ライフサイエンスコーパス: Macaca

1 edical research currently are from the genus Macaca.

2 nfer the phylogenetic relationships of genus Macaca.

3 red specific for PD as it was not present in Macaca fascicularis (7 MPTP and 8 controls) with similar

4 Burmese long-tailed macaques (Macaca fascicularis aurea) are one of a limited number o

5 ess and strain values in a finite model of a Macaca fascicularis cranium.

6 oagulation factors IX (hFIX) or X (hFX) into Macaca fascicularis fetuses at ~0.4 gestation.

7 e-unit activity was recorded from V6A in two Macaca fascicularis fixating real targets in darkness.

8 Twenty-four female Macaca fascicularis monkeys divided into groups by age (

9 re, we tested whether C-group motoneurons in Macaca fascicularis monkeys receive a direct cMRF input

10 Two Macaca fascicularis monkeys were trained to perform an i

11 basal [Ba], and accessory basal [AB]) in six Macaca fascicularis monkeys.

12 amine the GABAergic innervation of the CG in Macaca fascicularis monkeys.

13 Borneo) and, in Borneo, their macaque host (Macaca fascicularis or M. nemestrina).

14 as it was upregulated in carotid arteries of Macaca fascicularis subjected to atherosclerosis regress

15 prefrontal cortices of Macaca nemestrina and Macaca fascicularis to analyze the organization of termi

16 ellular composition of the Old World primate Macaca fascicularis via scanning and transmission electr

17 Intravenous inoculation of Macaca fascicularis with Escherichia coli produced mild

18 from aorta of young versus old male monkeys (Macaca fascicularis) (n=7/group), where aortic stiffness

19 d a learning paradigm for nonhuman primates (macaca fascicularis) and recorded the activity of single

20 mutations of SHANK3 in cynomolgus macaques (Macaca fascicularis) and their F1 offspring.

21 We find that LFS in the nonhuman primate (Macaca fascicularis) dACC, when combined with extinction

22 ic signatures, in female cynomolgus macaque (Macaca fascicularis) displaying naturally occurring depr

23 l area V2 of the macaque (Macaca nemestrina, Macaca fascicularis) for the orientation of texture-defi

24 arkers were detected in cynomolgus macaques (Macaca fascicularis) from Mauritius Island only, and, re

25 We directly compared macaque (Macaca fascicularis) functional connectivity (FC) assess

26 raging on shellfish by long-tailed macaques (Macaca fascicularis) in Khao Sam Roi Yot National Park,

27 Compared to cynomolgus macaques (Macaca fascicularis) infected with the same virus, the s

28 the proteome response in cynomolgus macaque (Macaca fascicularis) lung tissue over 7 days of infectio

29 male rhesus (Macaca mulatta) and cynomolgus (Macaca fascicularis) macaques with a minimally passaged

30 ring locomotion in a nonhuman primate (NHP) (Macaca fascicularis) model of bipedal locomotion.

31 We used the cynomolgus macaque (Macaca fascicularis) model of HIV-Mycobacterium tubercul

32 The cynomolgus macaque (Macaca fascicularis) model of M. tuberculosis infection

33 tradermal (ID) challenge cynomolgus macaque (Macaca fascicularis) model of scrub typhus, the leading

34 -H.1 lines readily invade human and macaque (Macaca fascicularis) normocytes with a preference for re

35 Thirty-four male monkeys (Macaca fascicularis) received bilateral 0.7-mg DEX impla

36 cortex in an additional control monkey (male Macaca fascicularis) that had no surgical intervention.

37 imary visual cortex in male macaque monkeys (Macaca fascicularis) to achromatic grating stimuli that

38 Using the cynomolgus macaque (Macaca fascicularis) to assess primate-specific imprinti

39 (rsFC) obtained using BOLD-fMRI in macaques (Macaca fascicularis) to structural connectivity derived

40 We used primate (Macaca nemestrina/Macaca fascicularis) tracing studies and 3D reconstructi

41 Telemetered cynomolgus macaques (Macaca fascicularis) were challenged by the aerosol rout

42 Monkeys (male Macaca fascicularis) were given 5-bromo-2-deoxyuridine (

43 In this study, eight monkeys (Macaca fascicularis) who were subjects in a separate exe

44 nfected groups of 5 or 6 cynomolgus monkeys (Macaca fascicularis) with either a wild-type MV or its "

45 que (Macaca mulatta) and cynomolgus macaque (Macaca fascicularis), all male.

46 mice (Mus musculus) and cynomolgus macaques (Macaca fascicularis), and-concomitantly-protective immun

47 r experiments undertaken in macaque monkeys (Macaca fascicularis), cMRF neurons labeled retrogradely

48 uman primate species, the cynomolgus monkey (Macaca fascicularis), in a realistic social ethological

49 nowlesi, a parasite of long-tailed macaques (Macaca fascicularis), is an important cause of human mal

50 In dog and monkey (Macaca fascicularis), Pax2 is expressed by astrocytes th

51 P dynamics and glaucoma: cynomolgus macaque (Macaca fascicularis), rhesus macaque (Macaca mulatta), p

52 multibody computer model of a primate skull (Macaca fascicularis), that aims to predict muscle recrui

53 l human donor eye and 2 normal primate eyes (Macaca fascicularis).

54 in a research colony of cynomolgus monkeys (Macaca fascicularis).

55 female and 1 male Macaca mulatta; and 2 male Macaca fascicularis).

56 ammillary bodies of five cynomolgus monkeys (Macaca fascicularis).

57 primate (NHP) model, the cynomolgus macaque (Macaca fascicularis).

58 apacity in adult female cynomolgus macaques (Macaca fascicularis).

59 visual cortex (V1) of anesthetized macaque (Macaca fascicularis).

60 were obtained from the retinae of macaques (Macaca fascicularis).

61 ivity (DTH) model in the cynomolgus macaque (Macaca fascicularis).

62 SM-denuded bladder of the cynomolgus monkey (Macaca fascicularis).

63 mpared to Old World species (Macaca mulatta, Macaca fascicularis).

64 sion of the epiblast during embryogenesis in Macaca fascicularis, but shows greater divergence from m

65 acaque models, principally Macaca rhesus and Macaca fascicularis, experimentally infected with the re

66 een found in four species of Asian macaques, Macaca fascicularis, M. mulatta, M. nemestrina, and M. l

67 ing in nonhuman primates (Macaca nemestrina, Macaca fascicularis, Macaca mulatta) to examine the orga

68 rt that Mauritian cynomolgus macaques (MCM), Macaca fascicularis, vaccinated with unmodified SIV gag

69 The cynomolgus macaque, Macaca fascicularis, was introduced onto the island of M

70 PVS-RIPO, after intrathalamic inoculation in Macaca fascicularis.

71 een human and the cynomolgus macaque monkey, Macaca fascicularis.

72 neighbouring groups of long-tailed macaques (Macaca-fascicularis) could be explained by ecological an

73 ormal nonhuman-primate species [Papio-anubis/Macaca-fascicularis] to determine the impact of differen

74 res the offspring's intestinal microbiome in Macaca fuscata (Japanese macaque).

75 extensively characterized a primate model in Macaca fuscata (Japanese macaque).

76 Male Japanese macaques (Macaca fuscata) were castrated for 5-7 months and then t

77 Female Japanese macaques (Macaca fuscata) were ovariectomized or tubal-ligated (n=

78 s (N = 131) with different dominance styles (Macaca fuscata, M. fascicularis, M. sylvanus, M. maura).

79 nted 7 Old World monkeys (Japanese macaques [Macaca fuscata], gray-cheeked mangabey [Lophocebus albig

80 The genus Macaca is an ideal model for investigating the biologica

81 l data from a group of moor macaque monkeys (Macaca maura), we used permutation-based linear regressi

82 postnatal development in comparison with the Macaca monkey, reaching a mature stage earlier than thes

83 a small population of DCs in rhesus macaque (Macaca mulata) mesenteric lymph node.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

266 ritoneal fibromatosis-associated herpesvirus Macaca nemestrina (RFHVMn), the pig-tailed macaque homol

267 sp. palliatus (the black and white colobus), Macaca nemestrina (southern pig-tailed macaque), and Man

268 cingulate, and dorsal prefrontal cortices of Macaca nemestrina and Macaca fascicularis to analyze the

269 of HHV-7, which we have provisionally named Macaca nemestrina herpesvirus 7 (MneHV7).

270 tex and V2 of six amblyopic macaque monkeys (Macaca nemestrina) and two visually normal controls.

271 n chronically catheterized pregnant monkeys (Macaca nemestrina) at 118-125 days gestation (term=172 d

272 ive analysis of two male pigtailed macaques (Macaca nemestrina) experimentally infected with XMRV.

273 We studied macaque monkeys (Macaca nemestrina) for which we have detailed psychophys

274 We found that pigtail macaque (Macaca nemestrina) hepatic cells derived from induced pl

275 eas V1 and V2 of six female macaque monkeys (Macaca nemestrina) made amblyopic by artificial strabism

276 ncy virus (SIV)-infected pig-tailed macaque (Macaca nemestrina) model, but this is poorly characteriz

277 0 chronically catheterized pregnant monkeys (Macaca nemestrina) with either group B streptococcus (GB

278 we evaluated DeltaGY in pig-tailed macaques (Macaca nemestrina), a species in which SIVmac239 infecti

279 ex of anesthetized amblyopic monkeys (female Macaca nemestrina), using 96-channel "Utah" arrays to re

280 this interaction in the pig-tailed macaque (Macaca nemestrina), which is used in preclinical evaluat

281 KIR-MHC interactions in pigtailed macaques (Macaca nemestrina).

282 dorsal roots from mice and pigtail monkeys (Macaca nemestrina).

283 xtrastriate cortical area V2 of the macaque (Macaca nemestrina, Macaca fascicularis) for the orientat

284 atomical tract-tracing in nonhuman primates (Macaca nemestrina, Macaca fascicularis, Macaca mulatta)

285 t sizes from an animal society model system (Macaca nemestrina, n=48).

286 d hes2 human embryonic stem cells (hESC) and Macaca nemestrina-induced PSC (iPSC) line-7 with cytokin

287 l, a P-gp substrate, in the nonhuman primate Macaca nemestrina.

288 We used primate (Macaca nemestrina/Macaca fascicularis) tracing studies a

289 ropriate model, such as the pigtail macaque (Macaca nemestrina; Mn), is crucial.

290 mary motor (M1) cortex of nonhuman primates (Macaca radiata) are modulated by reward expectation duri

291 visual cortex of awake monkeys (three female Macaca radiata).

292 s macaques [Macaca mulatta], bonnet macaque [Macaca radiate], and olive baboon [Papio anubis]), 3 chi

293 bbon and synaptic markers in fetal human and Macaca retina.

294 ade using common macaque models, principally Macaca rhesus and Macaca fascicularis, experimentally in

295 nd recording in isolated peripheral primate (Macaca sp.) retina using multi-electrode arrays.

296 To confirm infectivity of this isolate, 3 Macaca sylvanus were inoculated with a pool of M. fascic

297 es) stressors in wild male Barbary macaques (Macaca sylvanus) in Morocco.

298 ovation in a wild group of Barbary macaques (Macaca sylvanus).

299 much simpler society in the Tibetan macaque (Macaca thibetana), which we have tracked for 30 consecut

300 pid, only taking 51% of gestation whereas in Macaca this takes 81%.