ライフサイエンスコーパス: contact between @1 and

1 nce of a decline in household SAR for direct contact between 1976 and 2014 (P = .018).

2 re sustained without further intervention or contact between 3 and 6 months.

3 negative charges, but the result of specific contacts between gp120 and a well defined sulfation in s

4 The morphology and duration of contacts between cells and adhesive surfaces play a key

5 tated binding provides evidence for a direct contact between CooA and alpha-CTD of RNAP during activa

6 that these substitutions interfere with the contact between CRP and alpha but do not affect the posi

7 ctured backbone and an asymmetric pattern of contacts between T4L and alpha-crystallin.

8 Contact between lymphocytes and AM reduced inhibitory C/

9 terfere with van der Waals and hydrogen bond contacts between p27 and amino acids in the catalytic cl

10 These results indicate that contacts between PTF and amino acids in the POU-specific

11 tes a coordinated antiviral response through contact between gB and an as-yet-unidentified cell surfa

12 Benefits include lack of contact between solutions and an apparatus and a lack of

13 hropological expansion increases the risk of contact between human and animal populations and, as a r

14 These arene complexes show no close contacts between cations and anions.

15 wever, locally, we see evidence for improved contacts between antibody and antigen, and two mutations

16 an auxiliary role in facilitating productive contacts between tyrosine and antigen.

17 Heme was the central molecule mediating contact between HCCS and apocytochrome c.

18 with the beta-domains via an intramolecular contact between Phe86 and Arg183.

19 However, van der Waals contact between Trp330 and Arg308 may also be important

20 To assess neurovascular encasement, contact between tumor and arteries, between tumor and ve

21 barrier dominated resistance and the direct contact between ZnO and Au electrodes.

22 Analysis of dipolar contacts between heme and axial His and between heme and

23 Synapse formation requires contact between dendrites and axons.

24 eron and residual CpG, and requires physical contact between pDCs and B cells.

25 oduction, showing the importance of physical contact between T and B lymphocytes in the Th2-mediated

26 s studies have provided evidence that direct contact between nanoparticles and bacterial cell membran

27 ple A/E lesion on infected cells and loss of contact between enterocytes and basement membrane.

28 l packing interaction replicates the lateral contacts between alpha- and beta-tubulins in the microtu

29 We explored the contacts between alpha and beta1 by determining the exte

30 lpha2 domains results in significantly fewer contacts between alpha3 and beta2-microglobulin compared

31 Family processes involving contact between adoptive and birth family members, co-pa

32 y is caused by increasing the probability of contact between molecules and by stretching the molecule

33 The direct protein to protein contact between Egr1 and c/EBPbeta is also demonstrated

34 FVIII x-ray structures show close contacts between A1 and C2 domains.

35 rystalline form of TiO2 NSA, and an intimate contact between TiO2 and carbon cloth resulted from dire

36 p, in beta-turns, and in specific intrachain contacts between amino- and carboxyl domains.

37 Contacts between PNP and catalytic site ligands are shor

38 We suggest how F52/R54 contacts between regulatory and catalytic subunits might

39 of R5 HIV-1 isolates and localize a critical contact between gp120 and CCR5.

40 from guanidinium chloride, ten major, stable contacts between tubulin and CCT are involved.

41 We hypothesized that direct contact between ASM and CD4(+) T cells facilitated the t

42 ) gene and protein expression, and 3) direct contact between FC and CD4(+)25(-) T cells is required f

43 Additional contacts between gp120 and CD4 give the CD4-gp120 comple

44 By precluding direct contacts between TCR and CD4, the structure explains how

45 be measured by methods that require a direct contact between probe and cell.

46 Instead, direct cell-cell contact between macrophages and cells engineered to expr

47 These findings suggest that CD40-CD40 ligand contacts between fibroblasts and cells secreting IL-4 ma

48 n capture (Hi-C) analysis revealed prominent contacts between telomeres and chromosomal arm regions c

49 gration in the corneal stroma involves close contact between keratocytes and collagen.

50 hesion molecules, which were involved in the contact between eosinophils and Colo-205 cells.

51 ane beneath the pedicles, including apparent contacts between telodendria and cone pedicles.

52 cross our sites, changing abruptly at mapped contacts between plutons and correlating with bedrock co

53 arlier report in an animal model of physical contact between melanocytes and cutaneous nerves and for

54 mately 15-A resolution revealed two sites of contact between aNT and d that are mediated by highly co

55 Contacts between actin and DBP throughout their extensiv

56 is referred to as the wrench; ATP modulates contact between beta and delta among other functions.

57 of communication at synapses, the points of contact between axons and dendrites.

58 n older cells, were localized to a subset of contacts between axons and dendrites.

59 rogressive loss of Tregs, impaired cell-cell contact between Tregs and dendritic cells (DCs), as well

60 logy modeling suggests that there is minimal contact between protein and DNA, that the nascent base p

61 We examined the contacts between EVI1 and DNA by methylation interferenc

62 d by chromatin immunoprecipitations, loss of contacts between histones and DNA occurs at both promote

63 ounterpart revealed major divergences in the contacts between protein and DNA and in the enzyme orien

64 initiation complex and that establishment of contacts between RNAP and downstream DNA can be coupled

65 lled tumor cells to DCs depends on cell-cell contact between DCs and dying tumor cells and is mediate

66 AMs required tumor cell death and the direct contact between MPhi and dying cancer cells via Mer tyro

67 ols formation of a distinct type of adhesive contact between mesoderm and ectoderm cells that shows p

68 Contacts between afferents and efferents were observed f

69 The stimulatory effect depends on the contact between DHX29 and eIF1A.

70 nt of the ternary complex; however, physical contact between eIF3 and eIF2 has not been observed.

71 We analyzed close contacts between halogens and electron-rich moieties.

72 atherosclerotic arteries with minimal direct contact between balloon and endothelium.

73 is tRNA has been created and used to examine contacts between tRNA and Escherichia coli alanyl-tRNA s

74 activity to the number density of catalytic contacts between Au and FeO(x).

75 Direct contact between macrophages and fibroblasts was not requ

76 d in treatments where the membrane prevented contact between dinospores and fish.

77 ytoplasmic rod and ring substructures places contacts between FliG and FliMFliN at the periphery of t

78 ure showed that, although both had extensive contacts between PDZ and FN3 domains, they exhibited a l

79 ly specific binding, rather than nonspecific contact, between avidin and functionalized xenon leads t

80 While direct contacts between activators and general factors have bee

81 he N-terminus of UL25 localized the point of contact between UL25 and GFP.

82 inflammation was partly due to the cell-cell contacts between neurons and glia via neural cell adhesi

83 isplaced from the active site, restoring the contact between Cys707 and Glu673 and allowing the latte

84 the AMPA receptor GluR4 subunit to sites of contact between axons and GluR4-transfected nonneuronal

85 -terminal tail of gp43, providing a point of contact between gp45 and gp43.

86 er acetylation is involved in regulating the contacts between SIR3 and H4.

87 in time and function and the close physical contact between LVs and HEVs in the remodeling process a

88 model in which D1 and D2 make the principal contacts between KIR3DL1 and HLA-B while D0 acts through

89 Both decreased contact between people and horses, and the concomitant i

90 ction of cascades of virulence factors after contact between bacteria and host cells was investigated

91 al type III secretory mechanism activated by contact between bacteria and host cells.

92 ategies may include increasing the amount of contact between vector and host, reducing vector reprodu

93 These effects require direct cell:cell contact between FC and HSC.

94 g and hydrolysis, and suggest that molecular contacts between HslU and HslV vary dynamically througho

95 Such coupling is embodied in contacts between Hsp90 and Hsp70 in the GR:Hsp70:Hsp90:H

96 inal side of the V3 stem as critical for the contact between SU and HSPG.

97 ical) and the fully conserved catalytic site contacts between BtPNP and HsPNP, crystal structures rev

98 Inactivation requires cell-to-cell contact between CTL and HSV-infected cells.

99 ybrid analysis now indicates protein-protein contact between Polbeta and human AP endonuclease (Ape p

100 tion experiment further indicates that these contacts between F19 and I31 are intermolecular, contrar

101 d colocalization of beta-catenin in areas of contact between KC and immature (Langerhans cell-like) d

102 In contrast, contact between B19 and inappropriate muscle targets fai

103 pecies transmissions of STLV-1, suggest that contact between humans and infected nonhuman primates (N

104 with mixed acyl constituents at the point of contact between vesicle and interface then facilitate fu

105 dimerization of this RTK induces an extended contact between juxtamembrane and intramembrane alpha he

106 closed conformation and bolstering of cross contacts between CcpA and its other corepressor, HPr-Ser

107 terference studies, which revealed extensive contacts between EVI1 and its binding site.

108 To begin to identify contacts between P and its partners, we assessed the exp

109 d cargo-bound Xpot and functionally critical contacts between Xpot and its cargo.

110 de of the L2 structure, supporting extensive contact between E1 and L2 domain.

111 (13)C NMR chemical shifts and by side chain contacts between F19 and L34 residues, is qualitatively

112 nd highly localized to subcellular points of contact between myoblasts and laminin-coated 2.8-microm

113 27R or W105R plus W138R, thereby pinpointing contacts between HC and LCb.

114 Physical contact between ECs and LCs or T cells was not required

115 results suggest that the extensive physical contact between peroxisomes and lipid bodies promotes th

116 es from HIV-infected individuals, and direct contact between macrophages and lymphocytes is required.

117 d M145, with an essentially complete loss of contacts between C28W and M144 and M145.

118 A direct contact between bacteria and macrophage and not Mtb-rele

119 We postulate that Emp-mediated contact between erythroblasts and macrophages promotes t

120 If contact between lymphocytes and macrophages was prevente

121 The ARP-HSA interactions are reminiscent of contacts between actin and many binding partners and are

122 l-like) dendritic cells, but not in areas of contact between KC and mature (lymph node dendritic cell

123 At contacts between fibroblasts and MC/9 mast cells, mb-Kit

124 The main contact between Cdc6 and MCM occurs via the N-terminal p

125 flexible, and highly conductive due to good contacts between spheres and metallic conductivity of MX

126 s can markedly alter evolutionarily selected contacts between TCR and MHC ("CDR3 editing").

127 We reevaluated contacts between TCRs and MHC in the solved structures o

128 nts of indoor human environments, where most contact between humans and microbes occurs.

129 icate the Ndc80 complex as a direct point of contact between kinetochores and microtubules, but these

130 and tail domains of Hec1 generate essential contacts between kinetochores and microtubules in cells,

131 uggest that protein-lipid complexes form via contacts between proteins and mixed lipid/detergent mice

132 h17 polarization mostly depended on physical contacts between ASCs and MNCs-with a contribution of in

133 cate that IL-8 induction results from direct contact between bacteria and monocytes.

134 Interruption of intercellular contact between platelets and monocytes dramatically inh

135 erated high density of nanoscale interfacial contact between CZTS and MoS2-rGO hybrid.

136 Cross-linking of all domain-swapping contacts between NBDs and MSD cytoplasmic loops in oppos

137 of zebrafish and maintains, over days, close contact between head and multiple surface electrodes, en

138 Importantly, direct contact between osteocytes and multiple myeloma cells re

139 nduction of transmitter release initiated by contact between nerve and muscle is presented.

140 he protective effect was dependent on direct contact between Mvarphis and myeloma cells.

141 Physical contact between OCs and myeloma cells was required for t

142 ion efficiency, and the abrogation of direct contact between infected and naive animals through the e

143 No transmission by direct contact between infected and naive ferrets was observed.

144 cross-linking techniques to define molecular contacts between actin and ND8, a two-module nebulin fra

145 tion of the prehairpin is triggered by local contacts between F- and neighboring viral receptor-bindi

146 ypothesis that van der Waals and hydrophobic contacts between Y265 and neighboring residues are impor

147 The contacts between antigen and neutralizing antibody defin

148 of growth-delayed enterocytes and prolonged contact between ISCs and newly formed daughters.

149 vidence for the existence of direct synaptic contacts between CFs and NG2-expressing glia cells, addi

150 We conclude that contact between neural and non-neural ectoderm is capabl

151 Direct physical contact between transformed and nontransformed cells was

152 the majority (81%) of the total 263 synaptic contacts between MOR- and NR1-labeled neuronal profiles.

153 dicating the presence of a high frequency of contact between mitochondrial and nuclear DNA in some so

154 is consistent with the hypothesis of direct contact between EL2 and nucleotide ligands.

155 5l-associated sequences are sites of initial contact between homologues and of localized DNA synthesi

156 trait related to the intimate physiological contact between mother and offspring during gestation.

157 The proximity and possible contact between P66 and OspA (or other Osp proteins) may

158 This effect was maintained when direct contact between M1 and osteoclast precursors was interru

159 c reticulum and a second organelle, although contacts between mitochondria and other organelles have

160 distinguish contacts amongst promoters from contacts between promoters and other genomic elements.

161 This suggests that specific, unique contacts between SecA2 and other components of the acces

162 ha and nitric oxide, but does require direct contact between host and pathogen.

163 skeletal reorganization triggered by initial contact between TCR and peptide-bearing APC precede, and

164 f intermolecular complementarity at sites of contact between SK and Pg may represent a competitive ev

165 The cell wall is the initial point of contact between Candida and phagocytes, but isolated cel

166 in AgNM-exposed plants, showing that direct contact between AgNMs and plant seeds/roots is a require

167 These activities may require intimate contact between astrocyte and plaque.

168 mbrane curvature that would promote a closer contact between vesicle and plasma membrane.

169 wever, it is perhaps the specific and direct contact between Rat1 and Pol II that transmits the signa

170 The formation of stable adhesive contacts between pre- and post-synaptic neurons represen

171 Adhesive contact between pre- and postsynaptic neurons initiates

172 ns unaltered, consistent with the absence of contacts between Sox2 and POU(HD).

173 of preterm birth can be reduced by frequent contact between nurses and pregnant women or home monito

174 ld will enhance the number of encounters or "contacts" between predators and prey.

175 lytic behaviour, in which there is no direct contact between reagents and products, and our approach

176 The model predicts hydrogen bonding contacts between ligand and protein at S237 and D299 as

177 Approximately 65% of identified synaptic contacts between DbH- and PRV-positive profiles were cla

178 The majority of identified contacts between DbH- and PRV-positive profiles were cla

179 ain Outcome Measure Duration of face-to-face contact between patient and psychiatrist.

180 ding, giving an initial estimate of the main contacts between peptides and receptor.

181 these plasmids from competent donors despite contact between donor and recipient cells.

182 ely contributes to DNA transfer and mediates contact between donor and recipient strains.

183 that the random, initial, long-range (12 nm) contact between merozoites and red cells occurs normally

184 late growth factor signaling with filopodial contact between signaling and responding cells, and sugg

185 n important role in establishing the initial contact between DCs and resting T cells.

186 cY-FtsY complex, which allows the subsequent contact between SecY and ribosomal protein uL23.

187 d in order to establish effective activating contacts between FNR and RNA polymerase.

188 We used cross-linking to determine if direct contacts between MerR and RNAP also occur during this pr

189 is is the first evidence for stable physical contacts between MerR and RNAP and for a Hg(II)-induced

190 We define the contacts between Myx and RNAP and the effects of Myx on

191 se features suggested that the IZ (i.e., the contact between photoreceptors and RPE) is the primary s

192 ons, beyond the observed hydrophobic surface contacts, between 4 and RT is quite perplexing given the

193 Contact between cells and S(0) was required for growth.

194 between S4 and S6 (and likely the analogous contact between S1 and S3) likely results in an extended

195 centrations; the disruption of this extended contact between S4 and S6 (and likely the analogous cont

196 ibrils matrix further away from the point of contact between probe and sample.

197 For example, contact between axons and Schwann cells triggers signals

198 It is observed that the intimate contact between graphene and Si is maintained during vol

199 protein, suggesting a direct protein-protein contact between MotA and sigma70.

200 ndicates that they identify a second site of contact between RhaS and sigma70.

201 is is regulated, at least in part, by direct contacts between syt and SNAP-25/syntaxin.

202 SS indicates that these factors may mediate contacts between RNAPII and snRNPs during the coupled tr

203 d real-time animal position data to describe contact between animals and specific environmental areas

204 highlighting the importance of base-specific contacts between ppGpp and specific cytosine residues du

205 binding antibodies, while we find additional contacts between 11F8 and ssDNA that involve amino acids

206 ion constant, consistent with multiple ionic contacts between protein and ssDNA phosphate residues an

207 ectionality of tip cells and by loss of cell contacts between tip and stalk cells.

208 The remaining contacts between oligomycin and subunit c are primarily

209 on in nature and industry, where the time of contact between droplet and surface influences the trans

210 VC polarity and migration, we quantified the contact between TVCs and surrounding tissues, and blocke

211 Many pathogens spread primarily via direct contact between infected and susceptible hosts.

212 mitted infections require some form of close contact between infectious and susceptible hosts to spre

213 populations or by changing the frequency of contacts between infected and susceptible individuals.

214 o support SVZ neurogenesis, direct cell-cell contact between astrocytes and SVZ neuronal precursors m

215 form of regulation did not require prolonged contact between CTLs and T(reg) cells but depended on CT

216 s factor alpha and was blocked by preventing contact between macrophages and T cells, suggesting that

217 production of NO were dependent on cell-cell contact between MDSCs and T cells, and upon IFN-gamma, a

218 tes to build the IS and to maintain adhesive contacts between APC and T cells, required for continuou

219 entation and an overall 50% reduction in the contacts between jSR and T-tubules.

220 infection mediated by iDCs and mDCs required contact between DCs and target cells.

221 n target cells provides an additional arm of contact between effector and target cells which is criti

222 l-mediated death of Colo-205 by facilitating contact between effector and target cells.

223 nsport, wherein tethering provides the first contact between vesicle and target membranes.

224 ls, but could detect only the repeated close contact between effectors and targets, which suggested t

225 Contact between LAKs and targets was required for p65 ph

226 ) results in disruption of a protein-protein contact between TFIIB and TATA binding protein (TBP), wh

227 g the TFIIA.TBP contact or creating a second contact between TFIIA and TBP that was not visible in th

228 U or, in the case of glnHp2, by IHF to allow contact between activator and the sigma 54-RNA polymeras

229 ibition also requires direct protein-protein contact between AsiA and the RNAP core.

230 ary to the prevailing view that there was no contact between Australia and the rest of the world.

231 are bactericidal proteins that limit direct contact between bacteria and the intestinal epithelium a

232 unoprecipitation data revealed that physical contact between CAF1 and the LRR is blocked by mutation

233 nd integrin receptors to form areas of close contact between cells and the extracellular matrix refer

234 cellular factors that accumulate at sites of contact between cells and the extracellular matrix.

235 In addition to the contact between eIF2 and the N-terminal domain (NTD) of

236 During this conversion, total hydrophobic contact between enzyme and the peptide is preserved.

237 P-convertase complex suggests that the major contact between FP and the AP convertase is mediated by

238 No direct contact between gamma and the c ring seems to be require

239 The mucus layer is critical in limiting contact between host and the complex bacterial consortia

240 he HSGAG structure, thereby enabling maximum contact between HSGAG and the protein.

241 MCM3 suggests that MCM3 is a point of direct contact between KEAP1 and the MCM hexamer.

242 truncated the beta3-beta4 loop, eliminating contact between Lys65 and the gamma-phosphate of dNTP.

243 pepsin) showed that there are two regions of contact between PI3 and the enzyme.

244 he role of Arg-47 may be to maximize surface contact between PTP1B and the peptide, which contributes

245 Breaking contact between SecA and the sides of SecB results in re

246 rthermore, the binding mode also circumvents contact between TCR and the peptide presented by MHC, wh

247 The major contact between YidC and the lateral gate was lost in th

248 ot cause a substantial change on interfacial contacts between Arp3 and the ArpC2, ArpC3 and ArpC4 sub

249 at this activation does not require specific contacts between C and the carboxyl-terminal region of t

250 ing of Ca(2+) to the NaV CTD and uncover new contacts between CaM and the NaV CTD.

251 Contacts between endosomes and the endoplasmic reticulum

252 nd affinity much more susceptible to packing contacts between F4 and the heme group.

253 ; and 2) that in both cases binding involves contacts between gp59 and the acidic C-terminal domain o

254 act with the seipin complex, which regulates contacts between LDs and the endoplasmic reticulum (ER).

255 NA retardation analysis to: (i) evaluate the contacts between MarA and the marboxes of five different

256 through additional direct and water-mediated contacts between oligosaccharides and the protein surfac

257 A binding domains, aiming to establish novel contacts between p53 and the DNA phosphate backbone.

258 e poles from the outset and led to symmetric contacts between poles and the bud, effectively disrupti

259 -(15)N correlation spectra, revealing direct contacts between povidone and the API.

260 tein-protein interaction assays demonstrated contacts between SKIP and the SMRT, CIR, Sin3A, and HDAC

261 lecules bridge several of the intermolecular contacts between spermine and the enzyme and form a "pro

262 ta3 cytoplasmic domain and identify specific contacts between talin and the integrin tail required fo

263 in is modulated primarily by the strength of contacts between telethonin and the two titin chains, an

264 this conformational change requires specific contacts between transposase and the flanking TA dinucle

265 The anti-LFA-1 treatment led to fewer contacts between Tregs and the remaining CD11c(+) cells

266 designed to test the importance of specific contacts between VP1 and the carbohydrate moieties of th

267 these complexes would exclude van der Waals contacts between W and the Br atoms.

268 ors associated with placement, the nature of contact between caregivers and their institutionalized r

269 Premature disruption of cell contact between ISCs and their progeny leads to increase

270 gen atom transfer by enforcing van der Waals contact between radicals and their reacting partners.

271 Little is known about how patterns of contact between SWs and their clients influence the pers

272 computational analysis of the point of first-contact between viruses and their hosts, namely viral tr

273 en as an ecological "catalyst" by increasing contacts between chloroviruses and their hosts, zoochlor

274 Synaptic contacts between neurons and their targets are dynamic e

275 Virus population growth depends on contacts between viruses and their hosts.

276 The intimate contact between H3R2 and these domain types leads to the

277 lex is predominantly mediated by hydrophobic contacts between SSL3 and TLR2 and does not involve inte

278 (EL2) and the smaller subpocket "B" forming contacts between TM6 and TM7.

279 ting a survey of the major sequence-specific contacts between GlnRS and tRNAGln.

280 be formulated, and thus optimal interfacial contacts between actin and tropomyosin remain unknown.

281 The growth inhibition requires contact between DCs and tumor cells while LPS treatment

282 n important role for establishing a physical contact between UL8 and UL52.

283 type 1 (HIV-1) can initiate infections, but contact between infected and uninfected T cells can enha

284 portal of entry for transmission by physical contact between infected and uninfected tissues to other

285 mation of virological synapses during stable contacts between infected and uninfected T cells greatly

286 on, is a visual signal that acts to minimize contact between predator and unprofitable prey.

287 hin the dermis, therefore, enabling physical contact between bacteria and various cells below the bas

288 eins, and nerves should be diagnosed, if the contact between tumor and vascular or neural circumferen

289 densities and by processes of saturation in contacts between hosts and vectors.

290 Interobserver agreement in quantifying contact between tumor and vessels and between tumor and

291 results help to define important regions of contact between integrase and viral DNA, and assist in t

292 cording to the Bell model, at short times of contact between cell and virion, the gp120-CD4 bond is a

293 Based on the observations that physical contact between nanorods and virus particles was not req

294 Limiting the contact between vegetables and water or using steaming s

295 her delivered remotely, without face-to-face contact between participants and weight-loss coaches, ob

296 Together, this work unveils multipoint contacts between PNKP and XRCC4-LigIV that regulate PNKP

297 The contacts between Zalpha and Z-DNA are made primarily wit

298 QDs, TSPP, and Zn(2+), preventing the direct contact between QDs and Zn(2+) but affording fluorescenc