ライフサイエンスコーパス: marmoset

1 fects small New World primates (tamarins and marmosets).

2 fects small New World primates (tamarins and marmosets).

3 nd cattle, and at least twice in rodents and marmoset.

4 immune encephalomyelitis (EAE) in the common marmoset.

5 r existing disease models established in the marmoset.

6 sponses in the New World primate, the common marmoset.

7 eplicate efficiently upon passage to a naive marmoset.

8 ithelial stem/progenitor cells in the common marmoset.

9 l exchanges with a visually occluded virtual marmoset.

10 throughout the entire LGN, in anaesthetized marmosets.

11 cipient microaneurysms in retinas of gal-fed marmosets.

12 sity were observed in the retinas of gal-fed marmosets.

13 dial temporal (MT) area of anesthetized male marmosets.

14 D and +5 D single vision contact lens-reared marmosets.

15 requency, amplitude, and time in A1 of awake marmosets.

16 ric virus was passaged four times through 24 marmosets.

17 rge from a freeze response than right-handed marmosets.

18 rus failed to adapt during serial passage in marmosets.

19 er prefrontal damage in a comparable task in marmosets.

20 GB virus B (GBV-B), in infections of common marmosets.

21 higher amounts of pulmonary viral antigen in marmosets.

22 blishment of persistent chimera infection in marmosets.

23 fection with a hepacivirus, GBV-B, in common marmosets.

24 ymes, metabolic stability, and inhibition of marmoset 17beta-HSD1 and 17beta-HSD2.

25 In marmosets a sex-linked dichotomy results in dichromatic

26 ye growth and refractive state of the common marmoset, a New World primate that compensates for eithe

27 and during self-initiated vocalizations when marmosets, a highly vocal New World primate species, eng

28 unique to humans but new data indicate that marmosets, a new world monkey, take turns when vocalizin

29 It can infect common marmosets, a New World small primate, and induces viral

30 n in a series of behavioral studies in which marmosets, a vocal nonhuman primate species, were traine

31 Vif and Env that arise during adaptation to marmoset A3G and BST2 allow the virus to replicate in th

32 virus-resistant animals were susceptible to marmoset-adapted WT virus during rechallenge studies.

33 autoimmune encephalomyelitis (EAE) in common marmosets, allowing detailed analysis of secondary lymph

34 Both marmosets also performed an orientation discrimination t

35 e that approximately 70% of lemur and 16% of marmoset Alu elements belong to lineage-specific subfami

36 One major difference between the marmoset and human studies has been the level of trainin

37 encephalomyelitis (EAE) models in the common marmoset and rhesus monkey to model the association of E

38 In contrast, both marmosets and African green monkeys (AGM) proved suscept

39 inflammatory signs were observed in infected marmosets and CD46-transgenic mice; although viral repli

40 Virus adapted to the marmosets and eventually exhibited robust infections in

41 Fever onset was earlier with the marmosets and had a biphasic pattern similar to what has

42 n peak in the common ancestor of current day marmosets and has since moderately declined.

43 Thus, marmosets and humans may share similar pitch perception

44 l similarities between trait-like anxiety in marmosets and humans, and set the stage for further inve

45 highly correlated hypothalamic expression in marmosets and humans, suggesting co-regulation of 2 para

46 e findings allow for the development of both marmosets and macaques as neurobiological model systems

47 ptor, dipeptidyl peptidase 4, was similar in marmosets and macaques.

48 Moreover, marmosets and other callitrichid primates are very vocal

49 nonymous changes found exclusively in common marmosets and other tested callitrichine species that tw

50 he Wisconsin Card Sorting Test, developed in marmosets and recently adapted to rats, is a behavioral

51 nst Lassa virus challenge in guinea pigs and marmosets and virus-specific cell-mediated immunity in b

52 V and LCVs from NHPs (chimpanzee, orangutan, marmoset, and siamang) were selected for multifunctional

53 re more severe and of longer duration in the marmosets, and developed bronchointerstitial pneumonia.

54 y reported for cooperatively breeding common marmosets, and indicate that prosocial preferences in a

55 with encephalitis were noted in both AGM and marmosets; animals of both species succumbed between day

56 Here, we show that the common marmoset APOBEC3G (A3G) and BST2 proteins block HIV-1 in

57 In this study, we observed that common marmoset APOBEC3G and BST2, two known restriction factor

58 educe expression levels and encapsidation of marmoset APOBEC3G, while the changes in Env increase vir

59 nctional difference between A. nancymaae and marmoset APOBEC3Gs mapped to residue 128, previously sho

60 For example, marmosets are among only a handful of primates that, lik

61 Marmosets are diurnal New World monkeys that show sex-li

62 The findings also identify the marmoset as a viable animal model system for studying sp

63 ee, and orangutan genomes, using macaque and marmoset as outgroups.

64 osets as one lineage and two times through 6 marmosets as a second lineage.

65 was serially passaged five times through 14 marmosets as one lineage and two times through 6 marmose

66 jections, placed in the frontal lobe of nine marmosets as part of earlier studies.

67 for encoding sound onsets and offsets in the marmoset auditory cortex.

68 hat is able to escape the restriction in the marmoset B-LCLs.

69 The high manganese uptake in the marmoset basal ganglia and visual cortex can be explaine

70 mental paradigms that optimally tap into the marmosets' behavioral and cognitive capacities.

71 a on connections of cortical areas into a 3D marmoset brain template, generated from Nissl-stained se

72 ualize neuronal projections in a whole adult marmoset brain.

73 d for such "claustrum-enriched" genes in the marmoset brain.

74 ytes was a major consequence of infection of marmosets by the i.v. and s.c. exposure routes.

75 d amacrine cells in the retina of the common marmoset Callithrix jacchus.

76 d in the inner retinal neurons in the common marmoset Callithrix jacchus.

77 ositive retinal ganglion cells in the common marmoset Callithrix jacchus.

78 a full-length TRPML3 channel from the common marmoset (Callithrix jacchus) at an overall resolution o

79 vity and pathogenicity of RVFV in the common marmoset (Callithrix jacchus) by i.v., subcutaneous (s.c

80 ation of frontoparietal cortex in the common marmoset (Callithrix jacchus) by using intracortical mic

81 driven by both the sequencing of the common marmoset (Callithrix jacchus) genome and a growing deman

82 The sequencing of the common marmoset (Callithrix jacchus) genome offers the opportun

83 The common marmoset (Callithrix jacchus) has garnered interest rece

84 In the past decade, the New World common marmoset (Callithrix jacchus) has taken a seminal positi

85 ded the responses of up to 61 neurons in the marmoset (Callithrix jacchus) middle temporal area to a

86 umans, we experimentally infected the common marmoset (Callithrix jacchus) with diverse strains of My

87 To determine whether the common marmoset (Callithrix jacchus) would be an appropriate mo

88 during natural vocal exchanges in the common marmoset (Callithrix jacchus), a highly vocal New World

89 amental frequency of 440 Hz, that the common marmoset (Callithrix jacchus), a New World monkey with a

90 quantify the visual topography of V1 in the marmoset (Callithrix jacchus), a small diurnal monkey.

91 The common marmoset (Callithrix jacchus), a small-bodied New World

92 sts in New World monkeys, such as the common marmoset (Callithrix jacchus), a species of growing inte

93 are used for pitch extraction in the common marmoset (Callithrix jacchus), a vocal primate species,

94 a highly vocal New World primate, the common marmoset (Callithrix jacchus), across the entire hearing

95 A. nancymaae, but not marmoset (Callithrix jacchus), APOBEC3G was partially do

96 the inner nuclear layer in the retina of the marmoset (Callithrix jacchus).

97 roduced by spinal cord lesions in the common marmoset (Callithrix jacchus).

98 ion in a closely related species, the common marmoset (Callithrix jacchus).

99 ion in a closely related species, the common marmoset (Callithrix jacchus).

100 in response to hawk calls, in 18 Geoffroy's marmosets (Callithrix geoffroyi).

101 Here, we investigated whether hyperhexosemic marmosets (Callithrix jacchus) develop characteristic re

102 i, a large population of A1 neurons in awake marmosets (Callithrix jacchus) responded to rapid time-v

103 Six adult common marmosets (Callithrix jacchus) were acclimated to light,

104 time the successful generation of transgenic marmosets (Callithrix jacchus), an important nonhuman pr

105 In chimpanzees (Pan troglodytes) and common marmosets (Callithrix jacchus), left-handed individuals

106 Using single-unit recordings from awake marmosets (Callithrix jacchus), we validate several mode

107 Nissl-stained sections from the LGN of adult marmosets (Callithrix jacchus; 10 trichromatic females;

108 and anterior cingulate cortex of the common marmoset (Callithrx jacchus).

109 While conditioned task performance of a marmoset can compare unfavorably with rhesus monkey perf

110 However, a critical unknown is whether marmosets can perform visual tasks under head restraint.

111 Surface models of the marmoset, capuchin, and macaque monkey cortex were regis

112 requires a team of personnel experienced in marmoset care and handling, and small-animal neurosurger

113 We studied the susceptibility of common marmoset cells to HIV-1 infection and observed the prese

114 alues, and is likely the result of a smaller marmoset cochlea.

115 gms are well suited to isolate components of marmoset cognition that are highly relevant to humans.

116 trichromatic genotypes, rendering most male marmosets color-blind.

117 ene in human, chimpanzee, rhesus monkey, and marmoset contains a number of mutations common to all fo

118 The marmoset could be a valuable nonhuman primate model for

119 itioning techniques to determine whether the marmoset could control fixation for liquid reward.

120 Two marmosets could fixate a central point and ignore periph

121 mpus and thalamus of rat, mouse, macaque and marmoset, demonstrating error rates as low as 5%.

122 The chimera-infected marmosets described can be used as a suitable small-prim

123 n mice, but their cortical expression in the marmoset differed from the mouse pattern.

124 f the vlPFC affected the coping style that a marmoset displayed in the presence of the human intruder

125 od rewards to others, although capuchins and marmosets do deliver food rewards to others in similar k

126 usively that the koniocellular layers of the marmoset dorsal lateral geniculate nucleus have binocula

127 s study provides compelling evidence that in marmoset EAE, which forms lesions strongly resembling th

128 yo culture experiments further indicate that marmoset embryos utilize WNT signaling during early line

129 or subunit gamma (IL2RG) in pronuclear stage marmoset embryos.

130 s of frontal cortex neurons as freely moving marmosets engaged in conversational exchanges with a vis

131 nges in neural activity that occurred before marmosets even heard a conspecific vocalization that, as

132 acquired before and after EAE induction in 5 marmosets (every other week before lesions appeared, wee

133 Here, we demonstrate that marmosets exhibit two phenotypes upon infection with GBV

134 Six of seven HCV NS2 to -4A chimera-infected marmosets exhibited consistent viremia and one showed tr

135 macaques developed mild disease, and common marmosets exhibited moderate to severe, potentially leth

136 A recent study of marmoset frontal cortex observed modulated neural activi

137 elements across 62 subfamilies in the common marmoset genome.

138 d Platy-1, in the Callithrix jacchus (common marmoset) genome that arose around the time of the diver

139 Marmosets had lower proportions of midget bipolar and ro

140 The marmoset has been shown to be an outstanding model for s

141 ensity of Alu repeats (55 repeats/Mb), while marmoset has the greatest abundance (188 repeats/Mb).

142 Studies in the anesthetized marmoset have detailed the anatomy and physiology of the

143 Marmosets have a rich vocal repertoire and a similar hea

144 Marmosets have been reported to employ a circling patter

145 Excitotoxic lesions of analogous regions in marmosets have revealed, however, that although the OFC

146 We find that marmosets have significantly larger T1-weighted image en

147 Additionally, recent studies in marmosets have underscored that even in the absence of v

148 ed population of frontal cortex neurons when marmosets heard a conspecific vocalization, and that the

149 ected tamarin hepatic cell lines and primary marmoset hepatocyte cultures through the use of the simi

150 rus secretion following infection of primary marmoset hepatocyte cultures with a highly cell culture-

151 to achieve a complete viral cycle in primary marmoset hepatocyte cultures, providing a promising basi

152 eudoparticles were able to infect tamarin or marmoset hepatocytes efficiently, demonstrating that the

153 recorded in the central nucleus of the awake marmoset IC.

154 recordings from single neurons in ferret and marmoset in the previous mini-review.

155 Common marmosets in particular have significantly reduced diver

156 The common marmoset is a new world primate belonging to the Callitr

157 These data suggest that the marmoset is a viable model for studies of active vision

158 The marmoset is an emerging animal model for large-scale att

159 clude that cytoarchitectural area 6Va in the marmoset is similar to ventral premotor areas identified

160 Resolvability in marmosets is different from that in humans, where the fi

161 esults suggest that frontoparietal cortex in marmosets is organized in a similar fashion to that of o

162 rain structure before, during and after four marmosets learnt to use a rake, over a long period of 10

163 characterize a sparse population of cells in marmoset LGN that show orientation and spatial frequency

164 this function is not possessed by New World marmoset lymphocryptovirus BILF1.

165 ion factors able to block HIV-1 infection in marmoset lymphocytes.

166 or Alu elements in primates including lemur, marmoset, macaque, baboon, and chimpanzee as compared to

167 Marmosets maintained on 30% galactose (gal)-rich diet fo

168 Our findings demonstrate that common marmoset mammary stem/progenitor cells can be isolated a

169 hinae, or callitrichines) such as the common marmoset manifesting diminutive size and unique reproduc

170 or selective dopaminergic depletions of the marmoset medial caudate nucleus on serial discrimination

171 he failure of the chimeric virus to adapt in marmosets might be due to a bottleneck that occurs at th

172 Based on our results, the common marmoset model more closely resembles severe human RVF d

173 of autopsy data, a rhesus macaque and common marmoset model of MERS-CoV disease were analyzed.

174 Here, we describe the generation of a marmoset model of severe combined immunodeficiency (SCID

175 n the key similarities to human infection, a marmoset model of ZIKV infection may be useful for testi

176 c viruses and established a chimera-infected marmoset model.

177 alyses show that the typical mouse, rat, and marmoset models of DEHP toxicity cannot accurately profi

178 Together, the rhesus macaque and common marmoset models of MERS-CoV span the wide range of disea

179 The New World marmoset monkey (Callithrix jacchus) has a relatively sh

180 In particular, the common marmoset monkey (Callithrix jacchus) with a relatively s

181 In marmoset monkey auditory cortex, the latter type of adap

182 Thus, using the marmoset monkey Callithrix jacchus we characterize here

183 With a biomechanical model of the marmoset monkey vocal apparatus and behavioral developme

184 lume correlates of trait-like anxiety in the marmoset monkey.

185 also known as F2 and F7) were studied in the marmoset monkey.

186 ment of LGN and PIm inputs to area MT in the marmoset monkey.

187 We show that, in marmoset monkeys (a nonhuman primate that has far greate

188 show that neurons in the auditory cortex of marmoset monkeys (Callithrix jacchus) are sensitive to a

189 of two awake and passively listening female marmoset monkeys (Callithrix jacchus).

190 ime-varying acoustic and CI signals in awake marmoset monkeys (Callithrix jacchus).

191 rom single units in area MT of anaesthetised marmoset monkeys and examined responses to two-dimension

192 electively depleted dopamine from the OFC of marmoset monkeys and measured striatal extracellular dop

193 as about primate vocalizations and show that marmoset monkeys are a compelling model system for early

194 ows that vocal sequences produced by newborn marmoset monkeys are driven by slow fluctuations in phys

195 As marmoset monkeys are on a different branch of the evolut

196 Using marmoset monkeys as a model system, we first addressed w

197 ess contingent vocal feedback to twin infant marmoset monkeys over their first 2 months of life, the

198 nactivation of these regions were studied in marmoset monkeys performing an instrumental approach-avo

199 cortex of freely moving, naturally behaving, marmoset monkeys that may facilitate natural primate con

200 dy of the middle temporal area (MT) of adult marmoset monkeys that received unilateral V1 lesions wit

201 We used marmoset monkeys to explore whether another primate spec

202 ling, we showed that vocalizations in infant marmoset monkeys undergo dramatic changes that cannot be

203 esponses with acoustic and CI stimulation in marmoset monkeys unilaterally implanted with a CI electr

204 Here we show that when marmoset monkeys vocalize in the presence of masking noi

205 in the primary auditory cortex (A1) of awake marmoset monkeys were in fact highly selective for compl

206 Marmoset monkeys with unilateral lesions of either the a

207 ssels in human and nonhuman primates (common marmoset monkeys) and the feasibility of noninvasively i

208 d CI stimulation in auditory cortex of awake marmoset monkeys, we discovered that neurons unresponsiv

209 By using healthy common marmoset monkeys, Yamada et al traced the retinogenicula

210 Here, we explicitly test in marmoset monkeys-a very vocal and cooperatively breeding

211 ordings from cerebral cortex in anesthetized marmoset monkeys.

212 single-cell activity in dLGN of anesthetized marmoset monkeys.

213 lateral frontal cortex, areas 6Va and 8C, in marmoset monkeys.

214 y visual cortex, in sufentanil-anaesthetized marmoset monkeys.

215 jections in different locations within M1 of marmoset monkeys.

216 e fields previously described in macaque and marmoset monkeys.

217 spatial tuning in the BIN of unanesthetized marmoset monkeys.

218 identified in non-primary auditory cortex of marmoset monkeys.

219 in the primary auditory cortex (A1) of awake marmoset monkeys.

220 stream of the thalamus in naturally sleeping marmoset monkeys.

221 In this Primer, we describe key facets of marmoset natural social behavior and demonstrate that em

222 Similar to foveal development, marmoset neuronal generation was rapid, only taking 51%

223 lysis of video recordings showed that common marmosets (New World monkeys) differentiated between wel

224 In marmosets, nurr1 and netrinG2 genes exhibited highly con

225 Marmosets of both sexes were included in this study.

226 These results suggest that the marmoset offers an attractive small-animal model of huma

227 5,7-DHT-induced PFC serotonin depletions in marmosets on SSOST performance.

228 e-specific Alu subfamilies in lemur (seven), marmoset (one), and baboon/macaque (one) containing mult

229 a major block to HIV-1 replication in common marmosets operates at the level of viral entry and that

230 ynamics in the lineage leading to the common marmoset over the last 40 million years.

231 We speculate that the marmoset partially resistant phenotype may be due to a p

232 actors responsible for the blocks present in marmoset PBLs and B-LCLs are different.

233 rontal dopamine depletion, markedly impaired marmoset performance on a spatial self-ordered sequencin

234 unters additional postentry blocks in common marmoset peripheral blood mononuclear cells.

235 During passage, two marmoset phenotypes were observed: susceptible and parti

236 Marmoset photoreceptor development was studied to determ

237 2009), Ensembl supports 51 species including marmoset, pig, zebra finch, lizard, gorilla and wallaby,

238 henotype may be due to a polymorphism in the marmoset population that affects critical virus-host int

239 esence of polymorphic elements within common marmoset populations, suggests ongoing retrotranspositio

240 we identified a subpopulation of neurons in marmoset premotor cortex that was activated or suppresse

241 Comparison to inner cell masses of marmoset primate blastocysts identifies a similar comple

242 HCV NS2 to -4A chimera-infected marmosets provide a small-animal model for evaluating no

243 The marmoset provides the advantages of a small animal model

244 mm) and the effects were similar to those in marmosets raised on +5 D single vision contact lenses (e

245 ter extensive training in reversal learning, marmosets received an excitotoxic lesion of the VLPFC, O

246 The striking similarities between the marmoset retina and the human retina, and the exceptiona

247 In summary, secretagogin cells in marmoset retina are medium-field amacrine cells that sha

248 that three types of thorny ganglion cells in marmoset retina can be identified with antibodies agains

249 observed in the inner retinal neurons in the marmoset retina through intravitreal delivery.

250 inner nuclear and the ganglion cell layer of marmoset retina, however, the specific cell type(s) expr

251 cy of Buffer AVL (Qiagen) was tested against marmoset serum (EBOV concentration of 1 x 10(8) 50% tiss

252 Marmosets share with humans a cooperative breeding strat

253 Neurally, high-anxious marmosets showed reduced amygdala serotonin levels, and

254 mera) was produced and used to infect common marmosets, since HCV NS2 to NS4A proteins are critical p

255 We first sequenced the marmoset SLC6A4 promoter and identified a double nucleot

256 rformance on conventional testing paradigms, marmosets' social behavior and cognition are more simila

257 died simian foamy viruses (SFVs) from common marmosets, spider monkeys, and squirrel monkeys, New Wor

258 ed a drop in platelet counts in both AGM and marmosets suggestive of thrombosis, as well as leukocyto

259 In marmoset T cells transformed by Herpesvirus saimiri (HVS

260 In latently infected marmoset T cells, Herpesvirus saimiri (HVS) expresses si

261 Sm class U RNAs (HSURs) in latently infected marmoset T cells.

262 generated from two of the founder transgenic marmosets that reached sexual maturity.

263 In the V1 of anaesthetized marmosets, the EEG frequency spectrum undergoes transien

264 In marmosets, the pneumonia was more extensive, with develo

265 stripes may be functionally distinct, and in marmosets they also differ anatomically in the laminar o

266 y also heightened the anxiety responses of a marmoset to a human intruder.

267 together have provided a path for transgenic marmosets to contribute to the study of disease as well

268 Here we used trichromatic female marmosets to examine the intrinsic signal response in V1

269 ared the free viewing behavior of head-fixed marmosets to that of macaques, and found that their sacc

270 neural responses in the brain of four awake marmosets trained to fix their gaze upon images of faces

271 Such effects were not detected in EAE marmosets treated with mAb against BLyS or APRIL, where

272 However, we have found that marmoset TRIM5alpha does not block HIV-1.

273 ve highlighted that the complex fovea of the marmoset undergoes a more rapid postnatal development in

274 In sum, these results show that marmosets use two mechanisms to extract pitch (harmonic

275 We found that marmosets used temporal envelope information to discrimi

276 We further measured frequency resolution in marmosets using a psychophysical task in which pure tone

277 We find that pitch is extracted by marmosets using temporal envelope cues for lower pitch s

278 small brain regions of the infant and adult marmoset, using an MRI-guided approach.

279 gies, we hypothesized a critical role of the marmoset VLPFC in performance of a serial reversal learn

280 By measuring the natural statistics of marmoset vocal exchanges, we observed that they take tur

281 response to HCV NS3 in this viremia-resolved marmoset was boosted by rechallenging, but no viremia wa

282 trast to previous optical imaging studies in marmosets, we find clearly segregated color domains, sim

283 cording technique that we developed in awake marmosets, we found that the two types of rate-coding ne

284 auditory cortex of naturally sleeping common marmosets, we show that slow-wave sleep (SWS) alters neu

285 The hand preferences of 11 marmosets were assessed over their adult life span using

286 Seven marmosets were inoculated intrahepatically with HCV NS2

287 Marmosets were more susceptible to RVFV than rhesus maca

288 Ten marmosets were reared with multizone contact lenses of a

289 ccordance with these hypotheses, left-handed marmosets were slower to explore novel foods and slower

290 Marmosets were susceptible to lower doses of RVFV than A

291 We believe these transgenic marmosets will be invaluable non-human primate models in

292 arallel technical and paradigmatic advances, marmosets will become an essential model of human social

293 Re-challenge of a previously infected marmoset with a contemporary outbreak strain SPH2015 fro

294 When comparing marmosets with both capuchins and macaques, we found a h

295 ased on the composition of white matter from marmosets with experimental allergic encephalomyelitis (

296 novel animal model for in vivo infection of marmosets with HIV-1-like viruses.

297 Here we experimentally infected 4 male marmosets with ZIKV (prototype 1947 African strain) and

298 hes mark the occipitotemporal pathway of the marmoset, with the most anterior patches showing the str

299 been exploring the blocks to HIV-1 in common marmosets, with the ultimate goal of developing a new an

300 Both AGM and marmosets would serve as useful models of aerosol infect