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 t are explored to show a homologue exists in marmoset.

4 l exchanges with a visually occluded virtual marmoset.

5 ed activity in central (lemniscal) IC of the marmoset.

6 ithelial stem/progenitor cells in the common marmoset.

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

8 iocellular layers in the geniculates of four marmosets.

9 racellular recordings in the cortex of awake marmosets.

10 throughout the entire LGN, in anaesthetized marmosets.

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

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

13 tative high-level face processing network in marmosets.

14 higher amounts of pulmonary viral antigen in marmosets.

15 blishment of persistent chimera infection in marmosets.

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

17 cipient microaneurysms in retinas of gal-fed marmosets.

18 logically distinct near the time of birth in marmosets.

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

20 itory thalamus of awake, passively-listening marmosets.

21 ervations in single-unit recordings in awake marmosets.

22 ipp is associated with high-trait anxiety in marmosets.

23 of the optic tract (NOT) in the pretectum of marmosets.

24 ung and old rhesus macaques, baboons and old marmosets.

25 as9 has not been extensively investigated in marmosets.

26 ical (area MT) visual areas in anaesthetised marmosets.

27 ng the development of lens-induced myopia in marmosets.

28 In this study, we used 5 marmosets (4 males, 1 female).

29 ions from three primates (human, macaque and marmoset), a rodent (mouse) and a weasel (ferret).

30 That the marmoset, a physiologically- and genetically-accessible

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

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

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

34 While we could match several marmoset and human resting-state networks based on their

35 While we could match several marmoset and human RSNs based on their functional finger

36 common organizational motif (also evident in marmoset and macaque anatomical circuits) that might sup

37 pelling evidence supporting homology between marmoset and macaque FEF and suggest that the marmoset i

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

39 rovide compelling evidence for an FEF in the marmoset and suggest that the marmoset is a useful model

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

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

42 Thus, marmosets and humans may share similar pitch perception

43 anization of cortico-subcortical networks in marmosets and humans using ultra-high field fMRI.

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 tuted around 30% of striatal interneurons in marmosets and humans.

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

48 d the lateral intraparietal area of two male marmosets and recorded neural activity during performanc

49 ent was administered to both male and female marmosets and reduced peripheral levels of estradiol (E2

50 ty of inducing monogenic mutations in common marmosets and support the use of this species for genera

51 es the ventrolateral posterior area (VLP) in marmosets and the dorsolateral posterior area (DLP) in o

52 r females, three males) lightly anesthetized marmosets and used a data-driven hierarchical clustering

53 g ultra high field fMRI data to compare rat, marmoset, and human MFC functional connectivity.

54 imensions of architecture in the mouse, cat, marmoset, and macaque monkey.

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

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

57 o urban area was detected mainly in resident marmosets, and synanthropic mosquitoes were likely invol

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

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

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

61 Overall, these results support the view that marmosets are a promising preclinical modeling species f

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

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

64 Marmosets are neotropical primates with a modified OXT l

65 Marmosets are New World diurnal foveate monkeys, and are

66 ese results corroborate the viability of the marmoset as a preclinical model of human MFC dysfunction

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

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

69 activity in the hippocampus of freely moving marmosets as they naturally explored a spatial environme

70 in research-including rats, pigs, bears, and marmosets-as well as in humans, providing a translationa

71 undaries of frontal cortex were described in marmosets at the start of the 20th century (Brodmann, 19

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

73 higher affinity than OXT across AVPR1a, and marmoset AVPR1a show a 10-fold lower OXT binding affinit

74 ndogenous human AVPR1a signaling and enhance marmoset AVPR1a signaling.

75 and higher efficacious response than AVP at marmoset AVPR1a.

76 8)-OXT and Leu(8)-OXT at human, macaque, and marmoset AVPR1a.

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

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

79 e anatomical data made available through the Marmoset Brain Architecture Project are explored to show

80 Our results provide evidence that the marmoset brain has a greater neuronal activation after i

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

82 ualize neuronal projections in a whole adult marmoset brain.

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

84 es and trajectories of fiber pathways in the marmoset brain.

85 across the neocortex of humans, macaques and marmosets but not mice or ferrets.

86 tical networks in humans are also present in marmosets, but that small, potentially functionally rele

87 bcortical RSNs in humans are also present in marmosets, but that small, potentially functionally rele

88 Starting from randomly chosen marmoset call features, we use a greedy search algorithm

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

90 ectural organization of the EC in the common marmoset Callithrix jacchus.

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

92 The New World common marmoset (Callithrix jacchus) has become popular as a no

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

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

95 a largely lissencephalic cortex, the common marmoset (Callithrix jacchus) is a promising alternative

96 The common marmoset (Callithrix jacchus) is a small New World prima

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

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

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

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

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

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

103 e mostly lissencephalic cortex of the common marmoset (Callithrix jacchus).

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

105 ifferences in trait anxiety using the common marmoset (Callithrix jacchus, mixed sexes) as a model.

106 members of the Callitrichidae family, common marmosets (Callithrix jacchus) and red-bellied tamarins

107 Common marmosets (Callithrix jacchus) are susceptible to intest

108 itive flexibility, in unanaesthetized common marmosets (Callithrix jacchus) at two time points during

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

110 Single-unit studies in awake marmosets (Callithrix jacchus) have shown that a sub-pop

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

112 Nineteen Wistar rats and 21 marmosets (Callithrix jacchus) were distributed among co

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

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

115 xtrastriate visual cortex of awake, behaving marmosets (Callithrix jacchus).

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

117 In marmosets (Callithrix), a nonsynonymous nucleotide subst

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

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

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

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

122 procedures for construction of a custom-made marmoset chair, head-cap implantation, preparation of th

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

124 Most marmoset connectomic research, however, has exclusively

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

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

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

128 s strong dlPFC but weak mPFC connectivity in marmoset differs markedly from the stereotypical DMN in

129 These same marmosets displayed an anxiogenic, dose-dependent respon

130 Individually, marmosets displayed marked differences in behavioral sen

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

132 truncation of the LRRK2 kinase domain, into marmoset embryonic and induced pluripotent stem cells.

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

134 cacies of CRISPR/mRNA and CRISPR/nuclease in marmoset embryos were examined.

135 rthermore, optimal conditions to generate KI marmoset embryos were investigated using CRISPR/Cas9 and

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

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

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

139 We show that AI-treated male and female marmosets exhibit behavioral changes consistent with the

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

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

142 Male marmosets exhibited remarkably similar patterns of stron

143 while they view socially relevant videos of marmoset faces.

144 A critical step in the development of marmosets for such models is to characterize functional

145 ., 2012), the broad functional boundaries of marmoset frontal cortex have yet to be established.

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

147 electrode arrays into areas 8Ad-the putative marmoset frontal eye field-and the lateral intraparietal

148 elements across 62 subfamilies in the common marmoset genome.

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

150 Marmosets had a c-Fos expression that was notably more w

151 Eight marmosets had lenses removed for 30 mins twice/day durin

152 Marmosets had lower proportions of midget bipolar and ro

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

154 Marmosets have a rich vocal repertoire and a similar hea

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

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

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

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

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

160 We report place cells in marmoset hippocampus during free navigation that exhibit

161 ugh theta oscillations were prevalent in the marmoset hippocampus, the patterns of activity were nota

162 ate reduced anxiety levels in highly anxious marmosets in two uncertainty-based tests of anxiety: exp

163 motor functions), which was not observed for marmosets (in which no clear pattern could be drawn, and

164 Argentine hemorrhagic fever-like disease in marmosets infected with the New World mammarenavirus Jun

165 The common marmoset is a New World primate species ideally placed t

166 n diseases.SIGNIFICANCE STATEMENT The common marmoset is a New World primate that has garnered recent

167 The common marmoset is a promising alternative primate model due to

168 an FEF in the marmoset and suggest that the marmoset is a useful model for investigating FEF microci

169 armoset and macaque FEF and suggest that the marmoset is a useful primate model for investigating FEF

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

171 nces exist.SIGNIFICANCE STATEMENT The common marmoset is becoming increasingly popular as an addition

172 The common marmoset is envisioned as a candidate nonhuman primate s

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

174 ysiological investigation in awake, behaving marmosets is necessary to physiologically locate this ar

175 ght to functionally derive boundaries of the marmoset lateral frontal cortex (LFC) using ultra-high f

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

177 he unique ability to compare the rat MFC and marmoset LFC, which have often been suggested to be func

178 in primate brain, we generated a transgenic marmoset line in which EGFP is expressed under the contr

179 We found that, similar to humans, marmoset LRRK2 G2019S resulted in elevated kinase activi

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

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

182 digestion in three mixed-sex groups of adult marmosets maintained on three commercial base diets.

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

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

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

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

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

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

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

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

191 influences perinatal outcomes in the common marmoset monkey (Callithrix jacchus), using a combinatio

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

193 The New World marmoset monkey occupies an intriguing niche, displaying

194 The marmoset monkey offers a unique composition of ancestral

195 Therefore, the marmoset monkey represents a previously understudied pos

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

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

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

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

200 n of the middle temporal (MT) visual area in marmoset monkeys and studied the distribution and morpho

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

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

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

204 demonstrate that increased trait anxiety in marmoset monkeys correlates with reduced hippocampal glu

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

206 e into the medial caudate of male and female marmoset monkeys performing a touchscreen-based serial d

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

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

209 cardiovascular and behavioral monitoring in marmoset monkeys to show that over-activation of primate

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

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

212 Marmoset monkeys with unilateral lesions of either the a

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

214 We review studies in marmoset monkeys, songbirds, and other vertebrates.

215 Here, we provide evidence that, in marmoset monkeys, the size of a domestication phenotype-

216 Using infant marmoset monkeys, we densely sampled vocal, postural and

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

218 , we investigated laminar neural activity in marmoset monkeys, which have a smooth cortex.

219 anges in the contact vocalizations of infant marmoset monkeys, which transition from noisy, low frequ

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

221 but this relation is attenuated in mice and marmoset monkeys.

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

223 ordings from cerebral cortex in anesthetized marmoset monkeys.

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

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

226 ulate nucleus (LGN) and cortical area MT, in marmoset monkeys.

227 and the corresponding network topologies in marmoset monkeys.

228 connectivity profiles of the SN across rats, marmosets (n = 10), and humans (n = 30).

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

230 s of 143 retrograde tracer injections in the marmoset neocortex.

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

232 In marmosets, nurr1 and netrinG2 genes exhibited highly con

233 Marmosets of both sexes were included in this study.

234 ty in the inferior colliculus (IC) of common marmosets of both sexes while they performed a tone-in-n

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

236 Chinese hamster ovary cells expressing marmoset or human oxytocin receptors (mOTRs or hOTRs, re

237 evolutionary separation between macaques and marmosets, our results suggest this frontal network spec

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

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

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

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

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

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

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

245 test similarity with premotor regions in the marmoset, rather than dorsolateral prefrontal regions, w

246 Tamarins and marmosets represent viable New World models for ZIKV pat

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

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

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

250 area 8Ad, the putative frontal eye field in marmosets, rhythmic alpha-band activity (9-14 Hz) was hi

251 The EC layers and subfields in the marmoset seem to be architectonically similar to those t

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

253 Like Old World primates, marmosets show differential activation in anterior cingu

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

255 nses within the nonhuman primate, the common marmoset, similar to that seen in mood and anxiety disor

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

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

258 ntified sequence polymorphisms in the common marmoset SLC6A4 repeat region (AC/C/G and CT/T/C) associ

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

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

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

262 mode network with the superior colliculus in marmosets that was much weaker in humans.

263 ntal cortex in healthy, normally functioning marmosets, that is, how these circuitries are functional

264 Here, we found that, in common marmosets, the dorsolateral prefrontal cortex (dlPFC; pe

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

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

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

268 icrostimulation in frontal cortical areas in marmosets to physiologically identify FEF.

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

270 e model of human cognitive aging, the common marmoset, to examine the effects of a 4-week daily admin

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

272 Accordingly, we correlated marmoset trait anxiety scores to their postmortem aHipp

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

274 nge of frontal cortical areas in three adult marmosets (two males, one female).

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

276 more, the koniocellular geniculate layers in marmosets, unlike those in the geniculate of commonly st

277 n in more neocortical structures of rats and marmosets using a more robust quantitative technique and

278 tical resting-state networks (RSNs) in awake marmosets using resting-state fMRI and then compared the

279 ith cortical resting-state networks in awake marmosets using resting-state fMRI, then to compare thes

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

281 CRISPR/Cas9 may be utilized to produce KO/KI marmosets via gene editing.

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

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

284 cardiovascular and behavioral monitoring in marmosets, we show that over-activation of sgACC/25 redu

285 Seven marmosets were inoculated intrahepatically with HCV NS2

286 Sixteen marmosets were reared with a -5D contact lens on their r

287 was monitored by measuring refraction while marmosets were seated at the center of a 1 m radius view

288 In this study, four adult marmosets were trained to perform a series of visually-g

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

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

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

292 We implanted marmosets with 96-channel Utah arrays and applied micros

293 Moreover, treatment of Mtb-infected marmosets with a cytochrome bc1-aa3 oxidase inhibitor co

294 In adult marmosets with experimental autoimmune encephalomyelitis

295 ions that was mirrored in 72 lesions from 13 marmosets with experimental autoimmune encephalomyelitis

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

297 d RNA gene expression in 16 SLC6A4 genotyped marmosets with responsivity to 5HT(2A) antagonism during

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

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

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