ライフサイエンスコーパス: gibbon

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

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

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

4 tains Saitohin in chimpanzees, gorillas, and gibbons.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

37 4-enriched marrow cells were cocultivated on gibbon ape leukemia virus (GALV)-based retrovirus vector

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

65 Gibbon ape leukemia virus-pseudotyped vector yielded pri

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

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

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

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

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

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

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

73 Gibbons are small arboreal apes that display an accelera

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

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

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

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

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

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

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

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

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

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

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

85 The gibbon genome exhibits extensive karyotypic diversity wi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

122 Gibbons, which are flanked in evolution by rhesus monkey