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1 Intron positions and phasing were conserved between ZmMRP1 and 2 and their closest Ar

2 tor, indicating that this virulence strategy is conserved between a bacterial and a protozoan pathoge

3 lutamate transporters to interact with Tl(+) is conserved between GltPh and a mammalian member of the

4 fic recognition in the minor groove of dsRNA are conserved between NF90 and ADAR2.

5 The function of aflR appears to be conserved between ST- and AF-producing aspergilli, as

6 Two biologically relevant modules were conserved between AD and aging, one related to mito

7 he molecular identities of V2a and V2b cells are conserved between zebrafish and amniotes.

8 hter chromatid separation and cell expansion are conserved between gymnosperms and angiosperms.

9 clusion of histone H2A.Z from methylated DNA is conserved between plants and animals, and we present

10 genomes and found that gene body methylation is conserved between plants and animals, whereas selecti

11 from maize, indicating that this interaction is conserved between plants and animals.

12 sts that similar nuclear migration machinery is conserved between plants and animals.

13 e structural core of the protein is shown to be conserved between ZnCP and another large family of hy

14 ropose that bif2/PID sequence and expression are conserved between grasses and Arabidopsis, attesting

15 Thus, although the targets of the AP2 genes are conserved between maize and Arabidopsis, the genes t

16 Collinearity of genes flanking RPM1 is conserved between B. napus and Arabidopsis.

17 Our findings indicate that CCC function is conserved between grapevine and Arabidopsis, but neit

18 tic analysis indicates that the gating motif is conserved between eubacterial and archaebacterial Sec

19 The end-terminal sequences of QRFV are conserved between segments and are different from th

20 alysis, and hence to identify the genes that are conserved between B. cereus and B. anthracis, and th

21 als that, for 7 human autosomes, locus order is conserved between humans and baboons.

22 Both of these structural features are conserved between the eukaryotic and bacterial intro

23 ies (and their binding sites in target RNAs) are conserved between angiosperms and basal plants, sugg

24 Several key residues in the active site are conserved between CarA and beta-LS, supporting propo

25 gH/gL homodimerization may be conserved between alpha- and betaherpesviruses, becau

26 he mechanism of anterior pituitary induction is conserved between mammals and birds, using the same,

27 operator shows a protein-DNA interface that is conserved between both mec and bla targets.

28 regulation of Hh signal transduction by Nrps is conserved between mammals and bony fish, as we show t

29 lyses revealed that functions of these genes are conserved between C. elegans and C. briggsae.

30 iRNAs and the tendency for piRNAs to cluster is conserved between C. briggsae and C. elegans.

31 the core circuit topology of the Fix network is conserved between the rhizobia and C. crescentus, a f

32 o the ideal gas, and its geometric structure is conserved between C16 and C24.

33 amphipathic helix whose hydrophobic surface is conserved between CAF1 and CAF2.

34 of chromosomes in the interphase nucleus can be conserved between normal and cancer cells and our dat

35 ane domain of the CB2 receptor (K109), which is conserved between the CB1 and CB2 receptors, was muta

36 Domain topography is conserved between hemichordates and chordates despite

37 rate that the physiological role of Prominin is conserved between rhabdomeric and ciliated photorecep

38 ory event in Notch signaling that appears to be conserved between insects and crustaceans.

39 A histidine-rich stretch, which is conserved between CycT1 and CycT2 in this region, bou

40 equence of the translational control element are conserved between D. melanogaster and D. virilis.

41 be delimited to a 41 nucleotide domain that is conserved between D. melanogaster and D. virilis, and

42 parate location, between aa 83 and 92, which is conserved between D2V and D4V.

43 e (At)NPR1-mediated SAR defense response may be conserved between monocots and dicots.

44 studies, we find evidence that FAMA function is conserved between monocots and dicots, despite their

45 wth phenotype, indicating that gene function is conserved between mono- and dicotyledonous species.

46 cells, depending on functional domains that are conserved between Drosophila melanogaster and Drosop

47 ns but also certain features of the cis PREs are conserved between mammals and Drosophila.

48 hat a Deformed/Hoxb4 autoregulatory loop has been conserved between mouse and Drosophila.

49 interact in a sequence-specific fashion that is conserved between mammals and Drosophila.

50 in vivo in a sequence-specific fashion that is conserved between mammals and Drosophila.

51 ation of maternally deposited microRNAs that is conserved between Tribolium and Drosophila.

52 Most of the peptides are conserved between E. muris and E. chaffeensis OMP-19

53 While the -10 promoter element appears to be conserved between Chlamydia and E.coli, the structure

54 menon of FtsH-dependent PspC destabilization is conserved between Y. enterocolitica and E. coli.

55 se A and the arrangement of the active sites is conserved between the archaeal and eucaryal enzymes.

56 e suggests that the C- and B-class functions are conserved between monocots and eudicots, with B-clas

57 mpelling evidence that B-class gene function is conserved between monocots and eudicots.

58 unction, which explains how OMP assembly can be conserved between prokaryotes and eukaryotes.

59 NA anticodon recognition domain that has not been conserved between bacteria and eukaryotes; and 3) a

60 sting that the molecular basis of inhibition is conserved between archaea and eukaryotes.

61 The ribotoxic stress response, which is conserved between prokaryotes and eukaryotes, is a ce

62 res around the active-site histidine residue are conserved between the prokaryotic and eukaryotic kin

63 Thus, the process of protein mannosylation is conserved between M. tuberculosis and eukaryotic orga

64 orientation of EGLN1, TSNAX, and DISC1 genes are conserved between mammals and F. rubripes.

65 siological regulation of the OT and IT genes are conserved between mammals and fish.

66 echanisms that direct Pax6 ocular expression are conserved between mice and flies.

67 epidermal appendage regulatory pathways has been conserved between mice and flies.

68 g, identifying 24 coregulated complexes that were conserved between yeast and fly.

69 a tight 1:1 complex, and these interactions are conserved between mammals and fruit flies.

70 non-coding elements in the human genome that are conserved between human and Fugu.

71 ing accelerated evolution in mouse and those being conserved between human and fugu.

72 l constituents required for mODC degradation are conserved between animals and fungi, and that both m

73 at the mechanism of postsynaptic scaffolding is conserved between neuronal cholinergic and glutamater

74 tial order of the disulfide bridge formation is conserved between VEGF and glycoprotein alpha-subunit

75 2+) signalling in response to osmotic stress is conserved between land plants and green algae, but th

76 eraction sites with the 40S subunit and eIF3 are conserved between HCV and HCV-like IRESs.

77 These positions are conserved between CCT and HEME ACTIVATOR PROTEIN2 (H

78 aspects of the checkpoint control mechanism are conserved between fission yeast and higher eukaryote

79 -dependent) protein translocation mechanisms are conserved between prokaryotes and higher plant chlor

80 This ligand-binding mode is conserved between XEEL and hIntL-1.

81 Interestingly, this epitope is conserved between SIV and HIV-1 and exhibits a delaye

82 mavirus DNA packaging signal exists, then it is conserved between the BPV and HPV16 genomes; (iii) fu

83 he first intron of the murine CD21 gene that are conserved between mouse and human CD21 intronic sequ

84 crete sequences within the 21 kb region that are conserved between mouse and human, and are sufficien

85 esidues important to assembly of the protein are conserved between mouse and human, permitting the fo

86 ve sites, and two stretches of sequence that are conserved between mouse and human.

87 at roughly half of the measured interactions are conserved between mouse and human.

88 in other family members (TNFR and CD40) but are conserved between murine and human Fas.

89 shorter than the human PAP7 gene, all exons are conserved between the mouse and human.

90 the yku80(tel) alleles mutate residues that are conserved between the yeast and human Ku80 proteins,

91 key elements of this highly unusual strategy are conserved between yeast and human Rev1, including th

92 transcription factor binding sites appear to be conserved between bovine and human genes.

93 IIbeta-2, are novel variants that appear to be conserved between chicken and human.

94 dy suggests that the function of LCs may not be conserved between mouse and human and supports human

95 The genomic organization was found to be conserved between mouse and human IKCa1 as shown by c

96 se that binding to TG-rich DNA sequences has been conserved between the mouse and human proteins.

97 only demonstrate that chromosome instability is conserved between bovine and human cleavage embryos,

98 Ube3a isoform 2 is conserved between mouse and human and known to play k

99 BIM and BMF, and their proapoptotic function is conserved between mouse and human stem and progenitor

100 s role in the coordinate expression of genes is conserved between mouse and human, and indicate that

101 Since CXCR4 is conserved between mouse and human, the newfound role

102 ring embryogenesis and that protein function is conserved between mouse and human.

103 ve cis-acting element, the sequence of which is conserved between the mouse and human GATA-3 genes.

104 Genomic organization is conserved between the murine and human H(+)-ATPase B1

105 ese results thus indicate that the HSC niche is conserved between the murine and human species and su

106 This E-box is conserved between the rat and human GAP-43 promoter s

107 Point mutation of an amino acid that is conserved between the yeast and human proteins compro

108 onclude that singularity regulation by Cdc42 is conserved between yeast and human and that this regul

109 sfection experiments; this enhancing ability was conserved between mouse, rat, and human CE1 present

110 rgistic effect of synthetic OMP and IFN-beta was conserved between murine AMphi and human AMphi for I

111 han 130 of these gene expression differences were conserved between mouse and human monocyte subsets.

112 t signaling and cell-cycle control, and most were conserved between mouse and human.

113 Although some PcG protein domains are conserved between flies and humans, substantial regi

114 we define regions of noncoding sequence that are conserved between mice and humans.

115 ffer between S. pombe and S. cerevisiae, but are conserved between S. pombe and humans.

116 ge family of histone acetyltransferases that are conserved between yeast and humans.

117 turbations of its lipid environment that may be conserved between bacteria and humans.

118 n, tissue alignment, and lumen formation may be conserved between Drosophila and humans, but little i

119 at FOXO1 regulation of LHB transcription may be conserved between rodents and humans.

120 tivity of sirtuin 1, a mechanism we found to be conserved between zebrafish and humans.

121 -6 protein, suggesting that BTB function has been conserved between Drosophila and humans.

122 Interestingly, this interaction is conserved between flies and humans.

123 in the regulation of mitochondrial function is conserved between flies and humans.

124 The core enhancer is conserved between mice and humans and contains a crit

125 he Bcl-6 response element in intron 5, which is conserved between mice and humans, was studied in det

126 s (P = 0.04), suggesting that this phenotype is conserved between mice and humans.

127 Adamts16 is conserved between rats and humans.

128 onal regulation by lysine acetylation, which is conserved between yeast and humans and that, we show,

129 tly, the eIF3 role in programmed readthrough is conserved between yeast and humans.

130 ly, we present evidence that Ku p70 function is conserved between yeast, Drosophila, and humans.

131 Pex7p function is conserved between yeasts and humans, with defects in

132 ehavioral transitions between sleep and wake are conserved between mammals and insects.

133 ss and engrailed at the parasegment boundary is conserved between myriapods and insects; suggesting t

134 or high affinity DHP binding, even though it is conserved between DHP-sensitive and -insensitive Ca2+

135 A tyrosine residue (Y1048) in IIIS6 that is conserved between DHP-sensitive and -insensitive Ca2+

136 r data suggest that this crosstalk mechanism is conserved between vertebrate and invertebrate homolog

137 architecture of the substrate binding sites is conserved between sucrose and lac permeases.

138 patterns suggest that this direct repression is conserved between Diptera and Lepidoptera, but is abs

139 This repeat is conserved between species and located in a region whi

140 nts a distinct modular domain whose function is conserved between higher and lower eukaryotes.

141 some determinants for SecA2-dependent export are conserved between M. smegmatis and M. tuberculosis.

142 ER-to-LD targeting and function in LD growth are conserved between Drosophila and mammalian cells.

143 s to DNA topoisomerase I-mediated DNA damage are conserved between yeast and mammalian cells.

144 er the sequence nor location of this element is conserved between teleost and mammalian Col2a1.

145 ly occurs in an ordered pathway in vitro and is conserved between yeast and mammalian systems.

146 Although most circadian clock components are conserved between Drosophila and mammals, the roles

147 d and that genes within these feedback loops are conserved between Drosophila and mammals.

148 repair and suggest that DNA repair functions are conserved between Drosophila and mammals.

149 Chromosomal segments that are conserved between fishes and mammals are also conser

150 h as hyperactivity, sedation, and tolerance, are conserved between flies and mammals [3, 4], as are t

151 oan animals is composed of three clades that are conserved between flies and mammals and are referred

152 that mediate lymphocyte-specific expression are conserved between teleosts and mammals.

153 molecular mechanism of mRNA 3'-end formation are conserved between yeast and mammals, but also highli

154 As many stress-defense proteins are conserved between yeast and mammals, these data shed

155 el cross-intron protein-protein interactions are conserved between yeast and mammals.

156 d that bacterial drivers of disease severity are conserved between zebrafish and mammals.

157 asion and triggering apoptosis may therefore be conserved between insects and mammals.

158 y in regulating epithelial morphogenesis has been conserved between insects and mammals.

159 These aspects of Maf1 function have been conserved between yeast and mammals and are therefo

160 hanism of co-translational protein targeting is conserved between bacteria and mammals.

161 ired for proliferation, and this requirement is conserved between birds and mammals.

162 iated apoptotic DNA degradation pathway that is conserved between C. elegans and mammals.

163 hort cytoplasmic tail containing a site that is conserved between Caenorhabditis elegans and mammals.

164 w that an essential role of CKIdelta/epsilon is conserved between Drosophila and mammals, but CKIdelt

165 nclude that the underlying mechanism of RNAi is conserved between flies and mammals and that RNA-depe

166 bitory activity of certain BEN-solo proteins is conserved between flies and mammals.

167 ion of UBC32 (or UBE2J1) by the HRD1 complex is conserved between plants and mammals.

168 bserved, suggesting that the target molecule is conserved between S. cerevisiae and mammals.

169 suggesting that this aspect of TOR signaling is conserved between yeast and mammals.

170 evealing that a major sub-complex of the NPC is conserved between yeast and mammals.

171 echanism of meiotic recombination initiation is conserved between yeast and mammals.

172 The CpG-ODN binding function of DEC-205 is conserved between mouse and man, although human DEC-2

173 e point mutations were made in residues that are conserved between hCaR and metabotropic glutamate re

174 chanisms mediating DNA accessibility by FACT are conserved between yeast and metazoans.

175 nvolved in the initiation of DNA replication are conserved between yeasts and metazoans, the structur

176 Because regulatory elements are conserved between humans and mice, a thorough annota

177 h an additional transcription factor(s) that are conserved between humans and mice, are required for

178 lular machinery required for NoV replication are conserved between humans and mice.

179 placenta-specific transcription factors that are conserved between humans and mice.

180 The binding sites of NRF-2 are conserved between rats and mice.

181 nctions of polaris and pkd2 in LR patterning are conserved between zebrafish and mice and that Kupffe

182 fundamental biology of stem cells and niches is conserved between Drosophila and mice.

183 -dependent feedback control of Hh morphogens is conserved between flies and mice, but this role is sh

184 Genomic imprinting in most cases is conserved between human and mice.

185 cognized anatomical site where TM expression is conserved between humans and mice and may exert a cri

186 ans and, although vascular expression of DP1 is conserved between humans and mice, platelet DP1 is no

187 Around 40% of genes of unknown function that are conserved between plants and microbes are probably m

188 by global translation initiation sequencing are conserved between human and mouse cells, implying ph

189 tem-loop RNA structure elements in UTRs that are conserved between human and mouse orthologs and exis

190 opes recognized by both synthetic antibodies are conserved between human and mouse VEGF, and they mat

191 measurable facets of higher order structure are conserved between human and mouse, across the vast m

192 ally no overlap with intronic sequences that are conserved between human and mouse, and thus are geno

193 es alternative 3'-end processing events that are conserved between human and mouse, suggesting a func

194 ch are associated with intronic regions that are conserved between human and mouse.

195 ontaining 2 or more BRE-like sequences which are conserved between human and mouse.

196 d probably most, alternative splicing events are conserved between human and mouse.

197 that any host factors required for targeting are conserved between human and mouse.

198 ation and juxtaposition of the Surfeit genes are conserved between human and mouse.

199 ription factor binding is twice as likely to be conserved between human and mouse than typical enhanc

200 We show that this function is conserved between Drosophila and mouse PRC1 complexes

201 Sequence analysis reveals that this protein is conserved between human and mouse and contains the si

202 ion and aggregate formation on collagen that is conserved between human and mouse platelets.

203 tio of translation over 5' leaders and CDSes is conserved between human and mouse, and correlates wit

204 PPRE is conserved between human and mouse, and WY-14643 stimu

205 This polypeptide is conserved between human and mouse, is localized to th

206 The open reading frame of ApoE AS1 is conserved between human and mouse.

207 regulation of KILLER/DR5-mediated apoptosis is conserved between human and mouse.

208 DR1d, but not DR1p, is conserved between human and mouse.

209 its sorting and cellular retention function is conserved between human and mouse.

210 t the key regulation of Th17 differentiation is conserved between human and mouse.

211 While the ERK1/2 regulatory motif is conserved between rat and mouse beta-arrestin-2, it i

212 Of these, only the accessory factor site was conserved between the rat and mouse S(14) genes.

213 cation between the MBD and the ATPase domain is conserved between Msh2-Msh3 and Msh2-Msh6.

214 ing growth factor (interleukin-3) withdrawal is conserved between human and murine BAD.

215 nsufficiency for antagonizing Notch activity is conserved between human and murine cancers.

216 wed that 758 (88.2%) of protein-coding genes are conserved between N. risticii and N. sennetsu.

217 iated apoptotic DNA degradation pathway that is conserved between mammals and nematodes.

218 the B-Raf protein kinase to the cochaperone is conserved between mammals and nematodes.

219 es in segment IIIS6 and the pore region that are conserved between L-type and non-L-type channels (Ty

220 reveals that the amino acids (534)LPIYE(538) are conserved between all primate and nonprimate CMVs.

221 the molecular mechanisms of myoblast fusion are conserved between Drosophila and other animals, as f

222 Our results indicate that some LOS epitopes are conserved between H. somnus and other Haemophilus an

223 Assuming that Sec insertion mechanisms are conserved between nematodes and other eukaryotes, th

224 regulate the second heart field development are conserved between zebrafish and other vertebrates in

225 Over half of the chromosome break sites are conserved between Ascaris and Parascaris, whereas on

226 lysis with mouse showed tissue DC subsets to be conserved between species and permitted close alignme

227 The fold of inner and middle layers is conserved between T6SS and phage sheaths.

228 nd demonstrated that the catalytic mechanism is conserved between human and plant enzymes.

229 ct that many features of cell death strategy are conserved between animals and plants; however, some

230 jor aspects of meiotic recombination seem to be conserved between yeast and plants, especially the fa

231 ramming during male germline differentiation is conserved between animals and plants.

232 that the p21WAF1-interaction domain of PCNA is conserved between humans and plants.

233 e mechanisms regulating membrane trafficking are conserved between nonpolarized and polarized cells.

234 e molecular mechanisms of mesoderm induction are conserved between gastrula and post-gastrula stages

235 region facilitates a dimerization mode that is conserved between PEAK1 and pragmin.

236 R, thus proving that structure and mechanism are conserved between HisA and PriA.

237 the regulation of GABAergic gene expression, are conserved between the rodent and primate brain, and

238 Residues critical for adenine binding are conserved between species and provide a code that al

239 ndicated that the mode of fatty acid binding is conserved between tablysin-15 and Pry1.

240 g sites, all tryptophans and histidines that are conserved between PsaA and PsaB in the region of the

241 The CEL carries at least seven ORFs that are conserved between Psy B728a and Pto DC3000.

242 mitogenic factor promoting self-renewal that is conserved between rodent and rabbit SSCs; with an evo

243 Most of these regions are conserved between human, mouse, and rat GAD 65.

244 etermined to be important for FAAH catalysis were conserved between the Arabidopsis and rat protein s

245 nd two ALDHs (ALDH1 and RALDH2) all of which are conserved between humans and rodents.

246 SP regulation of rpoS is conserved between E. coli and S. enterica.

247 This gene organization is conserved between E. coli and S. typhimurium.

248 nds, suggesting that the observed regulation is conserved between E. coli and S. typhimurium.

249 strate that this protein-protein interaction is conserved between Btn1p and Sdo1p, the respective yea

250 ified 406 potential stem-loops, of which 110 were conserved between chimpanzee cytomegalovirus and se

251 d promoter recognition and melting steps may be conserved between sigma(70) and sigma(54), the domain

252 est that while the multiple functions of vpr are conserved between HIV-1 and SIVagm, the mechanisms l

253 d the composition of intronic sequences that are conserved between human and six eutherian mammals.

254 nal domain interface by which VP40 dimerizes is conserved between Ebola virus and SUDV, the C-termina

255 lytic HAT subunit, in addition to p55/Gcn5p, is conserved between yeast and Tetrahymena.

256 Finally, we show that this regulation is conserved between species and that CDCA7 levels are r

257 Of the 12 residues identified, 11 are conserved between EcoRI and the isoschizomer RsrI (w

258 for protein homeostasis, and ClpP proteases are conserved between eubacteria and the organelles of e

259 sequence, structure, and reaction mechanism are conserved between Hh-C17 and the self-splicing regio

260 d the positions of the intron/exon junctions are conserved between the human and the rodent genes.

261 identified several regulatory elements that are conserved between the murine and the human promoters

262 re and the organization of the gene locus to be conserved between the mouse and the human chromosomes

263 positions of four coding region splice sites were conserved between Drosophila per and the human para

264 The exon-intron borders were conserved between the human and the chicken MCT3 ge

265 out 3% mBESs match ESTs and > 70% of matches were conserved between the mouse and the human or the ra

266 These pause sites are conserved between E. coli and Thermus thermophilus R

267 of the stem cell microenvironment, or niche, are conserved between tissues, and this can be exploited

268 s competent to express engrailed, appears to be conserved between Drosophila and Tribolium.

269 We found that the role of prd is conserved between Drosophila and Tribolium; it is req

270 risingly show that the free energy landscape is conserved between knotted and unknotted protein, howe

271 al mechanisms of FLRT adhesion and repulsion are conserved between neurons and vascular endothelial c

272 To test whether such mechanisms are conserved between photosynthetic algae and vascular

273 ys an essential role in cilia formation that is conserved between Caenorhabditis elegans and vertebra

274 dramatically alter known functional domains are conserved between amphioxus and vertebrates, suggest

275 addition, several transcriptional enhancers are conserved between amphioxus and vertebrates--a very

276 nstrate that the functions of these proteins are conserved between amphioxus and vertebrates.

277 onents and pathways of endocytic trafficking are conserved between C. elegans and vertebrates, and th

278 st that the functions of homeo proteins also are conserved between invertebrates and vertebrates.

279 nsmembrane spoke domain, and the transporter are conserved between yeast and vertebrates; hence, they

280 etic networks involved in cell migration may be conserved between nematodes and vertebrates.

281 ion of Id genes in the mesoderm and endoderm is conserved between amphioxus and vertebrates, expressi

282 heir domains of function along the body axis is conserved between arthropods and vertebrates.

283 nteract with different targets, one of which is conserved between Drosophila and vertebrates.

284 cognition by a protein in the sperm acrosome is conserved between invertebrates and vertebrates, even

285 have a role in motor neuron development that is conserved between invertebrates and vertebrates.

286 Strikingly, DNA-contacting residues are conserved between ARFs, and we discover that monomer

287 The three loop bases that are conserved between the mutant and wild-type hairpins

288 st of the mutations altered amino acids that were conserved between yeast, human, and Xenopus RPA1.

289 esponses to changes in sphingolipid balance, are conserved between mammalian and yeast cells.

290 he pathways downstream of Bax and Bcl-xL may be conserved between vertebrates and yeast.

291 The model for kinetochore assembly is conserved between humans and yeast, and homologues of

292 aperones and other ER resident proteins, and is conserved between mammals and yeast.

293 function, F-actin and beta-catenin binding, are conserved between mouse and zebrafish.

294 Moreover, HIPK2 autophosphorylation is conserved between human and zebrafish and is importan

295 The relationship between APC and CtBP1 is conserved between humans and zebrafish and provides a