ライフサイエンスコーパス: Old World monkey

1 genomes of humans, apes and cercopithecoids (Old World monkeys).

2 mpanzee, one gorilla, one orangutan, and one Old World monkey.

3 95 bp Alu sequence of the rhesus monkey, an old world monkey.

4 as a cytoarchitectural homolog, area Tpt, in Old World monkeys.

5 of prosimian galagos, New World monkeys, and Old World monkeys.

6 G gene evolution from five hominoids and two Old World monkeys.

7 diminished the blindness in both humans and old world monkeys.

8 a primate panel that included great apes and Old World monkeys.

9 ft leads to the chromosome ancestral for all Old World monkeys.

10 only on the Y chromosomes of great apes and Old World monkeys.

11 ependent of their rate-decreasing effects in Old World monkeys.

12 rs in most cell lines and primary cells from Old World monkeys.

13 the catarrhine primates - the hominoids and Old World monkeys.

14 utionary divergence of the hominids from the Old World monkeys.

15 al cortex organization is similar in New and Old World monkeys.

16 ity in the last common ancestor of human and Old World monkeys.

17 in frontal cortex circuits across humans and Old World monkeys.

18 accelerated evolution in Hominini, apes, and Old World monkeys.

19 a regions in humans, great apes, and New and Old World monkeys.

20 te germ line after the split between New and Old World monkeys.

21 ion of the dorsal premotor cortex in New and Old World monkeys.

22 sing alpha-gal epitopes in humans, apes, and Old World monkeys.

23 a recombinant between two SIV lineages from Old World monkeys.

24 ancestral primate and the lineage leading to Old World monkeys.

25 that suggest greater specializations in the Old World monkeys.

26 tical areas in prosimian galagos than in the Old World monkeys.

27 oe-off, reminiscent of some Miocene apes and Old World monkeys.

28 no HBV infection has been reported in small, old-world monkeys.

29 ent among many African cercopithecoid (i.e., Old World) monkeys.

30 separation of the human/ape lineage from the Old World monkeys (10-20 million years ago).

31 5 primates including 8 New World monkeys, 10 Old World monkeys, 4 lesser apes, 17 great apes, and 6 h

32 We also examined 16 chimpanzees and various Old World monkeys: a pigtail macaque, a mangabey and 12

33 ctive than human A3C, and we determined that Old World Monkey A3C from rhesus macaque (rh) is not act

34 key antiviral activity we predict that other Old World Monkey A3Cs did not impart anti-lentiviral act

35 e required for cross-species adaptation from Old World monkey A3G to hominid A3G.

36 nes were incorporated into the genome of the Old World monkeys after the divergence of the Old World

37 rate of coding DNA in the catarrhine clade (Old World monkey and ape, including human) is much slowe

38 analysis of the nonsynonymous changes in the Old World Monkey and Great Ape lineages revealed a numbe

39 10 kbp in the 35 Myr since divergence of the Old World Monkey and hominid lineages.

40 ound in most mammalian cells, except for the Old World monkey and humans.

41 lthough virus has been isolated from various Old World monkey and New World monkey species, there has

42 The faces of Old World monkeys and apes (Catarrhini) exhibit every po

43 a1,4GlcNAc) is not expressed on the cells of Old World monkeys and apes (including humans) but is exp

44 alpha1,3GT gene was inactivated in ancestral Old World monkeys and apes by frameshift single-base del

45 w World monkeys) and another in catarrhines (Old World monkeys and apes).

46 the common ancestor of New World monkeys and Old World monkeys and apes, but then became vestigial in

47 s in anthropoid primates (New World monkeys, Old World monkeys and apes, including humans) have been

48 ys and catarrhines) and that of catarrhines (Old World monkeys and apes, including humans), a minimum

49 s not normally found in catarrhine primates (Old World monkeys and apes, including humans), all of wh

50 nes (New World monkeys) than in catarrhines (Old World monkeys and apes, including humans).

51 an LOC387715/ARMS2 gene were present only in Old World monkeys and apes.

52 n became vestigial in the common ancestor of Old World monkeys and apes.

53 t likely co-evolves with cortical folding in Old World monkeys and apes.

54 imate lentiviruses infect humans and several Old World monkeys and apes.

55 notably the earliest catarrhine ancestors of Old World monkeys and apes.

56 AS (catarrhine ancestor of snaR), limited to Old World Monkeys and apes; and ASR (Alu/snaR-related),

57 ng to LCVs of New World monkeys (clade A) or Old World monkeys and great apes (clades B and C).

58 a key node in the primate phylogeny between Old World monkeys and great apes.

59 ession is absent in catarrhines, that is, in Old World monkeys and hominids (apes, including humans),

60 rrhines (New World monkeys) and catarrhines (Old World monkeys and hominoids).

61 Like most Old World monkeys and humans, capuchin monkeys have high

62 rtical organization of LGN afferents between Old World monkeys and humans.

63 ion is reserved to only few mammals, such as Old World monkeys and humans.

64 es, of four non-human primate species (three Old World monkeys and one New World monkey).

65 ntron 1 of the red or green pigment genes of Old World monkeys and orangutans but was present in intr

66 recapitulated molecular signatures found in Old World monkeys and raises the possibility that APOL1

67 een natural antibodies present in humans and Old World monkeys and the Gal alpha(1-3)Gal epitope (xen

68 tribution are observed among cercopithecoid (Old World monkey) and hominoid genomes.

69 Myr for the split between Cercopithecoidea (Old World monkeys) and Hominoidea (apes), implying long

70 Catarrhine (humans, apes, and Old World monkeys) and platyrrhine (New World monkeys) p

71 sequenced the MSY of the rhesus macaque, an Old World monkey, and compared it to the human MSY.

72 ained relative to that of the orangutan, the Old World monkey, and the mouse, but not relative to tha

73 thropoid primate species (New World monkeys, Old World monkeys, and hominoids) to support greater met

74 er in lemurs and lorises, New World monkeys, Old World monkeys, and hominoids, lending support to the

75 nts of domains have been retained in New and Old World monkeys, and humans appear to have at least so

76 y of TRIM5alpha orthologs from humans, apes, Old World monkeys, and New World monkeys.

77 ha promoters from representative great apes, Old World monkeys, and New World monkeys.

78 evolution and regulation among humans, apes, Old World Monkeys, and New World Monkeys.

79 l area in humans, chimpanzees, an orangutan, Old World monkeys, and New World monkeys.

80 rican location of the common ancestor of the Old World monkeys, and suggests that the Asian colobine

81 in all Euarchontoglires other than apes and Old World monkeys, and that RLN2 derives from an ape-spe

82 isoform gene, COX8H, is absent in humans and Old World monkeys, and the other isoform gene, COX8L, is

83 nised among early Miocene catarrhines (apes, Old World monkeys, and their extinct relatives).

84 se may develop differently within species of old-world monkeys, and that the evidence of material cul

85 catarrhines-hominoids (apes and humans) and Old World monkeys-and are thus viewed as more primitive

86 ification of the key amino acids determining Old World Monkey antiviral activity we predict that othe

87 Trichromacy is the norm for all Old World monkeys, apes and humans, but in several gener

88 Y-located DAZ sequences were observed in all Old World monkeys, apes and humans.

89 olor vision among groupings of primates: (i) Old World monkeys, apes, and humans all enjoy trichromat

90 Pyrin-only proteins (POPs) are restricted to Old World monkeys, apes, and humans and have previously

91 in catarrhini (primate parvorder comprising old world monkeys, apes, and humans).

92 actions when compared with those observed in Old World monkeys, apes, and humans.

93 ble exceptions are higher primates including Old World monkeys, apes, and humans.

94 d before divergence of New World monkeys and Old World monkeys/apes.

95 ortly before the separation of hominoids and Old World monkeys approximately 23 million years ago, an

96 ion data in humans and gibbons as well as in Old World monkeys are inconsistent with a model of conve

97 Apes and Old World monkeys are prominent components of modern Afr

98 Most Old World monkeys are trichromats.

99 n the geniculate of commonly studied diurnal Old World monkeys, are well differentiated from the parv

100 chimpanzees and humans, but does not infect Old World monkeys because of replication blocks that occ

101 postmortem diffusion imaging scans from two Old World monkey brains.

102 and cytoarchitectonic analysis to show that old-world monkey brains have the same principles of orga

103 e structures (Gal) are present in humans and Old World monkeys but are negatively regulated in other

104 ) in humans, efficiently enters the cells of Old World monkeys but encounters a block before reverse

105 the RNRs from viruses that infect humans and Old World monkeys but not by the RNRs from viruses that

106 and neotame taste sweet to humans, apes, and Old World monkeys but not to New World monkeys and roden

107 s arose before the split between the New and Old World monkeys, but the ZNF91 subfamily has continued

108 Animal models, such as the infection of Old World monkeys by simian-human immunodeficiency virus

109 us type 1 (HIV-1) is blocked in the cells of Old World monkeys by TRIM5alpha, a tripartite motif (TRI

110 quences of non-human primates (apes, new and old world monkeys), canines and feline sequences.

111 ial/reproductive activities of hominoids and Old World monkeys (catarrhines).

112 immunodeficiency virus, type 1 infection in Old World monkey cells at the early post-entry step by p

113 hat HuTRS1 does not have these activities in Old World monkey cells.

114 Old World monkeys (Cercopithecoidea) are a highly succes

115 early members of their closest outgroup, the Old World monkeys (Cercopithecoidea).

116 lly, we report the oldest stem member of the Old World monkey clade, represented by a lower third mol

117 In humans, great apes, and Old World monkeys, cones make a poorly understood choice

118 available sequenced gorilla, orangutan, and Old World monkey counterparts, and, on a more limited ba

119 Old World monkeys diverged from apes perhaps 30 million

120 noids (apes and humans) and cercopithecoids (Old World monkeys) diverged around 23-25 Mya.

121 In Old World monkeys, diversification focuses on MHC-A and

122 As Old World monkeys (e.g., vervets) and humans share some

123 s of the only complete early cercopithecoid (Old World monkey) endocast currently known, that of 15-m

124 re needed to better understand early ape and Old World monkey evolution.

125 years of the catarrhine (i.e., hominoid and Old World monkey) evolution.

126 integration into cerebral germinal zones of Old World monkey fetuses.

127 a was present in 22 species (seven apes, two Old World monkeys, four New World monkeys, and nine stre

128 Here we describe a primitive Old World monkey from Nakwai, Kenya, dated at ~22 Ma, th

129 ht to have diverged before the divergence of Old World monkeys from great apes, are more similar to o

130 arrhines-i.e., the split of cercopithecoids (Old World monkeys) from hominoids (apes and humans)-is a

131 The TRIM5alpha proteins of humans and some Old World monkeys have been shown to block infection of

132 as been retained only in great apes, whereas Old World monkeys have disabled the gene in different wa

133 idea (apes and humans) and Cercopithecoidea (Old World monkeys) have a common ancestry as Catarrhini

134 Then, we tested Old World monkey, human, and engineered APOL1 variants f

135 y across captive, semifree ranging, and wild Old World monkeys, I investigated whether individuals ga

136 ubt on the role of the frontal cortex of the Old World monkeys in vocal communication.

137 nes, including-remarkably-between humans and old-world monkeys in MHC-DQB1.

138 A similar block to HIV-1 infection in Old World monkeys is attributable to the alpha isoform o

139 unodeficiency virus, which naturally infects Old World monkeys, is less susceptible to the TRIM5alpha

140 We presented 7 Old World monkeys (Japanese macaques [Macaca fuscata], g

141 of this gene inactivation, humans, apes, and Old World monkeys lack alpha-gal epitopes and naturally

142 their insertion occurred sequentially in the Old World monkey lineage prior to duplication of the anc

143 sable elements in this representative of the Old World monkey lineage, a group of diverse primates cl

144 he absence of DNA transposon activity in the Old World monkey lineage.

145 s that have followed its separation from the Old World monkey lineage.

146 rs ago, 5 million years before the human and Old World monkey lineages diverged.

147 ctively near the time when the New World and Old World monkey lineages split.

148 ersification and adaptation of great ape and Old World monkey lineages.

149 peats began before the human and cynomolgus (Old World) monkey lineages diverged.

150 ) before stabilizing since the separation of Old World monkeys (<50 MYA).

151 l New World monkey Aotus trivulgaris and the Old World monkey Macaca nemestrina by using immunocytoch

152 ed from orangutan (Pongo pygmaeus, oEDN) and Old World monkey (Macaca fascicularis, mcEDN) genomic DN

153 , chimpanzee, gorilla and orang-utan, and an Old World monkey, Macaca mulatta.

154 of the medial frontal cortex was assessed in Old World monkeys (macaque/baboon) and Hominoidea (chimp

155 the human lineage since it diverged from the Old World monkeys more than 25 million years ago.

156 In contrast to Old World monkeys, most New World monkeys (NWMs) are not

157 is and screening among NTCP orthologues from Old World monkeys, New World monkeys and prosimians, we

158 o 15 species/subspecies spanning great apes, old world monkeys, new world monkeys and prosimians.

159 usion in 56 primate species (including apes, Old World monkeys, New World monkeys, and strepsirrhines

160 rom orangutan, and species representative of Old-World monkeys, New-World monkeys, and lemurs were no

161 uggesting a divergence time between apes and Old World monkeys of 65 million years, too old to be con

162 igate this possibility, we injected 11 adult Old World monkeys of different ages (5-23 years) with th

163 simian arterivirus infections are common in Old World monkeys of many different species throughout A

164 s, CypA is required for HIV-1 restriction by Old World monkey orthologues of TRIM5alpha.

165 date, the only such example in hominoids and Old World monkeys outside of the major histocompatibilit

166 the RhCMV genome to those of several related Old World monkey (OWM) CMVs, we were able to filter out

167 panzee divergence is close to 20% of the ape-Old World monkey (OWM) divergence.

168 wild-caught chimpanzees and gorillas and 91 Old World monkey (OWM) species were screened for antibod

169 ct wild apes and several, primarily captive, Old World monkey (OWM) species.

170 using acute infections in humans and several Old World monkey (OWM) species.

171 resent new reference genome assemblies for 3 Old World monkey (OWM) species: Colobus angolensis ssp.

172 This member of the Old World monkey (OWM) superfamily is uniquely valuable

173 non-human primates--four great apes and one Old World Monkey (OWM)--and compared them with those of

174 of the primate species tested, specifically, Old World monkeys (OWM) and apes, have orthologues of hu

175 This clade is found in Old World monkeys (OWM), but not great apes, suggesting

176 genes as antiviral effectors, APOBEC3H from Old World monkeys (OWMs) has efficient antiviral activit

177 However, previous studies on TKO pigs using old world monkeys (OWMs) have been disappointing because

178 However, Old World monkeys (OWMs) have naturally-existing antibod

179 e genomes from 10 primate species, including Old World Monkeys (OWMs), New World Monkeys (NWMs), and

180 to those of cercopithecines, a subfamily of Old World monkey, particularly baboons, than to those of

181 curring plant protein that humans, apes, and Old World monkeys perceive as tasting sweet but that is

182 Among Old World monkeys, pig-tailed macaques (Pt) are uniquely

183 se results indicate that the adult brains of Old World monkeys produce new hippocampal neurons.

184 vidence from our own studies of both New and Old World monkeys, prosimian galagos, and close relative

185 n that also restores sequence alignment with Old World monkeys, protected against T. brucei rhodesien

186 distribution of these haplotypes in various Old World monkeys provides new insights about MHC-A evol

187 put contributes to information processing in Old World monkey retinas, we have been localizing histam

188 ution have some similarities to both New and Old World monkey retinas.

189 nabinoid receptor (CBR) agonist CP 55 940 in Old World monkeys (rhesus and cynomolgus), a species tha

190 subjects), (2) a new taxonomic group (i.e., Old World monkeys: rhesus macaques, Macaca mulatta), and

191 t in a single lysine residue that mimics the Old World monkey sequence, which augments trypanolytic a

192 ptases, and thus arose before great apes and Old World monkeys shared an ancestor, and before the alp

193 By comparison, Rhesus macaques (Old World monkeys) showed evidence for deeper levels of

194 The cells of most Old World monkey species exhibit early, postentry restri

195 ve infection (95%) among mandrills and other Old World monkey species inhabiting remote regions of Ca

196 Sampling within two geographically distinct Old World monkey species revealed extensive polymorphism

197 fected (15% combined frequency), while other Old world monkey species were negative.

198 s (a New World monkey species), macaques (an Old World monkey species), and humans using the same ind

199 we demonstrate that TRIM5alpha variants from Old World monkeys specifically associate with the HIV ty

200 lineage active at the divergence of apes and Old World monkeys, successive L1 subfamilies have emerge

201 identified this way are polymorphic in other Old World monkeys such as baboons.

202 Whether Old World monkeys such as macaques have consensus color

203 In the old world monkey, such a CD circuit for saccades has bee

204 Multiple signals in Old World monkeys suggest that the duplication events ma

205 s 15 and 16 in non-human primates, including Old World monkeys, suggesting that duplication of this r

206 Observation of recall in Old World monkeys suggests that it has been adaptive for

207 The modern Old World Monkeys (Superfamily Cercopithecoidea, Family

208 s prosimian primates, New World monkeys, and Old World monkeys support the concept that DM is a visua

209 s longus muscle was more like its homolog in Old World monkeys than in African apes.

210 Victoriapithecus represents a branch of Old World monkey that is intermediate between extant cer

211 Rhesus macaque is an Old World monkey that shared a common ancestor with huma

212 tested showed a single hybridization site in Old World monkeys that corresponded to one of the orthol

213 g gamma-herpesviruses that infect humans and Old World monkeys that encode this enzyme but absent in

214 Colobines are a unique group of Old World monkeys that principally eat leaves and seeds

215 reviously unknown level of AGL complexity in Old World monkeys that seems less evident in New World m

216 and highly divergent GBV-B-like virus in an Old World monkey, the black-and-white colobus (Colobus g

217 edial frontal cortex that can be traced from Old World monkeys to Hominoidea species, demonstrating a

218 n of apes in the late Miocene and failure of Old World monkeys to radiate into multiple species befor

219 To determine whether HIV-1 restriction by Old World monkey TRIM5alpha is modulated by the CA-CypA

220 only after these cells were transduced with Old World monkey TRIM5alpha.

221 onkey indicate that the initial radiation of Old World monkeys was first characterized by a reorganiz

222 e finds extend the fossil record of apes and Old World monkeys well into the Oligocene epoch of Afric

223 members after the human/ape divergence from Old World monkeys, while DA likely evolved from a Xiao b