ライフサイエンスコーパス: Macaca mulatta

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

24 of the amygdala on sleep in rhesus monkeys (Macaca mulatta).

25 tein, respectively, in adult rhesus monkeys (Macaca mulatta).

26 th cortico-pulvinar connections in macaques (Macaca mulatta).

27 e treated with xenogeneic pancreatic islets (Macaca mulatta).

28 ues (Macaca nemestrina) and rhesus macaques (Macaca mulatta).

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

30 rel monkeys (Saimiri sciureus) and macaques (Macaca mulatta).

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

32 ognitive development of male rhesus monkeys (Macaca mulatta).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

59 tral lateral nucleus (VL) of the thalamus in Macaca mulatta.

60 lla and orang-utan, and an Old World monkey, Macaca mulatta.

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

62 (1-85 years old) and two nonhuman primates (Macaca mulatta, 15 and 17 years old) were immunohistoche

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

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

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

66 The aged rhesus macaque monkey (Macaca mulatta), a species that develops beta-amyloid pl

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

68 performances of group-tested rhesus monkeys (Macaca mulatta) across various social contexts.

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

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

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

72 xperimental glaucoma was induced in monkeys (Macaca mulatta and M. fascicularis) by applying a laser

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

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

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

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

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

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

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

80 Macaque (Macaca mulatta) and human performance on feature and con

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

82 Rhesus macaques (Macaca mulatta) and pig-tailed macaques (Macaca nemestri

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

113 in 22 (16.7%) of 131 normal rhesus macaques (Macaca mulatta), compared to 18 (33.8%) of 53 rhesus mac

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

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

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

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

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

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

120 solates obtained from three species: rhesus (Macaca mulatta), cynomologus (Macaca fasicularis), and p

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

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

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

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

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

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

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

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

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

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

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

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

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

134 healthy simian HIV-infected rhesus monkeys (Macaca mulatta) expressing the 1F7 marker on anti-gp120

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

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

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

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

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

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

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

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

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

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

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

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

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

164 betaH-crystallin fraction of rhesus monkey (Macaca mulatta) lens.

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

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

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

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

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

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

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

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

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

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

175 ne regeneration experiments in 18 adult male Macaca mulatta monkeys to determine how long membranes m

176 d in the posterior maxilla and mandible in 4 Macaca mulatta monkeys.

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

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

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

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

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

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

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

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

185 However, in Macaca mulatta, only two FRG1 loci were identified, one

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

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

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

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

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

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

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

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

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

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

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

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

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

199 their coupling in old, healthy, nondiabetic Macaca mulatta primates (age 21 +/- 3.6 years).

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

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

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

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

204 ituations, was contrasted in rhesus monkeys (Macaca mulatta) reared individually with either canine c

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

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

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

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

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

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

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

212 Macaca mulatta retinas and optic nerves were fixed overn

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

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

215 herpesvirus-Macaca nemestrina (RFHVMn) and -Macaca mulatta (RFHVMm).

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

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

218 receptor CCR5 in humans and rhesus macaques (Macaca mulatta) serves as the primary coreceptor for cel

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

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

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

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

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

224 associated with exposure to rhesus macaques (Macaca mulatta), suggesting that BV isolates from rhesus

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

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

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

228 iciency virus (SIV)-infected rhesus macaque (Macaca mulatta) that developed a multicentric lymphoprol

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

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

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

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

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

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

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

236 lesioned bilaterally in six rhesus monkeys (Macaca mulatta) through microinjection of the neurotoxin

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

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

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

240 tro and then inoculated into rhesus monkeys (Macaca mulatta) to determine their neutralizing ability.

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

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

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

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

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

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

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

248 D8 cells in peripheral blood in six infected Macaca mulatta treated with OKT8F.

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

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

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

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

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

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

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

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

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

258 RF2 receptor binding sites in rhesus monkey (Macaca mulatta) was assessed by using iodine 125 ([125I)

259 edal reaching in humans and rhesus macaques (Macaca mulatta) was examined, and the data were compared

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

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

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

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

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

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

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

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

268 Adult Rhesus monkey eyes (Macaca mulatta) were dissected, and 5-mm macula and peri

269 ations from infant and adult rhesus monkeys (Macaca mulatta) were immunolabeled by incubation overnig

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

271 Rhesus monkeys (Macaca mulatta) were infected with five strains of simia

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

273 living in a large group of rhesus macaques (Macaca mulatta) were recorded along with their behavior.

274 human allergen, three female rhesus monkeys (Macaca mulatta) were sensitized with house dust mite (De

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 Rhesus monkeys (Macaca mulatta) were trained to solve visual discriminat

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 This duplication is present in Macaca mulatta whose divergence from hominoids is though

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

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

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

300 he obesity and diabetes prone rhesus monkey (Macaca mulatta) would provide an excellent animal model