ライフサイエンスコーパス: New World monkey

1 ate species (three Old World monkeys and one New World monkey).

2 sample of other great apes and Old World and New World monkeys).

3 when Catarrhines diverged from Platyrrhines (New World monkeys).

4 amang) or lower-order primates (e.g., old or new world monkeys).

5 s, representing the first such analysis in a New World monkey.

6 and CXCR4 proteins of the common marmoset, a New World monkey.

7 ive cytogenetic marker for Saimiri and other New World monkeys.

8 cute leukemia, T-cell lymphoma, and death in New World monkeys.

9 gs from humans, apes, Old World monkeys, and New World monkeys.

10 CP expression in the testes and sperm of two New World monkeys.

11 n of extrastriate cortex in three species of New World monkeys.

12 be correlated with orientation preference in New World monkeys.

13 sentative great apes, Old World monkeys, and New World monkeys.

14 all similarities across these two species of New World monkeys.

15 n among humans, apes, Old World Monkeys, and New World Monkeys.

16 anzees, an orangutan, Old World monkeys, and New World monkeys.

17 logous to the DM described in prosimians and New World monkeys.

18 ter the divergence of the Old World from the New World monkeys.

19 ity of ocular dominance column expression in New World monkeys.

20 but not by the RNRs from viruses that infect New World monkeys.

21 different species, including five species of New World monkeys.

22 t ape tissues when compared to Old World and New World monkeys.

23 CMV) and owl monkey CMV (OMCMV), that infect New World monkeys.

24 tion of replication of human adenoviruses in New World monkeys.

25 ult stands in contrast to those reported for New World monkeys.

26 cessing in trichromats of both Old World and New World monkeys.

27 uch color domains have not yet been shown in New World monkeys.

28 human, chimpanzee, and various Old World and New World monkeys.

29 s compared with representative Old World and New World monkeys.

30 t transfers have occurred between humans and New World monkeys.

31 v1 region in Old World primates and in v3 in New World monkeys.

32 simium, which parasitizes several species of New World monkeys.

33 ected in a sample of 45 primates including 8 New World monkeys, 10 Old World monkeys, 4 lesser apes,

34 ers and anthropoids) to that of anthropoids (New World monkeys and catarrhines) and that of catarrhin

35 changes in the stem of anthropoid primates (New World monkeys and catarrhines), possibly setting the

36 arisons of an extensive set of Old World and New World monkeys and hominoids to identify functional r

37 ent virus budding and arose independently in New World monkeys and mice.

38 likely functional in the common ancestor of New World monkeys and Old World monkeys and apes, but th

39 ated evolution occurred before divergence of New World monkeys and Old World monkeys/apes.

40 in macaques with DM connections described in New World monkeys and prosimian galagos support the conc

41 ong NTCP orthologues from Old World monkeys, New World monkeys and prosimians, we determined key resi

42 cies spanning great apes, old world monkeys, new world monkeys and prosimians.

43 mans, apes, and Old World monkeys but not to New World monkeys and rodents.

44 previously less well represented groups, the New World monkeys and the Strepsirrhini.

45 netic evidence suggests that platyrrhine (or New World) monkeys and caviomorph rodents of the Western

46 more numerous in the spider monkey (another New World monkey) and the bushbaby (a distant relative).

47 ndent locus expansions, one in platyrrhines (New World monkeys) and another in catarrhines (Old World

48 mian lineage ancestral to both platyrrhines (New World monkeys) and catarrhines (Old World monkeys an

49 ene (PPG), is present in platyrrhines, i.e., New World monkeys, and catarrhines but not in prosimians

50 groups (e.g., non-primates, strepsirrhines, New World monkeys, and hominoids).

51 ies (seven apes, two Old World monkeys, four New World monkeys, and nine strepsirrhines).

52 tical projections across prosimian primates, New World monkeys, and Old World monkeys support the con

53 the hindlimb and tail of prosimian galagos, New World monkeys, and Old World monkeys.

54 species (including apes, Old World monkeys, New World monkeys, and strepsirrhines) by using either m

55 ons on the origins and spread of tool use in New World monkeys, and the mechanisms - social, ecologic

56 species representative of Old-World monkeys, New-World monkeys, and lemurs were not.

57 election on CD4 has been most intense in the New World monkeys, animals that have never been found to

58 retina has been compared with the nocturnal New World monkey Aotus trivulgaris and the Old World mon

59 aracteristic of people; (ii) most species of New World monkeys are highly polymorphic, with individua

60 The platyrrhine primates, or New World monkeys, are immigrant mammals whose fossil re

61 We report here three novel OXT forms in the New World monkeys, as well as a more extensive distribut

62 on encounters an early block in the cells of New World monkeys because the CD4 receptor does not effi

63 d the genome of a common ancestor of Old and New World monkeys between 42 million and 65 million year

64 Unlike other New World Monkeys, but much like the macaque monkey, ceb

65 Cebus monkeys stand out from other New World monkeys by their ability to perform fine hand

66 a circum-Caribbean tropical distribution of New World monkeys by this time, with ocean barriers not

67 Whereas other New World monkeys can be quite dexterous, and possess a

68 extended in Aotus compared with the diurnal New World monkey Cebus apella.

69 same is true for another primate species-the New World monkey Cebus apella.

70 he prolactin gene, and evidence from another New World monkey (Cebus albifrons) and from the chimpanz

71 metries correlated with hand preference in a New World monkey (Cebus apella) that does not display po

72 and fetal erythrocytes from three species of New World monkeys (Cebus apella, Aotus azarae, and Calli

73 Infection of most New World monkey cells by the simian immunodeficiency vi

74 By contrast, most New World monkey cells exhibited much lower titers for t

75 but not HIV-1, infection is blocked in most New World monkey cells.

76 hat can overcome some of the early blocks in New World monkey cells.

77 Unlike in other species of New World monkeys, cerebral arterial angiopathy was not

78 we argue that first proving efficacy in the New World monkey challenge model would accelerate develo

79 ned 3 BILF1 clades, corresponding to LCVs of New World monkeys (clade A) or Old World monkeys and gre

80 s, apes and humans, but in several genera of New World monkeys, colour vision is strikingly polymorph

81 Here, we report that New World monkey cytomegaloviruses have broadly captured

82 deo recordings showed that common marmosets (New World monkeys) differentiated between well formed, c

83 In cells of Old World and some New World monkeys, dominant factors restrict human immun

84 d in large amounts in nonprimate mammals and New World monkeys due to the intracellular activity of t

85 e investigate brain shape diversification of New World monkeys during their adaptive radiation in rel

86 sequences revealed an evolutionary trend in New World monkeys either to inactivate the gamma1 gene o

87 Furthermore, we found that some New World monkeys encode up to ten additional APOBEC3G (

88 e placental mammals, lemurs (prosimians) and New World monkeys, encoding the alpha1,3GT enzyme that s

89 In somatic tissues, New World monkeys express an alternatively spliced form

90 We now report that brains of adult old and new world monkeys express mRNA encoding EphA4 receptor a

91 In New World monkeys, FKBP51 has been implicated in cortiso

92 and were duplicated after the divergence of New World monkeys from pre-monkeys approximately 40-65 m

93 uman RNase k6 from Great Ape, Old World, and New World monkey genomes.

94 ckage found only in the Cebidae radiation of New World monkeys, give rise to efficiently processed GP

95 evolutionarily largely conserved in Old and New World monkeys given its surprisingly similar overall

96 that the stem platyrrhines, ancestral to all New World monkeys, had gamma2 as the primary fetally exp

97 A complete skeleton of a large-bodied New World monkey has been found in Pleistocene cave depo

98 These New World monkeys have become a popular model in studies

99 Until now, the oldest fossil records of New World monkeys have come from Salla, Bolivia, and dat

100 extends to betaretroviruses and suggest that New World monkeys have evolved additional mechanisms to

101 However, to date, lentiviruses infecting New World monkeys have not been described.

102 Although most New World monkeys have only one X-linked photopigment lo

103 , recent studies in marmosets - a species of new world monkey in which the overall organization of vm

104 ns including recent findings in anesthetized New World monkeys indicate that that the digit represent

105 First, cortex caudal to area 1 in New World monkeys is more like area 5 than area 2.

106 In normal New World monkeys, labeled neurons were predominately di

107 nd Hylobates pileatus (gibbons) and from the New World monkey, Lagothrix lagotricha (woolly monkey).

108 ys after the divergence of the Old World and New World monkey lineages.

109 e skeleton resembles species of two distinct New World monkey lineages.

110 inar has been extensively studied in old and new world monkeys, little is known about the organizatio

111 s (chimpanzee, gorilla, orangutan), Old- and New-World monkeys (macaque and marmoset), and a prosimia

112 set receptors might allow the development of New World monkey models of HIV-1 infection.

113 erceived as sweet by other species including New World monkeys, mouse, and rat.

114 aging has revealed similar features in MT of New World monkeys, MT appears to have retained these bas

115 The authors tested free-ranging New World monkeys (nocturnal owl monkeys [Aotus nancymai

116 reports concerning zoonotic transmission of New World monkey (NWM) SFV to humans and resulting infec

117 osets, spider monkeys, and squirrel monkeys, New World monkey (NWM) species that share geographic ran

118 the multiple GH-like genes of an additional New World monkey (NWM), the white-fronted capuchin, Cebu

119 t the first investigation of L1 evolution in New World monkeys (NWM).

120 New World monkeys (NWMs) are characterized by an extensi

121 In contrast to Old World monkeys, most New World monkeys (NWMs) are not susceptible to poliovir

122 species, including Old World Monkeys (OWMs), New World Monkeys (NWMs), and apes, focusing on putative

123 avioral phenotypes has been described in the New World Monkeys (NWMs).

124 and established itself as a repeat family in New World monkeys (NWMs).

125 sing sera from humans, several OWMs, and two New World monkeys (NWMs).

126 that family-level diversification of extant New World monkeys occurred in the tropics, with new dive

127 New World monkeys of the genus Aotus synthesize a fusion

128 sity in five species of Saguinus (a genus of New World monkey) of different ages to a comparative pri

129 New World monkeys offer attractive advantages over Old W

130 many of these genes in anthropoid primates (New World monkeys, Old World monkeys and apes, including

131 rison with other anthropoid primate species (New World monkeys, Old World monkeys, and hominoids) to

132 e successively larger in lemurs and lorises, New World monkeys, Old World monkeys, and hominoids, len

133 nucleolytically active chimeras of human and New World monkey orthologs of EDN and, by evaluating the

134 We suggest that some New World monkey OXT-OXTR forms can be correlated to mal

135 urred in the transmembrane domains among the New World monkey pigment variants but apparently have no

136 cting African apes (Plasmodium rodhaini) and New World monkeys (Plasmodium brasilianum), but its orig

137 New World monkeys (platyrrhines) are a diverse part of m

138 Old World anthropoids and extinct and extant New World monkeys (platyrrhines) support relationships o

139 pes, and Old World monkeys) and platyrrhine (New World monkeys) primates, but not prosimians, have di

140 cross 18 locations in the common marmoset, a New World monkey primed for genetic engineering, and exa

141 ength copy of retroCHMP3 in the ancestors of New World monkeys provides modest inhibition of virus bu

142 emonstrate that the CD4 and CCR5 proteins of New World monkeys represent the major restriction agains

143 course of acute infection with ZIKV in these New World monkeys resembles the human illness in many re

144 nymous substitutions (Ks) observed among the New World monkey RNase k6 genes.

145 several other vertebrates, including Old and New World monkeys, seahorses, axolotls, and Xenopus.

146 eviously that recombinant EDN derived from a New World monkey sequence ( Saguinus oedipus ) had signi

147 aris, mcEDN) genomic DNAs, and from a second New World monkey sequence (Aotus trivirgatus, omEDN) as

148 ion likely arose at least as far back as the New World monkeys, some 40 million years ago.

149 ontrary to previous arguments, a member of a New World monkey species can solve an analogical problem

150 Notably, TRIM5alpha proteins from several New World monkey species restricted infection by SIVmac

151 However, fibroblasts established from three New World monkey species specifically resisted infection

152 ellating the auditory cortex of marmosets (a New World monkey species), macaques (an Old World monkey

153 of experimenter-given directional cues by a New World monkey species, cotton top tamarins (Saguinus

154 ow an aversion to inequity, individuals of a New World monkey species, cotton top tamarins (Saguinus

155 also identified MHC-E alleles in five other New World monkey species, representing all extant platyr

156 n isolated from various Old World monkey and New World monkey species, there has been no report of en

157 ted the susceptibility of Aotus nancymaae, a New World monkey species, to ETEC infection.

158 caques to severe and even lethal for certain New World monkey species.

159 omologue of the HLA-E locus in six different New World monkey species.

160 a similar functional organization exists in New World monkeys, such as the common marmoset (Callithr

161 of baboons and high order primates, but not New World monkeys, suggesting that progenitor K222 infec

162 mans but new data indicate that marmosets, a new world monkey, take turns when vocalizing too.

163 se ocular dominance columns, when present in New World monkeys, tend to occur in later-maturing parts

164 t by a different trajectory in platyrrhines (New World monkeys) than in catarrhines (Old World monkey

165 Here we present results from a small New World monkey that allows for the characterization of

166 Capuchins are the only New World monkeys that have evolved an opposable thumb a

167 but absent in homologous viruses that infect New World monkeys that naturally lack the A3B gene.

168 Marmosets are diurnal New World monkeys that show sex-linked cone photopigment

169 leus (LGN) of the thalamus in two species of New World monkeys - the diurnal squirrel monkey (Saimiri

170 Inferotemporal ablations in the New World monkey, the common marmoset (Callithrix jacchu

171 ull trichromacy is present in one species of New World monkey, the howler monkey, in which separate M

172 the slow loris (Nycticebus pygmaeus), and a New World monkey, the marmoset (Callithrix jacchus).

173 encing the upstream region of this gene in a New World monkey, the marmoset, we have been able to dem

174 In both species of New World monkeys, the DM region was more heavily myelin

175 Human and New World monkey TRIM5alpha proteins associated less eff

176 New World monkeys typically have only one X-chromosome p

177 process of detoxification for retroCHMP3 in New World monkeys using a combination of ancestral recon

178 primates varies from ubiquitous to few with New World monkeys varying the most.

179 Only when a New World monkey was compared with hominoids were the ra

180 the ability of HIV-1 to infect the cells of New World monkeys was examined.

181 al tuning of X-linked pigments in humans and New World monkeys, we estimated that the Ala --> Ser, Il

182 Old World monkeys that seems less evident in New World monkeys, which are more distant evolutionary r

183 the common marmoset (Callithrix jacchus), a New World monkey with a hearing range similar to that of

184 re connections of premotor cortical areas of New World monkeys with those of Old World macaque monkey

185 has been a recent resurgence of interest in New World monkeys within the biomedical research communi