ライフサイエンスコーパス: rhesus monkey

1 0 muA, 100-300 Hz, n = 172 IC locations in 3 rhesus monkeys).

2 8)F-AV1451 ((18)F-T807) in mice, rats, and a rhesus monkey.

3 ng and quantifying the I2BS, in vivo, in the rhesus monkey.

4 rimental autoimmune encephalomyelitis in the rhesus monkey.

5 eneration and cell death in the normal aging rhesus monkey.

6 ed 50%-75% homology with mouse and >90% with rhesus monkey.

7 petitive, low-dose intrarectal challenges in rhesus monkeys.

8 neutralization-resistant virus challenges in rhesus monkeys.

9 memory T cells characterized as TRM cells in rhesus monkeys.

10 s and key cellular and molecular features in rhesus monkeys.

11 ctorization of three novel adenoviruses from rhesus monkeys.

12 neutralization-resistant virus challenges in rhesus monkeys.

13 used as a vaccine against DENV2 infection in rhesus monkeys.

14 ) and the lateral prefrontal cortex (PFC) of rhesus monkeys.

15 CNS pathology in the rhMOG/CFA EAE model in rhesus monkeys.

16 mental autoimmune encephalomyelitis (EAE) in rhesus monkeys.

17 ral immune responses in colorectal mucosa in rhesus monkeys.

18 onsistent with recent anatomical findings in rhesus monkeys.

19 ones from 34 cortical injection locations in rhesus monkeys.

20 ct on spatial working memory performances in rhesus monkeys.

21 fluenced vestibulo-ocular reflex learning in rhesus monkeys.

22 , boosted the plasma levels of decitabine in rhesus monkeys.

23 y) exhibited promising in vivo properties in rhesus monkeys.

24 lcus body patch, defined by fMRI in the same rhesus monkeys.

25 ghteen PET studies were performed in 3 adult rhesus monkeys.

26 axis function of male and female prepubertal rhesus monkeys.

27 multiple cortical areas, in freely behaving rhesus monkeys.

28 n immunodeficiency virus (SIV) challenges in rhesus monkeys.

29 ot also decrease food-reinforced behavior in rhesus monkeys.

30 on of PCK1 and G6PC upon glucose infusion in rhesus monkeys.

31 nd multiscale imaging of synaptic markers in rhesus monkeys.

32 on of ChIs in the postcommissural putamen of rhesus monkeys.

33 ered intra-amniotically at ~80% gestation in rhesus monkeys.

34 before and after corpus callosum section in rhesus monkeys.

35 ollowing both acute and chronic treatment in rhesus monkeys.

36 disrupts activity-based sleep parameters in rhesus monkeys.

37 of spatial and object WM tasks in adolescent rhesus monkeys.

38 e initiated to determine the effect of CR in rhesus monkeys.

39 e recognition by SIV Env-specific NAbs in 16 rhesus monkeys.

40 ne responses to 5 different Ad vectors in 26 rhesus monkeys.

41 n immunodeficiency virus (SIV) challenges in rhesus monkeys.

42 liably prolonged renal allograft survival in rhesus monkeys.

43 lly injected into the striatum of four adult rhesus monkeys.

44 e pairs of sites in primary visual cortex of rhesus monkeys.

45 schedule of cocaine and food availability in rhesus monkeys.

46 platforms protect against ZIKV challenge in rhesus monkeys.

47 that of HIV-infected humans and SIV-infected rhesus monkeys.

48 Uganda following blood analyses of sentinel Rhesus monkeys.

49 ed with better working memory performance in rhesus monkeys.

50 ex (V1) and the middle temporal area (MT) in rhesus monkeys.

51 two endovascular ischemic models in sixteen rhesus monkeys.

52 ttenuating in hamsters (10- to 100-fold) and rhesus monkeys (100- to 1,000-fold).

53 In rhesus monkeys, (11)C-LY2459989 displayed a fast rate of

54 In rhesus monkeys, (11)C-LY2795050 displayed a moderate rat

55 Gibbons, which are flanked in evolution by rhesus monkeys (12-lipoxygenating ALOX15) and orangutans

56 In baseline experiments in rhesus monkey, [(18)F]11 gave high brain radioactivity u

57 This study examined the hypothalamus of 51 rhesus monkeys (23 male, 18 female, 6.5-31 years old) us

58 imaging of [(18)F]mefway was performed on 58 rhesus monkeys (33 l/l, 25 s-carriers) to examine the re

59 al associated with 30% CR initiated in adult rhesus monkeys (7-14 years) and a preliminary report wit

60 In rhesus monkeys, a strongly additive immunogenic effect o

61 with peak concentration (SUVs of 1.5-1.8 in rhesus monkeys) achieved within 7 min after injection.

62 The seroprevalence of these novel rhesus monkey adenovirus vectors was extremely low in su

63 These rhesus monkey adenoviruses phylogenetically clustered wi

64 panzee adenoviruses, far less is known about rhesus monkey adenoviruses.

65 e isolation and vectorization of three novel rhesus monkey adenoviruses.

66 of bivalent HIV-1 mosaic antigens to protect rhesus monkeys against acquisition of infection followin

67 n of Ebola virus are able to protect 100% of rhesus monkeys against lethal challenge when treatment w

68 neutralizing antibodies (bNAbs) can protect rhesus monkeys against simian-human immunodeficiency vir

69 maging was conducted on 27 CR and 17 control rhesus monkeys aged 19-31 years from a longitudinal stud

70 We studied 11 rhesus monkeys (ages 6-27 years) and 12 human subjects (

71 and by midbrain electrical stimulation in 11 rhesus monkeys (ages 6-27 years).

72 periments were performed to compare, in five rhesus monkeys, amphetamine-induced DA release and [(11)

73 Neurons in the rhesus monkey amygdala and BF were therefore recorded si

74 esis, we pharmacogenetically inactivated the rhesus monkey amygdala, a subcortical region with distri

75 Rhesus monkey and baboon APC presented HMBPP and 20.1 to

76 Seven eyes of normal, healthy rhesus monkeys and 8 of old, atherosclerotic, hypertensi

77 type-specific channelrhodopsin expression in Rhesus monkeys and apply this technique to modulate dopa

78 expectedly, five of them are also present in rhesus monkeys and are still segregating.

79 an immunodeficiency virus (SIV) infection of rhesus monkeys and before systemic viraemia.

80 suring responses of MSTd neurons in two male rhesus monkeys and by applying a recently-developed meth

81 irus family, was isolated from the stools of rhesus monkeys and can be cultivated in vitro in monkey

82 fully protective dose of the bNAb PGT121 to rhesus monkeys and challenged them intravaginally with S

83 reas, PFC, and ventral intraparietal area of rhesus monkeys and found that adjacent neurons represent

84 ults are consistent with the hypothesis that rhesus monkeys and humans share a common neural shape re

85 t, flies, nematodes, rodents, and, arguably, rhesus monkeys and humans.

86 a brain-machine interface (BMI) paradigm in rhesus monkeys and novel statistical analyses of neural

87 form are altered with aging and menopause in rhesus monkeys and that these metrics may be coupled wit

88 infection (IAI) with Ureaplasma in pregnant rhesus monkeys and to explore concentration-response rel

89 sseminate following mucosal SIV infection of rhesus monkeys and trigger components of the inflammasom

90 s interrogated with sera from infected mice, rhesus monkeys, and humans and with glycan-binding prote

91 orrelates with lifespan when comparing mice, rhesus monkeys, and humans.

92 netic stimulation of cortical neurons within rhesus monkey arcuate sulcus, during the execution of a

93 mental studies involving pediatric patients, rhesus monkeys are an ideal laboratory animal model to i

94 cific monoclonal antibodies in SHIV-infected rhesus monkeys as well as an impact on host immune respo

95 ausally promotes social donation behavior in rhesus monkeys, as it does in more egalitarian and monog

96 In young rhesus monkeys, AT is analogous to the childhood risk ph

97 ed the severity of myelin deficit lesions in rhesus monkey brain induced by experimental autoimmune e

98 rmal aging; in particular, in area 46 of the rhesus monkey brain, the strength of microcolumns was sh

99 the whole-genome transcriptional profiles of rhesus monkey brains from birth to adulthood.

100 the severity of myelin deficit in mouse and rhesus monkey brains.

101 ssfully prevents islet allograft survival in rhesus monkeys, but induction with alefacept provides no

102 ranslated across species, including diabetic rhesus monkeys, but manifested with concomitant cardiac

103 le Gag-specific cellular immune responses in rhesus monkeys, but these responses were transient and w

104 etal, cingulate, and insular cortices in the rhesus monkey by using high-resolution anterograde trace

105 Blocking rhesus monkey CD28 with FR104 mitigated autoreactive T a

106 ment against human CD28, cross-reactive with rhesus monkey CD28.

107 observed in 5 of 5 SIV239Deltanef-immunized rhesus monkeys challenged at 5 weeks with SIV239, i.e.,

108 of plasma viraemia to undetectable levels in rhesus monkeys chronically infected with the pathogenic

109 Here we show in a male rhesus monkey cohort (N = 60) that infant performance in

110 her and more reproducible plasma exposure in rhesus monkeys compared to 5.

111 hemokine levels following the vaccination of rhesus monkeys compared to the vaccinia virus-based vect

112 Here we investigated whether rhesus monkeys could actively discriminate videos showin

113 Thus, we showed that rhesus monkeys could learn to categorize on the basis of

114 ta suggest that persistent EBOV infection in rhesus monkeys could serve as a model for persistent EBO

115 Similar transcriptional profiling in the rhesus monkey dentate gyrus across postnatal development

116 In particular, the inoculation of DTMUV into rhesus monkeys did not result in either viremia or appar

117 A new study finds that rhesus monkeys display self-recognition behaviors toward

118 rtical (brainstem and cerebellar) neurons in rhesus monkeys during a vestibular heading discriminatio

119 nal and translational stimuli experienced by rhesus monkeys during natural (e.g., walking, grooming)

120 d rapidly after intrarectal SIV infection of rhesus monkeys, during the 'eclipse' phase, and before d

121 tional measurement of lymphocryptovirus, the rhesus monkey EBV, demonstrated elevated levels in the b

122 ere we show that productive SIV infection in rhesus monkey ECs, but not TPs, is markedly restricted t

123 The current study assessed, in rhesus monkeys, effects of modulation of alpha1, alpha2/

124 These challenge stocks infected rhesus monkeys efficiently by both intrarectal and intra

125 Here, we demonstrate that rhesus monkey embryonic stem cells (ESCs) and isolated I

126 We demonstrate here that rhesus monkey ESCs also display monoallelic expression a

127 These findings show that while aged rhesus monkeys experience audiometric hearing deficits s

128 Twenty-two to 30-year-old rhesus monkeys exposed to 30% caloric restriction since

129 In contrast, lower primates (baboons, rhesus monkeys) express 12-lipoxygenating enzymes.

130 Dynamic PET experiments were performed on 4 rhesus monkeys (female; age range, 9-13 y) using a small

131 fluid (CSF) and lymph nodes (LN) of infected rhesus monkeys for weeks after virus has been cleared fr

132 okine effects on striatal DA function, eight rhesus monkeys (four male, four female) were administere

133 The lead vaccine was effective in rhesus monkeys, generating significant and sustained ant

134 Our initial results demonstrated that rhesus monkeys given the viral mimic synthetic double-st

135 coordination and resistance to sarcopenia in rhesus monkeys have recently been reported.

136 Therefore, we investigated in Rhesus monkeys how the representation of arm kinematics

137 When tested in rhesus monkeys implanted with motor cortical electrode a

138 Six rhesus monkeys, implanted with a chronic indwelling doub

139 To investigate this, we tested rhesus monkeys in a preferential-looking procedure, meas

140 rphisms associated with drusenoid lesions in rhesus monkeys in ARMS2 and HTRA1 were similar in freque

141 ly measured to quantify LPA1 in the lungs of rhesus monkeys in vivo.

142 that of HIV-infected humans and SIV-infected rhesus monkeys, including gp120-focused responses and ra

143 lar and humoral immune responses in neonatal rhesus monkeys, including mucosal responses that remaine

144 were subsequently challenged with thirty 50% rhesus monkey infectious doses of SIVmac251 6 weeks afte

145 The young rhesus monkey is ideal for studying the origin of human

146 Although the rhesus monkey is used widely as an animal model of human

147 ioides posadasii contamination in commercial rhesus monkey kidney (RhMK) cells and the subsequent nat

148 Two rhesus monkeys learned to use a virtual hand, which they

149 e a high-resolution transcriptional atlas of rhesus monkey (Macaca mulatta) brain development that co

150 ntrolateral prefrontal cortex (VLPFC) of the rhesus monkey (Macaca mulatta) respond to and integrate

151 h resolution electron micrographs from aging rhesus monkey (Macaca mulatta), provided by Alan Peters

152 a complex face-processing system [8-10]: the rhesus monkey (Macaca mulatta).

153 elationship between behavioral inhibition in rhesus monkeys (Macaca mulatta) and airway hyperresponsi

154 scharge in the oculomotor vermis of behaving rhesus monkeys (Macaca mulatta) and found neurons that i

155 tons are altered with aging and menopause in rhesus monkeys (Macaca mulatta) and that these metrics c

156 We find that most MT neurons in rhesus monkeys (Macaca Mulatta) are selective for depth

157 ssed this issue by investigating pathways in rhesus monkeys (Macaca mulatta) from the amygdala to pOF

158 Rhesus monkeys (Macaca mulatta) learned the ordering of

159 test this hypothesis, we trained four female rhesus monkeys (Macaca mulatta) to perform a multiple-fi

160 Rhesus monkeys (Macaca mulatta) were implanted with an i

161 Five adult rhesus monkeys (Macaca mulatta) were trained to self-adm

162 Five cocaine-experienced adult rhesus monkeys (Macaca mulatta) were trained to self-adm

163 ecorded single-unit activity in the VLPFC of rhesus monkeys (Macaca mulatta) while they produced voca

164 ted into the entorhinal cortex in 2-week-old rhesus monkeys (Macaca mulatta).

165 five cocaine- and nicotine-experienced adult rhesus monkeys (Macaca mulatta).

166 ) binding by positron emission tomography in rhesus monkeys (Macaca mulatta).

167 on physical and mental health in a sample of rhesus monkeys (Macaca mulatta).

168 erstone of the object-processing pathway, in rhesus monkeys (Macaca mulatta).

169 Seven pairs of male adolescent rhesus monkeys, matched for baseline cognitive performan

170 In a sample of 49 yearling rhesus monkeys (mean=1.25 years, n=24 behaviorally inhib

171 whether CD8(+) T lymphocytes from vaccinated rhesus monkeys mediate viral inhibition in vitro and whe

172 In rodents and rhesus monkeys, MK-8722-mediated AMPK activation in skel

173 The rhesus monkey model may be useful to explore the role of

174 A rhesus monkey model may lay the foundation to study EVD

175 In a rhesus monkey model of EVD, once-daily intravenous admin

176 sing the simian immunodeficiency virus (SIV)/rhesus monkey model of HIV rectal infection, we investig

177 In the rhesus monkey model, exposure to MIA at the end of the f

178 In this rhesus monkey model, MIA yields offspring with abnormal

179 Using the rhesus monkey model, we show that intramuscular immuniza

180 oxin synthase activity of 12-lipoxygenating (rhesus monkey, mouse, rat, pig, humIle418Ala) and 15-lip

181 Adult male rhesus monkeys (N = 11) self-administered cocaine (0.2 m

182 PDM to reduce cocaine self-administration by rhesus monkeys (N=4) using a novel procedure that featur

183 Rhesus monkeys (n=6) responded under a concurrent schedu

184 In one experiment, male rhesus monkeys (N=9) were trained to respond under a fix

185 se pathway-mediated processing of APP in the rhesus monkey (nonhuman primate; NHP) CNS is not underst

186 With brain tissues from longer-lived rhesus monkeys of different ages, we found that aging re

187 Rhesus monkeys offer a strong comparative model for the

188 To explore this possibility, we tested rhesus monkeys on a serial delayed match-to-sample (DMS)

189 o examine the effects of amygdala lesions in rhesus monkeys on attentional capture by specific facial

190 e of a marmoset can compare unfavorably with rhesus monkey performance on conventional testing paradi

191 om groups of neurons in visual area V4 while rhesus monkeys performed a contrast discrimination task

192 al cortex and the middle temporal area while rhesus monkeys performed an attention task.

193 urophysiology of social action for reward in rhesus monkeys performing a reward-giving task.

194 Rhesus monkeys possess a 5-HTTLPR length polymorphism si

195 affiliative interactions of 29 two-year-old rhesus monkeys, previously observed as yearlings, at the

196 immune responses of infant and adult lungs, rhesus monkey primary airway epithelial cell cultures we

197 Rhesus monkeys primed with Ad26 vectors expressing SIVsm

198 Rhesus monkeys provide a valuable model for studying the

199 The rhesus monkey provides an excellent model of normal agin

200 rea 46 of the prefrontal cortices of sixteen rhesus monkeys, ranging in age from 5 to 35 years.

201 a-amniotic inoculation of Ureaplasma parvum, rhesus monkeys received AZI (12.5 mg/kg every 12 hours i

202 ltered during in vivo adaptation in mice and rhesus monkeys, rendering the cagT4SS nonfunctional; how

203 pan and that caloric restriction in mice and rhesus monkeys results in attenuation of age-related met

204 A small-animal PET scan of a rhesus monkey revealed moderate initial brain uptake (SU

205 Further studies in conscious, rhesus monkeys revealed an emergent bradycardia and brad

206 Herpesviruses, including rhesus monkey rhadinovirus (RRV) and its close homolog,

207 Here we investigated whether recombinant rhesus monkey rhadinovirus (RRV) could be used as a vacc

208 In rhesus monkey rhadinovirus (RRV), a close relative of th

209 pacity of recombinant, replication-competent rhesus monkey rhadinovirus (RRV), a persisting herpesvir

210 sistent viruses (Rev of SIV and ORF57 of the rhesus monkey rhadinovirus) are dependent on the nature

211 ma and milk, whereas humans and SIV-infected rhesus monkeys (RMs), Asian-origin nonnatural SIV hosts,

212 Adult male/female rhesus monkeys self-administered methamphetamine (0.03 m

213 fected B cells and CD20(+) spleen cells from rhesus monkeys shows increased expression of genes encod

214 reaching behaviors of lemurs, tamarins, and rhesus monkeys similarly bear on the evolutionary origin

215 ted auditory brainstem responses (ABRs) from rhesus monkeys spanning in age from 10 to 35 years old,

216 Histological evidence from young rhesus monkeys suggests that HC development is character

217 ntigen-4 (CTLA4) expression by alloactivated rhesus monkey T cells in the presence of CTLA4 immunoglo

218 In a sample of 592 young rhesus monkeys that are part of an extended multigenerat

219 on of antiretroviral therapy in SIV-infected rhesus monkeys that began antiretroviral therapy during

220 We established transgenic PD rhesus monkeys that express mutant alpha-syn (A53T).

221 ammatory responses in otherwise asymptomatic rhesus monkeys that had survived infection in the absenc

222 in vivo using the rectal challenge model in rhesus monkeys that HIV-1-infected lymphocytes can trans

223 Here we show in rhesus monkeys that neurons encoding the identity or the

224 nv sequence variations in SIVmac251-infected rhesus monkeys that resulted in viral escape from NAbs.

225 re, we examine the activity of MT neurons in rhesus monkeys that were trained to discriminate depth s

226 f revealed preference theory, we measured in rhesus monkeys the frequency of repeated choices between

227 ons of two specialized cortical areas in the rhesus monkey, the high-order lateral prefrontal cortex

228 Here we report that in rhesus monkeys, there is independent selective pressure

229 on kinetics and competence in Vero-E6 cells (rhesus monkey), tissue tropism in cultures of ex-vivo hu

230 mal PET studies were performed in rats and a rhesus monkey to evaluate tracer pharmacokinetics in the

231 itis (EAE) models in the common marmoset and rhesus monkey to model the association of EBV and MS.

232 We trained Rhesus monkeys to associate 26 distinct symbols with 0-2

233 ministered at approximately 80% gestation in rhesus monkeys to cause chorioamnionitis and FIRS that i

234 and posterior orbitofrontal cortex (pOFC) in rhesus monkeys to compare their relationship with excita

235 properties of (11)C-BU99008 were assessed in rhesus monkeys to determine brain penetration, brain dis

236 er, (11)C-GR103545, and performed a study in rhesus monkeys to estimate the in vivo receptor concentr

237 We used fMRI in rhesus monkeys to identify brain regions underlying head

238 nyl]-4-yl)cyclopropane-1-carboxylic acid) in rhesus monkeys to image LPA1 in the lung in vivo with PE

239 delivered to two separate groups of pregnant rhesus monkeys to induce MIA: 1) late first trimester MI

240 We trained rhesus monkeys to make decisions based on a sequence of

241 To clarify this issue, we trained rhesus monkeys to perform a center-out task in which arm

242 tions in the medial premotor cortex (MPC) of Rhesus monkeys to represent in a time-varying fashion th

243 In rhesus monkeys trained to report the presence or absence

244 r full agonists, midazolam and lorazepam, in rhesus monkeys trained to self-administer midazolam or c

245 l cortical layers and the caudate-putamen of rhesus monkeys, trained in a spatial-versus-object, rule

246 erized a panel of RING domain mutants of the rhesus monkey TRIM5alpha (TRIM5alpha(rh)) protein.

247 RIM5alpha PRYSPRY domain, the PRYSPRY of the rhesus monkey TRIM5alpha that potently restricts HIV inf

248 A1 by protons was reversed in both mouse and rhesus monkey TRPA1 by exchange of distinct residues wit

249 Both rodent and rhesus monkey TRPA1 failed to respond to extracellular a

250 tivates rat and mouse TRPA1 but not human or rhesus monkey TRPA1.

251 ere performed in partially pancreatectomized rhesus monkeys (two autologous and four allogenic) witho

252 between CoB and mTOR inhibition, we studied rhesus monkeys undergoing MHC-mismatched islet allotrans

253 Four rhesus monkeys underwent 12 scans with (11)C-GR103545 on

254 in and plasma of mice and in the plasma of a rhesus monkey using high-performance liquid chromatograp

255 of blocking experiments were performed in 3 rhesus monkeys using (11)C-LY2795050 and (11)C-carfentan

256 micrographs from the fornix of young and old rhesus monkeys using a semi-automatic detection algorith

257 mouse and compared findings to those in the rhesus monkey (V1 and lateral prefrontal cortex [LPFC]).

258 V1, and the middle temporal area, MT) while rhesus monkeys viewed different visual stimuli in differ

259 al cortex and the middle temporal area while rhesus monkeys viewed different visual stimuli in differ

260 ly varying both eye and head positions while rhesus monkeys viewed optic flow stimuli depicting vario

261 RISPR/Cas9 application in a primate species (rhesus monkey), we selected the beta-hemoglobin gene (HB

262 Here, in young rhesus monkeys, we combined viral vector technology with

263 From a pool of 109 peri-adolescent rhesus monkeys, we formed groups characterized by high o

264 their postsynaptic sites in the amygdala in rhesus monkeys, we found that the anterior cingulate cor

265 In 24 young rhesus monkeys, we measured Ce messenger RNA (mRNA) leve

266 sections and validated in brain tissue from rhesus monkeys, we show that neuronal loss is inconsiste

267 diffusion tractography in healthy humans and rhesus monkeys, we show that, whereas the LMC structural

268 Twenty-five rhesus monkeys were challenged with a lethal dose of SUD

269 Nine rhesus monkeys were experimentally infected with ZEBOV-M

270 Infant rhesus monkeys were exposed, from 1 through 6 months, to

271 Pregnant rhesus monkeys were fed 400 mug of BPA per kg of body we

272 Rhesus monkeys were fed a standard diet (SD), or a high-

273 Seven adult rhesus monkeys were imaged on a FOCUS 220 PET scanner af

274 Lactating rhesus monkeys were intramuscularly primed with either r

275 Sixteen rhesus monkeys were lethally infected with MARV or RAVV

276 PET scans in rhesus monkeys were obtained on a small-animal scanner t

277 Rhesus monkeys were pulmonary exposed to 2009 pandemic H

278 At birth, 32 male rhesus monkeys were randomly assigned to either maternal

279 Two rhesus monkeys were scanned under the awake (n = 6 scans

280 Rhesus monkeys were trained on a task in which two diffe

281 Two rhesus monkeys were trained to align a light bar paralle

282 Two rhesus monkeys were trained to grasp 50 objects in a del

283 Rhesus monkeys were trained to make two mutually exclusi

284 responses in milk, hormone-induced lactating rhesus monkeys were vaccinated with a transmitted/founde

285 dia and bradyarrhythmia were not observed in rhesus monkeys when intravenous infusion of MK-3682 was

286 inding was observed in self-block studies in rhesus monkeys, which do not natively express NFTs.

287 fects of fluoxetine administered to juvenile rhesus monkeys who, as young adults, were imaged with po

288 2 reduction to cocaine abuse, we imaged four rhesus monkeys with [(11)C]DTBZ positron emission tomogr

289 y demonstrated that vaccination of lactating rhesus monkeys with a DNA prime/vector boost strategy in

290 demonstrated that immunization of lactating rhesus monkeys with a modified vaccinia Ankara (MVA) pri

291 ated the developmental stage of peripubertal rhesus monkeys with a series of morphometric, hormonal,

292 We perform two studies in rhesus monkeys with Ad35/Ad26 vectors expressing SIVmac2

293 Adult male rhesus monkeys with an extensive cocaine self-administra

294 ments with (11)C-LY2459989 were performed in rhesus monkeys with arterial input function measurement.

295 was injected into the cerebrospinal fluid of rhesus monkeys with chronic simian immunodeficiency viru

296 s in support of recognition memory we tested rhesus monkeys with prefrontal-inferotemporal (PFC-IT) c

297 utralization-resistant SIVsmE660 variants in rhesus monkeys with restrictive TRIM5alpha alleles.

298 ased on the intravaginal challenge of female rhesus monkeys with SHIV(SF162P3N) and sought to validat

299 achieve a high efficiency of gene editing in rhesus monkey zygotes, with no detected off-target effec

300 mitochondria after fertilization in pig and rhesus monkey zygotes.