ライフサイエンスコーパス: sapiens

1 revisiae, C. elegans, D. melanogaster and H. sapiens).

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

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

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

5 comparison to early and recent humans (Homo sapiens).

6 sociated with newly discovered remains of H. sapiens.

7 ll-length protein-coding transcripts from H. sapiens.

8 networks between Epstein-Barr virus and Homo sapiens.

9 abditis elegans, Loxodonta africana and Homo sapiens.

10 phila, Gallus gallus, Mus musculus, and Homo sapiens.

11 le supports its unequivocal assignment to H. sapiens.

12 l dissections and compare the data with Homo sapiens.

13 ral interactions between Neanderthals and H. sapiens.

14 likely characteristic of pre-modern era Homo sapiens.

15 krans, Homo neanderthalensis, and early Homo sapiens.

16 -predicted structural conservation with Homo sapiens.

17 ound in all kingdoms of life, including Homo sapiens.

18 , for some loci, predates the origin of Homo sapiens.

19 PL (nucleotide binding protein-like) in Homo sapiens.

20 of FBA models for Escherichia coli and Homo sapiens.

21 o be about 11 % between S. cerevisiae and H. sapiens.

22 ly identified as either Neanderthals or Homo sapiens.

23 aenorhabditis elegans, Mus musculus and Homo Sapiens.

24 y a gradual, although erratic, decline in H. sapiens.

25 ent a pathological microcephalic modern Homo sapiens.

26 richia coli, Pyrococcus horikoshii, and Homo sapiens.

27 rs: H. antecessor, Sima de los Huesos and H. sapiens.

28 ntal differences between Neanderthals and H. sapiens.

29 ore ape-like Australopithecus species and H. sapiens.

30 parietal expansion than is the case for Homo sapiens.

31 thaliana, C. elegans, D. melanogaster and H. sapiens.

32 ccupation of Europe by Upper Palaeolithic H. sapiens.

33 cies as diverse as Escherichia Coli and Homo sapiens.

34 erevisiae, Drosophila melanogaster, and Homo sapiens.

35 a from both Drosophila melanogaster and Homo sapiens.

36 genital and acquired channelopathies in Homo sapiens.

37 e Atapuerca fossils resembled more recent H. sapiens.

38 y symbolic communication and cognition in H. sapiens.

39 in BmPOUM2 and other genes in B. mori and H. sapiens.

40 striate cortex (V1) of normally sighted Homo sapiens.

41 g before the regional arrival of modern Homo sapiens.

42 and interneuron developmental states in Homo sapiens.

43 roRNAs have been publicly described for Homo sapiens.

44 Arabidopsis thaliana, Mus musculus, and Homo sapiens.

45 human remains are the oldest reported for H. sapiens.

46 gion during this period-Neandertals and Homo sapiens.

47 t also confers reproductive benefits in Homo sapiens.

48 temporaneous hominin lineages (that is, Homo sapiens(8,9), H. heidelbergensis/H. rhodesiensis and Hom

49 ner-city male and female youth (species Homo sapiens) 9-12 years of age followed by the Columbia Cent

50 for ecosystem engineering exhibited by Homo sapiens A crucial outcome of such behaviors has been the

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

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

53 xtinction events, and (iii) how humans (Homo sapiens) affected interactions among non-human species.

54 erectus was more dimorphic than modern Homo sapiens, although less so than highly dimorphic apes, su

55 The Homo sapiens and Arabidopsis thaliana genomes are believed to

56 interaction in PRC2 core complexes from Homo sapiens and Chaetomium thermophilum, for which crystal s

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

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

59 o presumed early symbolic traditions of Homo sapiens and how they evolved over a period of more than

60 relative to the finished chromosomes of Homo sapiens and key model organisms generated by the Human G

61 roteomic screening, assign these finds to H. sapiens and link the expansion of Initial Upper Palaeoli

62 Expression of subunit c homologues from Homo sapiens and Manduca sexta, both species sensitive to ben

63 conjecture in two pairs of species: (i) Homo sapiens and Mus musculus and (ii) Saccharomyces cerevisi

64 evelopmental time information from both Homo sapiens and Mus musculus.

65 ns in more than a dozen cell types from Homo sapiens and Mus musculus.

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

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

68 to ~0.4 million years (Ma), during which H. sapiens and Neandertal dental growth characteristics may

69 ll within the era of speciation between Homo sapiens and Neanderthals/Denisovans and around three tim

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

71 sgA from Escherichia coli and Dim1 from Homo sapiens and Plasmodium falciparum have been determined.

72 years to discover that it was specific to H. sapiens and present in non-Africans 45,000 years ago.

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

74 y all telomerase RNAs, including those of H. sapiens and S. cerevisiae, share four conserved structur

75 riptional regulatory networks of E. coli, H. sapiens and S. cerevisiae.

76 and Yeast from two different organisms (Homo Sapiens and Saccharomyces cerevisiae, respectively) are

77 ion of boundaries of variability in early H. sapiens and the interpretation of individual fossils.

78 mated adult rib cage, for comparison with H. sapiens and the Kebara 2 Neanderthal.

79 anogaster, a complex genome assembly of Homo sapiens and the low coverage Sanger sequence assembly of

80 rgent mammalian lineages represented by Homo sapiens and the marsupial, Monodelphis domestica.

81 4 (GLRA4) subunits were found in human (Homo sapiens) and guinea pig (Cavia porcellus) tracheal smoot

82 Previous research in humans (Homo sapiens) and in nonhuman animals suggests that males hav

83 log of the spliceosomal proteins TFP11 (Homo sapiens) and Ntr1p (Saccharomyces cerevisiae) involved i

84 log of the nucleoporin NUP214 in human (Homo sapiens) and Nup159 in yeast (Saccharomyces cerevisiae),

85 the representation that mediates human (Homo sapiens) and rat (Rattus norvegicus) movement characteri

86 s thaliana, rice (Oryza sativa), human (Homo sapiens), and mouse (Mus musculus), we found that these

87 ely, Escherichia coli, Mus musculus and Homo sapiens, and compared using randomized 10-fold cross-val

88 cerevisiae, Caenorhabditis elegans and Homo sapiens, and found that about 2-10% of proteins in the g

89 ichia coli, Drosophila melanogaster and Homo sapiens annotations and real gene expression data extrac

90 Humans (Homo sapiens) anticipate the consequences of their forthcomin

91 Based on the available fossils, H. sapiens appears to have originated from the coalescence

92 cts data on >6000 bitopic proteins from Homo sapiens, Arabidopsis thaliana, Dictyostelium discoideum,

93 Homo sapiens are genetically diverse, but dramatic demographi

94 that can be unequivocally attributed to Homo sapiens are lacking.

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

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

97 c and anatomical evidence suggests that Homo sapiens arose in Africa between 200 and 100 thousand yea

98 to a re-evaluation of the conception of Homo sapiens as the exclusive manufacturer of specialised bon

99 aeolithic contexts favoured the view of Homo sapiens as the only species of the genus Homo capable of

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

101 If these artifacts were made by Homo sapiens, as has been suggested, then our age indicates t

102 28 352 targets and 16 833 pathways for Homo sapiens, as well as interactions of 1978 miRNAs, 24 898

103 proximately 20% for the C.intestinalis and H.sapiens assemblies, which is significant, considering th

104 cation, 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/lymphoma 2)

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

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

108 osophila melanogaster, Mus musculus and Homo sapiens bound G4 structures in BmPOUM2 and other genes i

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

110 best ensemble predictors available for Homo sapiens, Caenorhabditis elegans and Arabidopsis thaliana

111 or predicting nucleosome positioning in Homo sapiens, Caenorhabditis elegans and Drosophila melanogas

112 arge, metabolically expensive brains of Homo sapiens can be energetically afforded.

113 e to H. erectus, H. neanderthalensis, and H. sapiens cannot be explained by the rate of craniodental

114 protein levels at different stages of the H. sapiens cell cycle.

115 rm (Caenorhabditis elegans), and human (Homo sapiens) cells exhibit an enrichment of 5' monophosphate

116 RNA-binding activity of EBP1 in human (Homo sapiens) cells, the overwhelming majority of EBP1 intera

117 y yeast-two-hybrid screening using both Homo sapiens centrin 2 (Hscen2) and Chlamydomonas reinhardtii

118 ctron microscopy (cryo-EM) structure of Homo sapiens CHD4 engaged with a nucleosome core particle in

119 located on the X-chromosomes of human (Homo sapiens), chimpanzee (Pan troglodytes), mouse (Mus muscu

120 Humans (Homo sapiens), chimpanzees (Pan troglodytes), and rhesus monk

121 Homo sapiens chromosome 17 (HSA17) has two juxtaposed HOR arr

122 that the two alpha satellite arrays of Homo sapiens Chromosome 17 (HSA17), D17Z1 and D17Z1-B, behave

123 n site that documents early stages of the H. sapiens clade in which key features of modern morphology

124 t fossil attributed to a modern form of Homo sapiens comes from eastern Africa and is approximately 1

125 hat the terminus of an rRNA tentacle of Homo sapiens contains 10 tandem G-tracts that form highly sta

126 ons, we solved the crystal structure of Homo sapiens COQ9 at 2.4 A.

127 etworks of five organisms, S. cerevisiae, H. sapiens, D. melanogaster, A. thaliana, and E. coli, and

128 l genomics data sets for three organisms--H. sapiens, D. melanogaster, and S. cerevisiae--and show th

129 or example, GTRAC is able to compress a Homo sapiens dataset containing 1092 samples in 1.1 GB (compr

130 nstrating that coral AdTNF1 activates the H. sapiens death receptor pathway.

131 on networks of E. coli, S. cerevisiae and H. sapiens, defined as subsets of proteins whereby each rem

132 tes, ranging from Xenopus tropicalis to Homo sapiens, demonstrating that there is strong selective pr

133 od agreement with dates for the origin of H. sapiens derived from modern molecular diversity).

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

135 bly the issue of whether Neanderthals and H. sapiens differ.

136 pothesized that sex of the human child (Homo sapiens), differences in physical activity, and time of

137 ound three times longer than the modern Homo sapiens divergence times.

138 el organisms: Saccharomyces cerevisiae, Homo sapiens, Drosophila melanogaster, Caenorhabditis elegans

139 The activities of Dnmt2 enzymes from Homo sapiens, Drosophila melanogaster, Schizosaccharomyces po

140 Here we report a 15,000 years-old H. sapiens (Dushan 1) in South China with unusual mosaic fe

141 ntly available for three model genomes (Homo sapiens, E. coli and baker's yeast), and the project wil

142 foci of the essential crossover factor Homo sapiens enhancer of invasion 10 (Hei10), occur at half t

143 ures of both Mus musculus (stromal) and Homo sapiens (epithelial) tissue origins.

144 esting on Nanopore reads of Homo sapiens (H. sapiens), Escherichia coli (E. coli) and pUC19 shows tha

145 Mutations in human (Homo sapiens) ETHYLMALONIC ENCEPHALOPATHY PROTEIN1 (ETHE1) re

146 expected to be highest in Africa where Homo sapiens evolved and has maintained a large population fo

147 dy shape of anatomically modern humans (Homo sapiens) evolved via changes in the thorax, pelvis and l

148 e represented only approximately 10% of Homo sapiens' existence.

149 urasia, Australia and the Americas, early H. sapiens experienced massive time-varying climate and sea

150 nt the crystal structure of full-length Homo sapiens fascin-1, and examine its packing, conformationa

151 treptomyces coelicolor) and eukaryotic (Homo sapiens) FGEs contain a copper cofactor.

152 p that is relevant for understanding when H. sapiens first appeared in southern Asia.

153 etroduplication-derived genes in human (Homo sapiens), fly (Drosophila melanogaster), rice (Oryza sat

154 y (Escherichia coli for prokaryotes and Homo sapiens for eukaryotes).

155 blage, now associated with directly dated H. sapiens fossils at this site, securely dates to 45,820-4

156 evidence points to an African origin of Homo sapiens from a group called either H. heidelbergensis or

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

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

159 medicine pertains to a single species, Homo sapiens, functional human variation often involves seque

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

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

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

163 Human (Homo sapiens) glioma tumor-suppressor candidate region gene2

164 Testing on Nanopore reads of Homo sapiens (H. sapiens), Escherichia coli (E. coli) and pUC

165 , Pan troglodytes, Gorilla gorilla, and Homo sapiens haplotypes using transient dual-luciferase trans

166 Homo sapiens harbor two distinct, medically significant speci

167 vidence now demonstrates, however, that Homo sapiens has actively manipulated tropical forest ecologi

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

169 rlier hominin taxa, both Neanderthals and H. sapiens have extended the duration of dental development

170 elopmental programme of pluripotency in Homo sapiens Here, we confirm that naive PSCs do not respond

171 ng well after the origin and dispersal of H. sapiens However, the presence of a 3-rooted lower second

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

173 3/H4 complexes have been determined for Homo sapiens (Hs) and the budding yeasts Saccharomyces cerevi

174 P. falciparum (Pf) and Homo sapiens (Hs) OPRTs are characterized by highly dissociat

175 ubcellular localizations of proteins in Homo sapiens (HS, human) and Arabidopsis thaliana (AT, thale

176 ysteine (AdoHcy) hydrolases (SAHH) from Homo sapiens (Hs-SAHH) and from the parasite Trypanosoma cruz

177 f the cofactor NAD+ from the enzymes of Homo sapiens (Hs-SAHH) and Trypanosoma cruzi (Tc-SAHH) are qu

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

179 etylase, using recombinant enzymes from Homo sapiens (human) and Danio rerio (zebrafish).

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

181 ier conversion and data integration for Homo sapiens (human), Mus musculus (mouse), Rattus norvegicus

182 questions about the mode of evolution of H. sapiens in Africa and whether H. heidelbergensis/H. rhod

183 model simulates the overall dispersal of H. sapiens in close agreement with archaeological and fossi

184 less than 3.5% occurrence) in non-Asian Homo sapiens In contrast, its presence in Asian-derived popul

185 op to the evolution and spread of early Homo sapiens in East Africa is known mainly from isolated out

186 of the overlap between Neanderthals and Homo sapiens in Eurasia.

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

188 earliest arrival of Upper Palaeolithic Homo sapiens in Europe.

189 MH1 midface superficially resembles some H. sapiens in the distribution of remodeling fields.

190 ce coincides with the first occurrence of H. sapiens in the Eurasian steppes, establishes an essentia

191 ic and adaptive history of our species, Homo sapiens, including its interbreeding with other hominins

192 ins many zoologically unusual traits in Homo sapiens, including our complex toolkit, wide range of ha

193 Many features associated with Homo sapiens, including our large linear bodies, elongated hi

194 t (Saccharomyces cerevisiae) and human (Homo sapiens), intermediate cleavage peptidase55 (ICP55) play

195 based on the arrival of multiple waves of H. sapiens into Europe coming into contact with declining N

196 reasons for the relatively late entry of H. sapiens into Europe.

197 aeolithic technologies with the spread of H. sapiens into the mid-latitudes of Eurasia before 45 thou

198 tionary processes behind the emergence of H. sapiens involved the whole African continent.

199 Homo sapiens is also the only species that has developed form

200 The postcranial skeleton of modern Homo sapiens is relatively gracile compared with other homino

201 t the extent of structural variation in Homo sapiens is still unclear.

202 Among animals, Homo sapiens is unique in its capacity for widespread coopera

203 outh Siberia) but where and when they met H. sapiens is yet to be determined.

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

205 In contrast, Middle Paleolithic H. sapiens juveniles show greater similarity to recent huma

206 One AS, designated Homo sapiens keratin 7 (KRT7-AS), was selected due to its mar

207 The sequence of the Homo sapiens Krr1 GXXGlp is evolutionarily conserved (165KRRQ

208 Homo sapiens kynureninase is a pyridoxal-5'-phosphate depende

209 We demonstrate that Homo sapiens laforin complements the sex4 phenotype and propo

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

211 We characterized rRNA of the H. sapiens large ribosomal subunit by computation, circular

212 ave investigated how the competition with H. sapiens may have caused Neanderthals' extinction.

213 tive association on chromosome 6 at the Homo sapiens mediator complex subunit 23 gene/arginase I locu

214 RNA editing sites identified in humans (Homo sapiens), mice (Mus musculus) and flies (Drosophila mela

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

216 t (Saccharomyces cerevisiae) and human (Homo sapiens) mitochondria, Oxidase assembly protein1 (Oxa1)

217 ns, Drosophila melanogaster, G. gallus, Homo sapiens, Mus musculus or Rattus norvegicus and identifie

218 genes, comparing methylated genomes of Homo sapiens, Mus musculus, and Danio rerio with nonmethylate

219 m specific comparison of eight species: Homo sapiens, Mus musculus, Arabidopsis thaliana, Caenorhabdi

220 omains from seven eukaryotic organisms (Homo sapiens, Mus musculus, Bos taurus, Rattus norvegicus, Da

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

222 d aspects of the information content of Homo sapiens, Mus musculus, Drosophila melanogaster, Caenorha

223 , Drosophila melanogaster, Danio rerio, Homo sapiens, Mus musculus, Oryza sativa, Solanum lycopersicu

224 years in the seven supported organisms (Homo sapiens, Mus musculus, Rattus norvegicus, Drosophila mel

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

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

227 ue compared with recent and prehistoric Homo sapiens, Neandertal humeri are characterised by a pronou

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

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

230 nase (Saccharomyces cerevisiae--Erg26p, Homo sapiens--NSDHL (NAD(P) dependent steroid dehydrogenase-l

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

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

233 ago (ka) among earlier representatives of H. sapiens or evolved gradually over the last 400 thousand

234 han to the derived parabolic arcades of Homo sapiens or H. erectus.

235 sponding regions of GGPP synthases from Homo sapiens or S. cerevisiae.

236 uence identity to the S. cerevisiae and Homo sapiens orthologs of Usb1, respectively.

237 and the timing of dispersals that spread H. sapiens out of Africa and across the Old World.

238 oads for understanding the dispersal of Homo sapiens out of Africa and into Asia and Oceania.

239 as been hypothesized that the exodus of Homo sapiens out of Africa and into Eurasia between ~50-120 t

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

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

242 Eighty adult human (Homo sapiens) participants were presented with a task previou

243 ional perspective to the paradox of why Homo sapiens, particularly agriculturalists, appear to be rel

244 ope that may be unequivocally assigned to H. sapiens (Pecstera cu Oase, Romania) date to this time pe

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

246 Homo sapiens phylogeography begins with the species' origin n

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

248 derably from the much shallower thorax of H. sapiens, pointing to a recent evolutionary origin of ful

249 evant shortly before Upper Palaeolithic Homo sapiens populated the region.

250 oups were present at this site-an early Homo sapiens population, followed by a Neanderthal population

251 ion of local Neanderthal populations by Homo sapiens populations of African origin(1).

252 ong link between archaic and recent Asian H. sapiens populations.

253 enorhabditis elegans, Mus musculus, and Homo sapiens PPI networks.

254 proteins were evolutionary related with Homo sapiens proteins to sort out the non-human homologs.

255 imally redundant, canonical database of Homo sapiens proteins.

256 identified a centrin-binding site within H. sapiens Prp40 homolog A (HsPrp40A), which contains a hyd

257 ed on piRNAs in three different species - H. sapiens, R. norvegicus, and M. musculus - obtained from

258 represents a pathological microcephalic Homo sapiens rather than a new species, (i.e., H. floresiensi

259 pose that it represents a microcephalic Homo sapiens rather than a new species.

260 s in the two eukaryotic reconstructions Homo sapiens Recon 1 and Yeast 5 are specified as irreversibl

261 iii) the implementation of the Reconstructed Sapiens Reference Sequence (RSRS) as mitochondrial refer

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

263 Homo sapiens' relationship with the tropical rainforests of S

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

265 the exact place and time of emergence of H. sapiens remain obscure because the fossil record is scar

266 gins of these developmental patterns in Homo sapiens remain unknown.

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

268 23 and 0.944 for E. coli, M. musculus and H. sapiens, respectively).

269 hia coli, Saccharomyces cerevisiae, and Homo sapiens, respectively, and the conclusions are consisten

270 hia coli, Saccharomyces cerevisiae, and Homo sapiens, respectively.

271 xtinct hominins, including pre-Holocene Homo sapiens, retain the high levels seen in nonhuman primate

272 r atlases have been created for humans (Homo sapiens), rhesus macaques (Macaca mulatta), and several

273 tested functional robustness of human (Homo sapiens), rice (Oryza sativa) and budding yeast (Sacchar

274 myces pombe Slx8-Rfp (founding member), Homo sapiens RNF4, Dictyostelium discoideum MIP1 and Saccharo

275 nd database search tools inferring from Homo sapiens, Saccharomyces cerevisiae, and Arabidopsis thali

276 lack bear (Ursus americanus) and human (Homo sapiens sapiens), used in point manufacture.

277 origin of 'anatomically modern humans' (Homo sapiens sapiens).

278 hia coli, Saccharomyces cerevisiae, and Homo sapiens sequences reveals how co- and post-translational

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

280 ication functions classify a pathological H. sapiens specimen that, like LB1, represents an approxima

281 ul minimax strategy employed by ancient Homo sapiens subpopulations in a one-player game against natu

282 within the timeframe dating the dawn of Homo sapiens, suggesting that P. falciparum may have undergon

283 rger in E. coli and S. cerevisiae than in H. sapiens, suggesting that promiscuous protein-protein int

284 a regulatory network of brain tumor in Homo sapiens takes 12 days with MEDUSA, FastMEDUSA obtained t

285 ne projects such as Escherichia coli or Homo sapiens, teams of scientists were employed to manually c

286 als was part of the plastic behavior of Homo sapiens that allowed it to rapidly colonize a series of

287 (Bradyrhizobium japonicum USDA 110 and Homo sapiens) that had available X-ray structures were purifi

288 of data for E. coli, M. tuberculosis and H. sapiens, that the updated algorithm and inclusion of nov

289 ng in organisms ranging from archaea to Homo sapiens under both normal and stressed cellular conditio

290 ultiple organisms, including Eukaryota, Homo sapiens, Viridiplantae, Gram-positive Bacteria, Gram-neg

291 te the distinctive physical appearance of H. sapiens was probably also responsible for the neural sub

292 bjects were used by preschool children (Homo sapiens) was examined by directly observing them across

293 that took place after the emergence of Homo sapiens We show converging evidence from paleoanthropolo

294 e 1q21.1 region during the evolution of Homo sapiens; we found this locus to be deleted or duplicated

295 .g., violence or food shortage), modern Homo sapiens were equipped with the potential to rapidly colo

296 pation from the occupation of the cave by H. sapiens, which extends to 34,000 cal BP.

297 panzees (Pan troglodytes) and children (Homo sapiens) who observed a model's errors and successes cou

298 es were shown to be conserved comparing Homo sapiens with the marsupial, Monodelphis domestica.

299 rt a complex process for the evolution of H. sapiens, with the recognition of different, geographical

300 sativa], soybean [Glycine max], human [Homo sapiens], yeast [Saccharomyces cerevisiae], fruit fly [D