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1 C-5 cells or to cause hepatitis in primates (tamarins).
2 ortant for wild Callitrichids (marmosets and tamarins).
3 sequenced in the saki monkey, capuchin, and tamarin.
4 ass I molecule expressed by every cotton-top tamarin.
5 at is no longer functional in the cotton-top tamarin.
6 est content of organic acids was detected in tamarind.
7 1.18, compared to 0.86 for Coir and 0.91 for Tamarind.
8 s of particular mirror-specific behaviors in tamarins.
9 ose in this gene during the first passage in tamarins.
10 V-B induces an acute, resolving hepatitis in tamarins.
11 creased biochemical evidence of hepatitis in tamarins.
12 were isolated from mystax, owl monkeys, and tamarins.
13 lification in cultured cells and in infected tamarins.
14 s compared to calls of unfamiliar, unrelated tamarins.
15 , Kralik, and Botto-Mahan's experiments with tamarins.
16 emonstration of the ESC effect in cotton-top tamarins.
17 closely related to HCV, causes hepatitis in tamarins.
18 including complete loss of 2-5A synthesis in tamarins.
19 dered an infectious GBV-B clone nonviable in tamarins.
20 MHC class I polymorphism like the cotton-top tamarin, a dependence on shared MHC class I molecules ma
22 stablishing persistent infections in healthy tamarins, a feature that substantially enhances its valu
23 ested two hypotheses with captive cotton-top tamarins: (a) Tamarins will demonstrate higher rates of
25 that was recognized by all individuals, two tamarins also made a response to the same epitope of the
27 mmatory disease using the colitic cotton-top tamarin, an animal model of human ulcerative colitis.
28 e, human habitations border the forest while tamarin and capuchin monkeys are also common to edge hab
29 were habituated to a series of calls from 1 tamarin and then played back a test call from a novel ta
33 Marmosets range over shorter distances than tamarins and feed primarily on tree exudates, a clumped
35 surrogate model for HCV, causes hepatitis in tamarins and is the virus phylogenetically most closely
38 d primates revealed that the Callitrichinae (tamarins and marmosets) are an exception to these rules
42 ain social avoidance of unpalatable foods in tamarins and the absence of social avoidance in less coo
43 ability of each recombinant virus to infect tamarins and to cause acute hepatitis was determined.
44 WMs with two kidney cell lines of NWMs, TMX (tamarin) and NZP-60 (marmoset), and characterized their
46 social inequity aversion will be assessed by tamarins, and possibly by other primates, only under con
47 idenced in the reaching behaviors of lemurs, tamarins, and rhesus monkeys similarly bear on the evolu
48 We have demonstrated the suitability of the tamarin as a host for GBV-B and as a surrogate nonhuman
49 tuation playback experiments to test whether tamarins attend to the encoded information about individ
51 health effects in C57BL/6 mice compared with tamarind beverages sweetened with glucose or fructose.
54 ion to induce shared attention in cotton top tamarins, both in a task that involved food getting and
55 nd then played back a test call from a novel tamarin; both opposite- and same-sex pairings were teste
56 ure was used to show that human newborns and tamarins can discriminate sentences from Dutch and Japan
57 stic analyses of individual identity and the tamarins' capacity to discriminate among vocal signature
58 the chimeric RNA replicated in the liver of tamarins, causing biochemical and histopathological chan
59 virus-B (GBV-B) causes an acute hepatitis in tamarins characterized by increased alanine transaminase
61 the potential of few natural fibres such as Tamarind, Coir, and Mesta as sustainable alternatives to
63 ues), two New World NHP species (red-bellied tamarins; common marmosets) and Syrian hamsters-followin
65 tioned tube is replaced by an occluded ramp, tamarins consistently search in the compartment below th
73 gene in the HAV/7 background was virulent in tamarins, demonstrating that the simian virus 2C gene al
77 In experimental settings, chimpanzees and tamarins do not consistently take advantage of opportuni
80 d ELATE demonstrated significant anisotropy: Tamarind exhibited high stiffness, Coir showed variable
82 esponses emitted to digitized photographs of tamarins (Experiment 1) and to videotapes of real-time o
85 mian hepatocytes failed to induce viremia in tamarins following intrahepatic inoculation, nor did the
89 e highly-endangered callitrichid golden lion tamarin (GLT-Leontopithecus rosalia) is a rare conservat
93 y, and the three alleles in the marmoset and tamarin have spectral peaks near 562, 556, and 543 nm, r
103 hown to be uniquely sensitive to the sera of tamarins infected with GBV-B, validating their usefulnes
104 r weakly reactive (positive by PCR-NA), only tamarins infected with highly reactive stool suspensions
106 action including reintroduction of zoo-born tamarins into forest fragments 1984-2000, increased numb
109 ) from litchi seeds and xyloglucan (XG) from tamarind kernels were recovered, and composite films wer
110 the color associated with 3 food items, the tamarins learned to pick the color associated with 1 foo
113 lue rewards requiring travel to acquire, but tamarin monkeys do not, despite the greater patience of
114 Using a new data set generated by cotton-top tamarin monkeys playing a repeated food-exchange game, w
115 e conducted on human newborns and cotton-top tamarin monkeys to assess their ability to discriminate
116 s from the vertical to the horizontal plane, tamarins no longer show systematic perseverative errors
118 that HCV pseudoparticles were able to infect tamarin or marmoset hepatocytes efficiently, demonstrati
119 xogenously expressing TRIM5alpha from either tamarin or squirrel monkeys in permissive cell lines res
122 teners in optimized VTCC consisted of velvet tamarind powder (40.5%), water (40%), stevia (6%), xylit
124 s, but does show some similarity to So-N1, a tamarin pseudogene from which no transcript has been fou
125 assion fruit, surinam cherry, sapodilla, and tamarind pulps were evaluated as well as their by-produc
131 s C virus (HCV), and thus GBV-B infection of tamarins represents a powerful surrogate model system fo
133 y more correct choices and fewer errors than tamarins rewarded based on color cues during initial lea
136 his end, the authors examined the cotton-top tamarin's (Saguinus oedipus) combination long call (CLC)
141 closely related to the expressed cotton-top tamarin's MHC class I genes, but does show some similari
142 fore, the functional diversity of cotton-top tamarin's MHC class I loci may be even more limited than
143 sults demonstrate that at least three of the tamarin's MHC class I molecules can present the same epi
145 , we show that small New World primates, the tamarins Saguinus mystax and Leontocebus nigrifrons, inc
148 the squirrel monkey (Saimiri sciureus), the tamarin (Saguinus oedipus), and the spider monkey (Atele
149 nes of the New World primate, the cotton-top tamarin (Saguinus oedipus), are an exception to the high
150 HC class I diversity, such as the cotton-top tamarin (Saguinus oedipus), are more susceptible to fata
151 rmosets (Callithrix jacchus) and red-bellied tamarins (Saguinus labiatus), were highly susceptible to
152 replication in cell culture and virulence in tamarins (Saguinus mystax) and chimpanzees (Pan troglody
153 spatial context on discounting in cotton-top tamarins (Saguinus oedipus) and common marmosets (Callit
156 ontrolled captive conditions that cotton-top tamarins (Saguinus oedipus) have a long-term memory for
157 istent GBV-B infection in one of two healthy tamarins (Saguinus oedipus) inoculated intrahepatically
158 g of MHC-EcDNAs in four unrelated cotton-top tamarins (Saguinus oedipus) revealed no evidence for pol
159 positioned S-shaped opaque tube, cotton-top tamarins (Saguinus oedipus) search for the food in the p
161 authors present 4 experiments on cotton-top tamarins (Saguinus oedipus) using a reverse-reward conti
162 ls of a New World monkey species, cotton top tamarins (Saguinus oedipus) were tested in an offering t
163 s), young children (Homo sapiens), and adult tamarins (Saguinus oedipus) while they discriminated glo
164 f prosocial behavior by presenting cottontop tamarins (Saguinus oedipus) with the option to provide f
167 e that is closely related to HCV and infects tamarins (Saguinus sp.), in which a functionally importa
168 C virus (HCV) and causes acute hepatitis in tamarins (Saguinus species), making it an attractive sur
170 from the primary forest matrix, we show that tamarin seed dispersal is effective and contributes to t
171 ity and diffusion of the acid solvent in the tamarind seed matrix, resulting a pectin recovery 32.9%.
172 maximal rate (Vmax) values for hydrolysis of tamarind seed xyloglucan (tamXG) are 2.4 micro m and 966
174 mango, orange and tangerine peels as well as tamarind seeds by using the acid hydrolysis method.
175 social inequity, which was demonstrated when tamarins' sensitivity to the difference in rewards incre
176 st dielectric constant at lower frequencies, Tamarind showed the highest impedance at low frequencies
180 canonical first exon of NOD2 of marmoset and tamarin species and their susceptibility to chronic coli
181 the demonstration that GBV-B can persist in tamarins strengthens its relevance as a surrogate model
183 extent of additional mortality, whether some tamarins survive the disease and acquire immunity, and t
186 lone pGBB had acute resolving infection, one tamarin transfected with the poly(U) deletion mutant bec
191 s study, the course of infection of GBV-B in tamarins was followed using a real-time 5' exonuclease (
195 tive vocal signatures, we found that not all tamarins were equally discriminable based on the habitua
197 st tested for individual discrimination when tamarins were habituated to a series of calls from 1 tam
199 inal half of 2C was partially attenuated for tamarins while one containing AGM-27 sequences only in t
200 theses with captive cotton-top tamarins: (a) Tamarins will demonstrate higher rates of initial learni
202 h serum collected at weeks 2 and 90 from the tamarin with persistent infection had an acute resolving
204 is outbred primate species, we infected five tamarins with influenza virus and defined the CTL epitop
206 was observed in vivo following treatment of tamarins with ribavirin during acute infection with GBV-
212 ivity toward five acceptors: non-fucosylated tamarind xyloglucan (TXyG), arabinotriose (Ara(3)), non-