ライフサイエンスコーパス: common marmoset

1 he striatum of cynomolgus monkeys and of the common marmoset.

2 al autoimmune encephalomyelitis (EAE) in the common marmoset.

3 fear responses in the New World primate, the common marmoset.

4 tal 6-hydroxydopamine (6-OHDA) lesion in the common marmoset.

5 he New World primate Callithrix jacchus, the common marmoset.

6 mary epithelial stem/progenitor cells in the common marmoset.

7 the extension of our investigations into the common marmoset.

8 ntal allergic encephalomyelitis (EAE) in the common marmoset.

9 n cell culture and for lymphoma induction in common marmosets.

10 S mutants were tested in cell culture and in common marmosets.

11 addition, HVS Deltaorf14 was nononcogenic in common marmosets.

12 Deltaorf14 was tested in cell culture and in common marmosets.

13 ving infection with a hepacivirus, GBV-B, in common marmosets.

14 ivirus, GB virus B (GBV-B), in infections of common marmosets.

15 2 independent growth and induced lymphoma in common marmosets.

16 Whether adolescent common marmosets (a new world primate) are susceptible t

17 expressing the CD4 and CXCR4 proteins of the common marmoset, a New World monkey.

18 n the eye growth and refractive state of the common marmoset, a New World primate that compensates fo

19 study, these same rhythms were sought in the common marmoset, a primate model of eye growth, to estab

20 prototypical lymphoblast cell line from the common marmoset, a vitamin D-resistant New World primate

21 It can infect common marmosets, a New World small primate, and induces

22 mental autoimmune encephalomyelitis (EAE) in common marmosets, allowing detailed analysis of secondar

23 TP/c-ras each induced lymphoma in one of two common marmosets, although onset of disease was more rap

24 immune encephalomyelitis (EAE) models in the common marmoset and rhesus monkey to model the associati

25 s nonsynonymous changes found exclusively in common marmosets and other tested callitrichine species

26 Primary cells derived from common marmosets and squirrel monkeys support every phas

27 yl-1,2,3,6-tetrahydropyridine (MPTP)-treated common marmosets, and in normal individuals and patients

28 recently reported for cooperatively breeding common marmosets, and indicate that prosocial preference

29 Here, we show that the common marmoset APOBEC3G (A3G) and BST2 proteins block H

30 In this study, we observed that common marmoset APOBEC3G and BST2, two known restriction

31 These findings identify the common marmoset as a promising nonhuman primate to study

32 The findings of this study identify the common marmoset as a useful model of human EEE for testi

33 These findings identify the common marmoset as an appropriate model of human Lassa f

34 tinin positive retinal ganglion cells in the common marmoset Callithrix jacchus.

35 isplaced amacrine cells in the retina of the common marmoset Callithrix jacchus.

36 valuated in the inner retinal neurons in the common marmoset Callithrix jacchus.

37 ure of a full-length TRPML3 channel from the common marmoset (Callithrix jacchus) at an overall resol

38 infectivity and pathogenicity of RVFV in the common marmoset (Callithrix jacchus) by i.v., subcutaneo

39 organization of frontoparietal cortex in the common marmoset (Callithrix jacchus) by using intracorti

40 munity, driven by both the sequencing of the common marmoset (Callithrix jacchus) genome and a growin

41 The sequencing of the common marmoset (Callithrix jacchus) genome offers the o

42 The common marmoset (Callithrix jacchus) has garnered intere

43 In the past decade, the New World common marmoset (Callithrix jacchus) has taken a seminal

44 de penetrations in the temporal gyrus of the common marmoset (Callithrix jacchus) to 1) compare the f

45 en in humans, we experimentally infected the common marmoset (Callithrix jacchus) with diverse strain

46 To determine whether the common marmoset (Callithrix jacchus) would be an appropr

47 cortex during natural vocal exchanges in the common marmoset (Callithrix jacchus), a highly vocal New

48 ng fundamental frequency of 440 Hz, that the common marmoset (Callithrix jacchus), a New World monkey

49 The common marmoset (Callithrix jacchus), a small-bodied New

50 ion exists in New World monkeys, such as the common marmoset (Callithrix jacchus), a species of growi

51 signal are used for pitch extraction in the common marmoset (Callithrix jacchus), a vocal primate sp

52 tex of a highly vocal New World primate, the common marmoset (Callithrix jacchus), across the entire

53 poral ablations in the New World monkey, the common marmoset (Callithrix jacchus), produced a persist

54 iatal and extrastriatal brain regions of the common marmoset (Callithrix jacchus).

55 loss produced by spinal cord lesions in the common marmoset (Callithrix jacchus).

56 infection in a closely related species, the common marmoset (Callithrix jacchus).

57 eplication in a closely related species, the common marmoset (Callithrix jacchus).

58 trode in vitro in striatal sections from the common marmoset (Callithrix jacchus).

59 NA versus SA viruses like humans, we tested common marmosets (Callithrix jacchus) by using intranasa

60 d AVP receptors was examined in the brain of common marmosets (Callithrix jacchus) using in situ hybr

61 Six adult common marmosets (Callithrix jacchus) were acclimated to

62 Twenty-four adult common marmosets (Callithrix jacchus) were followed with

63 this possibility, young to middle aged adult common marmosets (Callithrix jacchus) were injected with

64 We inoculated common marmosets (Callithrix jacchus) with the objective

65 In chimpanzees (Pan troglodytes) and common marmosets (Callithrix jacchus), left-handed indiv

66 n cotton-top tamarins (Saguinus oedipus) and common marmosets (Callithrix jacchus), species known to

67 d virus from spontaneous B cell lymphomas of common marmosets (Callithrix jacchus).

68 Common marmosets (Callithrix jacchus, n = 18) were train

69 ons of the brain of a non-human primate (the common marmoset, Callithrix jacchus) following four syst

70 frontal and anterior cingulate cortex of the common marmoset (Callithrx jacchus).

71 We studied the susceptibility of common marmoset cells to HIV-1 infection and observed th

72 These results demonstrate that in common marmosets D3 receptors are located in both striat

73 lymphocryptovirus (LCV) naturally infecting common marmosets demonstrated that gamma-1 herpesviruses

74 Rhesus macaques developed mild disease, and common marmosets exhibited moderate to severe, potential

75 laty-1 elements across 62 subfamilies in the common marmoset genome.

76 , termed Platy-1, in the Callithrix jacchus (common marmoset) genome that arose around the time of th

77 02 reversed motor disability in MPTP-treated common marmosets in a dose-dependent manner.

78 Common marmosets in particular have significantly reduce

79 The common marmoset is a new world primate belonging to the

80 y, this functional organization of AI in the common marmoset is similar to that in other mammalian sp

81 In fact, common marmoset lymphocytes immortalized by the HVS/Tip

82 p mSH3B, retained its ability to immortalize common marmoset lymphocytes in culture.

83 Subgroup A and C strains transform primary common marmoset lymphocytes to interleukin-2-independent

84 Our findings demonstrate that common marmoset mammary stem/progenitor cells can be iso

85 llitrichinae, or callitrichines) such as the common marmoset manifesting diminutive size and unique r

86 Based on our results, the common marmoset model more closely resembles severe huma

87 bsence of autopsy data, a rhesus macaque and common marmoset model of MERS-CoV disease were analyzed.

88 Together, the rhesus macaque and common marmoset models of MERS-CoV span the wide range o

89 imary auditory cortical neurons in the adult common marmoset monkey (Callithrix jacchus) were modifie

90 In particular, the common marmoset monkey (Callithrix jacchus) with a relat

91 atic vessels in human and nonhuman primates (common marmoset monkeys) and the feasibility of noninvas

92 By using healthy common marmoset monkeys, Yamada et al traced the retinog

93 AG, analysis of video recordings showed that common marmosets (New World monkeys) differentiated betw

94 n that a major block to HIV-1 replication in common marmosets operates at the level of viral entry an

95 Following MPTP treatment of common marmosets, OPN protein expression was decreased,

96 ation dynamics in the lineage leading to the common marmoset over the last 40 million years.

97 -1 encounters additional postentry blocks in common marmoset peripheral blood mononuclear cells.

98 the presence of polymorphic elements within common marmoset populations, suggests ongoing retrotrans

99 ation of the HIV-1 envelope glycoproteins to common marmoset receptors might allow the development of

100 Experimental infection of common marmosets resulted in fulminant lymphoma with bot

101 of the amygdala in a new world primate, the common marmoset, resulted in a progressive impairment in

102 -4A chimera) was produced and used to infect common marmosets, since HCV NS2 to NS4A proteins are cri

103 We studied simian foamy viruses (SFVs) from common marmosets, spider monkeys, and squirrel monkeys,

104 factors are implicated in immortalization of common marmoset T lymphocytes and may also be critical i

105 ental HVS subgroup C strain 488 immortalized common marmoset T lymphocytes in vitro to interleukin-2-

106 ental HVS subgroup C strain 488 immortalized common marmoset T lymphocytes in vitro to interleukin-2-

107 nant HVS deltaSTP/v-ras immortalized primary common marmoset T lymphocytes to interleukin-2-independe

108 tor neurons was investigated in the rat, the common marmoset, the rhesus monkey and man using the SMI

109 In common marmosets treated with the selective nigral neuro

110 in the hemispheres of left- and right-handed common marmosets using surface photography and histology

111 onhuman primate, Callithrix jacchus jacchus (common marmoset), we show that immunization with myelin

112 rimary auditory cortex of naturally sleeping common marmosets, we show that slow-wave sleep (SWS) alt

113 Twenty-four common marmosets were grouped by onset of deprivation (g

114 small nonhuman primate model of Lassa fever, common marmosets were subcutaneously inoculated with Las

115 Thirty-three common marmosets were used.

116 n 19 to 20 days of experimental infection of common marmosets, while HVS deltaSTP-C488 and HVS deltaT

117 n, globus pallidus, substantia nigra) in the common marmoset, with the highest levels being in substa

118 e have been exploring the blocks to HIV-1 in common marmosets, with the ultimate goal of developing a