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 in a highly translatable nonhuman model, the rhesus monkey.

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

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

7 nd multiscale imaging of synaptic markers in rhesus monkeys.

8 disrupts activity-based sleep parameters in rhesus monkeys.

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

10 schedule of cocaine and food availability in rhesus monkeys.

11 platforms protect against ZIKV challenge in rhesus monkeys.

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

13 Uganda following blood analyses of sentinel Rhesus monkeys.

14 ed with better working memory performance in rhesus monkeys.

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

16 two endovascular ischemic models in sixteen rhesus monkeys.

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

18 neutralization-resistant virus challenges in rhesus monkeys.

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

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

21 ctorization of three novel adenoviruses from rhesus monkeys.

22 neutralization-resistant virus challenges in rhesus monkeys.

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

24 mental autoimmune encephalomyelitis (EAE) in rhesus monkeys.

25 ral immune responses in colorectal mucosa in rhesus monkeys.

26 cacy of one of the short vaccine regimens in rhesus monkeys.

27 onsistent with recent anatomical findings in rhesus monkeys.

28 ones from 34 cortical injection locations in rhesus monkeys.

29 ct on spatial working memory performances in rhesus monkeys.

30 fluenced vestibulo-ocular reflex learning in rhesus monkeys.

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

32 s inoculation of two Mamu-A*01 (+) RRV-naive rhesus monkeys.

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

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

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

36 axis function of male and female prepubertal rhesus monkeys.

37 multiple cortical areas, in freely behaving rhesus monkeys.

38 diolabeled with (11)C and studied in vivo in rhesus monkeys.

39 e control of disjunctive saccades in trained rhesus monkeys.

40 c effects against SARS-CoV-2 are observed in rhesus monkeys.

41 pheral immune cells during EBOV infection in rhesus monkeys.

42 g against HIV infection, in hemiparkinsonian rhesus monkeys.

43 d brain metabolism were assessed in 46 young rhesus monkeys.

44 PET studies were performed on rhesus monkeys.

45 (infectious colitis) in 170 socially-housed rhesus monkeys.

46 occupancy of JNJ-54175446 was observed in 2 rhesus monkeys.

47 d METH intake on reversal learning in female rhesus monkeys.

48 tor antagonist JNJ-54175446 were obtained in rhesus monkeys.

49 ricular nucleus (PVN) were evaluated in male rhesus monkeys.

50 on tensor images were collected in 581 young rhesus monkeys (1.89 +/- 0.77 years old; 43.9% female).

51 tions were compared in 12 healthy young male rhesus monkeys (~1-2 y old, ~3 +/- 1 kg).

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

53 In rhesus monkeys, (11)C-LSN3172176 metabolized rapidly (29

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

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

56 ained from 28 healthy humans, 10 baboons, 12 rhesus monkeys, 20 Yorkshire pigs, 20 Sprague-Dawley rat

57 In rhesus monkeys, a strongly additive immunogenic effect o

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

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

60 These rhesus monkey adenoviruses phylogenetically clustered wi

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

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

63 ide PET and resting-state fMRI in awake male rhesus monkeys after oral administration of various dose

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

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

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

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

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

69 ACE2 of human/rhesus monkey and rat/mouse exhibited the highest and lo

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

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

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

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

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

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

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

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

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

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

80 matin architecture during spermatogenesis in rhesus monkeys and mice.

81 dioligand for imaging and quantifying OGA in rhesus monkeys and mice.

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

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

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

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

86 Female rhesus monkeys and women are subject to age- and menopau

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

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

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

90 duced comparable peak immune responses in 30 rhesus monkeys as in humans and resulted in an 83% (95%

91 Methods: PET imaging was performed on rhesus monkeys at baseline and after administration of e

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

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

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

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

96 tures that contact mitotic NPCs in the fetal rhesus monkey but not in rat.

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

98 s were characterized in brains of mice and a rhesus monkey by in vivo electrophysiology, calcium imag

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

100 Thus, aging rhesus monkeys can play a key role in AD research.

101 Blocking rhesus monkey CD28 with FR104 mitigated autoreactive T a

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

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

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

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

106 Two rhesus monkeys conducted instructed walk-and-reach movem

107 r characteristics in embryonic rat and fetal rhesus monkey cortex.

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

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

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

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

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

113 Rhesus monkeys drank a 4% ethanol solution 6 h per day,

114 We recorded from two male rhesus monkeys during a juice choice task.

115 ing neural responses in the visual cortex of rhesus monkeys during a motion direction change detectio

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

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

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

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

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

121 k, we used a visual cue to instruct two male rhesus monkeys either to repeat their most recent choice

122 Eighteen rhesus monkeys euthanized between 3 and 8 days post-infe

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

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

125 of viral rebound in chronically SIV-infected rhesus monkeys following ART discontinuation.

126 16 ART-suppressed, chronically SIV-infected rhesus monkeys following ART discontinuation.

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

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

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

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

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

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

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

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

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

136 n immunodeficiency virus (SHIV) infection of rhesus monkeys is an important preclinical model for hum

137 s mechanistic and neuroimaging work in young rhesus monkeys linked the central nucleus of the amygdal

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

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

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

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

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

143 Here we address whether rhesus monkeys (Macaca mulatta) can learn the abstract c

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

145 We tested four male rhesus monkeys (Macaca mulatta) in both the expression a

146 lices of ventral premotor cortex (vPMC) from rhesus monkeys (Macaca mulatta) of either sex, we demons

147 ion to social cognition is causal by testing rhesus monkeys (Macaca mulatta) on a vicarious reinforce

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

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

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

151 To address this gap, we compared male rhesus monkeys (Macaca mulatta) with bilateral excitotox

152 axon terminals to (inputs) the ACC of adult rhesus monkeys (Macaca mulatta).

153 experiments using electrical stimulation in rhesus monkeys (Macaca mulatta).

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

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

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

157 and delta) in the fore brain of three female rhesus monkeys (Macaca mulatta).

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

159 ngly, during oculomotor behavior in mice and rhesus monkeys, mean irregularity of Purkinje cell spiki

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

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

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

163 We describe here the development of a rhesus monkey model of AD using soluble oligomers of the

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

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

166 Here, using a rhesus monkey model, 16S rRNA sequencing, and weighted n

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

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

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

170 achieving protective immunity against it in rhesus monkey models.

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

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

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

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

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

176 Aging rhesus monkeys naturally develop cognitive deficits, amy

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

178 In rhesus monkeys of both sexes, we investigated how these

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

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

181 during the day in both healthy and diabetic rhesus monkeys, peaking between 12 noon - 6 pm.

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

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

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

185 smitter GABA in regulating delay activity in rhesus monkeys performing a delayed decision task requir

186 e recording cellular activity in PFC of male rhesus monkeys performing a delayed decision task requir

187 d posterior cingulate cortex (PCC) in 2 male rhesus monkeys performing a saccadic reward task.

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

189 Rhesus monkeys primed with Ad26 vectors expressing SIVsm

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

191 cal functional connectivity is altered after rhesus monkeys received extensive training to learn nove

192 y analyzed the gene expression profiles in 2 rhesus monkey recipients using peripheral blood RNA-sequ

193 This study, using a rhesus monkey renal transplantation model, sought to det

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

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

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

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

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

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

200 replication-competent, recombinant strain of rhesus monkey rhadinovirus (RRV) expressing the Gag prot

201 The related rhesus monkey rhadinovirus (RRV) has shown potential as

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

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

204 atitis virus (VSV), adenovirus type 5 (Ad5), rhesus monkey rhadinovirus (RRV), and DNA again.

205 erved for cell-free infection by the related rhesus monkey rhadinovirus (RRV), which is relatively ev

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

207 ection of BJAB cells by KSHV and the related rhesus monkey rhadinovirus.

208 ent methods of slow delivery immunization of rhesus monkeys (RMs) resulted in more robust T follicula

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

210 Two rhesus monkeys scanned pairs of visually identical scree

211 Four rhesus monkeys self-administered i.v. infusions of fenta

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

213 Whole-body imaging of rhesus monkeys showed high uptake in kidney, spleen, liv

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

215 on, attenuates heroin self-administration in rhesus monkeys, suggesting it could be an effective trea

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

217 mparative approach, we assessed capuchin and rhesus monkeys' susceptibility to sunk costs in a psycho

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

219 eral anxiolytic effect on the performance of rhesus monkeys tasked with matching face stimuli, or a m

220 zapine, and deschloroclozapine, in four male rhesus monkeys tested in a spatial delayed response task

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

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

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

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

225 We evaluated the effects of Chase in rhesus monkeys that had undergone C7 spinal cord hemisec

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

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

228 We recently showed, in aged female rhesus monkeys, that systemic administration of MSC-EVs

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

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

231 -4-phenyl-1,2,3,6-tetrahydropyridine-treated rhesus monkeys, the standard non-human primate model of

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

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

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

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

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

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

238 and we performed a pool competition study in rhesus monkeys to define the optimal variant for each SH

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

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

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

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

243 re microscopy and RNA sequencing in 47 young rhesus monkeys to investigate AT's molecular underpinnin

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

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

246 To address these questions, we trained rhesus monkeys to perform a novel decision-making task w

247 context modulate strategy, we trained 2 male rhesus monkeys to perform a novel perceptual decision-ma

248 We trained rhesus monkeys to perform a two-stage decision task desi

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

250 We also did a parallel preclinical study in rhesus monkeys to test the protective efficacy of the sh

251 Experiments used two adult male rhesus monkeys trained on a reaching task.

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

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

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

255 body imaging of (89)Zr-labeled antibodies in rhesus monkeys up to 30 d after injection.

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

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

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

259 idual neurons in the middle temporal area of rhesus monkeys using a task that allowed us to isolate t

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

261 Here, we model a worst-case scenario using rhesus monkeys vaccinated or unvaccinated with the rVSV-

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

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

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

265 ribution of GABA(A) receptor subunits in the rhesus monkey was highly heterogeneous indicating a high

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

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

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

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

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

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

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

273 Five of the diabetic rhesus monkeys were also administered the anti-diabetic

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

275 Nine rhesus monkeys were experimentally infected with ZEBOV-M

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

277 We describe a therapy trial in which four rhesus monkeys were infected with SHIV-AD8 for 86 weeks

278 activity using a strategy task in which two rhesus monkeys were instructed by a visual cue either to

279 Sixteen rhesus monkeys were lethally infected with MARV or RAVV

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

281 Rhesus monkeys were pulmonary exposed to 2009 pandemic H

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

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

284 Rhesus monkeys were trained to make two mutually exclusi

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 different levels of visual cortex of 2 male rhesus monkeys while the animals did a visual discrimina

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

289 2 reduction to cocaine abuse, we imaged four rhesus monkeys with [(11)C]DTBZ positron emission tomogr

290 o ethanol-enhanced GABA release in abstinent rhesus monkeys with a history of chronic ethanol self-ad

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

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

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

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

295 e instrumented four healthy and six diabetic rhesus monkeys with CGM probes in the carotid artery and

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

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

298 ions of periventricular microglia in rat and rhesus monkey, yet are consistent with the concept that

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.