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1 DTH) model in the cynomolgus macaque (Macaca fascicularis).
2 cer injections in cynomolgus monkeys (Macaca fascicularis).
3 dentate gyrus of young adult monkeys (Macaca fascicularis).
4 ctions of MITN in cynomolgus monkeys (Macaca fascicularis).
5 ve, premenopausal cynomolgus monkeys (Macaca fascicularis).
6 dult (age, 21.2+/-0.2 years) monkeys (Macaca fascicularis).
7 -beta subunit of cynomolgous macaque (Macaca fascicularis).
8 ion and motor speed in young monkeys (Macaca fascicularis).
9 ded bladder of the cynomolgus monkey (Macaca fascicularis).
10 rning and memory function in monkeys (Macaca fascicularis).
11 ansected in eight cynomolgus monkeys (Macaca fascicularis).
12 mulatta) and one cynomolgous monkey (Macaca fascicularis).
13 ex (V1) in six normal adult macaques (Macaca fascicularis).
14 d genes in living cynomolgus monkeys (Macaca fascicularis).
15 r undertaken by long-tailed macaques (Macaca fascicularis).
16 to Old World species (Macaca mulatta, Macaca fascicularis).
17 6 conscious obese cynomolgus monkeys (Macaca fascicularis).
18 synanthrope, the long-tailed macaque (Macaca fascicularis).
19 ddle-aged female cynomolgus macaques (Macaca fascicularis).
20 human health, the cynomolgus macaque (Macaca fascicularis).
21 Mauritian-origin cynomolgus macaque (Macaca fascicularis).
22 donor eye and 2 normal primate eyes (Macaca fascicularis).
23 esearch colony of cynomolgus monkeys (Macaca fascicularis).
24 and 1 male Macaca mulatta; and 2 male Macaca fascicularis).
25 ry bodies of five cynomolgus monkeys (Macaca fascicularis).
26 (NHP) model, the cynomolgus macaque (Macaca fascicularis).
27 in adult female cynomolgus macaques (Macaca fascicularis).
28 cortex (V1) of anesthetized macaque (Macaca fascicularis).
29 btained from the retinae of macaques (Macaca fascicularis).
30 an and the cynomolgus macaque monkey, Macaca fascicularis.
31 smission electron microscopy in adult Macaca fascicularis.
32 pain-2) in the nonhuman primate (Nhp) Macaca fascicularis.
33 ells from 45 tissues of the adult NHP Macaca fascicularis.
34 rgoing different loading protocols in Macaca fascicularis.
35 O, after intrathalamic inoculation in Macaca fascicularis.
36 macaque populations were also present in M. fascicularis.
37 29/57) of the rhesus SNPs were present in M. fascicularis.
38 cific for PD as it was not present in Macaca fascicularis (7 MPTP and 8 controls) with similar degree
41 isingly high conservation of SNPs between M. fascicularis and M. mulatta, suggesting that the relatio
44 ee monkeys with spontaneous IDDM (two Macaca fascicularis and one Ceropithecus aethiops) were treated
46 rning paradigm for nonhuman primates (macaca fascicularis) and recorded the activity of single neuron
48 nd SIVmac251 infection in cynomolgus (Macaca fascicularis) and rhesus macaques of Chinese origin.
51 us musculus) and cynomolgus macaques (Macaca fascicularis), and-concomitantly-protective immunity aga
52 ese results indicate that a proportion of M. fascicularis are able to effectively control the replica
53 ted from breeding centers in China (where M. fascicularis are not native) showed they were similar to
55 n existing data, cynomolgus macaques, Macaca fascicularis, are a viable alternative, but need further
56 have occurred between the Peninsular and M. fascicularis-associated groups, including in the DBP[For
61 in the premotor cortex of the monkey (Macaca fascicularis) brain by means of a convergence of visual
62 ection can cause fatal simian AIDS in Macaca fascicularis, but many individuals survive with few clin
64 the epiblast during embryogenesis in Macaca fascicularis, but shows greater divergence from mouse de
65 pia) was induced in six normal, adult Macaca fascicularis by disinserting the medial rectus muscles.
66 as induced in monkeys (Macaca mulatta and M. fascicularis) by applying a laser to the trabecular mesh
67 in adult monkeys (Macaca mulatta and Macaca fascicularis) by laser application to the trabecular mes
69 ned that the beta-subunit of macaque (Macaca fascicularis) chorionic gonadotropin (mCG-beta) is more
70 iments undertaken in macaque monkeys (Macaca fascicularis), cMRF neurons labeled retrogradely from in
72 uring groups of long-tailed macaques (Macaca-fascicularis) could be explained by ecological and envir
73 auditory cortices in macaque monkeys (Macaca fascicularis) could be used to identify homologous regio
74 t that timely detection of P. knowlesi in M. fascicularis, coupled with control of inflammation while
78 immunization in humans, we vaccinated Macaca fascicularis (Cynomolgus) monkeys with DNA encoding the
80 ind that LFS in the nonhuman primate (Macaca fascicularis) dACC, when combined with extinction traini
81 atures, in female cynomolgus macaque (Macaca fascicularis) displaying naturally occurring depressive-
82 arthenogenetic development of monkey (Macaca fascicularis) eggs to the blastocyst stage, and their us
83 arnegie stage 8-11 cynomolgus monkey (Macaca fascicularis) embryos and performed in-depth transcripto
85 ung tissues from cynomolgus macaques (Macaca fascicularis) experimentally infected with a low dose of
86 models, principally Macaca rhesus and Macaca fascicularis, experimentally infected with the relapsing
90 was evaluated in cynomolgus monkeys (Macaca fascicularis) for immunogenicity and safety as a vaccine
91 V2 of the macaque (Macaca nemestrina, Macaca fascicularis) for the orientation of texture-defined for
92 2 DNA-positive blood into groups of naive M. fascicularis from either a viremic or nonviremic donor a
95 were detected in cynomolgus macaques (Macaca fascicularis) from Mauritius Island only, and, remarkabl
96 SIV)-susceptible cynomolgus macaques (Macaca fascicularis) from the Indian Ocean island of Mauritius
98 es from 12 macaque species and show that the fascicularis group originated from an ancient hybridizat
100 iverged first, and members of the sinica and fascicularis groups share a common ancestor; 3) Macaca a
101 administered to cynomolgus macaques (Macaca fascicularis) had a profound effect on MCs without any o
102 Taken together, these data show that M. fascicularis has the most diverse array of TRIM5 restric
104 ia paraancora, Euphyllia paradivisa, Galaxea fascicularis, Herpolitha limax, Montipora confusa, Monit
105 , genomic sequencing of M. nemestrina and M. fascicularis identifies a CypA retrotransposition in the
106 on shellfish by long-tailed macaques (Macaca fascicularis) in Khao Sam Roi Yot National Park, Thailan
107 imate species, the cynomolgus monkey (Macaca fascicularis), in a realistic social ethological context
108 very of TRIMCyp in both M. nemestrina and M. fascicularis indicates that TRIMCyp expression may be mo
109 ular dominance columns in a sample of six M. fascicularis, indicating that the number of hypercolumns
110 ns) identified 2 cynomolgus macaques (Macaca fascicularis) infected with Ebola (subtype Reston) virus
111 Compared to cynomolgus macaques (Macaca fascicularis) infected with the same virus, the squirrel
112 y in a group of long-tailed macaques (Macaca fascicularis) inhabiting Koram Island, Thailand, and it
113 We found that cynomolgus macaques (Macaca fascicularis) inoculated with ZIKV or SPONV were suscept
115 nhibition of photosynthetic efficiency in G. fascicularis is exacerbated in the presence of prometryn
117 , a parasite of long-tailed macaques (Macaca fascicularis), is an important cause of human malaria.
118 teome response in cynomolgus macaque (Macaca fascicularis) lung tissue over 7 days of infection with
119 nd in four species of Asian macaques, Macaca fascicularis, M. mulatta, M. nemestrina, and M. leonina.
121 the saccular or utricular neuroepithelium of fascicularis (Macaca fascicularis) or rhesus (Macaca mul
122 nonhuman primates (Macaca nemestrina, Macaca fascicularis, Macaca mulatta) to examine the organizatio
123 himpanzee), Papio hamadryas (baboon), Macaca fascicularis (macaque), and Eulemur fulvus collaris (col
124 equency in Indonesian than in Indochinese M. fascicularis macaques and is also present in samples fro
126 apanese (Macaca fuscata) and long-tailed (M. fascicularis) macaques were selected for their highly de
127 esus (Macaca mulatta) and cynomolgus (Macaca fascicularis) macaques with a minimally passaged Brazili
128 pygmaeus, oEDN) and Old World monkey (Macaca fascicularis, mcEDN) genomic DNAs, and from a second New
132 al (ID) challenge cynomolgus macaque (Macaca fascicularis) model of scrub typhus, the leading cause o
135 racers into the amygdaloid complex of Macaca fascicularis monkeys and examining labeled boutons in ar
137 tested whether C-group motoneurons in Macaca fascicularis monkeys receive a direct cMRF input by inje
138 y and toxicity of MEGC-PEG-rMETase in Macaca fascicularis monkeys using an escalating-dose strategy.
139 ystem of the hippocampal formation of Macaca fascicularis monkeys was studied immunohistochemically w
147 rta of young versus old male monkeys (Macaca fascicularis) (n=7/group), where aortic stiffness increa
149 tly asymptomatic cynomolgus macaques (Macaca fascicularis), naturally infected with SRV type 2 (SRV-2
150 nes readily invade human and macaque (Macaca fascicularis) normocytes with a preference for reticuloc
151 MHC I alleles in Cynomolgus macaques (Macaca fascicularis) of Chinese, Vietnamese, and Mauritian orig
152 sulinopenic nonhuman primates (three Macacca fascicularis, one Ceropithecus aethiops, and one Macacca
157 premotor cortical sites in primates (Maccaca fascicularis) performing a motor task, while measuring t
158 olerance of six stony coral species (Galaxea fascicularis, Porites rus, Acropora muricata, Montipora
160 itro cultivation of P. cynomolgi-infected M. fascicularis primary hepatocytes during which hypnozoite
161 rocess, studies were carried out in a Macaca fascicularis primate model of experimental periodontitis
162 process, studies were conducted in a Macaca fascicularis primate model of experimental periodontitis
163 e of IL-1 in periodontal disease in a Macaca fascicularis primate model, using human soluble IL-1 rec
165 ller cells from the human and monkey (Macaca fascicularis) retina were studied with various configura
166 scanning electron microscopy of adult Macaca fascicularis retinae to examine the 3D structure of mito
167 ls (especially the cynomolgus monkey, Macaca fascicularis) reveals that chronic psychosocial stress c
168 ics and glaucoma: cynomolgus macaque (Macaca fascicularis), rhesus macaque (Macaca mulatta), pig (Sus
169 a sylvanus were inoculated with a pool of M. fascicularis serum and developed an acute HBV infection
171 as upregulated in carotid arteries of Macaca fascicularis subjected to atherosclerosis regression die
173 rons in the brain of macaque monkeys (Macaca fascicularis) that represent the auditory space surround
174 ly nephrectomized cynomolgus monkeys (Macaca fascicularis) that underwent splenectomy and were immuno
175 sues of 17 adult cynomolgus macaques (Macaca fascicularis) that were infected with Mtb strain Erdman
176 dy computer model of a primate skull (Macaca fascicularis), that aims to predict muscle recruitment p
177 site whose natural vertebrate host is Macaca fascicularis (the 'kra' monkey); however, it is now incr
178 s of studies in 19 nonhuman primates (Macaca fascicularis), the potential therapeutic advantage of an
179 warming on the stress-tolerant coral Galaxea fascicularis through physiological and omics analyses.
180 tal cortices of Macaca nemestrina and Macaca fascicularis to analyze the organization of terminals an
181 isual cortex in male macaque monkeys (Macaca fascicularis) to achromatic grating stimuli that varied
183 ivisions of MD in cynomolgus monkeys (Macaca fascicularis) to assess the relative proportions of conn
184 s, we studied 34 cynomolgus macaques (Macaca fascicularis) to compare a 2004 human H5N1 Vietnam isola
185 obtained using BOLD-fMRI in macaques (Macaca fascicularis) to structural connectivity derived from ma
186 onhuman-primate species [Papio-anubis/Macaca-fascicularis] to determine the impact of different adipo
187 We used primate (Macaca nemestrina/Macaca fascicularis) tracing studies and 3D reconstructions of
188 icle in six awake cynomolgus monkeys (Macaca fascicularis) trained to sit calmly in a primate chair.
191 tory effects of IL10 in M. mulatta, while M. fascicularis undergoes a transcriptional makeover toward
192 ated infections in Macaca mulatta and Macaca fascicularis using whole blood RNA-sequencing and transc
193 two MPTP-treated cynomolgus monkeys (macaca fascicularis) using a high-resolution PET imaging system
194 performed in 15 anesthetized monkeys (Macaca fascicularis) using extracellular single-unit recording
195 e right eye of 7 cynomolgous monkeys, Macaca fascicularis, using laser injury to the aqueous outflow
196 Mauritian cynomolgus macaques (MCM), Macaca fascicularis, vaccinated with unmodified SIV gag alone i
197 composition of the Old World primate Macaca fascicularis via scanning and transmission electron micr
200 ar injury model in nonhuman primates (Macaca fascicularis), we were able to demonstrate that CTRP-1 c
205 ne, 32 male adult cynomolgus monkeys (Macaca fascicularis) were randomized to an ad libitum (AL) diet
207 The wild-born long-tailed macaques (Macaca fascicularis) were recently recruited and used as breede
209 Twenty-four cynomolgus macaques (Macaca fascicularis) were studied for 46 weeks after inoculatio
212 ent images in two healthy macaque monkeys (M fascicularis) which showed the FUS beam within the brain
215 In this study, 3 cynomolgus monkeys (Macaca fascicularis) with bilateral perirhinal cortex ablations
216 groups of 5 or 6 cynomolgus monkeys (Macaca fascicularis) with either a wild-type MV or its "N4-blin
217 al PVs in female cynomolgus macaques (Macaca fascicularis) without breeding contact for at least 3.5
218 R of total RNA from M. nemestrina and Macaca fascicularis yielded three TRIMCyp amplification product