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

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

9 be correlated with orientation preference in New World monkeys.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

113 New World monkeys of the genus Aotus synthesize a fusion

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

115 New World monkeys offer attractive advantages over Old W

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

153 Human and New World monkey TRIM5alpha proteins associated less eff

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

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

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

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

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

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

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

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

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