ライフサイエンスコーパス: fascicularis

1 -beta subunit of cynomolgous macaque (Macaca fascicularis).

2 donor eye and 2 normal primate eyes (Macaca fascicularis).

3 ion and motor speed in young monkeys (Macaca fascicularis).

4 rning and memory function in monkeys (Macaca fascicularis).

5 ansected in eight cynomolgus monkeys (Macaca fascicularis).

6 mulatta) and one cynomolgous monkey (Macaca fascicularis).

7 ex (V1) in six normal adult macaques (Macaca fascicularis).

8 esearch colony of cynomolgus monkeys (Macaca fascicularis).

9 ry bodies of five cynomolgus monkeys (Macaca fascicularis).

10 (NHP) model, the cynomolgus macaque (Macaca fascicularis).

11 in adult female cynomolgus macaques (Macaca fascicularis).

12 cortex (V1) of anesthetized macaque (Macaca fascicularis).

13 btained from the retinae of macaques (Macaca fascicularis).

14 cer injections in cynomolgus monkeys (Macaca fascicularis).

15 dentate gyrus of young adult monkeys (Macaca fascicularis).

16 ctions of MITN in cynomolgus monkeys (Macaca fascicularis).

17 ve, premenopausal cynomolgus monkeys (Macaca fascicularis).

18 dult (age, 21.2+/-0.2 years) monkeys (Macaca fascicularis).

19 pain-2) in the nonhuman primate (Nhp) Macaca fascicularis.

20 O, after intrathalamic inoculation in Macaca fascicularis.

21 macaque populations were also present in M. fascicularis.

22 29/57) of the rhesus SNPs were present in M. fascicularis.

23 smission electron microscopy in adult Macaca fascicularis.

24 cific for PD as it was not present in Macaca fascicularis (7 MPTP and 8 controls) with similar degree

25 Two animals (M fascicularis and M mulatta) were used as a diabetic, non

26 isingly high conservation of SNPs between M. fascicularis and M. mulatta, suggesting that the relatio

27 imiri sciureus), and macaque monkeys (Macaca fascicularis and M. radiata).

28 ee monkeys with spontaneous IDDM (two Macaca fascicularis and one Ceropithecus aethiops) were treated

29 ons of the murine, non-human primate (Macaca fascicularis) and human GI tracts.

30 rning paradigm for nonhuman primates (macaca fascicularis) and recorded the activity of single neuron

31 nd SIVmac251 infection in cynomolgus (Macaca fascicularis) and rhesus macaques of Chinese origin.

32 In cynomolgus (Macaca fascicularis) and squirrel (Saimiri sciureus) monkey eye

33 ese results indicate that a proportion of M. fascicularis are able to effectively control the replica

34 ted from breeding centers in China (where M. fascicularis are not native) showed they were similar to

35 Burmese long-tailed macaques (Macaca fascicularis aurea) are one of a limited number of wild

36 in the premotor cortex of the monkey (Macaca fascicularis) brain by means of a convergence of visual

37 ection can cause fatal simian AIDS in Macaca fascicularis, but many individuals survive with few clin

38 pia) was induced in six normal, adult Macaca fascicularis by disinserting the medial rectus muscles.

39 as induced in monkeys (Macaca mulatta and M. fascicularis) by applying a laser to the trabecular mesh

40 in adult monkeys (Macaca mulatta and Macaca fascicularis) by laser application to the trabecular mes

41 ned that the beta-subunit of macaque (Macaca fascicularis) chorionic gonadotropin (mCG-beta) is more

42 iments undertaken in macaque monkeys (Macaca fascicularis), cMRF neurons labeled retrogradely from in

43 auditory cortices in macaque monkeys (Macaca fascicularis) could be used to identify homologous regio

44 strain values in a finite model of a Macaca fascicularis cranium.

45 Three adult Macaca fascicularis (cynomolgous) monkeys received unilateral f

46 Macaca fascicularis (cynomolgus or longtail macaques) is the mo

47 immunization in humans, we vaccinated Macaca fascicularis (Cynomolgus) monkeys with DNA encoding the

48 was highly immunogenic in mice and in Macaca fascicularis (cynomolgus) monkeys.

49 ind that LFS in the nonhuman primate (Macaca fascicularis) dACC, when combined with extinction traini

50 arthenogenetic development of monkey (Macaca fascicularis) eggs to the blastocyst stage, and their us

51 ung tissues from cynomolgus macaques (Macaca fascicularis) experimentally infected with a low dose of

52 models, principally Macaca rhesus and Macaca fascicularis, experimentally infected with the relapsing

53 activity was recorded from V6A in two Macaca fascicularis fixating real targets in darkness.

54 was evaluated in cynomolgus monkeys (Macaca fascicularis) for immunogenicity and safety as a vaccine

55 V2 of the macaque (Macaca nemestrina, Macaca fascicularis) for the orientation of texture-defined for

56 2 DNA-positive blood into groups of naive M. fascicularis from either a viremic or nonviremic donor a

57 In M. fascicularis from endemically SRV-2-infected colonies, v

58 he presence of a chronic HBV infection in M. fascicularis from Mauritius Island.

59 were detected in cynomolgus macaques (Macaca fascicularis) from Mauritius Island only, and, remarkabl

60 SIV)-susceptible cynomolgus macaques (Macaca fascicularis) from the Indian Ocean island of Mauritius

61 We directly compared macaque (Macaca fascicularis) functional connectivity (FC) assessed usin

62 iverged first, and members of the sinica and fascicularis groups share a common ancestor; 3) Macaca a

63 Taken together, these data show that M. fascicularis has the most diverse array of TRIM5 restric

64 , genomic sequencing of M. nemestrina and M. fascicularis identifies a CypA retrotransposition in the

65 on shellfish by long-tailed macaques (Macaca fascicularis) in Khao Sam Roi Yot National Park, Thailan

66 imate species, the cynomolgus monkey (Macaca fascicularis), in a realistic social ethological context

67 very of TRIMCyp in both M. nemestrina and M. fascicularis indicates that TRIMCyp expression may be mo

68 ular dominance columns in a sample of six M. fascicularis, indicating that the number of hypercolumns

69 ns) identified 2 cynomolgus macaques (Macaca fascicularis) infected with Ebola (subtype Reston) virus

70 Compared to cynomolgus macaques (Macaca fascicularis) infected with the same virus, the squirrel

71 M. fascicularis is commonly used as a model for AIDS resear

72 teome response in cynomolgus macaque (Macaca fascicularis) lung tissue over 7 days of infection with

73 nd in four species of Asian macaques, Macaca fascicularis, M. mulatta, M. nemestrina, and M. leonina.

74 the saccular or utricular neuroepithelium of fascicularis (Macaca fascicularis) or rhesus (Macaca mul

75 nonhuman primates (Macaca nemestrina, Macaca fascicularis, Macaca mulatta) to examine the organizatio

76 himpanzee), Papio hamadryas (baboon), Macaca fascicularis (macaque), and Eulemur fulvus collaris (col

77 equency in Indonesian than in Indochinese M. fascicularis macaques and is also present in samples fro

78 TRIMCyp is absent in Mauritian M. fascicularis macaques.

79 apanese (Macaca fuscata) and long-tailed (M. fascicularis) macaques were selected for their highly de

80 pygmaeus, oEDN) and Old World monkey (Macaca fascicularis, mcEDN) genomic DNAs, and from a second New

81 comotion in a nonhuman primate (NHP) (Macaca fascicularis) model of bipedal locomotion.

82 We used the cynomolgus macaque (Macaca fascicularis) model of HIV-Mycobacterium tuberculosis co

83 The cynomolgus macaque (Macaca fascicularis) model of M. tuberculosis infection closely

84 al (ID) challenge cynomolgus macaque (Macaca fascicularis) model of scrub typhus, the leading cause o

85 oviral restriction factors and the use of M. fascicularis models in AIDS research.

86 of the intrinsic connectivity of the Macaca fascicularis monkey hippocampal formation.

87 racers into the amygdaloid complex of Macaca fascicularis monkeys and examining labeled boutons in ar

88 Twenty-four female Macaca fascicularis monkeys divided into groups by age (10-12 y

89 tested whether C-group motoneurons in Macaca fascicularis monkeys receive a direct cMRF input by inje

90 y and toxicity of MEGC-PEG-rMETase in Macaca fascicularis monkeys using an escalating-dose strategy.

91 ystem of the hippocampal formation of Macaca fascicularis monkeys was studied immunohistochemically w

92 Two Macaca fascicularis monkeys were trained to perform an instruct

93 Macaque fascicularis monkeys were used in a double-blind, placeb

94 he GABAergic innervation of the CG in Macaca fascicularis monkeys.

95 entorhinal cortex was investigated in Macaca fascicularis monkeys.

96 racers into the amygdaloid complex of Macaca fascicularis monkeys.

97 rta of young versus old male monkeys (Macaca fascicularis) (n=7/group), where aortic stiffness increa

98 intracranially in cynomolgus monkeys (Macaca fascicularis); (n = 17) for up to 30 days.

99 tly asymptomatic cynomolgus macaques (Macaca fascicularis), naturally infected with SRV type 2 (SRV-2

100 nes readily invade human and macaque (Macaca fascicularis) normocytes with a preference for reticuloc

101 MHC I alleles in Cynomolgus macaques (Macaca fascicularis) of Chinese, Vietnamese, and Mauritian orig

102 sulinopenic nonhuman primates (three Macacca fascicularis, one Ceropithecus aethiops, and one Macacca

103 ular neuroepithelium of fascicularis (Macaca fascicularis) or rhesus (Macaca mulatta) monkeys.

104 e neurological lesions than M. mulatta or M. fascicularis (P = 0.048).

105 In dog and monkey (Macaca fascicularis), Pax2 is expressed by astrocytes that are

106 premotor cortical sites in primates (Maccaca fascicularis) performing a motor task, while measuring t

107 from three awake cynomolgus monkeys (Macaca fascicularis) prepared for chronic recording.

108 itro cultivation of P. cynomolgi-infected M. fascicularis primary hepatocytes during which hypnozoite

109 rocess, studies were carried out in a Macaca fascicularis primate model of experimental periodontitis

110 process, studies were conducted in a Macaca fascicularis primate model of experimental periodontitis

111 e of IL-1 in periodontal disease in a Macaca fascicularis primate model, using human soluble IL-1 rec

112 Thirty-four male monkeys (Macaca fascicularis) received bilateral 0.7-mg DEX implants.

113 ller cells from the human and monkey (Macaca fascicularis) retina were studied with various configura

114 ls (especially the cynomolgus monkey, Macaca fascicularis) reveals that chronic psychosocial stress c

115 a sylvanus were inoculated with a pool of M. fascicularis serum and developed an acute HBV infection

116 Thirty six (52%) of the M. fascicularis SNPs were overlapping in both species.

117 as upregulated in carotid arteries of Macaca fascicularis subjected to atherosclerosis regression die

118 in an additional control monkey (male Macaca fascicularis) that had no surgical intervention.

119 rons in the brain of macaque monkeys (Macaca fascicularis) that represent the auditory space surround

120 ly nephrectomized cynomolgus monkeys (Macaca fascicularis) that underwent splenectomy and were immuno

121 sues of 17 adult cynomolgus macaques (Macaca fascicularis) that were infected with Mtb strain Erdman

122 dy computer model of a primate skull (Macaca fascicularis), that aims to predict muscle recruitment p

123 site whose natural vertebrate host is Macaca fascicularis (the 'kra' monkey); however, it is now incr

124 s of studies in 19 nonhuman primates (Macaca fascicularis), the potential therapeutic advantage of an

125 tal cortices of Macaca nemestrina and Macaca fascicularis to analyze the organization of terminals an

126 Using the cynomolgus macaque (Macaca fascicularis) to assess primate-specific imprinting, we

127 ivisions of MD in cynomolgus monkeys (Macaca fascicularis) to assess the relative proportions of conn

128 s, we studied 34 cynomolgus macaques (Macaca fascicularis) to compare a 2004 human H5N1 Vietnam isola

129 obtained using BOLD-fMRI in macaques (Macaca fascicularis) to structural connectivity derived from ma

130 onhuman-primate species [Papio-anubis/Macaca-fascicularis] to determine the impact of different adipo

131 We used primate (Macaca nemestrina/Macaca fascicularis) tracing studies and 3D reconstructions of

132 icle in six awake cynomolgus monkeys (Macaca fascicularis) trained to sit calmly in a primate chair.

133 Neither M. nemestrina nor M. fascicularis TRIMCyp could restrict HIV-1 or simian immu

134 n 7 is absent from both M. nemestrina and M. fascicularis TRIMCyp.

135 two MPTP-treated cynomolgus monkeys (macaca fascicularis) using a high-resolution PET imaging system

136 performed in 15 anesthetized monkeys (Macaca fascicularis) using extracellular single-unit recording

137 e right eye of 7 cynomolgous monkeys, Macaca fascicularis, using laser injury to the aqueous outflow

138 composition of the Old World primate Macaca fascicularis via scanning and transmission electron micr

139 The cynomolgus macaque, Macaca fascicularis, was introduced onto the island of Mauritiu

140 In the nonhuman primate (Macaque fascicularis), we analyzed a collection of bidirectional

141 ar injury model in nonhuman primates (Macaca fascicularis), we were able to demonstrate that CTRP-1 c

142 Telemetered cynomolgus macaques (Macaca fascicularis) were challenged by the aerosol route with

143 The monkeys (Macaca fascicularis) were chronically instrumented.

144 Monkeys (male Macaca fascicularis) were given 5-bromo-2-deoxyuridine (BrdU) i

145 Cynomolgus monkeys (Macaca fascicularis) were immunized systemically with nMOMP, an

146 ne, 32 male adult cynomolgus monkeys (Macaca fascicularis) were randomized to an ad libitum (AL) diet

147 Eleven monkeys (Macaca fascicularis) were rendered diabetic with streptozotocin

148 Twenty-four cynomolgus macaques (Macaca fascicularis) were studied for 46 weeks after inoculatio

149 Monkeys (Macacca fascicularis) were tested for their ability to perform l

150 Cynomolgus macaques (Macaca fascicularis) were transplanted with mismatched kidney a

151 In this study, eight monkeys (Macaca fascicularis) who were subjects in a separate exercise s

152 Intravenous inoculation of Macaca fascicularis with Escherichia coli produced mild to seve

153 In this study, 3 cynomolgus monkeys (Macaca fascicularis) with bilateral perirhinal cortex ablations

154 groups of 5 or 6 cynomolgus monkeys (Macaca fascicularis) with either a wild-type MV or its "N4-blin

155 al PVs in female cynomolgus macaques (Macaca fascicularis) without breeding contact for at least 3.5

156 R of total RNA from M. nemestrina and Macaca fascicularis yielded three TRIMCyp amplification product