ライフサイエンスコーパス: Macaca

1 nfer the phylogenetic relationships of genus Macaca.

2 edical research currently are from the genus Macaca.

3 We named the new enzyme MACase (Macaca Acidic Chitinase) to emphasize its differences fr

4 otoreceptor development differs from that in Macaca and humans.

5 cicularis groups share a common ancestor; 3) Macaca arctoides are classified in the sinica group.

6 tively late, at 56% gestation, compared with Macaca at 32% gestation.

7 Genus Macaca (Cercopithecidae: Papionini) is one of the most s

8 topology of our tree suggests that: 1) genus Macaca contains four monophyletic species groups; 2) wit

9 rs of primers were chosen from exon 2 of the Macaca DRB1 gene and another three pairs were chosen fro

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

11 Macaca fascicularis (cynomolgus or longtail macaques) is

12 ia parasite whose natural vertebrate host is Macaca fascicularis (the 'kra' monkey); however, it is n

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

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

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

16 nalysis of the intrinsic connectivity of the Macaca fascicularis monkey hippocampal formation.

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

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

19 Two Macaca fascicularis monkeys were trained to perform an i

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

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

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

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

24 Intravenous inoculation of Macaca fascicularis with Escherichia coli produced mild

25 RT-PCR of total RNA from M. nemestrina and Macaca fascicularis yielded three TRIMCyp amplification

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

27 ll regions of the murine, non-human primate (Macaca fascicularis) and human GI tracts.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

44 cs tools, we studied 34 cynomolgus macaques (Macaca fascicularis) to compare a 2004 human H5N1 Vietna

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

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

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

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

49 Cynomolgus monkeys (Macaca fascicularis) were immunized systemically with nM

50 baseline, 32 male adult cynomolgus monkeys (Macaca fascicularis) were randomized to an ad libitum (A

51 Eleven monkeys (Macaca fascicularis) were rendered diabetic with strepto

52 Cynomolgus macaques (Macaca fascicularis) were transplanted with mismatched k

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

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

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

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

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

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

59 a series of studies in 19 nonhuman primates (Macaca fascicularis), the potential therapeutic advantag

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

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

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

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

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

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

66 ade tracer injections in cynomolgus monkeys (Macaca fascicularis).

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

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

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

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

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

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

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

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

75 res the offspring's intestinal microbiome 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 nted 7 Old World monkeys (Japanese macaques [Macaca fuscata], gray-cheeked mangabey [Lophocebus albig

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

260 Macaca nemestrina do not express TRIM5alpha; therefore,

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

262 Here we show that Macaca nemestrina monkeys can directly control stimulati

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

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

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

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

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

268 efficient transduction of pigtailed macaque (Macaca nemestrina) long-term repopulating cells using VS

269 replication in vitro in pig-tailed macaque (Macaca nemestrina) lymphocytes.

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

271 signal used by monkeys (pigtailed macaques: Macaca nemestrina) means submission (immediate behavior)

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

273 cy virus (SIV)-infected pig-tailed macaques (Macaca nemestrina) were treated with four antiretroviral

274 0 chronically catheterized pregnant monkeys (Macaca nemestrina) with either group B streptococcus (GB

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

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

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

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

279 e-body PET of the pregnant nonhuman primate (Macaca nemestrina).

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

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

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

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

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

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

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

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

288 quence is also different from that of either Macaca or human.

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

290 her-reared, socially-housed bonnet macaques (Macaca radiata) in three age groups: juvenile, adolescen

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

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

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

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

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

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

297 looking behavior between 15 Barbary macaque (Macaca sylvanus) infants and their mothers in the presen

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

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

300 ovide a robust molecular phylogeny for genus Macaca with stronger statistical support than previous s