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1 he New World primate Callithrix jacchus, the common marmoset.
2 the extension of our investigations into the common marmoset.
3 ntal allergic encephalomyelitis (EAE) in the common marmoset.
4 he striatum of cynomolgus monkeys and of the common marmoset.
5 mary epithelial stem/progenitor cells in the common marmoset.
6 al autoimmune encephalomyelitis (EAE) in the common marmoset.
7 fear responses in the New World primate, the common marmoset.
8 tal 6-hydroxydopamine (6-OHDA) lesion in the common marmoset.
9 2 independent growth and induced lymphoma in common marmosets.
10 n cell culture and for lymphoma induction in common marmosets.
11 S mutants were tested in cell culture and in common marmosets.
12 addition, HVS Deltaorf14 was nononcogenic in common marmosets.
13 Deltaorf14 was tested in cell culture and in common marmosets.
14 ases are the most common diseases in captive common marmosets.
15 arger estimated effective population size of common marmosets.
16 signed for studying cooperative behaviors in common marmosets.
17 ivirus, GB virus B (GBV-B), in infections of common marmosets.
18 ving infection with a hepacivirus, GBV-B, in common marmosets.
19                           Whether adolescent common marmosets (a new world primate) are susceptible t
20 llion brain cells across 18 locations in the common marmoset, a New World monkey primed for genetic e
21 expressing the CD4 and CXCR4 proteins of the common marmoset, a New World monkey.
22 e demonstrate that during 3D navigation, the common marmoset, a new world primate adapted to daylight
23 n the eye growth and refractive state of the common marmoset, a New World primate that compensates fo
24 study, these same rhythms were sought in the common marmoset, a primate model of eye growth, to estab
25              We address this question in the common marmoset, a small arboreal New World primate with
26  prototypical lymphoblast cell line from the common marmoset, a vitamin D-resistant New World primate
27 mental autoimmune encephalomyelitis (EAE) in common marmosets, a model of MS that recapitulates focal
28                                It can infect common marmosets, a New World small primate, and induces
29 mental autoimmune encephalomyelitis (EAE) in common marmosets, allowing detailed analysis of secondar
30 TP/c-ras each induced lymphoma in one of two common marmosets, although onset of disease was more rap
31 pes of the central nervous system of healthy common marmoset and mapped 87 subclusters spatially onto
32 immune encephalomyelitis (EAE) models in the common marmoset and rhesus monkey to model the associati
33 dings in multiple cortical areas in both the common marmoset and the rhesus macaque.
34 racterizes the microbiome of healthy captive common marmosets and demonstrates that source-specific m
35 s nonsynonymous changes found exclusively in common marmosets and other tested callitrichine species
36 underpin reproductive performance in captive common marmosets and provides novel insights into the po
37                   Primary cells derived from common marmosets and squirrel monkeys support every phas
38 asibility of inducing monogenic mutations in common marmosets and support the use of this species for
39 New World NHP species (red-bellied tamarins; common marmosets) and Syrian hamsters-following single-d
40 yl-1,2,3,6-tetrahydropyridine (MPTP)-treated common marmosets, and in normal individuals and patients
41 recently reported for cooperatively breeding common marmosets, and indicate that prosocial preference
42 alian species: humans, long-tailed macaques, common marmosets, and rats.
43                       Here, we show that the common marmoset APOBEC3G (A3G) and BST2 proteins block H
44              In this study, we observed that common marmoset APOBEC3G and BST2, two known restriction
45                  These findings identify the common marmoset as a promising nonhuman primate to study
46      The findings of this study identify the common marmoset as a useful model of human EEE for testi
47                  These findings identify the common marmoset as an appropriate model of human Lassa f
48 sh a short-lived nonhuman primate (NHP), the common marmoset, as a key model of age-related cognitive
49 oarchitectural organization of the EC in the common marmoset Callithrix jacchus.
50 tinin positive retinal ganglion cells in the common marmoset Callithrix jacchus.
51 isplaced amacrine cells in the retina of the common marmoset Callithrix jacchus.
52 valuated in the inner retinal neurons in the common marmoset Callithrix jacchus.
53 ure of a full-length TRPML3 channel from the common marmoset (Callithrix jacchus) at an overall resol
54 infectivity and pathogenicity of RVFV in the common marmoset (Callithrix jacchus) by i.v., subcutaneo
55 organization of frontoparietal cortex in the common marmoset (Callithrix jacchus) by using intracorti
56 munity, driven by both the sequencing of the common marmoset (Callithrix jacchus) genome and a growin
57                        The sequencing of the common marmoset (Callithrix jacchus) genome offers the o
58                                The New World common marmoset (Callithrix jacchus) has become popular
59                                          The common marmoset (Callithrix jacchus) has garnered intere
60            In the past decade, the New World common marmoset (Callithrix jacchus) has taken a seminal
61    With a largely lissencephalic cortex, the common marmoset (Callithrix jacchus) is a promising alte
62                                          The common marmoset (Callithrix jacchus) is a small New Worl
63                                          The common marmoset (Callithrix jacchus) is increasingly rec
64                                          The common marmoset (Callithrix jacchus) is known for its hi
65                                          The common marmoset (Callithrix jacchus) is of considerable
66             As a nonhuman primate (NHP), the common marmoset (Callithrix jacchus) shares many feature
67 de penetrations in the temporal gyrus of the common marmoset (Callithrix jacchus) to 1) compare the f
68 en in humans, we experimentally infected the common marmoset (Callithrix jacchus) with diverse strain
69                     To determine whether the common marmoset (Callithrix jacchus) would be an appropr
70 cortex during natural vocal exchanges in the common marmoset (Callithrix jacchus), a highly vocal New
71 ng fundamental frequency of 440 Hz, that the common marmoset (Callithrix jacchus), a New World monkey
72 tool, we analyzed breathing behaviors of the common marmoset (Callithrix jacchus), a New World non-hu
73 onses of emotional facial expressions in the common marmoset (Callithrix jacchus), a New World primat
74 sis of social interaction observation is the common marmoset (Callithrix jacchus), a small New World
75                                          The common marmoset (Callithrix jacchus), a small-bodied New
76 ion exists in New World monkeys, such as the common marmoset (Callithrix jacchus), a species of growi
77  signal are used for pitch extraction in the common marmoset (Callithrix jacchus), a vocal primate sp
78 tex of a highly vocal New World primate, the common marmoset (Callithrix jacchus), across the entire
79 A sequencing to profile retinal cells of the common marmoset (Callithrix jacchus), an early divergent
80 dependently at the chromosome level, for the common marmoset (Callithrix jacchus), an primate model s
81                                          The common marmoset (Callithrix jacchus), due to its small s
82 poral ablations in the New World monkey, the common marmoset (Callithrix jacchus), produced a persist
83 trode in vitro in striatal sections from the common marmoset (Callithrix jacchus).
84 iatal and extrastriatal brain regions of the common marmoset (Callithrix jacchus).
85 ting the mostly lissencephalic cortex of the common marmoset (Callithrix jacchus).
86  loss produced by spinal cord lesions in the common marmoset (Callithrix jacchus).
87  infection in a closely related species, the common marmoset (Callithrix jacchus).
88 eplication in a closely related species, the common marmoset (Callithrix jacchus).
89 idual differences in trait anxiety using the common marmoset (Callithrix jacchus, mixed sexes) as a m
90 ed video cameras to capture the movements of common marmosets (Callithrix jacchus) and crickets stere
91    Two members of the Callitrichidae family, common marmosets (Callithrix jacchus) and red-bellied ta
92                                              Common marmosets (Callithrix jacchus) are susceptible to
93 nd cognitive flexibility, in unanaesthetized common marmosets (Callithrix jacchus) at two time points
94  Medical Centre/2012, were used to challenge common marmosets (Callithrix jacchus) by three routes of
95  NA versus SA viruses like humans, we tested common marmosets (Callithrix jacchus) by using intranasa
96 ity Neuropixels probes in freely moving male common marmosets (Callithrix jacchus) engaged in an anti
97 d AVP receptors was examined in the brain of common marmosets (Callithrix jacchus) using in situ hybr
98                                    Six adult common marmosets (Callithrix jacchus) were acclimated to
99                            Twenty-four adult common marmosets (Callithrix jacchus) were followed with
100 this possibility, young to middle aged adult common marmosets (Callithrix jacchus) were injected with
101                                We inoculated common marmosets (Callithrix jacchus) with the objective
102  examined this link in both sexes of captive common marmosets (Callithrix jacchus), a cooperatively b
103 istinct biomechanical ability(4)(,)(5)(,)(6)-common marmosets (Callithrix jacchus), Humboldt's squirr
104         In chimpanzees (Pan troglodytes) and common marmosets (Callithrix jacchus), left-handed indiv
105 n cotton-top tamarins (Saguinus oedipus) and common marmosets (Callithrix jacchus), species known to
106 s used as a long-lasting opioid analgesic in common marmosets (Callithrix jacchus), there are no publ
107 d virus from spontaneous B cell lymphomas of common marmosets (Callithrix jacchus).
108 ases are the most common diseases in captive common marmosets (Callithrix jacchus).
109  126 rhesus macaques (Macaca mulatta) and 72 common marmosets (Callithrix jacchus).
110                                              Common marmosets (Callithrix jacchus, n = 18) were train
111 ons of the brain of a non-human primate (the common marmoset, Callithrix jacchus) following four syst
112 frontal and anterior cingulate cortex of the common marmoset (Callithrx jacchus).
113             We studied the susceptibility of common marmoset cells to HIV-1 infection and observed th
114            These results demonstrate that in common marmosets D3 receptors are located in both striat
115  lymphocryptovirus (LCV) naturally infecting common marmosets demonstrated that gamma-1 herpesviruses
116  Rhesus macaques developed mild disease, and common marmosets exhibited moderate to severe, potential
117                                     Overall, common marmoset foraging association networks were cohes
118 ted by facial expressions in awake New World common marmosets from both male and female sex, and to d
119 laty-1 elements across 62 subfamilies in the common marmoset genome.
120 , termed Platy-1, in the Callithrix jacchus (common marmoset) genome that arose around the time of th
121                                          The common marmoset has enormous promise as a nonhuman prima
122 02 reversed motor disability in MPTP-treated common marmosets in a dose-dependent manner.
123 modulin-encoding E. coli colonize laboratory common marmosets in a manner dependent on the source, po
124                                              Common marmosets in particular have significantly reduce
125 erimental field study of four wild groups of common marmosets in which we controlled food distributio
126 ues were resistant to disease, we infected 3 common marmosets intranasally with LACV.
127                                          The common marmoset is a new world primate belonging to the
128                                          The common marmoset is a New World primate species ideally p
129 an brain diseases.SIGNIFICANCE STATEMENT The common marmoset is a New World primate that has garnered
130                                          The common marmoset is a promising alternative primate model
131 differences exist.SIGNIFICANCE STATEMENT The common marmoset is becoming increasingly popular as an a
132                                          The common marmoset is envisioned as a candidate nonhuman pr
133 y, this functional organization of AI in the common marmoset is similar to that in other mammalian sp
134                                     In fact, common marmoset lymphocytes immortalized by the HVS/Tip
135 p mSH3B, retained its ability to immortalize common marmoset lymphocytes in culture.
136   Subgroup A and C strains transform primary common marmoset lymphocytes to interleukin-2-independent
137                Our findings demonstrate that common marmoset mammary stem/progenitor cells can be iso
138 llitrichinae, or callitrichines) such as the common marmoset manifesting diminutive size and unique r
139 pmental timing of the cooperatively breeding common marmoset maps onto behavioral milestones.
140                    Based on our results, the common marmoset model more closely resembles severe huma
141 bsence of autopsy data, a rhesus macaque and common marmoset model of MERS-CoV disease were analyzed.
142             Together, the rhesus macaque and common marmoset models of MERS-CoV span the wide range o
143 imary auditory cortical neurons in the adult common marmoset monkey (Callithrix jacchus) were modifie
144                           In particular, the common marmoset monkey (Callithrix jacchus) with a relat
145 litters influences perinatal outcomes in the common marmoset monkey (Callithrix jacchus), using a com
146 atic vessels in human and nonhuman primates (common marmoset monkeys) and the feasibility of noninvas
147 ocal development of three different mammals: common marmoset monkeys, Egyptian fruit bats, and humans
148                             By using healthy common marmoset monkeys, Yamada et al traced the retinog
149 AG, analysis of video recordings showed that common marmosets (New World monkeys) differentiated betw
150  activity in the inferior colliculus (IC) of common marmosets of both sexes while they performed a to
151 n that a major block to HIV-1 replication in common marmosets operates at the level of viral entry an
152                  Following MPTP treatment of common marmosets, OPN protein expression was decreased,
153 ation dynamics in the lineage leading to the common marmoset over the last 40 million years.
154 -1 encounters additional postentry blocks in common marmoset peripheral blood mononuclear cells.
155  the presence of polymorphic elements within common marmoset populations, suggests ongoing retrotrans
156   The Old World macaque monkey and New World common marmoset provide fundamental models for human vis
157                                          The common marmoset provides a unique opportunity to study t
158 ation of the HIV-1 envelope glycoproteins to common marmoset receptors might allow the development of
159                    Experimental infection of common marmosets resulted in fulminant lymphoma with bot
160  of the amygdala in a new world primate, the common marmoset, resulted in a progressive impairment in
161 d responses within the nonhuman primate, the common marmoset, similar to that seen in mood and anxiet
162 -4A chimera) was produced and used to infect common marmosets, since HCV NS2 to NS4A proteins are cri
163 tly identified sequence polymorphisms in the common marmoset SLC6A4 repeat region (AC/C/G and CT/T/C)
164  We studied simian foamy viruses (SFVs) from common marmosets, spider monkeys, and squirrel monkeys,
165 factors are implicated in immortalization of common marmoset T lymphocytes and may also be critical i
166 ental HVS subgroup C strain 488 immortalized common marmoset T lymphocytes in vitro to interleukin-2-
167 ental HVS subgroup C strain 488 immortalized common marmoset T lymphocytes in vitro to interleukin-2-
168 nant HVS deltaSTP/v-ras immortalized primary common marmoset T lymphocytes to interleukin-2-independe
169 tor neurons was investigated in the rat, the common marmoset, the rhesus monkey and man using the SMI
170                      Here, we found that, in common marmosets, the dorsolateral prefrontal cortex (dl
171 haracterization of selective dynamics in the common marmoset, thus provides important insights into t
172                                   We trained common marmosets to perform spatial self-ordered sequenc
173  chimpanzees, gorillas, rhesus macaques, and common marmosets to understand human-specific features o
174  primate model of human cognitive aging, the common marmoset, to examine the effects of a 4-week dail
175                                           In common marmosets treated with the selective nigral neuro
176 in the hemispheres of left- and right-handed common marmosets using surface photography and histology
177 onhuman primate, Callithrix jacchus jacchus (common marmoset), we show that immunization with myelin
178 rimary auditory cortex of naturally sleeping common marmosets, we show that slow-wave sleep (SWS) alt
179                                  Twenty-four common marmosets were grouped by onset of deprivation (g
180 small nonhuman primate model of Lassa fever, common marmosets were subcutaneously inoculated with Las
181                                 Thirty-three common marmosets were used.
182 n 19 to 20 days of experimental infection of common marmosets, while HVS deltaSTP-C488 and HVS deltaT
183 s during pregnancy in a total of four female common marmosets with five or six fetuses per group.
184 n, globus pallidus, substantia nigra) in the common marmoset, with the highest levels being in substa
185 e have been exploring the blocks to HIV-1 in common marmosets, with the ultimate goal of developing a

 
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