ライフサイエンスコーパス: rhesus

1 thine dehydrogenase and ammonia transporter (Rhesus 50 glycoprotein) were significantly increased in

2 Here we show that both rhesus and cynomolgus macaques are highly susceptible to

3 ctivated rabies virus-based EBOV vaccine, in rhesus and cynomolgus monkeys.

4 CBR) agonist CP 55 940 in Old World monkeys (rhesus and cynomolgus), a species that has been used ext

5 sure time to clot formation (r-time) in both rhesus and human blood, comparing TLN versus HLL (withou

6 cell lines (LCLs) from human, chimpanzee and rhesus, and we identify patterns of m(6)A evolution amon

7 hypothesized that inefficient Env binding to rhesus CD4 (rhCD4) limits virus entry and replication an

8 (huCD4-Ig) than by the same molecule bearing rhesus CD4 domains 1 and 2 (rhCD4-Ig).

9 It has been shown that HIV-1 utilizes rhesus CD4 less efficiently than human CD4.

10 39 envelope glycoprotein (Env) that utilized rhesus CD4 more efficiently, while retaining its resista

11 442Y variant) also infected cells expressing rhesus CD4 with markedly greater efficiency than did una

12 increased its neutralization sensitivity to rhesus CD4-Ig without altering neutralization by human C

13 himeric alphaCD154, n = 5), or 2C10R4 (mouse-rhesus chimeric alphaCD40, n = 6) monotherapy using a co

14 s were only elicited by a fibroblast-adapted rhesus CMV vector with limited tissue tropism; a repaire

15 sceptibilities of the three macaque species (rhesus, cynomolgus, and bonnet) used.

16 eukin-10 (vIL-10) ortholog of both human and rhesus cytomegalovirus (HCMV and RhCMV, respectively) su

17 data were also obtained that indicated that rhesus cytomegalovirus is able to persist due to upregul

18 found that vaccinating rhesus macaques with rhesus cytomegalovirus vectors in which genes Rh157.5 an

19 bs, but alloantibodies against, for example, Rhesus D (RhD) and platelet Ags frequently have reduced

20 rom healthy donors immunized against foreign rhesus D alloantigen or vaccinia virus.

21 We conclude that the unknown rhesus factor values were likely to be missing not at ra

22 The mother's school-leaving-age and rhesus factor were not associated with the diabetes stat

23 elivery type) and 1 with missing values (her rhesus factor), while incorporating previous type 1 diab

24 porcine islet (NPI) xenografts compared with rhesus islet allografts at 1 hour, 24 hours, and 7 days.

25 However, whereas rhesus M-MDSCs lacked expression of CD33, PMN-MDSCs were

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

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

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

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

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

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

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

33 Rhesus macaque dams at approximately 80% gestation were

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

58 well as reference genomes of Chimpanzee and Rhesus Macaque.

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

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

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

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

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

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

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

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

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

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

69 Rhesus macaques (RMs) were immunized with NPs containing

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

90 Rhesus macaques are used to model human immunodeficiency

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

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

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

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

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

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

97 Rhesus macaques developed mild disease, and common marmo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

129 Four rhesus macaques received a single vaccination with a mix

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

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

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

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

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

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

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

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

138 Rhesus macaques underwent multiple scans including coinj

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

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

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

142 Rhesus macaques were inoculated with a variant of the pa

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

177 onferred protection against ZIKV in mice and rhesus macaques.

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

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

180 temporal lobe of cognitively assessed, aged rhesus macaques.

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

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

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

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

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

186 in boost vaccination regimens were tested in rhesus macaques.

187 V1 neutralizing sera from immunized mice and rhesus macaques.

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

189 irus transmission through mucosal contact in rhesus macaques.

190 l plasma cell frequency in vaccinated female rhesus macaques.

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

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

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

194 enhance protection from a SHIV challenge in rhesus macaques.

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

196 This Env can be used to make the rhesus model more similar in some ways to human infectio

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

215 mitochondria after fertilization in pig and rhesus monkey zygotes.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

256 Nine rhesus monkeys were experimentally infected with ZEBOV-M

257 Sixteen rhesus monkeys were lethally infected with MARV or RAVV

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

259 Rhesus monkeys were trained to make two mutually exclusi

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

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

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

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

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

265 0 muA, 100-300 Hz, n = 172 IC locations in 3 rhesus monkeys).

266 In rhesus monkeys, a strongly additive immunogenic effect o

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

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

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

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

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

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

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

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

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

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

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

278 schedule of cocaine and food availability in rhesus monkeys.

279 platforms protect against ZIKV challenge in rhesus monkeys.

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

281 Uganda following blood analyses of sentinel Rhesus monkeys.

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

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

284 nd multiscale imaging of synaptic markers in rhesus monkeys.

285 disrupts activity-based sleep parameters in rhesus monkeys.

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

287 -to-I editing sites in lncRNAs across human, rhesus, mouse, and fly, and observed an appreciable numb

288 Both TLN- and HLL-treated rhesus or human whole blood result in significantly prol

289 exhibited an expanded host range in primary rhesus peripheral blood mononuclear cells that included

290 to be missing not at random and were mainly rhesus-positive.

291 a novel analysis of population recordings in rhesus primate visual area V4 showing that a single biop

292 Livers from rhesus rota virus-infected mice with BA had 7-fold more

293 Rhesus rotavirus (RRV) can also lead to biliary atresia

294 In neonatal mice, rhesus rotavirus (RRV) can induce biliary atresia (BA),

295 The murine model of BA, employing rhesus rotavirus (RRV), parallels human disease and has

296 BA was induced in balb/cAnNCrl mice by rhesus rotavirus infection; uninfected mice were used as

297 During entry of rhesus rotavirus, VP8* interacts with cell surface gangl

298 leukocyte recruitment, and biliary injury in rhesus rotavirus-induced BA.

299 The nonhuman TRIM5 variants, rhesus TRIM5alpha (RhT5) and TRIM-cyclophilin A (TCyp),

300 expression of two nonhuman TRIM5 orthologs, rhesus TRIM5alpha (RhT5) and TRIM-cyclophilin A (TCyp),