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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

20 that suggest greater specializations in the Old World monkeys.

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

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

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

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

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

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

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

28 5 primates including 8 New World monkeys, 10 Old World monkeys, 4 lesser apes, 17 great apes, and 6 h

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

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

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

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

33 10 kbp in the 35 Myr since divergence of the Old World Monkey and hominid lineages.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

84 Most Old World monkeys are trichromats.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

171 The modern Old World Monkeys (Superfamily Cercopithecoidea, Family

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

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

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

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

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

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

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

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

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

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

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

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