ライフサイエンスコーパス: rhesus macaque

1 well as reference genomes of Chimpanzee and Rhesus Macaque.

2 rons in the BNSTALG from the mouse, rat, and rhesus macaque.

3 owing low-dose, repeated rectal challenge of rhesus macaques.

4 uman MD system using fMRI connectivity in 35 rhesus macaques.

5 o a CD4-mimetic miniprotein (gp140-M64U1) in rhesus macaques.

6 ency virus (SHIV)-infected and 16 uninfected rhesus macaques.

7 -producing cells in chronically SIV-infected rhesus macaques.

8 in boost vaccination regimens were tested in rhesus macaques.

9 V1 neutralizing sera from immunized mice and rhesus macaques.

10 anti-IL-15 mAb on T and NK cell dynamics in rhesus macaques.

11 deficiency virus (HIV) vaccine strategies in rhesus macaques.

12 tion of corticothalamic projections in awake rhesus macaques.

13 aining formulation of RiVax and tested it in rhesus macaques.

14 e of the parental bNAbs when administered to rhesus macaques.

15 ion in mouse colitis models and SIV-infected rhesus macaques.

16 ein (Env)-specific B and T cell responses in rhesus macaques.

17 of progression to AIDS in SIVmac251-infected rhesus macaques.

18 s of leukocyte gene regulation in humans and rhesus macaques.

19 n AMs in BAL fluid and IMs in lung tissue of rhesus macaques.

20 using scalp electroencephalography (EEG) in rhesus macaques.

21 B cell infection on oral viral challenge in rhesus macaques.

22 d to more rapid disease progression than are rhesus macaques.

23 ematopoietic macrophages from adult, healthy rhesus macaques.

24 immunodeficiency virus (SHIV) replication in rhesus macaques.

25 virus responsible for simian AIDS (SAIDS) in rhesus macaques.

26 lsion (CNE) delivery system was evaluated in rhesus macaques.

27 without gp140 boost in aluminum hydroxide in rhesus macaques.

28 ctal and intravaginal SIVsmE660 challenge of rhesus macaques.

29 rsistent infection after oral inoculation of rhesus macaques.

30 R) to characterize drusenoid lesions in aged rhesus macaques.

31 irus transmission through mucosal contact in rhesus macaques.

32 l plasma cell frequency in vaccinated female rhesus macaques.

33 r levels of Gag-specific immune responses in rhesus macaques.

34 ficiency Virus (SIV)-infected and uninfected rhesus macaques.

35 s; 5 mg/kg, oral, twice daily) and untreated rhesus macaques.

36 enhance protection from a SHIV challenge in rhesus macaques.

37 lays ZIKV replication to peak viral loads in rhesus macaques.

38 es than RD-Ad vectors in Syrian hamsters and rhesus macaques.

39 ctively, and performed a protection study in rhesus macaques.

40 onferred protection against ZIKV in mice and rhesus macaques.

41 t of the Mamu-B*008 allotype in SIV-infected rhesus macaques.

42 MDSC frequency and function in SIV-infected rhesus macaques.

43 temporal lobe of cognitively assessed, aged rhesus macaques.

44 The treatment also protected 33% of rhesus macaques (1 of 3) when given at 24 hours.

45 However, in marked contrast to rhesus macaques, 19 of 21 pig-tailed macaques controlled

46 unodeficiency virus (anti-SIV) activity into rhesus macaques 3 days following an intrarectal SIV inoc

47 f elite control in SIV-infected Mamu-B*08(+) rhesus macaques-a model of HLA-B*27-mediated elite contr

48 and measured noise correlations (rnoise) in rhesus macaque A1 during task performance.

49 te the memory B cell Ig repertoires from two rhesus macaques after five serial immunizations with Env

50 allenge stock in vitro, protected 6 out of 7 rhesus macaques against infection while the antibody 3BN

51 otein (GP) to provide protective immunity to rhesus macaques against lethal EBOV challenge.

52 Idiopathic chronic diarrhea (ICD) in rhesus macaques also resembles ulcerative colitis, one f

53 orted from vaccine-draining lymph nodes from rhesus macaques also showed expression of HLA-DR and wer

54 of L. plantarum-containing healthy and SIV+ rhesus macaques also transcribed genes for host glycan m

55 Here, we review the KIR genes of the rhesus macaque, an important animal model for human immu

56 variation in the absence of autopsy data, a rhesus macaque and common marmoset model of MERS-CoV dis

57 Together, the rhesus macaque and common marmoset models of MERS-CoV sp

58 simian immunodeficiency virus (SIV)-infected rhesus macaques and acute ethanol intoxication in a muri

59 of mAbs elicited by a model Env immunogen in rhesus macaques and comprehensively characterized their

60 adaptation may allow robust HCV infection in rhesus macaques and creation of a new animal model for s

61 ssess vaccine-induced antibodies, from mice, rhesus macaques and human clinical trials, for their fun

62 human immunodeficiency virus (SHIV)-infected rhesus macaques and human immunodeficiency virus type 1

63 use functional magnetic resonance imaging in Rhesus macaques and humans to examine the brain regions

64 netic and physiological similarities between rhesus macaques and humans, our results provide novel in

65 tor limiting HBV infection in cynomolgus and rhesus macaques and in pigs.

66 constructed an arrayed library of ISGs from rhesus macaques and tested the ability of hundreds of in

67 these vectors into the cerebellar cortex of rhesus macaques and tested vector efficacy in three ways

68 Materials and Methods Gravid rhesus macaques and their offspring (n = 10) were mainta

69 bidity and mortality affecting the supply of rhesus macaques and, potentially, their responses to exp

70 ed rhesus macaques, the heart of one treated rhesus macaque, and adjacent to a peripheral nerve of an

71 d comparative epigenetic profiling of human, rhesus macaque, and mouse corticogenesis to identify pro

72 ary hepatocytes from mice, rats, dogs, pigs, rhesus macaques, and cynomolgus macaques were transduced

73 Four T/F virus strains were inoculated into rhesus macaques, and each exhibited typical SIV replicat

74 tudy, we isolated and identified exosomes in rhesus macaques, and investigated their effects on cell

75 arily, hepatocytes from cynomolgus macaques, rhesus macaques, and pigs became fully susceptible to HB

76 ulatory cells in lymphoid tissues of healthy rhesus macaques, and we studied their dynamics throughou

77 s a novel and significant enhancement to the rhesus macaque animal model where both the clinical util

78 Many of these efforts rely on the rhesus macaque animal model.

79 Primary hepatocytes from rhesus macaques are also permissive for HCV-RNA replicat

80 onhuman primate model of VZV infection where rhesus macaques are intrabronchially challenged with the

81 Consequently, rhesus macaques are one of the most thoroughly studied n

82 Here we show that rhesus macaques are susceptible to infection by an Asian

83 Given that rhesus macaques are the animal model of choice for evalu

84 Rhesus macaques are used to model human immunodeficiency

85 ting function in lymph nodes of SIV-infected rhesus macaques associated with diminished IL-12 and IFN

86 cy virus (SIV) infection, we necropsied male rhesus macaques at 1, 3, 7, and 14 days after penile SIV

87 reening assessment was performed on 10 adult rhesus macaques at baseline and every 4-6 months for 2 y

88 in the rectal draining lymph nodes (dLNs) of rhesus macaques at different times after intrarectal ino

89 e our understanding of why EBV cannot infect rhesus macaques by proving that viral attachment through

90 We tested this prediction in two healthy rhesus macaques by recording single-unit spiking activit

91 virus with the restored pentameric complex, rhesus macaques can develop broadly neutralizing antibod

92 Here, we show that male rhesus macaques can learn categories by a transitive inf

93 for testing in the Ebola virus intramuscular rhesus macaque challenge model.

94 longitudinally-collected plasma samples from rhesus macaques challenged via intramuscular and aerosol

95 infections with diverse viruses in a captive rhesus macaque colony and identifies several viruses pos

96 f broadly neutralizing antibodies (bnAbs) in rhesus macaques, commonly used to assess vaccine immunog

97 ently accumulate in chronically SIV-infected rhesus macaques compared with those infected with less p

98 Immunization of rhesus macaques confers protection against MERS-CoV-indu

99 Importantly, immunization of rhesus macaques consistently gave superior B-cell (P < 0

100 stinct spatial behaviors from young and aged rhesus macaques: constrained space (CAGE), head-restrain

101 paring network organization of the mouse and rhesus macaque cortical connectome derived from complete

102 Rhesus macaque dams at approximately 80% gestation were

103 acious in delaying the onset of SIVmac251 in rhesus macaques, despite the higher immunogenicity of th

104 evelop disease, while nonnatural hosts, like rhesus macaques, develop AIDS.

105 Rhesus macaques developed mild disease, and common marmo

106 that PFC cells recorded from male and female rhesus macaques during a complex task show a moderate le

107 and cytokines were assessed in therapy-naive rhesus macaques during early and chronic stages of SIV i

108 A single immunization of rhesus macaques elicited a rapid and robust antibody res

109 ity in both PMd and PMv simultaneously while rhesus macaques engaged in a reach-to-grasp task.

110 elicit more potent and balanced responses in rhesus macaques, even with various simpler immunization

111 as obtained from 110 PMv neurons in two male rhesus macaques executing four reach-grasp-manipulate ta

112 Rhesus macaques exhibit 2.5-fold higher overall nucleoti

113 Here we report that uninfected infant rhesus macaques exhibited a higher physiological baselin

114 ced sex bias: vaccinated female but not male rhesus macaques exhibited delayed SIV acquisition.

115 We observed that uninfected infant rhesus macaques exhibited higher physiologic baseline mo

116 We evaluated one of the variants in rhesus macaques expressing permissive and restrictive TR

117 IM5alpha restriction when it was passaged in rhesus macaques expressing restrictive TRIM5alpha allele

118 eviously reported that in mice, gerbils, and rhesus macaques, expression of babA is lost, either by p

119 We show that microstimulation of the rhesus macaque FEF alters the magnitude of the PLR in a

120 le beneficial cognitive effects in aged, OVX rhesus macaque females.

121 ct using serial in utero MRI measurements of rhesus macaque fetuses, from which macroscopic and cellu

122 ortex is longitudinally characterized in the rhesus macaque, focusing on gestation day (G85) through

123 sequentially imaged CD4(+) cell recovery in rhesus macaques following total body irradiation (TBI) a

124 ian ZIKV clinical isolate (HS-2015-BA-01) in rhesus macaques for up to 142 d.

125 es to multiple virus and vaccine antigens in rhesus macaques for years after sustained memory B cell

126 before and following SIV infection protected rhesus macaques from developing AIDS and partially from

127 d from a human subject (AD358) and a Chinese rhesus macaque (GB40) displayed no or limited neutralizi

128 elevated rate of recent retroposition in the rhesus macaque genome.

129 The curve for rhesus macaques has a similar shape but is shifted down,

130 erstanding of extant genomic variation among rhesus macaques has implications for the use of this spe

131 c T follicular helper (TFH) cell activity in rhesus macaques has not previously been reported.

132 nt replication in vivo, we engrafted primary rhesus macaque hepatocytes into immunocompromised xenore

133 l deprivation (peer-rearing, PR) in archived rhesus macaque hippocampal samples (male, n = 13).

134 ons up to 25-valent in mice and 50-valent in rhesus macaques, HRV vaccine immunogenicity was related

135 Performance was compared for rhesus macaques, humans, and the betasort algorithm, as

136 monocyte-derived macrophages (MDMs) between rhesus macaques, i.e., experimental SIV hosts in which t

137 cell sorting from the peripheral blood of a rhesus macaque immunized with YU2gp140-F trimers in adju

138 lar and humoral immune responses elicited in rhesus macaques immunized with two poxvirus vectors (NYV

139 e-cell recordings from the IO of young adult rhesus macaques in acutely prepared brainstem slices, ou

140 and bronchoalveolar lavage fluid of AGMs and rhesus macaques (in which CD4 downregulation is not obse

141 lonization of the upper respiratory tract of rhesus macaques, in some cases associated with stimulati

142 Earlier we reported that in adult rhesus macaques, increasing monocyte turnover reflected

143 during persistent infection was analyzed in rhesus macaques infected long term with RhCMV to determi

144 This concept was evaluated in rhesus macaques infected long term with rhesus cytomegal

145 evaluated the pathogenicity and shedding in rhesus macaques infected with 1 of 2 West African isolat

146 s the viral kinetics and immune responses in rhesus macaques infected with a clinical ZIKV Brazilian

147 al of VSV-EBOV for postexposure treatment of rhesus macaques infected with EBOV-Makona.

148 s were measured in longitudinal samples from rhesus macaques infected with either SIVmac251 (progress

149 Infant humans and rhesus macaques infected with the human or simian immuno

150 some aspects of human infections.IMPORTANCE Rhesus macaque infection with simian immunodeficiency vi

151 Rhesus macaques inoculated with an AAV vector stably exp

152 previously showed that in early SIV-infected rhesus macaques intestinal dysfunction is initiated with

153 Paradoxically, control of this virus in rhesus macaques is only partial, and progression to AIDS

154 Moreover, using SVV infection of rhesus macaques, it will be possible to study how increa

155 In rhesus macaque lymphocytes, however, infection occurs en

156 lso detected on a small population of DCs in rhesus macaque (Macaca mulata) mesenteric lymph node.

157 A 3.5-year-old adult female rhesus macaque (Macaca mulatta) manifested swelling of t

158 patocytes from a small nonhuman primate, the rhesus macaque (Macaca mulatta).

159 Indian rhesus macaques (Macaca mulatta) are routinely used in p

160 Rhesus macaques (Macaca mulatta) are the most widely use

161 or cortical and forearm muscular activity of rhesus macaques (Macaca mulatta) as they reached, graspe

162 patterns and motor cortical spiking data in rhesus macaques (Macaca mulatta) handling objects of var

163 Consistent with MVT, rhesus macaques (Macaca mulatta) spent more time foragin

164 we measured the looking time of 3-month-old rhesus macaques (Macaca mulatta) viewing macaque faces v

165 s and consequences of natal dispersal age in rhesus macaques (Macaca mulatta), a species with male di

166 We investigated, in infant rhesus macaques (Macaca mulatta), whether newborns' capa

167 ity of saccade trajectories observed in five rhesus macaques (Macaca mulatta).

168 munodeficiency virus (SIV)-infected juvenile rhesus macaques (Macaca mulatta).

169 o a striking perturbation in pathogenesis in rhesus macaques (Macaca mulatta).

170 ses to scratching in a group of free-ranging rhesus macaques (Macaca mulatta).

171 ystem of humans, the squirrel monkey and the rhesus macaque, making comparisons with past results fro

172 We analyzed rhesus macaque MAOA (rhMAOA) expression in blood from ma

173 The SIV-infected rhesus macaque model closely resembles HIV-1 immunopatho

174 ody transfer and oral virus challenge in the rhesus macaque model for EBV infection.

175 ccines have shown remarkable efficacy in the rhesus macaque model of acquired immune deficiency syndr

176 challenge with wild-type (WT) SIV in the SIV-rhesus macaque model of HIV-1 transmission to women.

177 (+) T cells in situ by using an SIV-infected rhesus macaque model of HIV.

178 In the present study, we used a relevant rhesus macaque model of infection with simian immunodefi

179 Here, we present a novel rhesus macaque model of placental rhesus CMV (rhCMV) tra

180 In this study, we used a rhesus macaque model to assess the contributions of HMW1

181 ells now opens an opportunity to use the SIV/rhesus macaque model to further elucidate the potential

182 Using the rhesus macaque model we show that prior infection with Z

183 When tested in the larger rhesus macaque model, SC-Ad6 induces higher transgene-sp

184 Using the rhesus macaque model, this work was performed to address

185 Using the rhesus macaque model, which is critical for late-stage v

186 n patterns of these cells in a myeloablative rhesus macaque model.

187 ease of aerosol MARV Angola infection in the rhesus macaque model.

188 efficacy in the gold standard cynomolgus or rhesus macaque models of filovirus infection.

189 within the brain from two well-characterized rhesus macaque models of the neurological complications

190 Here, utilizing both human and rhesus macaque models, we show the impact of HIV and SIV

191 in 2F5 bnAb VHDJH and VLJL knock-in mice and rhesus macaques modified KYNU activity or disrupted tiss

192 tory cortex (A1) under two conditions: while rhesus macaque monkeys (Macaca mulatta) actively perform

193 Here, we used fMRI in rhesus macaque monkeys to map the superior temporal sulc

194 t-tonic neurons in the nucleus prepositus of rhesus macaque monkeys using eight-channel linear microe

195 of seven species-human, chimpanzee, gorilla, rhesus macaque, mouse, rat, and dog-to investigate epige

196 stered vaccines to six groups of infant male rhesus macaques (n = 12-16/group) using a standardized t

197 similar to that of 10E8, and a half-life in rhesus macaques of approximately 10 days.

198 Here we cognitively tested aged female rhesus macaques on (1) the delayed response task of spat

199 erformed FMT on six chronically SIV-infected rhesus macaques on antiretroviral treatment.

200 ct between task goals and distractors in the rhesus macaque, particularly for biologically relevant s

201 Five rhesus macaques per group received two DNA primes at wee

202 otential (LFP) activity in the PPC while two rhesus macaques performed a decision-making task.

203 populations in primary auditory cortex while rhesus macaques performed a novel feature-selective atte

204 etal (LIP) and middle temporal (MT) areas of rhesus macaques performing a motion direction discrimina

205 ateral prefrontal cortex (dlPFC) of two male rhesus macaques performing a task that elicited key aspe

206 neurons in dorsolateral PFC (DLPFC) of male rhesus macaques performing rule-guided prosaccades and a

207 sion of hNTCP on hepatocytes in vivo renders rhesus macaques permissive to HBV infection.

208 cytic receptors on dendritic cells (DCs), in rhesus macaques primed with a poxvirus vector (NYVAC-KC)

209 simian immunodeficiency virus (SIV)-infected rhesus macaque provides a powerful model for the study o

210 Therefore, Asian-lineage ZIKV infection of rhesus macaques provides a relevant animal model for stu

211 Four rhesus macaques received a single vaccination with a mix

212 simian immunodeficiency virus (SIV)-infected rhesus macaques received antibiotics followed by FMT.

213 Using infant rhesus macaques receiving thimerosal-containing vaccines

214 virus (SIV) acquisition in three independent rhesus macaque repeated low-dose rectal challenge studie

215 e applied HIV-1 and SEVI to intact human and rhesus macaque reproductive tract tissues to determine h

216 All T/F viruses were pathogenic in rhesus macaques, resulting in progressive CD4(+) T cell

217 Zika virus directly to the tonsils of three rhesus macaques results in detectable plasma viremia in

218 Whole-genome sequencing analysis of 133 rhesus macaques revealed more than 43.7 million single-n

219 ization studies in mice, Guinea pigs, and in Rhesus macaques, revealed that LNPs induced high titers

220 lls from peripheral blood and the jejunum in rhesus macaques, revealing distinct expression patterns

221 d herpesvirus (KSHV) and the closely related rhesus macaque rhadinovirus (RRV) are the only viruses k

222 's sarcoma-associated herpesvirus (KSHV) and rhesus macaque rhadinovirus (RRV), are unique in that th

223 mpact HIV-specific vaccine immunogenicity in rhesus macaques (RhM).

224 mmon nonhuman primate species, Indian-origin rhesus macaques (RM) and Mauritian-origin cynomolgus mac

225 do not develop disease, whereas infection of rhesus macaques (RM) causes CD4(+) T cell loss and AIDS.

226 ly does not cause AIDS, whereas SIV-infected rhesus macaques (RM) typically develop AIDS.

227 simian immunodeficiency virus (SIV)-infected rhesus macaques (RM), CD4(+) TSCM are preserved in numbe

228 of IL-7 could reverse TN deficiency in aging rhesus macaques (RM), either by enhancement of the demon

229 ereas infection of nonnatural hosts, such as rhesus macaques (RM), is commonly pathogenic.

230 on and disease progression than SIV-infected rhesus macaques (RM).

231 Five groups of six rhesus macaques (RMs) each were vaccinated with DNA/EP-A

232 sive transfer of HIV-specific nAbs protected rhesus macaques (RMs) from subsequent mucosal challenge

233 simian immunodeficiency virus (SIV)-infected rhesus macaques (RMs) shows that these cells contribute

234 Rhesus macaques (RMs) were immunized with NPs containing

235 port show that intrabronchial inoculation of rhesus macaques (RMs) with VZV resulted in an abortive V

236 hown that during pathogenic SIV infection of rhesus macaques (RMs), rapid disease progression is asso

237 ccine induced a similar antibody response in rhesus macaques (RMs), which are commonly used as an ani

238 ns from primary HIV-1 strains fail to infect rhesus macaques (RMs).

239 vage (BAL) fluid of healthy and SIV-infected rhesus macaques (RMs).

240 rus persistence in ART-treated, SIV-infected rhesus macaques (RMs).

241 s (SHIV) adapted for pathogenic infection of rhesus macaques (SHIVAD8-EO).

242 Luciferase reporter assays validated rhesus macaque SIRT1 as a direct miR-34a target.

243 d the effects of hormone replacement in aged rhesus macaques, soon after surgically-induced menopause

244 m the major simian immunodeficiency virus of rhesus macaque, sooty mangabey, and HIV-2 (SIVsmm/SIVmac

245 aluated using 12 weekly rectal challenges in rhesus macaques subgrouped by tripartite motif-containin

246 (SIV) infection in vervet monkeys but not in rhesus macaques, suggesting that part of the signal refl

247 ifying selection has had stronger effects in rhesus macaques than in humans.

248 cells in a unique cohort of SIV-controlling rhesus macaques that maintained low to undetectable leve

249 twice-weekly rectal SHIV162p3 challenges in rhesus macaques that received either placebo (n = 7), MV

250 chemically induced colitis in SIV-uninfected rhesus macaques that we developed using dextran sulfate

251 e or in combination with the bnAb PGT121, in rhesus macaques that were chronically infected with SHIV

252 nal nerves, and dorsal root ganglia (DRG) of rhesus macaques that were inoculated intrathecally with

253 ain insight into these questions, we studied rhesus macaques that were vaccinated with SIVmac239 and

254 nstrate, in closed-loop experiments with two rhesus macaques, that after the loss of approximately 60

255 We tested, in rhesus macaques, the effects of a 500-fold range of an a

256 s were observed in the brains of two treated rhesus macaques, the heart of one treated rhesus macaque

257 g in the blood following aerosol exposure of rhesus macaques to a lethal dose of Marburg virus.

258 ewise, Mamu-B*08 expression also predisposes rhesus macaques to control simian immunodeficiency virus

259 py in simian immunodeficiency virus-infected rhesus macaques to determine whether decreased TZ fibros

260 , and the female reproductive tract (FRT) of rhesus macaques to determine whether these cells contrib

261 with a social status manipulation in female rhesus macaques to investigate how status alters immune

262 Rhesus macaque TRIM5alpha (rhTRIM5alpha) is a retroviral

263 keys are susceptible to resistance by common rhesus macaque TRIM5alpha alleles and result in reduced

264 riction of retroviruses by human TRIM5alpha, rhesus macaque TRIM5alpha, and owl monkey TRIM-Cyp remai

265 ction factors in primary CD4(+) T cells from rhesus macaques under various conditions, finding dynami

266 Rhesus macaques underwent multiple scans including coinj

267 re identified in SIV p27(Gag) Analysis of 31 rhesus macaques vaccinated with full-length SIV gag pDNA

268 V neutralization panel and samples from four rhesus macaque vaccine trials designed for cross compari

269 In mucosal tissues of normal rhesus macaques, we found CD4(+) pDCs to be the subset r

270 Here, using ART-treated, SIV-infected rhesus macaques, we show that CTLA-4(+)PD-1(-) memory CD

271 Matched rhesus macaques were either uninfected or intrarectally

272 gnaling and chemotaxis in vitro Six infected rhesus macaques were infused with differentially fluores

273 Age-matched SIV-infected rhesus macaques were injected with saline.

274 One-month-old rhesus macaques were inoculated orally with the simian-h

275 Rhesus macaques were inoculated with a variant of the pa

276 Fourteen pair-housed, juvenile male rhesus macaques were inoculated with SIVmac239 and, 4 wk

277 In this study, 15 rhesus macaques were sequentially sacrificed following a

278 Rhesus macaques were studied to directly address the pot

279 Three rhesus macaques were vaccinated via three DNA primes and

280 Rhesus macaques were vaccinated with aerosolized HPIV3/E

281 ficiently utilizes human CD4 than the CD4 of rhesus macaques, whereas the closely related virus SIVma

282 e effect of primate FH binding, we immunized rhesus macaques with a 4-component serogroup B vaccine (

283 In this study, we report that coimmunizing rhesus macaques with HIV-1 gp160 DNA and gp140 trimeric

284 from atraumatic rectal inoculation of Indian rhesus macaques with low doses of SIVmac251 or SIVsmE660

285 Further, vaccination of RhCMV-uninfected rhesus macaques with nonfunctional forms of RhCMV vIL-10

286 Our results demonstrate that immunization of rhesus macaques with NP adjuvants mixed with soluble SIV

287 for the prevention of Ebola virus disease in rhesus macaques with regards to reduction of viral load,

288 We found that vaccinating rhesus macaques with rhesus cytomegalovirus vectors in w

289 Intrabronchial inoculation of rhesus macaques with simian varicella virus (SVV) recapi

290 Infection of rhesus macaques with simian varicella virus (SVV), a hom

291 Here, we infected rhesus macaques with simian-human immunodeficiency virus

292 We propose that infections of rhesus macaques with SIVmac239 G382R/H442Y might better

293 After infection of rhesus macaques with SIVmac239, the expression of most c

294 We find that immunization of rhesus macaques with the pentavalent vaccine results in

295 rrent study, we evaluated the performance of rhesus macaques with ventral striatum (VS) lesions on a

296 VS) and amygdala to appetitive RL, we tested rhesus macaques with VS or amygdala lesions on determini

297 for 6 months after respiratory infection of rhesus macaques with wild type MeV.

298 Five repeated cervical inoculations of rhesus macaques with wild-type serovar D strain D/UW-3/C

299 We infect two cohorts of rhesus macaques with ZIKV; one cohort has been exposed t

300 antibodies to multiple neutralizing sites in rhesus macaques, with quality attributes comparable to t