ライフサイエンスコーパス: Homo sapiens

1 s) in comparison to early and recent humans (Homo sapiens).

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

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

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

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

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

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

8 Swartkrans, Homo neanderthalensis, and early Homo sapiens.

9 high-predicted structural conservation with Homo sapiens.

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

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

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

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

14 rsially identified as either Neanderthals or Homo sapiens.

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

16 epresent a pathological microcephalic modern Homo sapiens.

17 Escherichia coli, Pyrococcus horikoshii, and Homo sapiens.

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

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

20 ces cerevisiae, Drosophila melanogaster, and Homo sapiens.

21 n data from both Drosophila melanogaster and Homo sapiens.

22 o congenital and acquired channelopathies in Homo sapiens.

23 can cause congenital and acquired disease in Homo sapiens.

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

25 positive selection in the lineage leading to Homo sapiens.

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

27 eoglobus fulgidus, Arabidopsis thaliana, and Homo sapiens.

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

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

30 the striate cortex (V1) of normally sighted Homo sapiens.

31 e microRNAs have been publicly described for Homo sapiens.

32 s long before the regional arrival of modern Homo sapiens.

33 ulus and interneuron developmental states in Homo sapiens.

34 mbe, Arabidopsis thaliana, Mus musculus, and Homo sapiens.

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

36 hat it also confers reproductive benefits in Homo sapiens.

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

38 enorhabditis elegans, Loxodonta africana and Homo sapiens.

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

40 omical dissections and compare the data with Homo sapiens.

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

42 e contemporaneous hominin lineages (that is, Homo sapiens(8,9), H. heidelbergensis/H. rhodesiensis an

43 y, inner-city male and female youth (species Homo sapiens) 9-12 years of age followed by the Columbia

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

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

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

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

48 rom extinction events, and (iii) how humans (Homo sapiens) affected interactions among non-human spec

49 Homo erectus was more dimorphic than modern Homo sapiens, although less so than highly dimorphic ape

50 The Homo sapiens and Arabidopsis thaliana genomes are believ

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

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

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

54 Observations in Homo sapiens and Drosophila melanogaster have revealed a

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

56 Africa was the birth-place of Homo sapiens and has the earliest evidence for symbolic

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

58 w into presumed early symbolic traditions of Homo sapiens and how they evolved over a period of more

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

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

61 olog conjecture in two pairs of species: (i) Homo sapiens and Mus musculus and (ii) Saccharomyces cer

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

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

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

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

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

67 data set and from a comparison of tissues in Homo sapiens and Mus musculus.

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

69 The Homo sapiens and other eukaryotic constitutive kynurenin

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

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

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

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

74 sues and Yeast from two different organisms (Homo Sapiens and Saccharomyces cerevisiae, respectively)

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

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

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

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

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

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

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

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

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

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

85 , namely, Escherichia coli, Mus musculus and Homo sapiens, and compared using randomized 10-fold cros

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

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

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

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

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

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

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

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

94 Homo sapiens are genetically diverse, but dramatic demog

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

96 during the Middle Pleistocene epoch, such as Homo sapiens, are highly debated(1-5).

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

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

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

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

101 suggesting that it is likely the product of Homo sapiens as they dispersed eastward out of Africa.

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

103 RNAs, 28 352 targets and 16 833 pathways for Homo sapiens, as well as interactions of 1978 miRNAs, 24

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

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

106 lution trace-element geochemical analysis of Homo sapiens (both modern and fossil), Homo neanderthale

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

108 i, Drosophila melanogaster, Mus musculus and Homo sapiens bound G4 structures in BmPOUM2 and other ge

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

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

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

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

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

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

115 Metazoans (Homo sapiens, Ceanorhabditis elegans and Drosophila mela

116 ), worm (Caenorhabditis elegans), and human (Homo sapiens) cells exhibit an enrichment of 5' monophos

117 anded RNA-binding activity of EBP1 in human (Homo sapiens) cells, the overwhelming majority of EBP1 i

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

119 o-electron microscopy (cryo-EM) structure of Homo sapiens CHD4 engaged with a nucleosome core particl

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

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

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

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

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

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

126 how that the terminus of an rRNA tentacle of Homo sapiens contains 10 tandem G-tracts that form highl

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

142 ty is expected to be highest in Africa where Homo sapiens evolved and has maintained a large populati

143 ow body shape of anatomically modern humans (Homo sapiens) evolved via changes in the thorax, pelvis

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

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

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

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

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

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

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

151 In human (Homo sapiens), fruit fly (Drosophila melanogaster), and

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

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

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

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

156 Human (Homo sapiens) glioma tumor-suppressor candidate region g

157 Testing on Nanopore reads of Homo sapiens (H. sapiens), Escherichia coli (E. coli) an

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

159 Homo sapiens harbor two distinct, medically significant

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

161 Using only the information that Homo sapiens has existed at least 200,000 years, we conc

162 e developmental programme of pluripotency in Homo sapiens Here, we confirm that naive PSCs do not res

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

164 Body odour is a characteristic trait of Homo sapiens, however its role in human behaviour and ev

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

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

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

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

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

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

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

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

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

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

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

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

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

178 edges and the second is a network of PPI in Homo sapiens (Human) with 20,644 nodes and 241,008 edges

179 entifier conversion and data integration for Homo sapiens (human), Mus musculus (mouse), Rattus norve

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

181 are (less than 3.5% occurrence) in non-Asian Homo sapiens In contrast, its presence in Asian-derived

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

183 tion of the overlap between Neanderthals and Homo sapiens in Eurasia.

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

185 t the earliest arrival of Upper Palaeolithic Homo sapiens in Europe.

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

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

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

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

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

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

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

193 Homo sapiens is also the only species that has developed

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

195 s, but the extent of structural variation in Homo sapiens is still unclear.

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

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

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

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

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

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

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

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

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

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

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 yeast (Saccharomyces cerevisiae) and human (Homo sapiens) mitochondria, Oxidase assembly protein1 (O

209 Homo sapiens mitochondrial transcription factor B1 (h-mt

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

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

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

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

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

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

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

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

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

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

220 alf a million splice sites from five species-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 f twelve phylogenetically diverse organisms: Homo sapiens, Mus musculus, Takifugu rubripes, Ciona int

225 nalysis (XMAn)' database is a compilation of Homo sapiens mutated peptides in FASTA format, that was

226 Here we show that the Homo sapiens NAD(+) synthetase (hsNadE) lacks substrate

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

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

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

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

231 ia coli RppH, Legionella pneumophila Sde and Homo sapiens NudT16 (HsNudT16).

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

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

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

235 % sequence identity to the S. cerevisiae and Homo sapiens orthologs of Usb1, respectively.

236 rossroads for understanding the dispersal of Homo sapiens out of Africa and into Asia and Oceania.

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

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

244 Homo sapiens phylogeography begins with the species' ori

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

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

247 an groups were present at this site-an early Homo sapiens population, followed by a Neanderthal popul

248 sorption of local Neanderthal populations by Homo sapiens populations of African origin(1).

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 a minimally redundant, canonical database of Homo sapiens proteins.

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 Defining the distinctive capacities of Homo sapiens relative to other hominins is a major focus

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

259 The origin of Homo sapiens remains a matter of debate.

260 1 renin RT-PCR product is 100% homologous to Homo sapiens renin.

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

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

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

264 icular atlases have been created for humans (Homo sapiens), rhesus macaques (Macaca mulatta), and sev

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

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

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

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

269 bly black bear (Ursus americanus) and human (Homo sapiens sapiens), used in point manufacture.

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

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

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

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

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

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

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

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

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

279 mammals was part of the plastic behavior of Homo sapiens that allowed it to rapidly colonize a serie

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

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

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

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

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

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

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

287 anges that took place after the emergence of Homo sapiens We show converging evidence from paleoanthr

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

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

290 ns (e.g., violence or food shortage), modern Homo sapiens were equipped with the potential to rapidly

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

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

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

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

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

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

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

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