI in two monkeys (Macaca mulatta) during continuous, self-paced movements

128 pulated IFN-I signalling in rhesus macaques (Macaca mulatta) during simian immunodeficiency virus (SI

129 FPs recorded in V1 of anesthetized macaques (Macaca mulatta) during the presentation of color movies.

130 n the middle temporal area (MT) of macaques (Macaca mulatta) during the slow phase of optokinetic nys

131 h eyes of four adult rhesus macaque monkeys (Macaca mulatta) during two baseline sessions, and again

132 ostsurgically in 6 groups of rhesus monkeys (Macaca mulatta), each consisting of 1 sham-operated cont

133 how in this study that aging rhesus monkeys (Macaca mulatta) exhibit poor CD8 T cell and B cell respo

134 We show that rhesus macaques (Macaca mulatta) experimentally infected with P. coatneyi

135 t human eye bank eyes and 10 rhesus macaque (Macaca mulatta) eyes were measured.

136 ity, we hypothesized that in Rhesus monkeys (Macaca mulatta) fed a high fat diet and who subsequently

137 ined the genome sequence of an Indian-origin Macaca mulatta female and compared the data with chimpan

138 Additionally, five Macaca mulatta female monkeys ( approximately 5.5-7 year

139 Three monkeys (Macaca mulatta) fixated five vertically displaced target

140 experiments on free-ranging rhesus monkeys (Macaca mulatta), focusing specifically on their capacity

141 region of one optic nerve of rhesus monkeys (Macaca mulatta) for 1.5 years.

142 by investigating pathways in rhesus monkeys (Macaca mulatta) from the amygdala to pOFC at the level o

143 ing approximately 24% of the rhesus macaque (Macaca mulatta) genome onto 4178 homologous loci in the

144 object association, in which rhesus monkeys (Macaca mulatta) had to first learn to discriminate betwe

145 or cortical spiking data in rhesus macaques (Macaca mulatta) handling objects of variable shape and s

146 e (OPRM1) of both humans and rhesus macaques Macaca mulatta has been associated with differential aff

147 ontrast in area V4d of the behaving macaque (Macaca mulatta), i.e., narrow bandpass filter neurons wi

148 s did not impair the performance of monkeys (Macaca mulatta) immediately after errors, but made them

149 dala-lesioned and unoperated rhesus monkeys (Macaca mulatta) in 2 contexts.

150 We trained animals (Macaca mulatta) in a challenging perceptual task in whic

151 ed this problem by training 2 monkeys (male, Macaca mulatta) in a postural perturbation task while re

152 To test this, we engaged monkeys (Macaca mulatta) in a reward-based decision task in which

153 We tested four male rhesus monkeys (Macaca mulatta) in both the expression and identity task

154 ctivity from the amygdala of 2 male monkeys (Macaca mulatta) in response to visual, tactile, and audi

155 rum apical membrane Ag 1 in rhesus macaques (Macaca mulatta), including the chimpanzee adenovirus 63

156 llected from 253 free-ranging rhesus macaque Macaca mulatta infants on Cayo Santiago, Puerto Rico, we

157 Rhesus macaques (Macaca mulatta) infected intravenously with a lethal dos

158 ants in visual oddball sequences in macaque (Macaca mulatta) inferior temporal (IT) cortex, a higher-

159 ythmic activity in V1 of the macaque monkey (macaca mulatta) is affected by top-down visual attention

160 The rhesus macaque (Macaca mulatta) is an abundant primate species that dive

161 Although the rhesus macaque (Macaca mulatta) is commonly used for biomedical research

162 ippocampal gyrus (PHG) of the rhesus monkey (Macaca mulatta) is comprised of three distinct cortical

163 our displayed by laboratory rhesus macaques (Macaca mulatta) is often used as an indicator of stress.

164 ough the SIV-infected Indian rhesus macaque (Macaca mulatta) is the animal model most widely used for

165 The rhesus macaque (Macaca mulatta) is the most widely studied nonhuman prim

166 organism in biomedicine, the rhesus macaque (Macaca mulatta) is the most widely used nonhuman primate

167 The species examined included rhesus (Macaca mulatta), Japanese (M. fuscata), pigtailed (M. ne

168 Four sophisticated macaque monkeys (Macaca mulatta) learned 6 different, 15-item ordinal lis

169 Two monkeys (Macaca mulatta) learned a color change-detection task wh

170 Rhesus monkeys (Macaca mulatta) learned the ordering of stimulus lists u

171 r calcium accumulation in cultured human and Macaca mulatta lenses results in proteolysis of crystall

172 performed in Indian-origin rhesus macaques (Macaca mulatta), little is known about lentiviral pathog

173 identify the core region in macaque monkeys (Macaca mulatta, M. nemestrina) could be used to identify

174 w World hosts compared to Old World species (Macaca mulatta, Macaca fascicularis).

175 rvegicus (rat), Danio rerio (zebrafish), and Macaca mulatta (macaque), as well as perform orthologous

176 ved the 67-week health of SIVsmE660-infected Macaca mulatta macaques.

177 ns from visual area V5/MT while two monkeys (Macaca mulatta) made perceptual decisions about the rota

178 neurons to oriented gratings in two monkeys (Macaca mulatta) making delayed saccades to targets dista

179 A 3.5-year-old adult female rhesus macaque (Macaca mulatta) manifested swelling of the left upper ey

180 iciency virus (SIV)-infected rhesus macaque (Macaca mulatta) model to examine whether disseminated M.

181 ead candidate in two in vivo rhesus macaque (Macaca mulatta) models.

182 rminals of prefrontal cortical area 9 in the Macaca mulatta monkey.

183 Longitudinal studies in Macaca mulatta monkeys show that insulin resistance is a

184 -Hz ERGs were evoked from four adult rhesus (Macaca mulatta) monkeys using sine-wave, square-wave, an

185 ascicularis (Macaca fascicularis) or rhesus (Macaca mulatta) monkeys.

186 Male rhesus macaque (Macaca mulatta) morphological traits are likely to refle

187 Here, we found that in rhesus monkeys (Macaca mulatta) most axon terminals labeled from tracers

188 ive behavior of group-living rhesus macaque (Macaca mulatta) mothers with a history of abusive parent

189 ions where others look), in infant macaques (Macaca mulatta; n = 119).

190 ala of naive rats (n=32) and rhesus monkeys (Macaca mulatta; n=6).

191 premotor cortex (vPMC) from rhesus monkeys (Macaca mulatta) of either sex, we demonstrate that MSC-E

192 samples of captive juvenile rhesus macaques (Macaca mulatta) of the Tulane National Primate Research

193 The authors tested 90 rhesus monkeys (Macaca mulatta) on a task of spatial memory, the spatial

194 gnition is causal by testing rhesus monkeys (Macaca mulatta) on a vicarious reinforcement task before

195 ected in different parts of the putamen in 3 Macaca mulatta (one male) and the laminar distribution o

196 s of SIVmac239-infected rhesus macaques (RM; Macaca mulatta), one with chronic infection, the other w

197 tly available genomes from Canis familiaris, Macaca mulatta, P. troglodytes and Rattus norvegicus, an

198 Our study investigated Macaca mulatta, Pan troglodytes, Gorilla gorilla, and Ho

199 l in AIP and F5 while three macaque monkeys (Macaca mulatta) performed a delayed grasping task.

200 cordings in V1 while rhesus macaque monkeys (Macaca mulatta) performed a task that demanded top-down

201 e recorded from VLPFC while rhesus macaques (Macaca mulatta) performed an audiovisual working memory

202 ngle CGp neurons was recorded while monkeys (Macaca mulatta) performed delayed-saccade trials initiat

203 ary BG output nucleus, in nonhuman primates (Macaca mulatta) performing a motor associative learning

204 i-unit activity in two male macaque monkeys (Macaca mulatta) performing an attention task.

205 four seminal, published studies in monkeys (Macaca mulatta) performing multialternative tasks.

206 us-tuned MSTd neurons in two rhesus monkeys (Macaca mulatta) performing pursuit eye movements across

207 caque (Macaca fascicularis), rhesus macaque (Macaca mulatta), pig (Sus scrofa), and mouse (Mus muscul

208 eport that gene transfer into rhesus monkey (Macaca mulatta) preimplantation embryos gives rise to tr

209 Three adult male monkeys (Macaca mulatta), previously behaviorally and genetically

210 ccuracy of population coding in the macaque (Macaca mulatta) primary visual cortex (V1).

211 ified IgG from convalescent rhesus macaques (Macaca mulatta) protects naive recipient macaques agains

212 ectron micrographs from aging rhesus monkey (Macaca mulatta), provided by Alan Peters and his colleag

213 The rhesus monkey (Macaca mulatta) provides a compelling model to study age

214 genomic markers mapped in a rhesus macaque (Macaca mulatta) radiation hybrid panel with the human ge

215 Whereas mammals (Pan troglodytes, Macaca mulatta, Rattus norvegicus, and Mus musculus) sho

216 In the first group, six adult monkeys (Macaca mulatta) received a single injection of the thymi

217 Six adult monkeys (Macaca mulatta) received a unilateral lesion of the late

218 labeling experiments, four macaque monkeys (Macaca mulatta) received injections of biotinylated dext

219 d its neural substrate, 10-12-d-old monkeys (Macaca mulatta) received sham operations or neurotoxic h

220 s in the lateral intraparietal area (LIP) of Macaca mulatta reflect learned associations between dire

221 frontal cortex (VLPFC) of the rhesus monkey (Macaca mulatta) respond to and integrate conspecific voc

222 that our TGI model in adult Rhesus macaques (Macaca mulatta) results in marked neuronal cell loss in

223 Wholemounts of rhesus monkey (Macaca mulatta) retinas with the choroid removed but the

224 nd the four homologues described in macaque (Macaca mulatta) revealed very high conservation with onl

225 o those of the well-studied related species, Macaca mulatta (rhesus macaque).

226 The abundant protein was identified as Macaca mulatta serum albumin precursor (67 kDa) from eig

227 We show that putative interneurons in FEF of Macaca mulatta show stronger attentional rate modulation

228 of tissue from a series of macaque monkeys (Macaca mulatta) showed that cells in the region of both

229 Consistent with MVT, rhesus macaques (Macaca mulatta) spent more time foraging for social info

230 nstrating that free-ranging rhesus macaques (Macaca mulatta) spontaneously discriminate between facia

231 Previous nonhuman primate (Macaca mulatta) studies suggest that this neuronal toler

232 activity in the deep layers of the macaque (Macaca mulatta) superior colliculus (SC) and the underly

233 ediated social cognition in rhesus macaques (Macaca mulatta), supplemented by discussion of recent wo

234 entify a pathway in the brain of the primate Macaca mulatta that conveys corollary discharge signals.

235 tex, and supplementary eye field of monkeys (Macaca mulatta) that performed a metacognitive visual-oc

236 nance hierarchy of juvenile macaque monkeys (Macaca mulatta) that received bilateral ibotenic acid le

237 virus (SIV) inoculation of rhesus macaques (Macaca mulatta) that were followed throughout their cour

238 ng and aged, male and female rhesus monkeys (Macaca mulatta) that were tested for cognitive status th

239 ording neurons in attending macaque monkeys (Macaca mulatta), that attention modulates visual signals

240 rence genome sequence of the rhesus macaque (Macaca mulatta), the most widely studied non-human prima

241 elated regions in the awake behaving monkey (Macaca mulatta): the parietal reach region (PRR) and the

242 ty in primary motor cortex (M1) of macaques (Macaca mulatta) to arm, wrist, and hand postures during

243 uthors trained 3 adult male rhesus macaques (Macaca mulatta) to categorize pairs of unknown conspecif

244 We trained two monkeys (Macaca mulatta) to determine the direction of visual mot

245 tes (Macaca nemestrina, Macaca fascicularis, Macaca mulatta) to examine the organization of specific

246 ons impaired the ability of macaque monkeys (Macaca mulatta) to learn conditional motor associations

247 esis, we trained four female rhesus monkeys (Macaca mulatta) to perform a multiple-fixation visual co

248 modulation during rest, we trained monkeys (Macaca mulatta) to perform a reaching task with their ow

249 to re-examine the ability of rhesus monkeys (Macaca mulatta) to recover from FDM.

250 The tendency for rhesus macaques, Macaca mulatta, to be tied affiliatively to others via c

251 tor and dorsal premotor cortices of monkeys (Macaca mulatta) trained to perform an instructed-delay r

252 fferences between M. nemestrina TRIM5eta and Macaca mulatta TRIM5alpha, some of which are at or near

253 ques (Macaca nemestrina) and rhesus monkeys (Macaca mulatta), two nonhuman primate species commonly u

254 Neurons were recorded in areas V1 and V2 of Macaca mulatta under behaviorally induced fixation.

255 ied prosthetic control; we show how monkeys (Macaca mulatta) use their motor cortical activity to con

256 bly (rheMacS) of the Chinese rhesus macaque (Macaca mulatta) using long-read sequencing and multiplat

257 were acquired from 40 normal rhesus monkeys (Macaca mulatta) using spectral domain optical coherence

258 de novo mutation rate in the rhesus macaque (Macaca mulatta) using whole-genome sequence data from 32

259 m young, adult, and aged non-human primates (Macaca mulatta), using the GeneChip(R) Rhesus Macaque Ge

260 at approximately 50% of rhesus macaques (RM; Macaca mulatta) vaccinated with SIV protein-expressing r

261 looking time of 3-month-old rhesus macaques (Macaca mulatta) viewing macaque faces varying in their d

262 social interactions of adult rhesus monkeys (Macaca mulatta) was assessed after bilateral ibotenic ac

263 When a group of six rhesus monkeys (Macaca mulatta) was inoculated intranasally with STAT1-b

264 When a group of six rhesus monkeys (Macaca mulatta) was inoculated intranasally with the SLA

265 l blood of captive juvenile rhesus macaques (Macaca mulatta) was observed following rotavirus infecti

266 natural human infection in rhesus macaques (Macaca mulatta), was used.

267 human SPL shifting region exists in monkeys (Macaca mulatta), we adopted an event-related fMRI paradi

268 ce adult risk of disease in rhesus macaques (Macaca mulatta), we analyze changes in basal leukocyte g

269 In two male rhesus macaque monkeys (Macaca mulatta), we found that lateral MD neurons carryi

270 in frontal eye field (FEF) of awake monkeys (Macaca mulatta), we probed the visual field with small s

271 nd electron microscopy in nonhuman primates (Macaca mulatta), we tested the hypothesis that the oppos

272 Fifty-two rhesus macaques (Macaca mulatta) were immunized with Ad26 vectors that en

273 Rhesus monkeys (Macaca mulatta) were implanted with an intracortical mic

274 Young adult rhesus macaques (Macaca mulatta) were intravenously administered 2.0 to 2

275 Adult female rhesus monkeys (Macaca mulatta) were spayed and either treated with plac

276 Rhesus monkeys (Macaca mulatta) were taught a large number of visual dis

277 neurons in MIo and SIo as two naive monkeys (Macaca mulatta) were trained in a novel tongue-protrusio

278 Five rhesus monkeys (Macaca mulatta) were trained to learn novel conditional

279 Four rhesus monkeys (Macaca mulatta) were trained to learn novel sets of visu

280 Monkeys (Macaca mulatta) were trained to order visual arrays base

281 Five adult rhesus monkeys (Macaca mulatta) were trained to self-administer cocaine

282 ve cocaine-experienced adult rhesus monkeys (Macaca mulatta) were trained to self-administer nicotine

283 sular microstructural features, confirmed in Macaca mulatta, were linked to behavior and predicted in

284 We investigated, in infant rhesus macaques (Macaca mulatta), whether newborns' capacity to imitate f

285 e hypotheses are valid, then rhesus monkeys (Macaca mulatta)--which share some homologies in the voca

286 nit activity in the VLPFC of rhesus monkeys (Macaca mulatta) while they produced vocalizations on com

287 reality system to translate macaque monkeys (Macaca mulatta) while they viewed motion parallax displa

288 Here we report that infant monkeys (Macaca mulatta) who engaged in more neonatal face-to-fac

289 ies was examined in juvenile rhesus monkeys (Macaca mulatta) who, at 2 weeks of postnatal age, receiv

290 uman primates, we immunized rhesus macaques (Macaca mulatta) with a DNA vaccine plasmid encoding Pfs2

291 nodeficiency virus-infected rhesus macaques (Macaca mulatta) with AIDS.

292 s this gap, we compared male rhesus monkeys (Macaca mulatta) with bilateral excitotoxic lesions restr

293 od choices of six adult male rhesus monkeys (Macaca mulatta) with bilateral, neurotoxic amygdala lesi

294 LGN to visual functions of macaque monkeys (Macaca mulatta) with chronic V1 lesions.

295 ustic startle in 2 groups of rhesus monkeys (Macaca mulatta) with different rearing experiences.

296 ting by inactivating the SC in two macaques (Macaca mulatta) with local muscimol injections.

297 Amaral (2006) reported that macaque monkeys (Macaca mulatta) with neonatal neurotoxic amygdala lesion

298 ions to behavior, we studied rhesus monkeys (Macaca mulatta) with restricted excitotoxic lesions targ

299 in the intestinal tract of rhesus macaques (Macaca mulatta) with SIV/AIDS.

300 rmance on the CSST by 7 young adult monkeys (Macaca mulatta) with surgically induced hypertension was