ライフサイエンスコーパス: gibbon

1 rimates (chimpanzee, gorilla, orangutan, and gibbon).

2 a primate brain the mass of that of the lar gibbon.

3 MICs), in the brain of a lesser ape, the lar gibbon.

4 ha2-globin-containing unit in both human and gibbon.

5 d by application to an empirical dataset for gibbons.

6 esting interspecies transmission from OWM to gibbons.

7 uses (GALVs) have been isolated from captive gibbons.

8 igate environmental predictors of calling in gibbons.

9 he absence of its putative ligand, MHC-G, in gibbons.

10 t also in bonobos, gorillas, orangutans, and gibbons.

11 tains Saitohin in chimpanzees, gorillas, and gibbons.

12 culia ( Latrunculia) austini Samaai, Kelly & Gibbons, 2006 (class Demospongiae, order Poecilosclerida

13 We found that gibbons acted more often in the two conditions involving

14 ock I occur in both duplication units of the gibbon alpha-globin locus.

15 or recognition site in the Alu repeat of the gibbon and a G-->A substitution in the last position of

16 in, whereas in primates (macaque monkey, lar gibbon and human) the highest proportion of inhibitory W

17 e duplication and dispersion taking place in gibbon and involving loci corresponding to human chromos

18 In this issue of the JID, Fitz-Gibbons and colleagues present strain-based resolution o

19 polymorphic LAVA insertions across multiple gibbons and found 96 LAVA elements overlapping enhancer

20 suggesting that KoRV predates GALV and that gibbons and koalas acquired the virus at different times

21 iate host whose range overlaps those of both gibbons and koalas.

22 11 bonobos, 48 gorillas, 37 orangutans and 2 gibbons and observed undescribed variation in great apes

23 comparing our results with those of captive gibbons and other free-feeding captive primates, we foun

24 is closer to great apes than to hylobatids (gibbons and siamangs), which are convergent with other s

25 ), Nomascus nastusus and Hylobates pileatus (gibbons) and from the New World monkey, Lagothrix lagotr

26 into the last common ancestor of hylobatids (gibbons) and hominids (great apes and humans).

27 compare the additive model, due to Mesterton-Gibbons, and the multiplicative model, due to Parker, of

28 trovirus (binds Pit-2 receptor) but not with gibbon ape leukemia retrovirus (binds Pit-1 receptor), i

29 The membrane receptors for the gibbon ape leukemia retrovirus and the amphotropic murin

30 y (CHO) cells are resistant to infections by gibbon ape leukemia virus (GALV) and amphotropic murine

31 The mammalian gammaretroviruses gibbon ape leukemia virus (GALV) and feline leukemia vir

32 Gibbon ape leukemia virus (GALV) and koala retrovirus (K

33 press distinct but related receptors for the gibbon ape leukemia virus (GALV) and the amphotropic mur

34 Gibbon ape leukemia virus (GALV) and the koala retroviru

35 kemia virus (MuLV), the related protein from gibbon ape leukemia virus (GaLV) does not form functiona

36 der the direction of MoMSV LTR and using the gibbon ape leukemia virus (GALV) Env for internalization

37 virus (F-MLV) Env, but not with the related gibbon ape leukemia virus (GaLV) Env or with a chimeric

38 ant retroviruses pseudotyped with either the gibbon ape leukemia virus (GaLV) envelope or the vesicul

39 structed functional immunologically reactive gibbon ape leukemia virus (GALV) envelope proteins, tagg

40 g an optimized transduction protocol using a gibbon ape leukemia virus (GaLV) envelope-containing pac

41 e genes from each of the five members of the gibbon ape leukemia virus (GALV) family of type C retrov

42 The Env protein from gibbon ape leukemia virus (GaLV) has been shown to be in

43 has remained the only sequence implicated in gibbon ape leukemia virus (GALV) infection, and an acidi

44 ic murine retrovirus-related virus (XMRV) or gibbon ape leukemia virus (GALV) infection, even when th

45 were significantly higher than the level of gibbon ape leukemia virus (GaLV) receptor mRNA in cells

46 s targeting the amphotropic receptor and the gibbon ape leukemia virus (GALV) receptor Pit-1 were use

47 virus preparations of murine leukemia virus, gibbon ape leukemia virus (GALV), and simian sarcoma-ass

48 ity with the exogenous and highly infectious gibbon ape leukemia virus (GALV), the infectivity of KoR

49 y::Fur)] and the fusogenic glycoprotein from gibbon ape leukemia virus (GALV), which it was hoped wou

50 HPG is a close relative of KoRV and the gibbon ape leukemia virus (GALV), with virion morphology

51 4-enriched marrow cells were cocultivated on gibbon ape leukemia virus (GALV)-based retrovirus vector

52 aging cells FLYRD (LgGLSN and LNX) or by the gibbon ape leukemia virus (GALV)-pseudotype packaging ce

53 nto baboon marrow repopulating cells using a gibbon ape leukemia virus (GALV)-pseudotype retroviral v

54 tors having an envelope protein derived from gibbon ape leukemia virus (GALV).

55 a receptor not only for A-MuLVs but also for gibbon ape leukemia virus (GALV).

56 Murine cells are typically resistant to gibbon ape leukemia virus (GALV).

57 eplaced the native env sequence with that of gibbon ape leukemia virus (GALV).

58 otide identity with another gammaretrovirus, gibbon ape leukemia virus (GALV).

59 A notable exception is gibbon ape leukemia virus (GALV).

60 eptor-binding subdomain (RBD) derived from a gibbon ape leukemia virus (GALV).

61 photropic murine leukemia virus (A-MuLV) and gibbon ape leukemia virus (GALV); E36 cells are highly s

62 e greatest nucleic acid sequence identity to gibbon ape leukemia virus and murine leukemia virus.

63 ted protein that functions as a receptor for gibbon ape leukemia virus but not for A-MuLV.

64 g of both tetherin and a viral glycoprotein, gibbon ape leukemia virus envelope (GaLV Env).

65 n packaging cell lines containing either the gibbon ape leukemia virus envelope (PG13 cells), the mur

66 Of the FeLV, murine leukemia virus, and gibbon ape leukemia virus envelopes tested, we found tha

67 ectofusin-1 variants to promote the modified gibbon ape leukemia virus glycoprotein-pseudotyped lenti

68 s virus glycoproteins and also with modified gibbon ape leukemia virus glycoproteins.

69 Transfection of Hep3B cells with the Gibbon Ape leukemia virus hyperfusogenic envelope protei

70 Here we show that MDEV is also not in the gibbon ape leukemia virus or RD114 virus interference gr

71 ones expressing ZAP-70 were generated in the Gibbon ape leukemia virus packaging line PG13.

72 generated a human packaging cell line with a gibbon ape leukemia virus pseudotype (Phoenix-GALV), and

73 ll surface phosphate transport proteins, the gibbon ape leukemia virus receptor Glvr-1 (Pit-1) or the

74 B feline leukemia viruses (FeLV-Bs) use the gibbon ape leukemia virus receptor, Pit1, as a receptor

75 sions and was demonstrated with amphotropic, gibbon ape leukemia virus, and vesicular stomatitis viru

76 trast, the slightly different sequences from Gibbon ape leukemia virus, Moloney leukemia virus, PSAPP

77 (c) gene IL2RG pseudotyped with amphotropic, gibbon ape leukemia virus, or RD114 envelopes.

78 For numerous gammaretroviruses, such as the gibbon ape leukemia virus, woolly monkey virus, feline l

79 Gibbon ape leukemia virus-pseudotyped vector yielded pri

80 quences are most closely related to those of gibbon ape leukemia virus.

81 The gibbon ape leukemia viruses (GALVs) are among the most m

82 Gibbon ape leukemia viruses (GALVs) are part of a larger

83 West of the Wallace Line, gibbon ape leukemia viruses (GALVs) have been isolated f

84 Transduction with gibbon-ape leukemia virus pseudotyped Moloney murine leu

85 iruses (MuLVs), feline leukemia viruses, and gibbon-ape leukemia virus, encode an alternate, glycosyl

86 lication of somatic gene therapy by use of a gibbon-ape-leukaemia-virus pseudotyped gammaretroviral v

87 EATO (GALV-S), were originally isolated from gibbon apes, whereas the fifth member of this family, si

88 d, groups compared to other social primates, gibbons are not exempt from these conflicts in their eve

89 Gibbons are small arboreal apes that display an accelera

90 ad that genetic variation data in humans and gibbons as well as in Old World monkeys are inconsistent

91 KIR genes in great apes has not occurred in gibbons because they lack MHC-C.

92 within the infracortical white matter of the gibbon brain, indicating that the WMICs are a numericall

93 A substantial number (11/24) of human-NLE gibbon breakpoints showed new insertions of gibbon-speci

94 eding captive primates, we found that Hainan gibbons can obtain sufficient energy for growth and repr

95 Smith MT, Guyton KZ, Gibbons CF, Fritz JM, Portier CJ, Rusyn I, DeMarini DM,

96 neuron number in the LP-pulvinar complex in gibbon, chimpanzee, and gorilla compared to humans, howe

97 Given that gibbons dance in various behavioral contexts, and appear

98 he Sonic Hedgehog (SHH) gene associated with gibbons' elongated limbs.

99 conducted a comprehensive analysis of Hainan gibbons' energy intake and expenditure, reproductive par

100 These findings advance understanding of gibbon evolution, biology, and conservation.

101 n orangutan two sites were identified, while gibbon exhibited only a single site.

102 Gibbons (family Hylobatidae), small apes closely related

103 In other species, such as the orangutan and gibbon, FISH signals were only identified at the distal

104 The four strains of GALV isolated from gibbons formed a monophyletic clade that was closely rel

105 isolates most likely stem from infection of gibbons from a human source.

106 We further show that the gibbon genera (Nomascus, Hylobates, Hoolock and Symphala

107 ce of the highly rearranged structure of the gibbon genome by disrupting transcription of cell cycle

108 The gibbon genome exhibits extensive karyotypic diversity wi

109 TR-Alu (LIKE)), which is still active in the gibbon genome.

110 HBV variants, including evidence for a novel gibbon/genotype C recombinant among HBV variants from Vi

111 are 1, 4, 13, 13, 17, and 17 repeats in the gibbon, gorilla, orangutan, bonobo, neanderthal, and hum

112 HBVs previously isolated from a chimpanzee, gibbons, gorillas, and orangutans.

113 ough diverse and irregular in structure, the gibbon haplotypes are unusually small, containing only t

114 ke sequence, whereas gorilla, orangutan, and gibbon have a single copy.

115 is a GALV strain that likely originated in a gibbon host.

116 on of the entire adult alpha-globin locus of gibbon (Hylobates lar).

117 akey and others in roller pump design and by Gibbon in oxygenator development.

118 elevant to the cross-species transmission to gibbons in Southeast Asia and broadens the known distrib

119 mpanzees, bonobos, gorillas, orangutans, and gibbons, including siamangs) are of great scientific int

120 ed 55 faecal samples from 50 orangutan and 5 gibbon individuals from Borneo and Sumatra.

121 lar proviruses in white-cheeked gibbons; the gibbon insertions cluster within the OWM recombinant cla

122 ) consisting of the mature coding portion of gibbon interleukin-3 (IL-3) and full-length FAC in Esche

123 t cross-species infection between koalas and gibbons is unlikely.

124 Phylogenetic analysis indicated that the gibbon isolates lie within the human HBV family, indicat

125 hominoid KIR haplotype indicates that modern gibbon KIR haplotypes were formed by a series of deletio

126 the KIR locus, is present and intact on all gibbon KIR haplotypes.

127 ces shaping the size and organization of the gibbon KIR locus differed from those acting upon the KIR

128 ith advanced computational tools such as the GIBBON library and FEBio, our approach minimizes manual

129 noids lived in an environment that favored a gibbon-like size, but a series of selective regime shift

130 Functional experimentation identified gibbon LinARs, which could have participated in the deve

131 Two of these insertions were fixed in the gibbon lineage and overlapped with enhancer chromatin st

132 r mechanism for the genome plasticity of the gibbon lineage.

133 ZNF461), that have been disrupted in the NLE gibbon lineage.

134 ntain gorilla was incorrectly referred to as Gibbon lymphocryptovirus 1 in Table 1.

135 s of chimpanzee, bonobo, gorilla, orangutan, gibbon, macaque, owl monkey, and marmoset.

136 These results suggest that while gibbons may strategize to maximize benefits in a competi

137 Hainan gibbon (Nomascus hainanus) is the world's rarest primate

138 pecies were added in the last year including gibbon (Nomascus leucogenys) and Tasmanian devil (Sarcop

139 bly and analysis of a northern white-cheeked gibbon (Nomascus leucogenys) genome.

140 teny breakpoint regions in the white-cheeked gibbon (Nomascus leucogenys, NLE) in the form of high-qu

141 plays performed by four adult female cao vit gibbons (Nomascus nasutus) residing in four polygynous g

142 frame in chimpanzee and gorilla, but not in gibbon or macaque.

143 A to H and species-associated chimpanzee and gibbon/orangutan groups.

144 Gibbons participated in three conditions: a control cond

145 ling analyses suggest historical dynamics in gibbon population size and habitat suitability, which ar

146 Gibbons present a suitable model to study these contribu

147 t the non-human HBV clades in orangutans and gibbons resulted from cross-species transmission events

148 es from the human and from the orangutan and gibbon revealed wide overlap of elements across species,

149 A serological analysis of 30 captive gibbons revealed that 47% were positive for at least one

150 Following Gibbon's historic successful closure of an atrial septal

151 s and the great apes but not in lesser apes (gibbon, siamang) or lower-order primates (e.g., old or n

152 gibbon breakpoints showed new insertions of gibbon-specific repeats and mosaic structures formed fro

153 We describe the propensity for a gibbon-specific retrotransposon (LAVA) to insert into ch

154 er levels of gene expression in cis We found gibbon-specific signatures of purifying/positive selecti

155 cluster in a hand-over-hand fashion, like a gibbon swinging through the branches of a tree.

156 Pongo abelii)) and a lesser ape (the siamang gibbon (Symphalangus syndactylus)), and untangled the in

157 ies were 99.5% for gorilla tau and 99.0% for gibbon tau.

158 ree closely related species of wild Nomascus gibbons that live in polygynous groups.

159 entified similar proviruses in white-cheeked gibbons; the gibbon insertions cluster within the OWM re

160 may have been involved in the adaptation of gibbons to their arboreal habitat.

161 between members of genotypes A, D, F/H, and gibbon variants but not in B, C, or the Asian B/C recomb

162 n of an ancestral retrovirus into koalas and gibbons via one or more intermediate as-yet-unknown host

163 s of the core and surface genes of human and gibbon virus isolates were very similar.

164 In this regard, gibbon vocalizations offer an instructive model to under

165 s of four KIR haplotypes from two species of gibbon, we find that the smaller apes do not conform to

166 Gibbons, which are flanked in evolution by rhesus monkey

167 We presented dyads of gibbons with a situation in which they could decide whet

168 the current task, we asked whether dyads of gibbons would solve a conflict of interest over food rew