ライフサイエンスコーパス: share a common

1 hesizing of a novel series of analogues that share a common 2-amino-3-(4-chlorobenzoyl)thiophene nucl

2 rather than being static pore formers, AMPs share a common ability to lower interfacial tensions tha

3 >/=68% of syndromic and idiopathic ASD cases shared a common acetylome signature at >5,000 cis-regula

4 For a given neuron, these elements tended to share a common alignment in eye-centered coordinates.

5 ins such that colonies reject if they do not share a common allele at either locus, fuse temporarily

6 cally distinct synthetic interactions, which share a common altered gene, may prove to be a novel and

7 nomes indicate that the TPA strains examined share a common ancestor after the fifteenth century, wit

8 assertions that type I and type III systems share a common ancestor and reveal how a conserved struc

9 s are diverse in their overall reactions yet share a common ancestor and some conserved active site f

10 riophages and herpesviruses almost certainly share a common ancestor in their evolution.

11 haplotype indicated that these four families share a common ancestor sufficiently distant to have per

12 es, red algae, green algae, and land plants, share a common ancestor that lived approximately 1.9 Bya

13 t if the seven language families we consider share a common ancestor then that common ancestor likely

14 cquired through horizontal gene transfer and share a common ancestor with proteins in other plant pat

15 Small basic proteins present in most Archaea share a common ancestor with the eukaryotic core histone

16 he Placozoa have opsins, and that the opsins share a common ancestor with the melatonin receptors.

17 ch FEVR family that subsequently appeared to share a common ancestor with the original family.

18 Breeds share a common ancestor, the gray wolf.

19 Eukaryotes and prokaryotes last shared a common ancestor 2 billion years ago, and while

20 hellia, two island endemic species that last shared a common ancestor approximately 300,000 years ago

21 e distinct from that of the 1979 isolate and shared a common ancestor around 1987.

22 om the 2006-2007 outbreak in East Africa and shared a common ancestor around 2003 to 2004.

23 ary analysis indicated that all the isolates shared a common ancestor dating back approximately 50 ye

24 ion and maintained between species that last shared a common ancestor more than 400 million years ago

25 human pathogen Candida albicans (which last shared a common ancestor with S. cerevisiae some 300 mil

26 The 1979 Madagascar isolate shared a common ancestor with strains on the mainland ar

27 owed that at least two of the three families shared a common ancestor.

28 as changed since mosses and angiosperms last shared a common ancestor.

29 nserved since O. sativa and A. thaliana last shared a common ancestor.

30 flecting the time when the walnut genus last shared a common ancestor.

31 Although Nef of SIVcpz shares a common ancestor with that of SIVrcm, an SIV in

32 Enzymes sharing a common ancestor as defined by sequence and str

33 gle common ancestor; by extension, they also share a common ancestral habitat.

34 era velia and Vitrella brassicaformis, which share a common ancestry with Apicomplexa, provided an op

35 They are thought to share a common ancestry, and, in particular, T-type calc

36 dard laboratory strains that are reported to share a common ancestry, but exhibit substantial phenoty

37 They also share a common ancestry, MRL being formed from a multi-s

38 nd imply that animal nociceptive systems may share a common ancestry, tracing back to a progenitor th

39 ated virophage strongly suggest that PgV-16T shares a common ancestry with the largest known dsDNA vi

40 VIII) are structurally conserved domains and share a common and essential function in membrane bindin

41 t bacterial and archaeal head-tailed viruses share a common architectural principle.

42 These bacterial microcompartments share a common architecture of an enzymatic core encapsu

43 d that the mechanically resistant structures share a common architecture, with similarities to the fo

44 We find that all TFNs share a common assortativity signature and that this sig

45 ligomeric form of different amyloid proteins share a common backbone conformation, but the amorphous

46 eads originating from each long DNA molecule share a common barcode.

47 t differ from Ub in amino acid sequence, yet share a common beta-grasp fold, also form isopeptide bon

48 e obtained SAR indicate that 2a and muscimol share a common binding mode, which deviates from the bin

49 al that these chemically distinct inhibitors share a common binding pocket on GPC.

50 p90RSK and CHIP share a common binding site in the ERK5 C-terminal domai

51 We show that both NS5B(Delta21) and CypA share a common binding site on NS5A that contains residu

52 Binding studies also showed that they share a common binding site that overlaps with that of c

53 ies, this suggests that all three regulators share a common binding surface on the catalytic subunit.

54 be attributed to a cluster of HLA-C alleles sharing a common binding groove F pocket with HLA-C*04:0

55 he pathogenesis of childhood ALL and allergy share a common biologic mechanism.

56 describe sets of genes or gene products that share a common biology.

57 is a highly sulfated glycosaminoglycan that shares a common biosynthetic pathway with heparan sulfat

58 e allosteric and redox partner binding sites share a common border.

59 It shares a common building layer with ITQ-22 and contains

60 These features share a common, but unexplained, origin--namely, pathway

61 3 isoform1 (i1), but not isoform3 (i3) which shares a common C-terminal region, suppresses these mali

62 Whereas sorghum and maize share a common C4 origin, C4 metabolism evolved independ

63 ed K(+) channels are voltage-independent and share a common calcium/calmodulin-mediated gating mechan

64 ion is a systemic inflammatory state and may share a common casual pathway for cancer development aft

65 sferases belonging to the DHHC family, which share a common catalytic Asp-His-His-Cys (DHHC) motif.

66 a divergent set of metabolosomes, BMCs that share a common catalytic core and process distinct subst

67 SCF enzymes share a common catalytic core containing Cul1Rbx1, which

68 s that have diverse biological functions but share a common catalytic core domain composed of six mem

69 Although the proteins share a common catalytic core, they have different speci

70 opose that the three pneumococcal sialidases share a common catalytic mechanism up to the final produ

71 tructure, indicating that they are likely to share a common catalytic mechanism.

72 sely related than previously thought and may share a common cell of origin.

73 rmore, aneurysm formation and cyst formation share a common cellular and molecular pathway involving

74 ore, both CA1 pyramidal and SOM interneurons shared a common cellular mechanism (reduction in SK chan

75 These applications share a common challenge(7) well-known in classical ecol

76 Neurodegenerative diseases share a common characteristic, the presence of intracell

77 metabolism and genetics had a common origin, shared a common chemical frame, and were embedded under

78 Mycobacteria share a common cholesterol degradation pathway initiated

79 nd pathological differences, asthma and COPD share a common clinical facet: raised airway ATP levels.

80 iology, prognosis, and treatment, CP and RCM share a common clinical presentation of predominantly ri

81 These classes share a common cobalamin-binding core, but use distinct

82 ucleus neuron are not selected at random but share a common complex-spike property.

83 se studies remain controversial because they share a common confound: the conspecific's line of gaze,

84 In contrast, multiarm studies efficiently share a common control arm while evaluating multiple exp

85 is response to anoxic and hypoxic treatments share a common core of genes related to the anaerobic me

86 The four glycoforms share a common core structure, and the differences are r

87 The structure shares a common core with paramyxovirus F proteins, impl

88 ssembly contained two multiprotein complexes sharing a common core consisting of RBP-J and RBP-K and

89 mechanisms governing the movements of nuclei sharing a common cytoplasm are not understood.

90 in that nuclei cycle asynchronously despite sharing a common cytoplasm.

91 ome number varies substantially among nuclei sharing a common cytoplasm.

92 mponents among these divergent T3SS subtypes sharing a common cytoplasmic milieu.

93 These cells share a common DC progenitor with conventional DCs, and

94 s of function in syd-1, liprin-alpha, or wrd shares a common defect in which a portion of synaptic ve

95 Thus, despite sharing a common deletion mechanism, these closely relat

96 ng behaviors of Tritonia and Pleurobranchaea share a common dependence on serotonergic neuromodulatio

97 f FFR-Guided Treatment of Coronary Disease), sharing a common design, were pooled as PRIME-FFR (Insig

98 chwann cells and olfactory ensheathing cells share a common developmental origin.

99 ver vessels derives from the endocardium and shares a common developmental origin with coronary arter

100 om four sympatric species of Drosophila that share a common diet of decaying mushrooms.

101 ough single-layer or bilayer graphene, which shares a common Dirac-cone feature in the band structure

102 , two distinct reaction paths originate that share a common diradical intermediate, however, without

103 actors (TFs) belong to protein families that share a common DNA binding domain and have very similar

104 Since monozygotic (MZ) twins share a common DNA sequence, their study represents an i

105 tors encoded in the human genome and, due to sharing a common DNA binding domain, they are all though

106 Three of the peptides that shared a common docking mode, where key TCR-MHC germline

107 They share a common domain architecture that features an N-te

108 PfhB2 shares a common domain architecture with IbpA and contai

109 two cortical projection neuron types that 1) share a common efferent target, 2) are known to exhibit

110 e of organic acid ligands but appear to only share a common electrostatic interaction between a conse

111 mechanisms discussed in this review seem to share a common element: prolonged increases in reactive

112 the proximal parts of the coronary arteries share a common embryonic origin, we hypothesized that CA

113 plate, notochord, hypochord and floor plate share a common embryonic origin.

114 opoietic system and the vascular endothelium share a common embryonic origin; interindividual variati

115 propose that Cryptomycota and microsporidia share a common endoparasitic ancestor, with the clade un

116 They share a common energy metabolism but represent a heterog

117 ly social but evolutionarily distant species sharing a common environment, these findings give new in

118 results suggest that coronavirus S1 subunits share a common evolutionary origin but have attained div

119 that is, positions in multiple genomes that share a common evolutionary origin, is a crucial, yet di

120 stems are regulated by genetic programs that share a common evolutionary origin.

121 he heterodimeric and homodimeric kinesin-14s share a common evolutionary structural and mechanochemic

122 jor clonal subpopulations in each tumor that shared a common evolutionary lineage.

123 cing leaves and petals, despite these organs sharing a common evolutionary origin.

124 dels of photosynthesis and leaf gas exchange share a common 'Farquhaur-model' core structure.

125 All nanomaterials share a common feature of large surface-to-volume ratio,

126 underlying causes and pathophysiology, they share a common feature, in that each disorder activates

127 MukB and canonical SMC proteins share a common five-domain structure in which globular N

128 How proteins sharing a common fold have evolved different functions i

129 mily is a versatile group of protein domains sharing a common fold.

130 teins from phylogenetically diverse bacteria share a common function in contact-dependent growth inhi

131 Current studies show that FlnA and FlnB share a common function in stabilizing the actin cytoske

132 ays in fly mutants, we show that these genes share a common function, which appears to be distinct fr

133 tion map, and it is suggested that both maps share a common functional architecture.

134 t members of the TULP family (TUB and TULP1) share a common functional interaction with MTAP1A.

135 Many essential processes in biology share a common fundamental step-establishing physical co

136 A large fraction of RepID-binding sites share a common G-rich motif and exhibit elevated replica

137 ium)-suggests that many eukaryotic organisms share a common gamete fusion mechanism.

138 All CLLs share a common gene expression profile that suggests der

139 essive cancers and embryonic stem (ES) cells share a common gene expression signature.

140 unique extant species with populations that share a common genetic background but blood feed in one

141 are key target tissues of estrogen, may thus share a common genetic basis underpinned by highly frequ

142 types exists, indicating that they plausibly share a common genetic basis.

143 nd other abilities (the extent to which they share a common genetic etiology) cannot be determined fr

144 at intersect, that is, they overlap and thus share a common genome interval.

145 MARV and EBOV share a common genome organization but show important di

146 All the complex rearrangement products share a common genomic organization, duplication-inverte

147 ), raising the question whether Kir channels share a common Golgi export mechanism.

148 The existence of two thermalization pathways sharing a common ground state suffices for power enhance

149 ten translationally regulated drivers of EMT sharing a common GU-rich cis-element within the 3'-untra

150 entially training participants on tasks that share a common high-level task structure can produce fas

151 ities may interact with infectious pathogens sharing a common host.

152 Although they share a common induction mechanism, it is not known how

153 Rho GTPases share a common inhibitor, Rho guanine nucleotide dissoci

154 These clusters are present in both sexes and share a common input pathway, but sex-specific wiring re

155 SRC and AURKA share a common interaction partner, NEDD9, which serves

156 Thus, ATL and AG do not share a common interest in semantic tasks, but, rather,

157 All proteins shared a common internalization pathway into lysosomal c

158 reveals that the four imido/iminyl complexes share a common iron oxidation level consistent with a fe

159 ing that plant peptide hormone receptors may share a common ligand binding mode and activation mechan

160 s adsorption in a porous crystal whose cages share a common ligand that can adopt two distinct rotati

161 ot necessary to generate new antibodies that share a common light chain, therefore allowing the immed

162 lthough the entire VMH including the VMH(vl) shares a common lineage, the VMH(vl) further differentia

163 humic substances suggests that they and BrC share a common link between pH and absorption, which we

164 ed in all eukaryotes and encode for proteins sharing a common MAGE homology domain.

165 eld of view by imaging 2 oblique planes that share a common major axis with the cell.

166 Haplogroups K and T, which share a common maternal ancestor, are shown as protectiv

167 ence identity, both ClpXP and the proteasome share a common mechanism by which substrate sequences re

168 processes in archaea and eukaryotic cytosols share a common mechanism dependent on a [3Fe-4S] cluster

169 dicate that Neurospora and higher eukaryotes share a common mechanism for the signal transduction of

170 , it remains unclear if all these chemotypes share a common mechanism of action.

171 0-dependent members of this family appear to share a common mechanism of hydride transfer from the re

172 Critically, Pol alpha and the CMG helicase share a common mechanism of interaction with Ctf4.

173 . target erythrocytes of different ages, but share a common mechanism of invasion.

174 ly that the PerR orthologs from streptococci share a common mechanism of metal binding, peroxide sens

175 ngs, we investigated whether oAbeta and oTau share a common mechanism when they impair memory and LTP

176 data indicate that the allosteric modulators share a common mechanism whereby they increase available

177 at pH inactivation and the external K sensor share a common mechanism, whereby E132, R128, and F127 s

178 tachycardias, whether atrial or ventricular, share a common mechanism.

179 ndicating that quelling and qiRNA production share a common mechanism.

180 suggests that members of the NDT superfamily share a common mechanism; however, the enzymes differ in

181 metabolic, or genetic, degeneration of axons shares a common mechanism involving mitochondrial dysfun

182 ely 4% of the mammalian genome whose members share a common membrane topology.

183 ar timing differences are maintained despite sharing a common milieu.

184 response pathway revealed that IAA and 2,4-D share a common mode of action to elicit downstream physi

185 Fimbriae share a common mode of biogenesis, orchestrated by a mol

186 ntibodies CH04 and PGT145 indicate that they share a common mode of glycan penetration by extended an

187 es, metabolism and immunity, have evolved to share a common modular architecture that allows extensiv

188 t that cold-induced suppression of TRPV1 may share a common molecular basis with heat-induced potenti

189 ngage different subsets of residues, despite sharing a common morphinan scaffold.

190 gnment corrections on spectral regions which share a common "most similar" spectrum.

191 is sequence specific, as these fragments all share a common motif that matches the YBX1 recognition s

192 highly homologous calcium-binding proteins, share a common motif with GIV for Galpha(i) binding and

193 ere derived from the same clone-all lineages shared a common mtDNA mutation.

194 Netrin G proteins share a common multi-domain architecture comprising a la

195 There are four homologous isoforms (HCN1-4) sharing a common multidomain architecture that includes

196 rlapping patterns of promiscuity result from sharing a common multifunctional ancestor.

197 One possibility is that muscles of a synergy share a common neural drive.

198 haptic perceptual systems are understood to share a common neural representation of object shape.

199 he hypothesis that rhesus monkeys and humans share a common neural shape representation that directly

200 erally infrequent, surprising (novel) events share a common neuroanatomical substrate.

201 ty to chemical and behavioral addictions may share a common neurobiological basis.

202 distinct, specialized niches or whether they share a common niche.

203 Both proteins share a common nucleation-elongation mechanism, whereby

204 ermis-resident antigen-presenting cells that share a common ontogeny with macrophages but function as

205 shows that caval vein and atrial myocardium share a common origin and demonstrates a clonal relation

206 s in eukaryotic/eukaryote-like IleRSs, which share a common origin but diverged through adaptation to

207 Multiple cell types that share a common origin cooperate to form a supportive nic

208 eveloping bone marrow HSC niche-forming MSCs share a common origin with sympathetic peripheral neuron

209 The first haematopoietic stem cells share a common origin with the dorsal aorta and derive f

210 upports the proposition that this center may share a common origin with the insect mushroom body desp

211 ted whether cells within a metaplastic gland share a common origin, whether glands clonally expand by

212 ra of phytochrome and phototropin, appear to share a common origin.

213 that tunicate and vertebrate hair cells may share a common origin.

214 dentified Ab10 variants (Ab10-I and Ab10-II) share a common origin.

215 uli is critical in determining which stimuli share a common origin.

216 IL-12 and IL-23 share a common p40 subunit encoded by Il12b, which is ne

217 Discovery of the cytokine IL-23, which shares a common p40 subunit with IL-12, prompted efforts

218 We sought to define whether both variants share a common pathogenesis.

219 All cancers, however, share a common pathogenesis.

220 esent a family of at least 80 illnesses that share a common pathogenesis: an immune-mediated attack o

221 hat diseases with different molecular causes share a common pathogenic mechanism or that dysregulated

222 d reduced generalized BMD in RA patients may share a common pathogenic mechanism.

223 r's, Parkinson's and polyglutamine diseases, share a common pathogenic mechanism: the abnormal accumu

224 Many neurodegenerative proteinopathies share a common pathogenic mechanism: the abnormal accumu

225 osttreatment reactions following DEC and IVM share a common pathophysiology.

226 ce and protomer structure these proteins may share a common pathway for amyloid nucleation and subseq

227 The findings suggest that CFH and ARMS2 share a common pathway in the pathogenesis of AMD.

228 , we evaluated whether TFFs and NHE isoforms share a common pathway to promote epithelial repair.

229 + 18 treatment, indicating these correctors shared a common pathway for rescue involving a network o

230 Patients with EOAD, lvPPA, and PCA shared a common pattern of WM damage that involved the b

231 Furthermore, cognitive control tasks shared a common performance factor related to set shifti

232 entricles (LV) do not function in isolation, sharing a common pericardial sac and interventricular se

233 Although fenethylline shares a common phenethylamine core with other amphetami

234 ascin-2 (p.R109H) or mice lacking beta-actin share a common phenotype including progressive, high-fre

235 First and second-generation DASAs share a common photoisomerization mechanism in chlorinat

236 They share a common physical basis, one aspect of which is a

237 studies show that adipocytes and fibroblasts share a common pool of progenitor cells, with Zinc finge

238 We assume that a population of V1 neurons shares a common pool of thalamic inputs, and consists of

239 epidemiologic data have shown that AD and MD share a common possible genetic cause.

240 suggests that most, if not all, Hox proteins share a common potential to induce cell segregation but

241 Both TA polymers share a common precursor synthesis pathway, but differ i

242 No larger difference between organisms that share a common prey could exist than between carnivorous

243 olution, and in some taxa limbs and genitals share a common primordium.

244 scientific approaches to the origin of life share a common problem: a chemical path to lipids as mai

245 100,000 genetic tags, we found that B1 cells share a common progenitor with embryonic cells of the co

246 elated to endocrine cells by lineage as they share a common progenitor.

247 ted that different kinds of self-control may share a common psychobiological component.

248 Yeast and human Top1 share a common reaction mechanism and domain structure.

249 imprinting status of Capsella rubella, which shared a common recent ancestor with Arabidopsis thalian

250 They both share a common receptor subunit, IL-4Ralpha, and signal

251 in terms of near-threshold decision-making, sharing a common recurrent (attractor) neural circuit me

252 These disparate pathways share a common regulatory GTPase Ypt1 (Rab1) that is act

253 ion across independent developmental modules shares a common regulatory 'logic', which has a predicta

254 ort the observation that MNSAID-UA, although sharing a common response with AERD to COX inhibitors, s

255 All RGS proteins share a common RGS domain that interacts with G protein

256 of types A and B are all centrosymmetric and share a common ring conformation.

257 the SAM clan, comprising three families that share a common SAM-binding core but differ radically in

258 These small molecule inhibitors share a common scaffold and have activity against both b

259 ring the induction of the UPR, some of which share a common sequence motif that may direct cleavage o

260 Candidate AgaR-binding motifs share a common sequence with consensus CTTTC that was fo

261 Imaging studies in brain, heart and islets share a common set of challenges, including developing n

262 works that have different types of links but share a common set of nodes) arise naturally in a wide s

263 We hypothesized that rat and human cells share a common signal-encoding mechanism but employ diff

264 We hypothesized that Osr1 and Tbx5 share a common signaling networking and downstream targe

265 Light and ACh share a common signaling pathway in sphincter muscle.

266 ax3-negative lineage origin, harbor SCs that share a common signature (Pax7(+), Ki67(-), Nestin-GFP(+

267 t human and mouse clusters are analogous and share a common signature of senescence and SASP.

268 oxide, and titania supports, apparently all sharing a common, similarly structured gold active site.

269 zed form of intercellular communication that shares a common SNARE-mediated fusion mechanism with oth

270 T and B cells share a common somatic gene rearrangement mechanism for

271 only in that they are both distressing--they share a common somatosensory representation as well.

272 Eosinophil receptors for IL-5 share a common ss-chain with IL-3 and GM-CSF receptors.

273 ase and the neuronal cell in Sydenham chorea share a common streptococcal epitope GlcNAc and target i

274 ogues from S. coelicolor and M. tuberculosis share a common structural core domain, with extensive, a

275 transmembrane segment family of ion channels share a common structural design.

276 involving phosphorylation or Ca(2+) binding--share a common structural mechanism for switching off th

277 n to cytotoxicity and amyloidogenicity, they share a common structural motif, and are channel forming

278 reveals separate receptor binding sites that share a common structural motif, thus suggesting a poten

279 oswitches are diverse, but we find that they share a common structural strategy in positioning their

280 EcXGPRT shares a common structural feature with other members of

281 ymporter (SSS) from Vibrio parahaemolyticus, shares a common structural fold with LeuT of the neurotr

282 bers of a superfamily of homologous proteins sharing a common structural core diverge into subgroups

283 Our study suggests that Mnk1 and Mnk2 share a common structure of the allosteric inhibitory bi

284 ethod for testing whether music and movement share a common structure that affords equivalent and uni

285 The liver and exocrine pancreas share a common structure, with functioning units (hepati

286 We speculate that LOXs share a common T-shaped substrate channel architecture t

287 amplified, creating sequence 'families' that share a common tag sequence derived from the two origina

288 hic sesquiterpenes, which we hypothesized to share a common target.

289 ocol that aims to generate spectral segments sharing a common target spectrum.

290 The studies presented shared a common theme in which a combination of physical

291 and narrow thermal niches, or if provenances share a common thermal niche.

292 Temporally close episodes shared a common timestamp regardless of the spatial cont

293 onal identities emerge from progenitors that share a common transcriptional code is not understood.

294 opographically related progenitor pools that share a common transcriptional code produce serotonergic

295 Four share a common translational start site encoded by exon

296 e discovered that all nontransverse patterns share a common underlying array architecture, having a c

297 ons among the traits, at least some of which share a common underlying genetic architecture.

298 we review evidence that these disorders may share a common underlying neuropathy: altered excitatory

299 Therefore, insofar as twins share a common upbringing, it appears that genes, rather

300 rms of decision-making and motor control may share a common utility in which the brain represents the