ライフサイエンスコーパス: Homo sapiens

1 , and PHA17 (HSA13) (PHA, P. hamadryas; HSA, Homo sapiens).

2 uitfly (Drosophila melanogaster), and human (Homo sapiens).

3 ons (about 1400 GO terms and 11,000 genes in Homo sapiens).

4 caques (Macaca nemestrina) and adult humans (Homo sapiens).

5 ed to identify homologous regions in humans (Homo sapiens).

6 tions by pigeons (Columba livia) and humans (Homo sapiens).

7 ogaster, Mus musculus, Rattus norvegicus and Homo sapiens).

8 in chimpanzees (Pan troglodytes) and humans (Homo sapiens).

9 er, Caenorhabditis elegans, Mus musculus and Homo Sapiens.

10 epresent a pathological microcephalic modern Homo sapiens.

11 Escherichia coli, Pyrococcus horikoshii, and Homo sapiens.

12 less parietal expansion than is the case for Homo sapiens.

13 n species as diverse as Escherichia Coli and Homo sapiens.

14 ces cerevisiae, Drosophila melanogaster, and Homo sapiens.

15 n data from both Drosophila melanogaster and Homo sapiens.

16 o congenital and acquired channelopathies in Homo sapiens.

17 can cause congenital and acquired disease in Homo sapiens.

18 bditis elegans, Drosophila, Mus musculus and Homo sapiens.

19 positive selection in the lineage leading to Homo sapiens.

20 he region during this period-Neandertals and Homo sapiens.

21 reading frames in Xenopus, Mus musculus, and Homo sapiens.

22 eoglobus fulgidus, Arabidopsis thaliana, and Homo sapiens.

23 g Drosophila melanogaster, Mus musculus, and Homo sapiens.

24 PPI) networks between Epstein-Barr virus and Homo sapiens.

25 y played a critical role in the evolution of Homo sapiens.

26 contextual circumstances of the emergence of Homo sapiens.

27 model organisms to understand the biology of Homo sapiens.

28 sis was most similar to that of contemporary Homo sapiens.

29 desaturases from Drosophila melanogaster to Homo sapiens.

30 ster, Arabidopsis thaliana, Mus musculus and Homo sapiens.

31 rmal physiological range of the Palaeolithic Homo sapiens.

32 ave recently been found in Fugu rubripes and Homo sapiens.

33 This range increase parallels that of Homo sapiens.

34 enorhabditis elegans, Loxodonta africana and Homo sapiens.

35 Drosophila, Gallus gallus, Mus musculus, and Homo sapiens.

36 omical dissections and compare the data with Homo sapiens.

37 most likely characteristic of pre-modern era Homo sapiens.

38 Swartkrans, Homo neanderthalensis, and early Homo sapiens.

39 high-predicted structural conservation with Homo sapiens.

40 rs, found in all kingdoms of life, including Homo sapiens.

41 s and, for some loci, predates the origin of Homo sapiens.

42 hat it also confers reproductive benefits in Homo sapiens.

43 s NUBPL (nucleotide binding protein-like) in Homo sapiens.

44 ction of FBA models for Escherichia coli and Homo sapiens.

45 rsially identified as either Neanderthals or Homo sapiens.

46 enes for speech after they first appeared in Homo sapiens 100,000-150,000 years ago.

47 It was localized on Homo sapiens 3q26 chromosomal locus, a region that has b

48 (29 members), Drosophila melanogaster (29), Homo sapiens (60) and Arabidopsis thaliana (57), and we

49 acity for ecosystem engineering exhibited by Homo sapiens A crucial outcome of such behaviors has bee

50 ith endocasts from great apes, Homo erectus, Homo sapiens, a human pygmy, a human microcephalic, spec

51 species that diverged from the ancestors of Homo sapiens about 25 million years ago.

52 a" model, which posits a dispersal of modern Homo sapiens across Eurasia as a single wave at 60,000

53 most prevalent chronic bacterial diseases of Homo sapiens afflict the skeleton.

54 The Homo sapiens and Arabidopsis thaliana genomes are believ

55 s type 1 (HIV-1) infectivity when particular Homo sapiens and Cercopithecus aethiops cell lines were

56 RNA interaction in PRC2 core complexes from Homo sapiens and Chaetomium thermophilum, for which crys

57 ests that it appeared after the emergence of Homo sapiens and contributed to the great success of our

58 Observations in Homo sapiens and Drosophila melanogaster have revealed a

59 pproximately 700 million years that separate Homo sapiens and Drosophila melanogaster.

60 ndida albicans, Drosophila melanogaster, and Homo sapiens and form a subgroup of a family of proteins

61 is conserved from Caenorhabditis elegans to Homo sapiens and has an undefined meiotic function in fe

62 standing of the evolutionary relationship of Homo sapiens and Homo neanderthalensis and signifies the

63 nted relative to the finished chromosomes of Homo sapiens and key model organisms generated by the Hu

64 Expression of subunit c homologues from Homo sapiens and Manduca sexta, both species sensitive t

65 vered a family of small secreted proteins in Homo sapiens and Mus musculus using a novel database sea

66 Two organisms are currently supported: Homo sapiens and Mus musculus.

67 vered a family of small secreted proteins in Homo sapiens and Mus musculus.

68 and developmental time information from both Homo sapiens and Mus musculus.

69 glycans in more than a dozen cell types from Homo sapiens and Mus musculus.

70 is well within the era of speciation between Homo sapiens and Neanderthals/Denisovans and around thre

71 The Homo sapiens and other eukaryotic constitutive kynurenin

72 orresponds to a few percent of the genome in Homo sapiens and other mammals, and up to half the genom

73 ner except for closely related species (i.e. Homo sapiens and Pan troglodytes) where gene-specific cl

74 of KsgA from Escherichia coli and Dim1 from Homo sapiens and Plasmodium falciparum have been determi

75 RHEX is well conserved in Homo sapiens and primates but absent from mouse, rat, an

76 for cluster transfer to apo Fd targets from Homo sapiens and S. pombe demonstrated that the identity

77 The repository (currently available for Homo sapiens and Saccharomyces cerevisiae) and computati

78 cluster transfer from ISU to apo Fd for both Homo sapiens and Schizosaccharomyces pombe proteins, and

79 The origin of anatomically modern Homo sapiens and the fate of Neanderthals have been fund

80 a melanogaster, a complex genome assembly of Homo sapiens and the low coverage Sanger sequence assemb

81 divergent mammalian lineages represented by Homo sapiens and the marsupial, Monodelphis domestica.

82 alpha4 (GLRA4) subunits were found in human (Homo sapiens) and guinea pig (Cavia porcellus) tracheal

83 Previous research in humans (Homo sapiens) and in nonhuman animals suggests that male

84 homolog of the spliceosomal proteins TFP11 (Homo sapiens) and Ntr1p (Saccharomyces cerevisiae) invol

85 homolog of the nucleoporin NUP214 in human (Homo sapiens) and Nup159 in yeast (Saccharomyces cerevis

86 productive condition, the findings in human (Homo sapiens) and other species may reflect similar proc

87 e of the representation that mediates human (Homo sapiens) and rat (Rattus norvegicus) movement chara

88 e differentially expressed during the human (Homo sapiens) and/or fruitfly (Drosophila melanogaster)

89 pared adults (Homo sapiens), young children (Homo sapiens), and adult tamarins (Saguinus oedipus) whi

90 ntified only in Yarrowia lipolytica, humans (Homo sapiens), and Arabidopsis (Arabidopsis thaliana).

91 dopsis thaliana, rice (Oryza sativa), human (Homo sapiens), and mouse (Mus musculus), we found that t

92 rolinensis), goat (Capra hircus), and human (Homo sapiens);and the MWS pigments of cave fish, gecko (

93 myces cerevisiae, Caenorhabditis elegans and Homo sapiens, and found that about 2-10% of proteins in

94 erved in M. tuberculosis, Rattus norvegicus, Homo sapiens, and Mus musculus.

95 scherichia coli, Drosophila melanogaster and Homo sapiens annotations and real gene expression data e

96 Humans (Homo sapiens) anticipate the consequences of their forth

97 patterns of genetic influences on behavior, Homo sapiens appears to be typical of other animal speci

98 roximately 80%) is much greater than that of Homo sapiens (approximately 59%); consequently, codon us

99 l repeats found using PILER are reported for Homo sapiens, Arabidopsis thalania and Drosophila melano

100 collects data on >6000 bitopic proteins from Homo sapiens, Arabidopsis thaliana, Dictyostelium discoi

101 obacter pylori, Saccharomyces cerevisiae and Homo sapiens are codon usage paradigms that can be bette

102 aneous de novo loss-of-function mutations in Homo sapiens are due to nucleotide substitutions within

103 Homo sapiens are genetically diverse, but dramatic demog

104 ears that can be unequivocally attributed to Homo sapiens are lacking.

105 Candida albicans and GlcNAc kinase NAGK from Homo sapiens, are required for rescue in this context.

106 enetic and anatomical evidence suggests that Homo sapiens arose in Africa between 200 and 100 thousan

107 led to a re-evaluation of the conception of Homo sapiens as the exclusive manufacturer of specialise

108 r Palaeolithic contexts favoured the view of Homo sapiens as the only species of the genus Homo capab

109 If these artifacts were made by Homo sapiens, as has been suggested, then our age indica

110 le location, by a hominin species other than Homo sapiens, at an as-yet unknown date.

111 Overexpression of BCL2 (Homo sapiens B-cell chronic lymphocytic leukemia/lymphom

112 aliana B-ZIP domains are homologous with any Homo sapiens B-ZIP domains.

113 Pigeons (Columba livia) and humans (Homo sapiens) both showed response time facilitation at

114 The target ODNs specific to Homo sapiens Breast and ovarian cancer cells were detect

115 s 2 enzymes, those from Escherichia coli and Homo sapiens, by determining kinetic isotope effects on

116 r the best ensemble predictors available for Homo sapiens, Caenorhabditis elegans and Arabidopsis tha

117 ped for predicting nucleosome positioning in Homo sapiens, Caenorhabditis elegans and Drosophila mela

118 he genome and transcriptome sequence data of Homo sapiens, Caenorhabditis elegans and Schizosaccharom

119 gree of mRNA up-regulation was observed in a Homo sapiens calpain-like protease.

120 the large, metabolically expensive brains of Homo sapiens can be energetically afforded.

121 Metazoans (Homo sapiens, Ceanorhabditis elegans and Drosophila mela

122 get by yeast-two-hybrid screening using both Homo sapiens centrin 2 (Hscen2) and Chlamydomonas reinha

123 t are located on the X-chromosomes of human (Homo sapiens), chimpanzee (Pan troglodytes), mouse (Mus

124 Humans (Homo sapiens), chimpanzees (Pan troglodytes), and rhesus

125 Homo sapiens chromosome 17 (HSA17) has two juxtaposed HO

126 howed that the two alpha satellite arrays of Homo sapiens Chromosome 17 (HSA17), D17Z1 and D17Z1-B, b

127 rliest fossil attributed to a modern form of Homo sapiens comes from eastern Africa and is approximat

128 bditis elegans, Drosophila melanogaster, and Homo sapiens completed and others to be finished in the

129 stion of whether the ancestors of all modern Homo sapiens comprised a single African population or an

130 ssue is of particular relevance to humans as Homo sapiens contains the active L1 Ta1 subfamily of the

131 unctions, we solved the crystal structure of Homo sapiens COQ9 at 2.4 A.

132 rall, among-population differences in extant Homo sapiens cranial morphology are proportional to amon

133 For example, GTRAC is able to compress a Homo sapiens dataset containing 1092 samples in 1.1 GB (

134 tebrates, ranging from Xenopus tropicalis to Homo sapiens, demonstrating that there is strong selecti

135 In contrast to our Homo sapiens-derived genes, the microbiome is much more

136 we hypothesized that sex of the human child (Homo sapiens), differences in physical activity, and tim

137 nd around three times longer than the modern Homo sapiens divergence times.

138 Here we show that the Homo sapiens DNA strand exchange protein, HsRad51, shows

139 RefSeq sequences for Homo sapiens, Drosophila melanogaster, and Caenorhabditi

140 hich the entire genomes have been sequenced: Homo sapiens, Drosophila melanogaster, Caenorhabditis el

141 d model organisms: Saccharomyces cerevisiae, Homo sapiens, Drosophila melanogaster, Caenorhabditis el

142 The activities of Dnmt2 enzymes from Homo sapiens, Drosophila melanogaster, Schizosaccharomyc

143 currently available for three model genomes (Homo sapiens, E. coli and baker's yeast), and the projec

144 uding foci of the essential crossover factor Homo sapiens enhancer of invasion 10 (Hei10), occur at h

145 ignatures of both Mus musculus (stromal) and Homo sapiens (epithelial) tissue origins.

146 Mutations in human (Homo sapiens) ETHYLMALONIC ENCEPHALOPATHY PROTEIN1 (ETHE

147 s have represented only approximately 10% of Homo sapiens' existence.

148 present the crystal structure of full-length Homo sapiens fascin-1, and examine its packing, conforma

149 ic (Streptomyces coelicolor) and eukaryotic (Homo sapiens) FGEs contain a copper cofactor.

150 , which includes: Danio rerio zFKHR (foxo5), Homo sapiens FKHR-L1 (FoxO3a) and Mus musculus FKHR2 (Fo

151 of retroduplication-derived genes in human (Homo sapiens), fly (Drosophila melanogaster), rice (Oryz

152 mistry (Escherichia coli for prokaryotes and Homo sapiens for eukaryotes).

153 Contemporary adult and juvenile Homo sapiens fossil crania manifest bone modifications i

154 The discovery of anatomically modern Homo sapiens fossils at Herto, Ethiopia, changes this.

155 ssil evidence points to an African origin of Homo sapiens from a group called either H. heidelbergens

156 tion ("the speciation event") that separated Homo sapiens from a prior hominid species.

157 cause medicine pertains to a single species, Homo sapiens, functional human variation often involves

158 Alignment of rpS5/rpS7 from metazoans (Homo sapiens), fungi (Saccharomyces cerevisiae) and bact

159 There were 252 reported Homo sapiens genes containing the repeats (AC)n, (GT)n,

160 The phenotype of the present day Homo sapiens genome is much different from that of our a

161 We first tested our method on Homo sapiens genome; using a very few known human miRNAs

162 latta, Pan troglodytes, Gorilla gorilla, and Homo sapiens haplotypes using transient dual-luciferase

163 Homo sapiens harbor two distinct, medically significant

164 cal evidence now demonstrates, however, that Homo sapiens has actively manipulated tropical forest ec

165 periments of chemically denatured cpn10 from Homo sapiens (hmcpn10) and Aquifex aeolicus (Aacpn10) we

166 /CenH3/H4 complexes have been determined for Homo sapiens (Hs) and the budding yeasts Saccharomyces c

167 P. falciparum (Pf) and Homo sapiens (Hs) OPRTs are characterized by highly diss

168 ) and compared them to the I-2 proteins from Homo sapiens (Hs), Saccharomyces cerevisiae (GLC8), and

169 t we describe the isolation of the wild-type Homo sapiens (Hs)ORC and variants containing a Walker A

170 The experiments described here show that Homo sapiens (Hs)Rad52 and yeast Rad52 proteins promote

171 mutations in the DNA helicase RecQ3 [a.k.a. Homo sapiens (hs)WRN].

172 the subcellular localizations of proteins in Homo sapiens (HS, human) and Arabidopsis thaliana (AT, t

173 homocysteine (AdoHcy) hydrolases (SAHH) from Homo sapiens (Hs-SAHH) and from the parasite Trypanosoma

174 ion of the cofactor NAD+ from the enzymes of Homo sapiens (Hs-SAHH) and Trypanosoma cruzi (Tc-SAHH) a

175 e sequence-based map of human chromosome 17 [Homo sapiens, (HSA) 17] were found to be highly consiste

176 cherichia coli and compared to the PNPs from Homo sapiens (HsPNP) and Plasmodium falciparum (PfPNP).

177 migratoria (LmRXR), Mus musculus (MmRXR) or Homo sapiens (HsRXR) to the VP16 activation domain.

178 deacetylase, using recombinant enzymes from Homo sapiens (human) and Danio rerio (zebrafish).

179 hree extant species and two subgenera, Homo (Homo) sapiens (humankind), Homo (Pan) troglodytes (commo

180 , MMP-3, interferon induced-15 [IFI-15], and Homo sapiens hypothetical protein MGC5566) and two downr

181 ackdrop to the evolution and spread of early Homo sapiens in East Africa is known mainly from isolate

182 The earliest credible evidence of Homo sapiens in Europe is an archaeological proxy in the

183 representing four continental populations of Homo sapiens in the context of four ape species.

184 ta, there is no unanimity over how to define Homo sapiens in the fossil record.

185 gia guttata, a songbird species) and humans (Homo sapiens) in AP tests that required classification o

186 graphic and adaptive history of our species, Homo sapiens, including its interbreeding with other hom

187 explains many zoologically unusual traits in Homo sapiens, including our complex toolkit, wide range

188 Many features associated with Homo sapiens, including our large linear bodies, elongat

189 g a wide range of species from caiman to the Homo sapiens, indicating that this glycosaminoglycan att

190 y that the resequencing of a large number of Homo sapiens individuals might be used to annotate the h

191 yeast (Saccharomyces cerevisiae) and human (Homo sapiens), intermediate cleavage peptidase55 (ICP55)

192 Homo sapiens is also the only species that has developed

193 The postcranial skeleton of modern Homo sapiens is relatively gracile compared with other h

194 Among animals, Homo sapiens is unique in its capacity for widespread co

195 Our species, Homo sapiens, is highly autapomorphic (uniquely derived)

196 One AS, designated Homo sapiens keratin 7 (KRT7-AS), was selected due to it

197 e syndrome 1 (Nibrin), ribosomal protein L4, Homo sapiens KIAA0419 gene product, eukaryotic initiatio

198 The sequence of the Homo sapiens Krr1 GXXGlp is evolutionarily conserved (16

199 Homo sapiens kynureninase is a pyridoxal-5'-phosphate de

200 We demonstrate that Homo sapiens laforin complements the sex4 phenotype and

201 cited as a critical step in the evolution of Homo sapiens, language, and human-level cognition.

202 teristics and perceptual studies with human (Homo sapiens) listeners.

203 xplain the telomere length differences among Homo sapiens, M. musculus, and M. spretus.

204 uggestive association on chromosome 6 at the Homo sapiens mediator complex subunit 23 gene/arginase I

205 233 identifications for 81 gel patterns for Homo sapiens, Methanococcus jannaschii, Pyro coccus furi

206 to-I RNA editing sites identified in humans (Homo sapiens), mice (Mus musculus) and flies (Drosophila

207 Human (Homo sapiens) micro-RNAs (hsa-miRNAs) regulate virus and

208 Homo sapiens mitochondrial transcription factor B1 (h-mt

209 evisiae, Caenorhabditis elegans, Drosophila, Homo sapiens, Mus musculus and Arabidopsis species as we

210 romoter, sharing 80% sequence identity among Homo sapiens, Mus musculus and Rattus norvegicus.

211 elegans, Drosophila melanogaster, G. gallus, Homo sapiens, Mus musculus or Rattus norvegicus and iden

212 actor genes, comparing methylated genomes of Homo sapiens, Mus musculus, and Danio rerio with nonmeth

213 ognizable doublets in the following genomes: Homo sapiens, Mus musculus, Arabidopsis thaliana, and Ca

214 d from specific comparison of eight species: Homo sapiens, Mus musculus, Arabidopsis thaliana, Caenor

215 ein domains from seven eukaryotic organisms (Homo sapiens, Mus musculus, Bos taurus, Rattus norvegicu

216 ein domain homology in the transcriptomes of Homo sapiens, Mus musculus, Drosophila melanogaster and

217 RNA22-GUI is currently available for Homo sapiens, Mus musculus, Drosophila melanogaster and

218 alyzed aspects of the information content of Homo sapiens, Mus musculus, Drosophila melanogaster, Cae

219 alf a million splice sites from five species-Homo sapiens, Mus musculus, Drosophila melanogaster, Cae

220 six entirely sequenced eukaryotic proteomes (Homo sapiens, Mus musculus, Drosophila melanogaster, Cae

221 liana, Drosophila melanogaster, Danio rerio, Homo sapiens, Mus musculus, Oryza sativa, Solanum lycope

222 ous proteins from nine eukaryotic organisms: Homo sapiens, Mus musculus, Rattus norvegicus, Arabidops

223 hree years in the seven supported organisms (Homo sapiens, Mus musculus, Rattus norvegicus, Drosophil

224 IMP currently supports seven organisms (Homo sapiens, Mus musculus, Rattus novegicus, Drosophila

225 f twelve phylogenetically diverse organisms: Homo sapiens, Mus musculus, Takifugu rubripes, Ciona int

226 previous methods (examples are provided for Homo sapiens/Mus musculus and Plasmodium falciparum/Plas

227 liaris; n=19) and 4- to 6-year-old children (Homo sapiens; n=24) were given a task wherein a desirabl

228 Unique compared with recent and prehistoric Homo sapiens, Neandertal humeri are characterised by a p

229 We show that HsNHA2 (Homo sapiens NHA2) resides on the plasma membrane and, i

230 These inhibitors are selective against Homo sapiens NMT1 (HsNMT), have excellent ligand efficie

231 drogenase (Saccharomyces cerevisiae--Erg26p, Homo sapiens--NSDHL (NAD(P) dependent steroid dehydrogen

232 n which the emergence of anatomically modern Homo sapiens occurred has proved difficult, particularly

233 4-, 7-, and 10-year-old children and adults (Homo sapiens) on a nonverbal serial-order task to respon

234 rhesus monkeys (Macaca mulatta) and humans (Homo sapiens) on adjacent pairs (e.g., AB, BC, CD, DE, E

235 sis than to the derived parabolic arcades of Homo sapiens or H. erectus.

236 corresponding regions of GGPP synthases from Homo sapiens or S. cerevisiae.

237 it has been hypothesized that the exodus of Homo sapiens out of Africa and into Eurasia between ~50-

238 gued to result from the expansion of archaic Homo sapiens out of Africa.

239 seums Lukenya Hill Hominid 1 (KNM-LH 1) is a Homo sapiens partial calvaria from site GvJm-22 at Luken

240 Eighty adult human (Homo sapiens) participants were presented with a task pr

241 additional perspective to the paradox of why Homo sapiens, particularly agriculturalists, appear to b

242 In this work, the cDNA encoding Homo sapiens PDF (HsPDF) has been cloned and a truncated

243 scribe here a new human peptide deformylase (Homo sapiens PDF, or HsPDF) that is localized to the mit

244 rial phytochrome with the effector module of Homo sapiens phosphodiesterase 2A.

245 Homo sapiens phylogeography begins with the species' ori

246 As in yeast and humans (Homo sapiens), plant U1-70K is coded by a single gene.

247 We apply our method to the Homo sapiens-Plasmodium falciparum host-pathogen system.

248 the Levant shortly before Upper Palaeolithic Homo sapiens populated the region.

249 r, Caenorhabditis elegans, Mus musculus, and Homo sapiens PPI networks.

250 inum proteins were evolutionary related with Homo sapiens proteins to sort out the non-human homologs

251 report the crystallographic structure of the Homo sapiens Pth2 at a 2.0-A resolution as well as its c

252 LB1 represents a pathological microcephalic Homo sapiens rather than a new species, (i.e., H. flores

253 s propose that it represents a microcephalic Homo sapiens rather than a new species.

254 ctions in the two eukaryotic reconstructions Homo sapiens Recon 1 and Yeast 5 are specified as irreve

255 Specifically, we first divided each Homo sapiens Refseq-derived gene's spliced nucleotide se

256 Homo sapiens' relationship with the tropical rainforests

257 e origins of these developmental patterns in Homo sapiens remain unknown.

258 1 renin RT-PCR product is 100% homologous to Homo sapiens renin.

259 herichia coli, Saccharomyces cerevisiae, and Homo sapiens, respectively, and the conclusions are cons

260 herichia coli, Saccharomyces cerevisiae, and Homo sapiens, respectively.

261 Extinct hominins, including pre-Holocene Homo sapiens, retain the high levels seen in nonhuman pr

262 y and tested functional robustness of human (Homo sapiens), rice (Oryza sativa) and budding yeast (Sa

263 charomyces pombe Slx8-Rfp (founding member), Homo sapiens RNF4, Dictyostelium discoideum MIP1 and Sac

264 ls, and database search tools inferring from Homo sapiens, Saccharomyces cerevisiae, and Arabidopsis

265 Analysis of the completed genomes of Homo sapiens, Saccharomyces cerevisiae, Caenorhabditis e

266 nary origin of 'anatomically modern humans' (Homo sapiens sapiens).

267 herichia coli, Saccharomyces cerevisiae, and Homo sapiens sequences reveals how co- and post-translat

268 The basic physiology and morphology of Homo sapiens sets boundaries to our eating habits, but w

269 ees' (Pan troglodytes) and human children's (Homo sapiens) skills at imitation with a 2-action test o

270 cessful minimax strategy employed by ancient Homo sapiens subpopulations in a one-player game against

271 Using a BLAST search against the Homo sapiens subset of the SWISS-PROT and TrEMBL databas

272 lies within the timeframe dating the dawn of Homo sapiens, suggesting that P. falciparum may have und

273 otes crassus, Schizosaccharomyces pombe, and Homo sapiens, suggesting that this protein is widely dis

274 otes crassus, Schizosaccharomyces pombe, and Homo sapiens suggests that related proteins are widely d

275 on of a regulatory network of brain tumor in Homo sapiens takes 12 days with MEDUSA, FastMEDUSA obtai

276 irectly to the N-terminal 163 amino acids of Homo sapiens TATA-binding protein-associated factor-1 (h

277 lestone projects such as Escherichia coli or Homo sapiens, teams of scientists were employed to manua

278 the latter including the rTS beta protein in Homo sapiens that has been implicated in regulating thym

279 urces (Bradyrhizobium japonicum USDA 110 and Homo sapiens) that had available X-ray structures were p

280 irginiana), mouse (Mus musculus), and human (Homo sapiens) to determine if their divergent imprint st

281 e types of sulfate activating complex (SAC) [Homo sapiens (type I); Mycobacterium tuberculosis (type

282 ficking in organisms ranging from archaea to Homo sapiens under both normal and stressed cellular con

283 of multiple organisms, including Eukaryota, Homo sapiens, Viridiplantae, Gram-positive Bacteria, Gra

284 and its evolution in the lineage leading to Homo sapiens was driven by strong positive selection.

285 ich objects were used by preschool children (Homo sapiens) was examined by directly observing them ac

286 r primary curational domain is pathways from Homo sapiens, we regularly create electronic projections

287 ncode proteins in Caenorhabditis elegans and Homo sapiens, we show that introns in highly expressed g

288 to the 1q21.1 region during the evolution of Homo sapiens; we found this locus to be deleted or dupli

289 bonucleases from cow (Bos taurus) and human (Homo sapiens) were produced in Escherichia coli and puri

290 Two groups of human participants (Homo sapiens) were tested for cognitive mapping using pr

291 rst enzyme of the biopterin (BH4) pathway in Homo sapiens, where it is encoded by a homologous folE g

292 r Neanderthals a subspecies or population of Homo sapiens, which contributed significantly to the evo

293 strong adaptive evolution in the descent of Homo sapiens, which is consistent with its putative role

294 chimpanzees (Pan troglodytes) and children (Homo sapiens) who observed a model's errors and successe

295 ariable experiment in the species closest to Homo sapiens with high intakes of calcium and potassium

296 quences were shown to be conserved comparing Homo sapiens with the marsupial, Monodelphis domestica.

297 gene shows sequence similarity to the human (Homo sapiens) XPD and yeast (Saccharomyces cerevisiae) R

298 entirely sequenced organisms, namely human (Homo sapiens), yeast (Saccharomyces cerevisiae), and wee

299 Oryza sativa], soybean [Glycine max], human [Homo sapiens], yeast [Saccharomyces cerevisiae], fruit f

300 This study compared adults (Homo sapiens), young children (Homo sapiens), and adult