ライフサイエンスコーパス: Callithrix

1 e OR subfamilies in two species of marmoset (Callithrix).

2 t C. pygmaea should be included in the genus Callithrix.

3 In marmosets (Callithrix), a nonsynonymous nucleotide substitution in

4 We sampled 59 wild and captive Callithrix across four species and their hybrids.

5 The Brazilian buffy-tufted-ear marmoset (Callithrix aurita), one of the world's most endangered p

6 t might have contributed to the evolution of Callithrix biological features.

7 , Alouatta gamma is inactive at term, and in Callithrix, gamma(1) is down-regulated fetally, whereas

8 e to hawk calls, in 18 Geoffroy's marmosets (Callithrix geoffroyi).

9 n captive marmosets prompted us to study the Callithrix gut microbiome composition and predictive fun

10 Wild Callithrix gut microbiomes were enriched for Bifidobacte

11 novel repeat family, termed Platy-1, in the Callithrix jacchus (common marmoset) genome that arose a

12 ates strongly supports the classification of Callithrix jacchus and C. geoffroyi into the jacchus gro

13 Callithrix jacchus is an outbred New World primate chara

14 development in the New World marmoset monkey Callithrix jacchus is similar to previous reports in Mac

15 Using the nonhuman primate, Callithrix jacchus jacchus (common marmoset), we show th

16 Thus, using the marmoset monkey Callithrix jacchus we characterize here a new neurobiolo

17 test, we cannulated 2 cohorts of marmosets (Callithrix jacchus) (N = 14) in either area 14 of the ve

18 o capture the movements of common marmosets (Callithrix jacchus) and crickets stereoscopically and ap

19 the Callitrichidae family, common marmosets (Callithrix jacchus) and red-bellied tamarins (Saguinus l

20 e auditory cortex of awake marmoset monkeys (Callithrix jacchus) are capable of firing in a sustained

21 in the auditory cortex of marmoset monkeys (Callithrix jacchus) are sensitive to auditory feedback d

22 Common marmosets (Callithrix jacchus) are susceptible to intestinal inflam

23 gth TRPML3 channel from the common marmoset (Callithrix jacchus) at an overall resolution of 2.9 A.

24 bility, in unanaesthetized common marmosets (Callithrix jacchus) at two time points during late middl

25 athogenicity of RVFV in the common marmoset (Callithrix jacchus) by i.v., subcutaneous (s.c.), and in

26 12, were used to challenge common marmosets (Callithrix jacchus) by three routes of infection: aeroso

27 rontoparietal cortex in the common marmoset (Callithrix jacchus) by using intracortical microstimulat

28 ses like humans, we tested common marmosets (Callithrix jacchus) by using intranasal infection and mo

29 vestigated whether hyperhexosemic marmosets (Callithrix jacchus) develop characteristic retinal vascu

30 ns in auditory cortex of the awake marmoset (Callithrix jacchus) encode temporal information with eit

31 obes in freely moving male common marmosets (Callithrix jacchus) engaged in an antiphonal calling par

32 of a non-human primate (the common marmoset, Callithrix jacchus) following four systemic injections o

33 both the sequencing of the common marmoset (Callithrix jacchus) genome and a growing demand for alte

34 The sequencing of the common marmoset (Callithrix jacchus) genome offers the opportunity to exp

35 The New World marmoset monkey (Callithrix jacchus) has a relatively short gestational p

36 The New World common marmoset (Callithrix jacchus) has become popular as a nonhuman pri

37 The common marmoset (Callithrix jacchus) has garnered interest recently as a

38 past decade, the New World common marmoset (Callithrix jacchus) has taken a seminal position in neur

39 Single-unit studies in awake marmosets (Callithrix jacchus) have shown that a sub-population of

40 ral retinal thickness profiles in marmosets (Callithrix jacchus) induced with myopia continuously for

41 lissencephalic cortex, the common marmoset (Callithrix jacchus) is a promising alternative primate m

42 The common marmoset (Callithrix jacchus) is a small New World primate species

43 The common marmoset (Callithrix jacchus) is increasingly recognized as an ide

44 The common marmoset (Callithrix jacchus) is known for its highly vocal nature

45 The common marmoset (Callithrix jacchus) is of considerable biomedical import

46 sponses of up to 61 neurons in the marmoset (Callithrix jacchus) middle temporal area to a sequence o

47 In marmoset monkeys (Callithrix jacchus) of both sexes, we labeled the axons

48 In marmoset monkeys (Callithrix jacchus) of both sexes, we visualized the axo

49 rld monkeys (Cebus apella, Aotus azarae, and Callithrix jacchus) representing three of the seven plat

50 population of A1 neurons in awake marmosets (Callithrix jacchus) responded to rapid time-varying CI s

51 nonhuman primate (NHP), the common marmoset (Callithrix jacchus) shares many features in common with

52 the lateral belt of awake marmoset monkeys (Callithrix jacchus) showed significant changes in firing

53 n the temporal gyrus of the common marmoset (Callithrix jacchus) to 1) compare the functional organiz

54 T in awake male and female marmoset monkeys (Callithrix jacchus) to compare brain activations to cons

55 ains of the striatum of a primate (marmoset; Callithrix jacchus) using fast-scan voltammetry at a car

56 s examined in the brain of common marmosets (Callithrix jacchus) using in situ hybridization, immunoc

57 Six adult common marmosets (Callithrix jacchus) were acclimated to light, comfortabl

58 Nineteen Wistar rats and 21 marmosets (Callithrix jacchus) were distributed among control group

59 Juvenile marmosets (Callithrix jacchus) were divided into two experimental g

60 Twenty-four adult common marmosets (Callithrix jacchus) were followed with regular behaviour

61 young to middle aged adult common marmosets (Callithrix jacchus) were injected with BrdU and perfused

62 s of adult primates, adult marmoset monkeys (Callithrix jacchus) were injected with BrdU and perfused

63 neurons in the adult common marmoset monkey (Callithrix jacchus) were modified by extensive exposure

64 In particular, the common marmoset monkey (Callithrix jacchus) with a relatively short life span is

65 Marmoset monkeys (Callithrix jacchus) with bilateral transections of the a

66 experimentally infected the common marmoset (Callithrix jacchus) with diverse strains of Mycobacteriu

67 We inoculated common marmosets (Callithrix jacchus) with the objective of developing a s

68 To determine whether the common marmoset (Callithrix jacchus) would be an appropriate model to ass

69 k in both sexes of captive common marmosets (Callithrix jacchus), a cooperatively breeding primate wi

70 This study explored how marmosets (Callithrix jacchus), a highly social primate species, pr

71 ural vocal exchanges in the common marmoset (Callithrix jacchus), a highly vocal New World primate.

72 equency of 440 Hz, that the common marmoset (Callithrix jacchus), a New World monkey with a hearing r

73 breathing behaviors of the common marmoset (Callithrix jacchus), a New World non-human primate model

74 l facial expressions in the common marmoset (Callithrix jacchus), a New World primate species sharing

75 nned intact skull in awake marmoset monkeys (Callithrix jacchus), a primate species featuring a smoot

76 the visual topography of V1 in the marmoset (Callithrix jacchus), a small diurnal monkey.

77 eraction observation is the common marmoset (Callithrix jacchus), a small New World primate that shar

78 The common marmoset (Callithrix jacchus), a small-bodied New World primate, o

79 World monkeys, such as the common marmoset (Callithrix jacchus), a species of growing interest as a

80 for pitch extraction in the common marmoset (Callithrix jacchus), a vocal primate species, by measuri

81 ocal New World primate, the common marmoset (Callithrix jacchus), across the entire hearing frequency

82 rofile retinal cells of the common marmoset (Callithrix jacchus), an early divergent in anthropoid ev

83 ccessful generation of transgenic marmosets (Callithrix jacchus), an important nonhuman primate model

84 e chromosome level, for the common marmoset (Callithrix jacchus), an primate model system that is wid

85 A. nancymaae, but not marmoset (Callithrix jacchus), APOBEC3G was partially downregulate

86 The common marmoset (Callithrix jacchus), due to its small size, prosocial na

87 This tropism extends to marmoset (Callithrix jacchus), enabling robust, non-invasive gene

88 cal ability(4)(,)(5)(,)(6)-common marmosets (Callithrix jacchus), Humboldt's squirrel monkeys (Saimir

89 in the auditory cortex of marmoset monkeys (Callithrix jacchus), in which the firing rate of a neuro

90 zees (Pan troglodytes) and common marmosets (Callithrix jacchus), left-handed individuals are less li

91 n the New World monkey, the common marmoset (Callithrix jacchus), produced a persistent impairment on

92 ins (Saguinus oedipus) and common marmosets (Callithrix jacchus), species known to differ in temporal

93 asting opioid analgesic in common marmosets (Callithrix jacchus), there are no published studies on p

94 atal outcomes in the common marmoset monkey (Callithrix jacchus), using a combination of physiologica

95 single-unit recordings from awake marmosets (Callithrix jacchus), we validate several model predictio

96 es (Macaca mulatta) and 72 common marmosets (Callithrix jacchus).

97 issencephalic cortex of the common marmoset (Callithrix jacchus).

98 ic and CI signals in awake marmoset monkeys (Callithrix jacchus).

99 nuclear layer in the retina of the marmoset (Callithrix jacchus).

100 spinal cord lesions in the common marmoset (Callithrix jacchus).

101 visual cortex of awake, behaving marmosets (Callithrix jacchus).

102 passively listening female marmoset monkeys (Callithrix jacchus).

103 losely related species, the common marmoset (Callithrix jacchus).

104 losely related species, the common marmoset (Callithrix jacchus).

105 aeus), and a New World monkey, the marmoset (Callithrix jacchus).

106 ank of the lateral sulcus in five marmosets (Callithrix jacchus).

107 etry in striatal sections from the marmoset (Callithrix jacchus).

108 aneous B cell lymphomas of common marmosets (Callithrix jacchus).

109 striatal sections from the common marmoset (Callithrix jacchus).

110 riatal brain regions of the common marmoset (Callithrix jacchus).

111 common diseases in captive common marmosets (Callithrix jacchus).

112 xamined social tolerance at feeding sites in Callithrix jacchus, a cooperatively breeding primate spe

113 The GH gene cluster in marmoset, Callithrix jacchus, comprises eight GH-like genes and ps

114 in trait anxiety using the common marmoset (Callithrix jacchus, mixed sexes) as a model.

115 Common marmosets (Callithrix jacchus, n = 18) were trained to discriminate

116 ising spontaneously in the New World primate Callithrix jacchus, the common marmoset.

117 rganization of the EC in the common marmoset Callithrix jacchus.

118 etinal ganglion cells in the common marmoset Callithrix jacchus.

119 e cells in the retina of the common marmoset Callithrix jacchus.

120 and selective inhibitor of 17beta-HSD1 from Callithrix jacchus.

121 inner retinal neurons in the common marmoset Callithrix jacchus.

122 ed sections from the LGN of adult marmosets (Callithrix jacchus; 10 trichromatic females; 2 dichromat

123 rs, we show here that chimerism in marmoset (Callithrix kuhlii) twins is not limited to blood-derived

124 The finding of YFV by RT-PCR in five Callithrix monkeys who were all YFV-negative by histopat

125 s, but allochthonous callitrichid marmosets (Callithrix) serve as principle ecological GLT threats.

126 T-qPCR and/or immunohistochemistry, being 22 Callithrix-spp. most from urban areas.

127 ulo is associated with different outcomes in Callithrix when compared to other monkeys.

128 ng that without the pygmy marmoset the genus Callithrix would be paraphyletic.