ライフサイエンスコーパス: sapiens

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

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

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

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

5 identify homologous regions in humans (Homo sapiens).

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

7 of FBA models for Escherichia coli and Homo sapiens.

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

9 ly identified as either Neanderthals or Homo sapiens.

10 aenorhabditis elegans, Mus musculus and Homo Sapiens.

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

12 ent a pathological microcephalic modern Homo sapiens.

13 richia coli, Pyrococcus horikoshii, and Homo sapiens.

14 ntal differences between Neanderthals and H. sapiens.

15 parietal expansion than is the case for Homo sapiens.

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

17 cies as diverse as Escherichia Coli and Homo sapiens.

18 erevisiae, Drosophila melanogaster, and Homo sapiens.

19 a from both Drosophila melanogaster and Homo sapiens.

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

21 genital and acquired channelopathies in Homo sapiens.

22 sociated with newly discovered remains of H. sapiens.

23 ause congenital and acquired disease in Homo sapiens.

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

25 ive selection in the lineage leading to Homo sapiens.

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

27 bus fulgidus, Arabidopsis thaliana, and Homo sapiens.

28 sophila melanogaster, Mus musculus, and Homo sapiens.

29 , in contrast to the six families found in H.sapiens.

30 yed a critical role in the evolution of Homo sapiens.

31 typically observed in the second heptad in H.sapiens.

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

33 networks between Epstein-Barr virus and Homo sapiens.

34 gion during this period-Neandertals and Homo sapiens.

35 abditis elegans, Loxodonta africana and Homo sapiens.

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

37 le supports its unequivocal assignment to H. sapiens.

38 l dissections and compare the data with Homo sapiens.

39 likely characteristic of pre-modern era Homo sapiens.

40 krans, Homo neanderthalensis, and early Homo sapiens.

41 -predicted structural conservation with Homo sapiens.

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

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

44 t also confers reproductive benefits in Homo sapiens.

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

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

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

48 ndocasts from great apes, Homo erectus, Homo sapiens, a human pygmy, a human microcephalic, specimen

49 he four or five heptads typically found in H.sapiens, a prediction experimentally verified by circula

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

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

52 The Homo sapiens and Arabidopsis thaliana genomes are believed to

53 e 1 (HIV-1) infectivity when particular Homo sapiens and Cercopithecus aethiops cell lines were used

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

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

56 Observations in Homo sapiens and Drosophila melanogaster have revealed a seco

57 imately 700 million years that separate Homo sapiens and Drosophila melanogaster.

58 ing of the evolutionary relationship of Homo sapiens and Homo neanderthalensis and signifies the dawn

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

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

61 a family of small secreted proteins in Homo sapiens and Mus musculus using a novel database searchin

62 sly characterized IFNA gene families from H. sapiens and Mus musculus, for the analysis of both whole

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

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

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

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

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

68 The Homo sapiens and other eukaryotic constitutive kynureninases

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

70 xcept for closely related species (i.e. Homo sapiens and Pan troglodytes) where gene-specific cluster

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

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

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

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

75 The repository (currently available for Homo sapiens and Saccharomyces cerevisiae) and computational

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

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

78 4 (GLRA4) subunits were found in human (Homo sapiens) and guinea pig (Cavia porcellus) tracheal smoot

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

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

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

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

83 adults (Homo sapiens), young children (Homo sapiens), and adult tamarins (Saguinus oedipus) while th

84 ed only in Yarrowia lipolytica, humans (Homo sapiens), and Arabidopsis (Arabidopsis thaliana).

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

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

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

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

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

90 erns of genetic influences on behavior, Homo sapiens appears to be typical of other animal species.

91 eats found using PILER are reported for Homo sapiens, Arabidopsis thalania and Drosophila melanogaste

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

93 er pylori, Saccharomyces cerevisiae and Homo sapiens are codon usage paradigms that can be better und

94 Homo sapiens are genetically diverse, but dramatic demographi

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

96 specify heterodimerizing B-ZIP proteins in H.sapiens are not present in A.thaliana.

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

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

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

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

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

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

103 cation, by a hominin species other than Homo sapiens, at an as-yet unknown date.

104 Overexpression of BCL2 (Homo sapiens B-cell chronic lymphocytic leukemia/lymphoma 2)

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

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

107 at Neanderthals represent a subspecies of H. sapiens by comparing the degree of their morphological d

108 nzymes, those from Escherichia coli and Homo sapiens, by determining kinetic isotope effects on flavi

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

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

111 nome and transcriptome sequence data of Homo sapiens, Caenorhabditis elegans and Schizosaccharomyces

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 Metazoans (Homo sapiens, Ceanorhabditis elegans and Drosophila melanogas

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

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

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

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

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

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

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

122 of whether the ancestors of all modern Homo sapiens comprised a single African population or an amal

123 is of particular relevance to humans as Homo sapiens contains the active L1 Ta1 subfamily of the huma

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

125 among-population differences in extant Homo sapiens cranial morphology are proportional to among-pop

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

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

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

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

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

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

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

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

134 The H. sapiens DHOD also appears to have a pKa near 9.4 control

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

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

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

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 Similar KIEs were obtained with the H. sapiens enzyme at a pH value below the pKa.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

160 Homo sapiens harbor two distinct, medically significant speci

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

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

163 ents of chemically denatured cpn10 from Homo sapiens (hmcpn10) and Aquifex aeolicus (Aacpn10) were mo

164 In a collection of 52 rodent-H. sapiens homologous mRNAs that had STRs, six (11.5%) STR-

165 3/H4 complexes have been determined for Homo sapiens (Hs) and the budding yeasts Saccharomyces cerevi

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

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

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

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

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

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

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

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

174 uence-based map of human chromosome 17 [Homo sapiens, (HSA) 17] were found to be highly consistent, w

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

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

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

178 -3, interferon induced-15 [IFI-15], and Homo sapiens hypothetical protein MGC5566) and two downregula

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

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

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

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

183 uttata, a songbird species) and humans (Homo sapiens) in AP tests that required classification of con

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

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

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

187 ide range of species from caiman to the Homo sapiens, indicating that this glycosaminoglycan attachme

188 t the resequencing of a large number of Homo sapiens individuals might be used to annotate the human

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

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

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

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

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

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

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

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

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

198 drome 1 (Nibrin), ribosomal protein L4, Homo sapiens KIAA0419 gene product, eukaryotic initiation fac

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

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

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

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

203 tics and perceptual studies with human (Homo sapiens) listeners.

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

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

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

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

208 Homo sapiens mitochondrial transcription factor B1 (h-mtTFB1)

209 ae, Caenorhabditis elegans, Drosophila, Homo sapiens, Mus musculus and Arabidopsis species as well as

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

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

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

213 able doublets in the following genomes: Homo sapiens, Mus musculus, Arabidopsis thaliana, and Caenorh

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

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

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

217 omain homology in the transcriptomes of Homo sapiens, Mus musculus, Drosophila melanogaster and Caeno

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

219 million splice sites from five species-Homo sapiens, Mus musculus, Drosophila melanogaster, Caenorha

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

221 roteins from nine eukaryotic organisms: Homo sapiens, Mus musculus, Rattus norvegicus, Arabidopsis th

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

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

224 lve phylogenetically diverse organisms: Homo sapiens, Mus musculus, Takifugu rubripes, Ciona intestin

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

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

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

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

229 -, and 10-year-old children and adults (Homo sapiens) on a nonverbal serial-order task to respond to

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

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

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

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

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

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

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

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

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

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

240 e here a new human peptide deformylase (Homo sapiens PDF, or HsPDF) that is localized to the mitochon

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

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

243 Homo sapiens phylogeography begins with the species' origin n

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

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

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

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

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

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

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

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

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

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

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

255 Homo sapiens' relationship with the tropical rainforests of S

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

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

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

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

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

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

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

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

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

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

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

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

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

269 of language that emphasizes the role of the sapiens-specific cerebral torque in determining the four

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

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

272 Using a BLAST search against the Homo sapiens subset of the SWISS-PROT and TrEMBL databases, w

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

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

275 In H. sapiens, TAFA-3 has two isoforms formed by alternative s

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

277 ly to the N-terminal 163 amino acids of Homo sapiens TATA-binding protein-associated factor-1 (hsTAF1

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

279 atter including the rTS beta protein in Homo sapiens that has been implicated in regulating thymidyla

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

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

282 In H. sapiens, the family is composed of four genes and two ps

283 es of sulfate activating complex (SAC) [Homo sapiens (type I); Mycobacterium tuberculosis (type II);

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

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

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

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

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

289 mary curational domain is pathways from Homo sapiens, we regularly create electronic projections of h

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

291 leases from cow (Bos taurus) and human (Homo sapiens) were produced in Escherichia coli and purified,

292 nzyme of the biopterin (BH4) pathway in Homo sapiens, where it is encoded by a homologous folE gene.

293 nderthals a subspecies or population of Homo sapiens, which contributed significantly to the evolutio

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

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

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

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

298 rely sequenced organisms, namely human (Homo sapiens), yeast (Saccharomyces cerevisiae), and weed (Ar

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

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