ライフサイエンスコーパス: Pan troglodytes

1 anual task were assessed in 109 chimpanzees (Pan troglodytes).

2 ologues in the MHC of the common chimpanzee (Pan troglodytes).

3 Homo sapiens) donors and common chimpanzees (Pan troglodytes).

4 of hand use in a sample of 187 chimpanzees (Pan troglodytes).

5 e was tested in a sample of 188 chimpanzees (Pan troglodytes).

6 ion was examined in 115 captive chimpanzees (Pan troglodytes).

7 tamarins (Saguinus mystax) and chimpanzees (Pan troglodytes).

8 uman brain, are also present in chimpanzees (Pan troglodytes).

9 ves: bonobos (Pan paniscus) and chimpanzees (Pan troglodytes).

10 area 10) cortices of developing chimpanzees (Pan troglodytes).

11 red helical filaments in an aged chimpanzee (Pan troglodytes).

12 llum from MRI brain scans of 53 chimpanzees (Pan troglodytes).

13 and maternal space use) in wild chimpanzees (Pan troglodytes).

14 ves, bonobos (Pan paniscus) and chimpanzees (Pan troglodytes).

15 our closest living relative, the chimpanzee (Pan troglodytes).

16 odeficiency virus (SIVcpz) from chimpanzees (Pan troglodytes).

17 pal and amygdalar volumes of 60 chimpanzees (Pan troglodytes).

18 mans in comparison to the common chimpanzee (Pan troglodytes).

19 precentral gyrus-morphology in chimpanzees (Pan troglodytes).

20 (TCRBV) repertoire of the common chimpanzee Pan troglodytes.

21 o and are significantly larger than those of Pan troglodytes.

22 llus sphinx, Allenopithecus nigroviridis and Pan troglodytes.

23 olive baboon [Papio anubis]), 3 chimpanzees (Pan troglodytes), 6 members of the parrot (Psittacinae)

24 mpared among a group of 4 adult chimpanzees (Pan troglodytes), a group of 2 adult orangutans (Pongo p

25 ted the ontogeny of tool use in chimpanzees (Pan troglodytes), a species known for its extensive and

26 In chimpanzees (Pan troglodytes), adult males are more gregarious than f

27 In three experiments, chimpanzees (Pan troglodytes) always chose between an option deliveri

28 In a series of experiments, chimpanzees (Pan troglodytes), an orangutan (Pongo pygmaeus), and hum

29 ure of the actively transcribed GLTP gene in Pan troglodytes and establish the intronless GLTP as a p

30 egies used to combine seriated cups by apes (Pan troglodytes and P. paniscus) and monkeys (Cebus apel

31 s (Macaca mulatta), chimpanzees and bonobos (Pan troglodytes and Pan paniscus).

32 ata are available for our closest relatives, Pan troglodytes and Pan paniscus, data from the nonrecom

33 Observations of chimpanzees (Pan troglodytes) and bonobos (Pan paniscus) provide valu

34 ariation using body weights for chimpanzees (Pan troglodytes) and bonobos (Pan paniscus), addressing

35 osest living primate relatives, chimpanzees (Pan troglodytes) and bonobos (Pan paniscus), exhibit not

36 mans' closest living relatives, chimpanzees (Pan troglodytes) and bonobos (Pan paniscus), with a dyad

37 closest phylogenetic relatives, chimpanzees (Pan troglodytes) and bonobos (Pan paniscus).

38 arative studies between humans, chimpanzees (Pan troglodytes) and bonobos (Pan paniscus).

39 k was used to determine whether chimpanzees (Pan troglodytes) and children (Homo sapiens) who observe

40 In chimpanzees (Pan troglodytes) and common marmosets (Callithrix jacchu

41 in the genomes of 20 wild-born chimpanzees (Pan troglodytes) and have compared the identified chimpa

42 Here we tested chimpanzees (Pan troglodytes) and human children on a modified ultima

43 eixidor, and K. A. Bard tested chimpanzees' (Pan troglodytes) and human children's (Homo sapiens) ski

44 milarity between BT displays of chimpanzees (Pan troglodytes) and human smiles varied in relation to

45 identify a homologous region in chimpanzees (Pan troglodytes) and humans (Homo sapiens).

46 In this study, chimpanzees (Pan troglodytes) and orangutans (Pongo abelii) either ha

47 L1HS72) that was also present in the common (Pan troglodytes) and pygmy (P. paniscus) chimpanzee geno

48 ologues described to date in the chimpanzee (Pan troglodytes) and the four homologues described in ma

49 nzees (Pan paniscus), 13 common chimpanzees (Pan troglodytes) and three Hylobatidae (one Hylobates la

50 e found Plasmodium infection in chimpanzees (Pan troglodytes) and western gorillas (Gorilla gorilla),

51 orangutans (Pongo pygmaeus), 14 chimpanzees (Pan troglodytes), and 4 bonobos (Pan paniscus).

52 in 2- and 3-year-old children, chimpanzees (Pan troglodytes), and orangutans (Pongo pygmaeus).

53 Humans (Homo sapiens), chimpanzees (Pan troglodytes), and rhesus monkeys (Macaca mulatta) co

54 caca mulatta, Gorilla gorilla, Pan paniscus, Pan troglodytes, and Homo sapiens.

55 ter than that between the common chimpanzee, Pan troglodytes, and the pygmy chimpanzee or bonobo, Pan

56 Populations of the common chimpanzee (Pan troglodytes) are in an impending risk of going extin

57 Chimpanzees (Pan troglodytes) are often divided into subspecies, but

58 Chimpanzees (Pan troglodytes) are, along with bonobos, humans' closes

59 paniscus), which, together with chimpanzees (Pan troglodytes), are humans' closest living relatives.

60 ves, bonobos (Pan paniscus) and chimpanzees (Pan troglodytes), as valuable sources of comparative dat

61 neopterin in 70 sexually mature chimpanzees (Pan troglodytes) at Ngogo, Kibale National Park, Uganda.

62 hypothesized to be homologous to chimpanzee (Pan troglodytes) border patrols.

63 ve been isolated from the common chimpanzee (Pan troglodytes), but only three such SIVcpz infections

64 ample of 80 preserved postmortem chimpanzee (Pan troglodytes) cerebral hemispheres.

65 five primate species, Homo sapiens (human), Pan troglodytes (chimpanzee), Papio hamadryas (baboon),

66 m Old World apes; Gorilla gorilla (gorilla), Pan troglodytes (chimpanzee), Pongo pygmaeus (orang-utan

67 nstitution of these two archaic hominins and Pan troglodytes (chimpanzee).

68 We have sequenced the Pan troglodytes class I (Patr) molecules from three comm

69 nera, Homo (Homo) sapiens (humankind), Homo (Pan) troglodytes (common chimpanzee), and Homo (Pan) pan

70 nzee research sites, we sampled a further 34 Pan troglodytes communities.

71 ere, using a dataset of 144 wild chimpanzee (Pan troglodytes) communities, we show that chimpanzees e

72 lthough this fossil is comparable in size to Pan troglodytes, computerized tomography scans of the ne

73 d since infancy, pairs of adult chimpanzees (Pan troglodytes) could trade between themselves to obtai

74 mans' closest living relatives, chimpanzees (Pan troglodytes), could punish an individual who stole f

75 Data from three African field sites on Pan troglodytes demonstrate an unambiguous pattern of a

76 t has been reported that common chimpanzees (Pan troglodytes) differ from humans in being capable of

77 Male chimpanzees, Pan troglodytes, differ from males in most other mammali

78 n-human primates, and show that chimpanzees (Pan troglodytes) do not take advantage of opportunities

79 Human (Homo sapiens) (m/f), chimpanzee (Pan troglodytes) (f), and rhesus macaque (Macaca mulatta

80 controversial, particularly for chimpanzees (Pan troglodytes), for which it is difficult to rule out

81 conspecific face recognition in chimpanzees (Pan troglodytes) from 2 primate centers that provided di

82 e display from a cDNA library of chimpanzee (Pan troglodytes) gamma1/kappa antibody genes.

83 sess the referential function of chimpanzee (Pan troglodytes) gestures to obtain food.

84 uman equivalent chromosome(s) of chimpanzee (Pan troglodytes), gorilla (Gorilla gorilla) and oranguta

85 Our study investigated Macaca mulatta, Pan troglodytes, Gorilla gorilla, and Homo sapiens haplo

86 in all four great ape species (Pan paniscus, Pan troglodytes, Gorilla gorilla, Pongo pygmaeus) by var

87 s on joint attention in 4 great ape species (Pan troglodytes, Gorilla gorilla, Pongo spp., and Pan pa

88 lla (Gorilla gorilla) and common chimpanzee (Pan troglodytes) habitats in East and West Africa, the r

89 Two chimpanzees (Pan troglodytes) had a direct view of an experimenter pl

90 pygmaeus) and were compared with chimpanzee (Pan troglodytes) hand preferences in subjects that were

91 sed - an approach which in wild chimpanzees (Pan troglodytes) has revealed cultural differences in th

92 sing number of field studies of chimpanzees (Pan troglodytes) have achieved long-term status across A

93 Chimpanzees (Pan troglodytes) have been known to exhibit rudimentary

94 Captive chimpanzees (Pan troglodytes) have been shown to learn the use of nov

95 , however, researchers studying chimpanzees (Pan troglodytes) have challenged this idea.

96 Even though recent studies in chimpanzees (Pan troglodytes) have demonstrated population-level righ

97 NCE STATEMENT Recent studies in chimpanzees (Pan troglodytes) have shown that some can learn to produ

98 Serum samples (n = 245) from chimpanzees (Pan troglodytes) housed at 32 European zoos were measure

99 g the play behavior of 57 adult chimpanzees (Pan troglodytes) in Tai National Park, Cote d'Ivoire, wh

100 res contagious yawning in adult chimpanzees (Pan troglodytes) in the presence of a non-biological hum

101 Common chimpanzees (Pan troglodytes) infected with hepatitis C virus (HCV) s

102 irus (SIVcpz) infection of wild chimpanzees (Pan troglodytes) is incomplete since few isolates, mostl

103 hereas our closest relative, the chimpanzee (Pan troglodytes), is often characterized as overly compe

104 ne of our closest relatives, the chimpanzee (Pan troglodytes), is viewed as a reluctant altruist, act

105 Whereas mammals (Pan troglodytes, Macaca mulatta, Rattus norvegicus, and

106 Two chimpanzees (Pan troglodytes) made numerousness judgments of nonvisib

107 al call variation in different subspecies of Pan troglodytes, measuring minimum f(0) as well as maxim

108 mosomes of human (Homo sapiens), chimpanzee (Pan troglodytes), mouse (Mus musculus) and rat (Rattus n

109 phere dominance, in three great ape species (Pan troglodytes, Pan paniscus and Gorilla gorilla).

110 to human alleles, we sequenced 18 different Pan troglodytes (Patr) alleles of 14 chimpanzees, 2 of t

111 e characterized CD4+ T cells targeting seven Pan troglodytes (Patr) class II-restricted epitopes duri

112 ects of modified procedures on chimpanzees' (Pan troglodytes) performance in a scale model comprehens

113 Using genome-edited human and chimpanzee (Pan troglodytes, Pt) neural progenitor cells and cortica

114 locations in the chromosomes of chimpanzee (Pan troglodytes, PTR), gorilla (Gorilla gorilla, GGO) an

115 s investigated whether juvenile chimpanzees (Pan troglodytes) recognize and use enforced statistical

116 lence study of SIVcpz infection in five wild Pan troglodytes schweinfurthii communities in east Afric

117 ive status in wild mature female chimpanzees Pan troglodytes schweinfurthii from two communities, Kan

118 ng several communities of chimpanzees of the Pan troglodytes schweinfurthii subspecies in Uganda.

119 eat ape vocal communication, the chimpanzee (Pan troglodytes schweinfurthii) 'pant hoot'.

120 nk trajectories in wild eastern chimpanzees (Pan troglodytes schweinfurthii) and find remarkable sex

121 Chimpanzees in east Africa (Pan troglodytes schweinfurthii) are also infected with S

122 d genetic data from the Kasekela chimpanzee (Pan troglodytes schweinfurthii) community in Gombe Natio

123 Vcpz sequence (TAN1) from a wild chimpanzee (Pan troglodytes schweinfurthii) from Gombe National Park

124 photographic study of subadult chimpanzees (Pan troglodytes schweinfurthii) in Kanyawara, Kibale Nat

125 cted from nonhabituated eastern chimpanzees (Pan troglodytes schweinfurthii) in the Issa Valley (n =

126 n a savanna-mosaic community of chimpanzees (Pan troglodytes schweinfurthii) in the Issa Valley, Tanz

127 two neighbouring communities of chimpanzees (Pan troglodytes schweinfurthii) in the Kalinzu Forest, U

128 ocal exchanges in immature wild chimpanzees (Pan troglodytes schweinfurthii) of the Sonso community o

129 lus samples recovered from wild chimpanzees (Pan troglodytes schweinfurthii) who died in Gombe Nation

130 ing quality (body size) in wild chimpanzees (Pan troglodytes schweinfurthii), a species with long per

131 uses by 36 infant and juvenile chimpanzees (Pan troglodytes schweinfurthii), over 15 months at Ngogo

132 Chimpanzee (Pan troglodytes) sclera appear much darker than the whit

133 ans, bonobos (Pan paniscus) and chimpanzees (Pan troglodytes), share many traits that are common in h

134 uthors previously reported that chimpanzees (Pan troglodytes) showed a striking bias to select the la

135 ur closest living relatives, the chimpanzee (Pan troglodytes), shows the ability to succeed in comple

136 e, we investigated how pairs of chimpanzees (Pan troglodytes) solved a problem of dynamically coordin

137 of 4 originally cross-fostered chimpanzees (Pan troglodytes), still living freely, but now in a labo

138 n our closest living relatives, chimpanzees (Pan troglodytes), suggest that among primates, regular i

139 sus monkey (Macaca mulatta), and chimpanzee (Pan troglodytes) suggested that 17 of these imprinted DM

140 en greater than that between P. paniscus and Pan troglodytes, suggesting that endocranial development

141 An 11-year-old female chimpanzee (Pan troglodytes) that had already learned a large number

142 4 was based on the finding that chimpanzees (Pan troglodytes) that have been trained on the concept o

143 We tested a chimpanzee (Pan troglodytes) that recognizes 128 spoken words, askin

144 Here we show that in Pan troglodytes the peak in root growth rate coincides w

145 hologous sequences in the common chimpanzee (Pan troglodytes ), the gorilla (Gorilla gorilla) and the

146 asure of psychopathy for use in chimpanzees (Pan troglodytes), the Chimpanzee Psychopathy Measure (CP

147 ted the inferior pulvinar of the chimpanzee (Pan troglodytes), the closest evolutionary relative of h

148 ocedure originally designed for chimpanzees (Pan troglodytes) to measure the reactions of Asian eleph

149 died experimentally by allowing chimpanzees (Pan troglodytes) to observe alternative patterns of acti

150 The ability of chimpanzees (Pan troglodytes) to recognize the correspondence between

151 d CC morphology from MRIs in 67 chimpanzees (Pan troglodytes) to see whether similar effects were pre

152 nhuman primate species, such as chimpanzees (Pan troglodytes), to a limited degree.

153 with bonobos (Pan paniscus) and chimpanzees (Pan troglodytes) (Total n = 119) to assess their motivat

154 Chimpanzees in west central Africa (Pan troglodytes troglodytes) are endemically infected wi

155 rains from west central African chimpanzees (Pan troglodytes troglodytes) but human viruses belonging

156 n this study, we show that wild chimpanzees (Pan troglodytes troglodytes) in the Goualougo Triangle t

157 valence in west central African chimpanzees (Pan troglodytes troglodytes) remain to be elucidated.

158 SIVcpz) from naturally infected chimpanzees (Pan troglodytes troglodytes) to man.

159 n a single community of Central chimpanzees (Pan troglodytes troglodytes).

160 captive members of the chimpanzee subspecies Pan troglodytes troglodytes.

161 We examined whether and how chimpanzees (Pan troglodytes) update their initial belief about the l

162 two wild populations of western chimpanzees (Pan troglodytes verus) in Cantanhez National Park, Guine

163 rmed ethanol (alcohol), by wild chimpanzees (Pan troglodytes verus) in Cantanhez National Park, Guine

164 etiology that affects sanctuary chimpanzees (Pan troglodytes verus) in Sierra Leone.

165 at eating among wild adult male chimpanzees (Pan troglodytes verus) in Tai National Park, Cote d'Ivoi

166 sult in the extirpation of local chimpanzee (Pan troglodytes verus) populations.

167 ool use comes from three Western chimpanzee (Pan troglodytes verus) sites in Cote d'Ivoire, aged betw

168 her a ripe-fruit specialist, the chimpanzee (Pan troglodytes verus), arrived earlier at breakfast sit

169 oppers, a captive female western chimpanzee (Pan troglodytes verus), who featured in the PG Tips tele

170 dity and modern forest-dwelling chimpanzees (Pan troglodytes verus).

171 n Critically Endangered western chimpanzees (Pan troglodytes verus).

172 nine-member pedigree of Western chimpanzees, Pan troglodytes verus.

173 t sequence data from 10 Western chimpanzees, Pan troglodytes verus.

174 red as infants in Reno, Nevada, chimpanzees (Pan troglodytes) Washoe, Moja, Tatu, and Dar freely conv

175 000 conflict interactions in 44 chimpanzees (Pan troglodytes), we provide evidence for relatively sta

176 and numerousness judgments by 2 chimpanzees (Pan troglodytes) were investigated when 2 quantities of

177 Six chimpanzees (Pan troglodytes) were presented with pairs of color phot

178 eat apes (bonobo (Pan paniscus), chimpanzee (Pan troglodytes), western lowland gorilla (Gorilla goril

179 osely related species (i.e. Homo sapiens and Pan troglodytes) where gene-specific clustering is evide

180 nd morphology of 16 hearts from chimpanzees (Pan troglodytes) which were either healthy or affected b

181 pointing in 3 adult, laboratory chimpanzees (Pan troglodytes) who have not received language training

182 rived from the liver of a common chimpanzee (Pan troglodytes) with hepatitis C, specifically recogniz

183 n liver biopsy specimens of two chimpanzees (Pan troglodytes) with previously resolved HCV infection