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1 Mtb challenge in non-human primates (Macaca mulatta).
2 ine-experienced adult rhesus monkeys (Macaca mulatta).
3 med reinstatement in rhesus macaques (Macaca mulatta).
4 mission tomography in rhesus monkeys (Macaca mulatta).
5 orded in auditory cortex of primates (Macaca mulatta).
6 ual cortices of anesthetized monkeys (Macaca mulatta).
7 bular loss in alert behaving monkeys (Macaca mulatta).
8 health in a sample of rhesus monkeys (Macaca mulatta).
9 -lymphocyte-depleted rhesus macaques (Macaca mulatta).
10 .) exposure route in rhesus macaques (Macaca mulatta).
11 ional processes in the primate brain (Macaca mulatta).
12 rtical areas in adult Rhesus monkeys (Macaca mulatta).
13 als in the visual cortex of macaques (Macaca mulatta).
14 selection process in rhesus macaques (Macaca mulatta).
15 y and behaviorally in rhesus monkeys (Macaca mulatta).
16 d periodontitis in nonhuman primates (Macaca mulatta).
17 related adult female rhesus macaques (Macaca mulatta).
18 ) to cortical area MT in the primate (Macaca mulatta).
19 andidate priority map in the macaque (Macaca mulatta).
20 middle aged, and old rhesus monkeys (Macaca mulatta).
21 tex of anaesthetized macaque monkeys (Macaca mulatta).
22 cutive function in the rhesus monkey (Macaca mulatta).
23 (Papio hamadryas) and rhesus monkeys (Macaca mulatta).
24 isual processing (area V1) in monkey (Macaca mulatta).
25 ys (Cebus apella) and rhesus monkeys (Macaca mulatta).
26 were inoculated into rhesus monkeys (Macaca mulatta).
27 nes in SIV(mac251)-infected macaques (Macaca mulatta).
28 erceptual strategies of two macaques (Macaca mulatta).
29 brain of three female rhesus monkeys (Macaca mulatta).
30 iously identified in rhesus macaques (Macaca mulatta).
31 on of infant abuse in rhesus monkeys (Macaca mulatta).
32 Vmac251 infection in rhesus macaques (Macaca mulatta).
33 tion against SIV in rhesus macaques (Macacca mulatta).
34 modium vivax malaria (P. cynomolgi in Macaca mulatta).
35 phocyte responses in rhesus macaques (Macaca mulatta).
36 ubjects and in 17 eyes of 13 monkeys (Macaca mulatta).
37 colonies of captive rhesus macaques (Macaca mulatta).
38 in PFC area 46 of 38 rhesus monkeys (Macaca mulatta).
39 ted this capacity in rhesus macaques (Macaca mulatta).
40 oth male and female macaque monkeys (Maccaca mulatta).
41 uts) the ACC of adult rhesus monkeys (Macaca mulatta).
42 cortex (V1; N = 15) of male monkeys (Macaca mulatta).
43 roup of free-ranging rhesus macaques (Macaca mulatta).
44 ing system [8-10]: the rhesus monkey (Macaca mulatta).
45 ies observed in five rhesus macaques (Macaca mulatta).
46 rocessing pathway, in rhesus monkeys (Macaca mulatta).
47 trical stimulation in rhesus monkeys (Macaca mulatta).
48 V)-infected juvenile rhesus macaques (Macaca mulatta).
49 ual exploration in nonhuman primates (Macaca mulatta).
50 n in pathogenesis in rhesus macaques (Macaca mulatta).
51 nonhuman primate, the rhesus macaque (Macaca mulatta).
52 timulation artifact in awake monkeys (Macaca mulatta).
53 cortex in 2-week-old rhesus monkeys (Macaca mulatta).
54 e turnover in Indian rhesus macaques (Macaca mulatta).
55 and MPTP-lesioned nonhuman primates (Macaca mulatta).
56 treatment on normal binocular infant Macaca mulatta.
57 ental wild-type MV in a natural host, Macaca mulatta.
58 revealed independent gene duplication in M. mulatta.
59 verge in single neurons of area V2 in Macaca mulatta.
60 iendships in juvenile rhesus monkeys (Macaca mulatta): (1) individual characteristics including sex,
61 years old) and two nonhuman primates (Macaca mulatta, 15 and 17 years old) were immunohistochemically
62 5 of 16 asymptomatic rhesus monkeys (Macaca mulatta) (31%) were positive for a curved gram-negative
63 -bred adolescent male rhesus monkeys (Macaca mulatta) (4-10 kg) were used as recipients and donors.
66 ite their presumed functional importance, M. mulatta Ab receptors are largely uncharacterized, posing
67 itions: while rhesus macaque monkeys (Macaca mulatta) actively performed a threshold amplitude modula
68 Subjects Twenty-eight rhesus monkeys (Macaca mulatta) aged 24 to 30 months were used for the study.
69 e trigeminal blink reflex in monkeys (Macaca mulatta) alters the effective balance between fixation a
70 ultiple locations within the primate (Macaca mulatta) amygdala spatially defined and statistically se
71 prototypic TRIMCyp alleles described for M. mulatta and M. nemestrina, restricts human immunodeficie
72 ases in 2 species of macaque monkeys (Macaca mulatta and Macaca arctoides) were explored over the cou
73 avioral inhibition in rhesus monkeys (Macaca mulatta) and airway hyperresponsiveness, but not atopy,
74 nfected a small group of male rhesus (Macaca mulatta) and cynomolgus (Macaca fascicularis) macaques w
75 hlorocebus aethiops), rhesus macaque (Macaca mulatta) and cynomolgus macaque (Macaca fascicularis), a
76 mographic history of rhesus macaques (Macaca mulatta) and document the extent of linkage disequilibri
77 in humans, chimpanzees and macaques (Macaca mulatta) and found a prominent temporal lobe projection
78 or vermis of behaving rhesus monkeys (Macaca mulatta) and found neurons that increased or decreased t
80 eriment 1, we trained rhesus monkeys (Macaca mulatta) and humans (Homo sapiens) on adjacent pairs (e.
81 ging and menopause in rhesus monkeys (Macaca mulatta) and that these metrics correlate with delayed r
82 , Old World monkeys: rhesus macaques, Macaca mulatta), and (3), the presentation of artificially sequ
83 visual cortex of the rhesus macaque (Macaca mulatta), and also show that, like in rodents, STDP is g
84 mans (Homo sapiens), rhesus macaques (Macaca mulatta), and several other nonhuman primate species, bu
85 mate species (Cercopithecus tantalus, Macaca mulatta, and Aotus trivirgatus) was not increased by As(
86 abolism in the brain of MPTP-lesioned Macaca mulatta, and in the serum and cerebrospinal fluid of PD
88 (NHP) model of Lyme disease, 16 adult Macaca mulatta animals inoculated with strain N40 of B. burgdor
90 SIV-infected Indian rhesus macaques (Macaca mulatta) are an important animal model for humans infect
93 at most MT neurons in rhesus monkeys (Macaca Mulatta) are selective for depth sign based on both disp
98 recorded single neuron responses from Macaca mulatta area V2 to a display of two bright and two dark
99 muscular activity of rhesus macaques (Macaca mulatta) as they reached, grasped, and carried objects o
100 e OFC encode the values that monkeys (Macaca mulatta) assign to different goods when they choose betw
102 ng of naturalistic sounds in primate (Macaca mulatta) auditory cortex we here investigate potential i
104 ophocebus albigena], rhesus macaques [Macaca mulatta], bonnet macaque [Macaca radiate], and olive bab
105 anscriptional atlas of rhesus monkey (Macaca mulatta) brain development that combines dense temporal
108 enteric plexus, of the rhesus monkey (Macaca mulatta) by immunohistochemistry and directly compare it
109 in mature non-human primate oocytes (Macaca mulatta) by spindle-chromosomal complex transfer from on
110 young, healthy, adult rhesus monkeys (Macaca mulatta) by tying 2.0 silk ligatures at the gingival mar
112 ns to examine whether rhesus monkeys (Macaca mulatta) can learn dominance relationships between unfam
113 re we address whether rhesus monkeys (Macaca mulatta) can learn the abstract concept of "middle" in a
114 rons in area V4 of the rhesus monkey (Macaca mulatta) can reliably predict large changes in an animal
115 th a meta-analysis of rhesus monkeys (Macaca mulatta), capuchin monkeys (Cebus apella), and pigeons (
118 m manual tracking task in the monkey (Macaca mulatta), climbing fiber discharge dynamically controls
119 Pan troglodytes), and rhesus monkeys (Macaca mulatta) completed the same relational matching-to-sampl
120 SIV-infected Indian rhesus macaques (Macaca mulatta), comprehensive CD8+ T cell epitope identificati
122 ng paradigm in which Rhesus macaques (Macaca mulatta) controlled a computer cursor by modulating neur
123 ates that adult female rhesus monkey (Macaca mulatta) coos are individually distinctive but their scr
124 to determine whether rhesus macaques (Macaca mulatta) could generalize successful performance on an e
126 ern, responses of neurons in macaque (Macaca mulatta) dorsal anterior cingulate cortex (dACC) to both
127 We found that neurons in primate (Macaca mulatta) dorsal anterior cingulate cortex, an area that
128 ivity of dopamine neurons in monkeys (Macaca mulatta) during a Pavlovian procedure with appetitive an
129 antia nigra pars compacta of monkeys (Macaca mulatta) during a reaching task in which the energetic c
130 ield potentials in MI in two monkeys (Macaca mulatta) during continuous, self-paced movements to seri
131 IFN-I signalling in rhesus macaques (Macaca mulatta) during simian immunodeficiency virus (SIV) tran
133 iddle temporal area (MT) of macaques (Macaca mulatta) during the slow phase of optokinetic nystagmus.
134 of four adult rhesus macaque monkeys (Macaca mulatta) during two baseline sessions, and again 1 week
135 ically in 6 groups of rhesus monkeys (Macaca mulatta), each consisting of 1 sham-operated control and
136 this study that aging rhesus monkeys (Macaca mulatta) exhibit poor CD8 T cell and B cell responses in
139 the most prevalent allotypic variants of M. mulatta FcgammaR for binding to both human and M. mulatt
140 hypothesized that in Rhesus monkeys (Macaca mulatta) fed a high fat diet and who subsequently receiv
141 e genome sequence of an Indian-origin Macaca mulatta female and compared the data with chimpanzees an
144 ments on free-ranging rhesus monkeys (Macaca mulatta), focusing specifically on their capacity to gen
146 stigating pathways in rhesus monkeys (Macaca mulatta) from the amygdala to pOFC at the level of the s
147 roximately 24% of the rhesus macaque (Macaca mulatta) genome onto 4178 homologous loci in the human g
148 association, in which rhesus monkeys (Macaca mulatta) had to first learn to discriminate between pair
149 ical spiking data in rhesus macaques (Macaca mulatta) handling objects of variable shape and size.
150 1) of both humans and rhesus macaques Macaca mulatta has been associated with differential affinity t
151 in area V4d of the behaving macaque (Macaca mulatta), i.e., narrow bandpass filter neurons with peak
153 ot impair the performance of monkeys (Macaca mulatta) immediately after errors, but made them unable
156 problem by training 2 monkeys (male, Macaca mulatta) in a postural perturbation task while recording
157 To test this, we engaged monkeys (Macaca mulatta) in a reward-based decision task in which they s
158 We tested four male rhesus monkeys (Macaca mulatta) in both the expression and identity task after
159 from the amygdala of 2 male monkeys (Macaca mulatta) in response to visual, tactile, and auditory st
160 cal membrane Ag 1 in rhesus macaques (Macaca mulatta), including the chimpanzee adenovirus 63 (AdCh63
161 from 253 free-ranging rhesus macaque Macaca mulatta infants on Cayo Santiago, Puerto Rico, we examin
163 visual oddball sequences in macaque (Macaca mulatta) inferior temporal (IT) cortex, a higher-order c
167 pal gyrus (PHG) of the rhesus monkey (Macaca mulatta) is comprised of three distinct cortical areas b
169 e SIV-infected Indian rhesus macaque (Macaca mulatta) is the animal model most widely used for studyi
172 The species examined included rhesus (Macaca mulatta), Japanese (M. fuscata), pigtailed (M. nemestrin
173 Four sophisticated macaque monkeys (Macaca mulatta) learned 6 different, 15-item ordinal lists (via
176 um accumulation in cultured human and Macaca mulatta lenses results in proteolysis of crystallins, th
177 med in Indian-origin rhesus macaques (Macaca mulatta), little is known about lentiviral pathogenicity
180 s (rat), Danio rerio (zebrafish), and Macaca mulatta (macaque), as well as perform orthologous conver
182 visual area V5/MT while two monkeys (Macaca mulatta) made perceptual decisions about the rotation di
183 to oriented gratings in two monkeys (Macaca mulatta) making delayed saccades to targets distant from
184 year-old adult female rhesus macaque (Macaca mulatta) manifested swelling of the left upper eyelid an
186 ficiency virus (SIV)-rhesus macaque (Macacca mulatta) model point to opportunities at the earliest st
187 virus (SIV)-infected rhesus macaque (Macaca mulatta) model to examine whether disseminated M. avium
190 s were evoked from four adult rhesus (Macaca mulatta) monkeys using sine-wave, square-wave, and 4-ms
193 ere, we found that in rhesus monkeys (Macaca mulatta) most axon terminals labeled from tracers inject
196 or cortex (vPMC) from rhesus monkeys (Macaca mulatta) of either sex, we demonstrate that MSC-EVs redu
197 of captive juvenile rhesus macaques (Macaca mulatta) of the Tulane National Primate Research Center.
198 The authors tested 90 rhesus monkeys (Macaca mulatta) on a task of spatial memory, the spatial Delaye
199 is causal by testing rhesus monkeys (Macaca mulatta) on a vicarious reinforcement task before and af
200 n different parts of the putamen in 3 Macaca mulatta (one male) and the laminar distribution of the l
201 Vmac239-infected rhesus macaques (RM; Macaca mulatta), one with chronic infection, the other with pri
202 ilable genomes from Canis familiaris, Macaca mulatta, P. troglodytes and Rattus norvegicus, and combi
205 s in V1 while rhesus macaque monkeys (Macaca mulatta) performed a task that demanded top-down spatial
206 ded from VLPFC while rhesus macaques (Macaca mulatta) performed an audiovisual working memory task.
207 p neurons was recorded while monkeys (Macaca mulatta) performed delayed-saccade trials initiated rand
208 output nucleus, in nonhuman primates (Macaca mulatta) performing a motor associative learning task.
211 d MSTd neurons in two rhesus monkeys (Macaca mulatta) performing pursuit eye movements across display
212 Macaca fascicularis), rhesus macaque (Macaca mulatta), pig (Sus scrofa), and mouse (Mus musculus).
215 gG from convalescent rhesus macaques (Macaca mulatta) protects naive recipient macaques against chall
216 micrographs from aging rhesus monkey (Macaca mulatta), provided by Alan Peters and his colleague, Cla
218 c markers mapped in a rhesus macaque (Macaca mulatta) radiation hybrid panel with the human genome, a
219 Whereas mammals (Pan troglodytes, Macaca mulatta, Rattus norvegicus, and Mus musculus) showed a h
220 n the first group, six adult monkeys (Macaca mulatta) received a single injection of the thymidine an
222 eural substrate, 10-12-d-old monkeys (Macaca mulatta) received sham operations or neurotoxic hippocam
223 e lateral intraparietal area (LIP) of Macaca mulatta reflect learned associations between directions
224 cortex (VLPFC) of the rhesus monkey (Macaca mulatta) respond to and integrate conspecific vocalizati
225 r TGI model in adult Rhesus macaques (Macaca mulatta) results in marked neuronal cell loss in the hip
226 four homologues described in macaque (Macaca mulatta) revealed very high conservation with only one a
228 he abundant protein was identified as Macaca mulatta serum albumin precursor (67 kDa) from eight non-
229 that putative interneurons in FEF of Macaca mulatta show stronger attentional rate modulation than p
230 sue from a series of macaque monkeys (Macaca mulatta) showed that cells in the region of both the ven
231 Consistent with MVT, rhesus macaques (Macaca mulatta) spent more time foraging for social information
232 ng that free-ranging rhesus macaques (Macaca mulatta) spontaneously discriminate between facial image
234 ation of SNPs between M. fascicularis and M. mulatta, suggesting that the relationship of these two s
235 ty in the deep layers of the macaque (Macaca mulatta) superior colliculus (SC) and the underlying ret
236 social cognition in rhesus macaques (Macaca mulatta), supplemented by discussion of recent work in h
237 d supplementary eye field of monkeys (Macaca mulatta) that performed a metacognitive visual-oculomoto
238 ierarchy of juvenile macaque monkeys (Macaca mulatta) that received bilateral ibotenic acid lesions o
239 (SIV) inoculation of rhesus macaques (Macaca mulatta) that were followed throughout their course of d
240 aged, male and female rhesus monkeys (Macaca mulatta) that were tested for cognitive status through t
241 neurons in attending macaque monkeys (Macaca mulatta), that attention modulates visual signals before
242 enome sequence of the rhesus macaque (Macaca mulatta), the most widely studied non-human primate in b
243 regions in the awake behaving monkey (Macaca mulatta): the parietal reach region (PRR) and the dorsal
244 rimary motor cortex (M1) of macaques (Macaca mulatta) to arm, wrist, and hand postures during movemen
245 trained 3 adult male rhesus macaques (Macaca mulatta) to categorize pairs of unknown conspecifics pre
247 caca nemestrina, Macaca fascicularis, Macaca mulatta) to examine the organization of specific cingula
248 aired the ability of macaque monkeys (Macaca mulatta) to learn conditional motor associations between
249 e trained four female rhesus monkeys (Macaca mulatta) to perform a multiple-fixation visual conjuncti
250 tion during rest, we trained monkeys (Macaca mulatta) to perform a reaching task with their own arm w
252 The tendency for rhesus macaques, Macaca mulatta, to be tied affiliatively to others via connecti
253 dorsal premotor cortices of monkeys (Macaca mulatta) trained to perform an instructed-delay reaching
254 ed from parietal neurons in monkeys (Macacca mulatta) trained to report the direction of an apparent
255 es between M. nemestrina TRIM5eta and Macaca mulatta TRIM5alpha, some of which are at or near locatio
256 acaca nemestrina) and rhesus monkeys (Macaca mulatta), two nonhuman primate species commonly used to
258 sthetic control; we show how monkeys (Macaca mulatta) use their motor cortical activity to control a
259 eMacS) of the Chinese rhesus macaque (Macaca mulatta) using long-read sequencing and multiplatform sc
260 quired from 40 normal rhesus monkeys (Macaca mulatta) using spectral domain optical coherence tomogra
261 mutation rate in the rhesus macaque (Macaca mulatta) using whole-genome sequence data from 32 indivi
262 , adult, and aged non-human primates (Macaca mulatta), using the GeneChip(R) Rhesus Macaque Genome Ar
263 oximately 50% of rhesus macaques (RM; Macaca mulatta) vaccinated with SIV protein-expressing rhesus c
264 time of 3-month-old rhesus macaques (Macaca mulatta) viewing macaque faces varying in their distance
265 When a group of six rhesus monkeys (Macaca mulatta) was inoculated intranasally with STAT1-blind MV
266 When a group of six rhesus monkeys (Macaca mulatta) was inoculated intranasally with the SLAM-blind
267 of captive juvenile rhesus macaques (Macaca mulatta) was observed following rotavirus infection.
269 PL shifting region exists in monkeys (Macaca mulatta), we adopted an event-related fMRI paradigm that
270 t risk of disease in rhesus macaques (Macaca mulatta), we analyze changes in basal leukocyte gene exp
271 In two male rhesus macaque monkeys (Macaca mulatta), we found that lateral MD neurons carrying CD s
272 tal eye field (FEF) of awake monkeys (Macaca mulatta), we probed the visual field with small spots of
273 tron microscopy in nonhuman primates (Macaca mulatta), we tested the hypothesis that the opposite sta
274 lated from leukapheresis products of Macacca mulatta were cultured in granulocyte-macrophage colony s
279 in MIo and SIo as two naive monkeys (Macaca mulatta) were trained in a novel tongue-protrusion task.
283 ine-experienced adult rhesus monkeys (Macaca mulatta) were trained to self-administer nicotine or nic
284 icrostructural features, confirmed in Macaca mulatta, were linked to behavior and predicted individua
285 estigated, in infant rhesus macaques (Macaca mulatta), whether newborns' capacity to imitate facial g
286 heses are valid, then rhesus monkeys (Macaca mulatta)--which share some homologies in the vocal produ
287 ivity in the VLPFC of rhesus monkeys (Macaca mulatta) while they produced vocalizations on command or
288 system to translate macaque monkeys (Macaca mulatta) while they viewed motion parallax displays that
289 Here we report that infant monkeys (Macaca mulatta) who engaged in more neonatal face-to-face inter
290 examined in juvenile rhesus monkeys (Macaca mulatta) who, at 2 weeks of postnatal age, received sele
291 imates, we immunized rhesus macaques (Macaca mulatta) with a DNA vaccine plasmid encoding Pfs25 or a
292 gap, we compared male rhesus monkeys (Macaca mulatta) with bilateral excitotoxic lesions restricted t
293 ces of six adult male rhesus monkeys (Macaca mulatta) with bilateral, neurotoxic amygdala lesions and
297 (2006) reported that macaque monkeys (Macaca mulatta) with neonatal neurotoxic amygdala lesions displ
298 behavior, we studied rhesus monkeys (Macaca mulatta) with restricted excitotoxic lesions targeting e
300 on the CSST by 7 young adult monkeys (Macaca mulatta) with surgically induced hypertension was compar