ライフサイエンスコーパス: E

1 E complex is the earliest spliceosome precursor in which

2 E-consults increased the breadth and volume of total con

3 E. histolytica encodes a homolog of the human cytokine m

4 We measured fitness of approximately 14,000 E. coli strains, each expressing a reporter gene with a

5 143 nonduplicate Enterobacter isolates (102 E. cloacae complex, 41 E. aerogenes) were tested, includ

6 Moreover, expression of D28A accumulated 18S-E in Bystin-associated pre-40S particles, suggesting tha

7 of PARN is necessary for the release of 18S-E from Bystin-associated pre-40S particles.

8 peroxide afforded [Cp*2Fe][PhC(O)OE(C6F5)3] (E = B 5, Al 6).

9 ethyl 8-(2-(benzoyloxy)-ethyl)-hexahydro-4-((E)-pent-2-enyl)-2H-chromene-6-carboxylate of polyketide

10 obacter isolates (102 E. cloacae complex, 41 E. aerogenes) were tested, including 136 collected from

11 Of the 649 E. coli clinical isolates, 5 (0.8%) consistently produce

12 rgy % [E%] fat) (UNSAT) or carbohydrates (80 E% carbohydrate) (CHO) as well as a eucaloric control di

13 Matrigel assay, we showed that ct-8,9-E-11-HET is proangiogenic, whereas ct-8,9-E-15-HET is no

14 ,9-E-11-HET is proangiogenic, whereas ct-8,9-E-15-HET is not active.

15 Accordingly, E+P treatment of breast cancer cells increased ER bindin

16 rong pheromone antagonist codlemone acetate (E,E)-8,10-dodecadien-1-yl acetate.

17 ial marine natural product bromophycoic acid E scaffold.

18 er, mutation that substituted glutamic acid (E) for glutamine (Q) at amino acid position 623 (E623Q)

19 th the application of JNJ-303 and additional E-4031 significantly increased APD.

20 somerisation of (all-E)-rubixanthin and (all-E)-lycopene using iodine-catalysed photoisomerisation sh

21 The isomerisation of (all-E)-rubixanthin and (all-E)-lycopene using iodine-catalys

22 The observation that the alpha4 E loop is involved suggests that physostigmine interacts

23 An enhancer with amalgamated E-box and GATA motifs (+9.5) controls expression of the

24 prgU gene pairs are widely distributed among E. faecalis isolates and other enterococcal and staphylo

25 These natural products have in common an E,Z-configured conjugated diene linked to a di- or triyn

26 crobial peptide activity developed either an E. faecalis or Pseudomonas aeruginosa urinary tract infe

27 vidence that NCX1 interacts with and anchors E-cadherin to the cell surface independent of NCX1 ion t

28 ly decreased the expression of Zonulin-1 and E-cadherin, whereas Nlrp3 knockdown increased the permea

29 H0 (66.14) than that of ES-FPC (52.63), and E-FPC (43.27) and was comparable to PPC (68.47).

30 S. aureus and E. coli antigens were detected in immune-blotted HDM ext

31 groove comprising two electronegative B- and E-pockets that coincide with the preference for P2 and P

32 cidity, sugars, organic acids, vitamin C and E, carotenoids, polyphenolics and volatile compounds dur

33 ed the abundance of FIB (Total coliforms and E. coli) and the Bacteroidales (HF183 marker) with bacte

34 , with the exception of E. lecanii-corni and E. lavatrina, for which there was considerable log score

35 that contains all carbon atoms of the D and E ring of the natural product could be installed in thre

36 CHK1 via Rb-E2F by upregulating cyclin D and E.

37 Crystal structures of P- and E-selectin suggest a two-state model in which ligand bin

38 thia, T. denticola, P. micra, C. rectus, and E. nodatum show statistically higher detection frequenci

39 It requires a Rho- and E-cadherin adhesion-dependent, substrate-parallel contra

40 els, important for localization of STIM1 and E-Syts at ER-PM junctions, were reduced in RASSF4-knockd

41 In foragers, BA and (E)-dec-2-en-1-yl acetate (DA) generated the strongest an

42 ostructured electrode by using specific anti-E.coli DNA aptamer (Kd 14nM), screened by new in-situ d

43 Information on the apolipoprotein E (Apo-E) phenotype was available for 1259 men.

44 Apolipoprotein E (apoE) plays a critical role in cholesterol transport

45 Apolipoprotein E isolated from human cerebrospinal fluid carries sulfat

46 fic deficiency of CXCR4 in an apolipoprotein E-deficient mouse model.

47 zheimer's disease risk factor apolipoprotein E (APOE) varepsilon3/4 allele.

48 s effects on atherogenesis in apolipoprotein E-deficient (ApoE(-/-)) mice.

49 Information on the apolipoprotein E (Apo-E) phenotype was available for 1259 men.

50 Here, we designed a genetic screen around E. coli that identified high-affinity cytochrome bd oxid

51 As E cell and gDN1 activity is necessary and sufficient for

52 As E. histolytica does not readily form cysts in vitro, we

53 g conjugates (NDCs) of monomethyl auristatin E (MMAE) significantly increase loading on a per-vehicle

54 gated duocarmycin- and monomethyl auristatin E (MMAE)-based anti-PSMA ADCs with drug-to-antibody rati

55 The AE.A244 gp120 in AIDSVAX B/E also bound to the unmutated ancestor of a V2-glycan br

56 tudy groups 1-3 received ALVAC-HIV+AIDSVAX B/E, AIDSVAX B/E, and ALVAC-HIV, respectively, or placebo.

57 -3 received ALVAC-HIV+AIDSVAX B/E, AIDSVAX B/E, and ALVAC-HIV, respectively, or placebo.

58 combinant HIV-1 gp120 subtype B/subtype E (B/E) proteins demonstrated 31% vaccine efficacy.

59 T4 in suppressing a model enteric bacterium (E. coli K-12) in mixtures with soil bacteria (Pseudomona

60 no acids using the transmembrane beta-barrel E. coli PagP as a scaffold protein.

61 The electrochemical, aptamer-based (E-AB) sensor platform provides a modular approach to the

62 Electrochemical aptamer-based (E-AB) sensors offer advantageous analytical detection ab

63 onality, and the incidence of UTIs caused by E coli vaccine serotypes in each group.

64 This is followed by E/Z separation in a fourth analytical column.

65 s are a class of cell-surface factor used by E. coli for adherence.

66 d G) and preserved TC-NER (category 2: XP-C, E, and V).

67 iformly express high levels of the canonical E-selectin binding determinant sialyl Lewis X (sLe(X)) a

68 uced ROS-induced degradation of beta-catenin/E-cadherin in vitro and ameliorated skin damage in roden

69 /Abl kinases and degradation of beta-catenin/E-cadherin.

70 oach for de novo sequencing using whole cell E. coli lysate.

71 We detected escherichelin during clinical E. coli urinary tract infection (UTI) and experimental h

72 ng rice yield in response to elevated [CO2] (E-[CO2]) by comparison to free-air CO2 enrichment (FACE)

73 connected network motifs, Escherichia coli (E. coli) appears to favor crosstalk wherein at least one

74 loped for the detection of Escherichia coli (E. coli) using the T7 bacteriophages engineered with lac

75 n in aerobically respiring Escherichia coli (E. coli).

76 In contrast, E. medicae strains have lpiA/acvB and ebpA/tcrA/tcsA/fsr

77 progression by binding cyclin A- and cyclin E-CDK2.

78 In contrast, ectopic Cyclin E overproduction uncouples short G1 from fast MCM loadin

79 e and low-molecular-weight isoform of cyclin E (cytoplasmic)-negative) is a reliable prognostic bioma

80 At embryonic day (E) 12.5, the mesenchymal precursor pool began to subdivi

81 steady-state hematopoiesis at embryonic day (E) 14.5 was not affected by homozygous Mof deletion desp

82 trogens can be tested during embryonic days (E)14 to 19.

83 Importantly, neurobehavioral deficits, E/I imbalance, and histological damage are all ameliorat

84 sa region of Pluto (220 degrees -250 degrees E, 0 degrees -20 degrees N).

85 Using a DeltasdhE E. coli strain, we show that the requirement for the ass

86 from genetically manipulated GSC depletion, E(z) knockdown germ cells also fail to replenish lost GS

87 this improvement comes the ability to deploy E-AB sensors directly in situ in the veins of live anima

88 Starting from dimethyl (E)-2-{[(1-tert-butoxycarbonyl)-1H-indol-3-yl]methylene}s

89 ts using a series of organic triplet donors (E((3)pipi*) from 1.83 to 0.78 eV).

90 l patients underwent PET/CT with (68)Ga-DOTA-E-[c(RGDfK)](2) radiotracer and blood-sample tests to qu

91 Allergic side effects during E-OIT were common but all were mild to moderate.

92 he safety of pure nicotine inhalation, i.e., E-cigarettes.

93 peptide) and rest/exercise echocardiography (E/e' ratio) to make this determination.

94 While electrophilicities E correlate poorly with the LUMO energies and with Parr'

95 ys, enriched in unsaturated FA (78 energy % [E%] fat) (UNSAT) or carbohydrates (80 E% carbohydrate) (

96 Btbd7 can enhance E-cadherin ubiquitination, internalization, and degradat

97 f phenotypic variability in enteropathogenic E. coli (EPEC), an important human pathogen, both in vir

98 lycosylation site within the viral envelope (E) protein, whereas many isolates of the African lineage

99 he outcomes of patients with BSI due to ESBL-E who received empiric therapy with such drugs (other ac

100 ohort study of patients with BSI due to ESBL-E who received empiric treatment with OADs or carbapenem

101 Finally, mRNA expression of several ESC/E(Z) complex genes were increased by progesterone in con

102 he plant volatile compound pear ester ethyl-(E,Z)-2,4-decadienoate, while CpomOR6a responds to the st

103 wo routes that failed to access eupalinilide E were triaged either as a result of providing an incorr

104 minimum amount of THF afforded exclusively (E)-1 as the other diastereomeric product and was mediate

105 Cells expressing E-selectinE88D rolled but detached faster.

106 n with an extremely high selectivity factor (E > 500), showing that the classical mechanism involving

107 g in deeper defects and hence a higher field E th is required for unpinning.

108 n factors SRY-box 10 (SOX10) and zinc finger E-box binding homeobox 2 (ZEB2).

109 e resistance development in four out of five E. faecium strains; however, increased resistance was ob

110 e developed methodology was then applied for E. coli quantification in water samples using nanomateri

111 Shape is an important biomarker for E. gracilis, serving as an indicator of biological clock

112 hought to be a major source of nutrients for E. coli in the gut.

113 eased from the nucleus and competes LGN from E-cadherin to locally form the LGN/NuMA complex.

114 ocyte-associated antigen (CLA), a functional E-selectin ligand (ESL), is selectively expressed on cir

115 ning methods for estimating the MCPD-E and G-E contents in the fish products.

116 ropropane-1,2-diol (MCPD-E), and glycidol (G-E).

117 Garcinone E (GE) was found to exhibit excellent anti-proliferative

118 etic features of bla KPC emergence in global E. coli, 2008-2013, using both long- and short-read whol

119 ets for therapy of senile dementias.-Goetzl, E.

120 and was mediated by a beneficial (Z)-1 --> (E)-1 interconversion.

121 Cellular removal was evaluated by H&E, DAPI and DNA quantification.

122 ), 614 had tumor tissue samples scored for H&E sTILs and 427 for CD8 biomarker assessments.

123 Although hepatitis E virus (HEV) is regarded as a self-limiting infection a

124 iral treatment options for chronic Hepatitis E Virus (HEV) infections are limited and immunological d

125 that can be exploited to alter heterogeneous E. faecalis populations.

126 We propose the high E eff value corresponds to the onset of high energy dyna

127 patients had the highest strain and highest E/e' ratio, were the oldest, were predominantly female,

128 HC-Ib molecule human leukocyte antigen (HLA)-E and specific for an epitope from UL40 (VMAPRTLIL), whi

129 Because HLA-E plays an important role in antiviral immunity by regul

130 +) T cells, epigenetic downregulation of HLA-E by high-risk HPV E7 may contribute to virus-induced im

131 omorphic nature in the human population, HLA-E is an attractive target for novel vaccine and immunoth

132 es of a TRBV9(+) TCR in complex with the HLA-E molecule presenting the two peptides.

133 Our results show how E-cadherin instructs the assembly of the LGN/NuMA comple

134 Further analysis identified E-cadherin as the top positive correlated gene, while he

135 en-specific serum/plasma immunoglobulin (Ig) E levels later in life.

136 n, IL-5 and IL-13), serum immunoglobulin (Ig)E and airway hyper-responsiveness (AHR).

137 ted anti-interleukin and anti-immunoglobulin E therapies, and in monitoring subsequent treatment resp

138 ic sensitization, serum total immunoglobulin E (IgE), forced expiratory volume in one-second (FEV1) a

139 In E. coli, activity of AasC was sensitive to triacsin C an

140 e glutamate is the major monovalent anion in E. coli, these results suggest that SSB likely binds to

141 1295 treatment reduced plasma LPS content in E. coli-challenged baboons, implying reduced complement-

142 to-deoxyoctulosonate (Kdo)-lipid A domain in E. coli was necessary to facilitate chemical structure a

143 drolysis activity of an amidase expressed in E. coli with three different substrates.

144 Heterologous gene expression in E. coli confirmed its functions for hydrolysis of AHLs,

145 Among several pathways implicated in E-T coupling, activation of voltage-gated L-type Ca(2+)

146 Predictive cysteine cross-linking in E. coli membranes and PELDOR measurements along the tran

147 Targeted mutations in E. chaffeensis were created to disrupt two genes, and al

148 defects in PM lipid homeostasis observed in E-Syts KO cells, delayed diacylglycerol clearance from t

149 of macrocyclic peptide libraries produced in E. coli cells.

150 systems support conjugative DNA transfer in E. coli and trigger P. aeruginosa T6SS killing, but not

151 iR-126* and miR-126 downregulation increased E-selectin and VCAM1, respectively, while miR-126 overex

152 ota, which leads to overgrowth of indigenous E. coli and facilitates colonization by opportunistic pa

153 T4 was more effective than PEf1 in infecting E. coli K-12 in pure cultures, PEf1 was 20-fold more eff

154 the wca operon caused a persistent-infection E. coli strain to become sensitive to complement-mediate

155 hat seen with a cysteine protease inhibitor, E-64 (I-1).

156 rom imbalances in excitatory and inhibitory (E/I) brain circuitry.

157 ects that disrupt the excitatory/inhibitory (E/I) balance.

158 increased ratio of excitatory to inhibitory (E/I) neurotransmission.

159 s a general approach to compatibly interface E-AB sensors with complex biological samples.

160 ely describe a mouse model for investigating E faecalis wound infection determinants, and suggest tha

161 fic jasmonate repressor that regulates JAs, (E)-alpha-bergamotene, TPIs, and a defensin.

162 lial cells with surface expression of PD-L1, E-cadherin, CD24, and VEGFR2 rapidly formed tumors outsi

163 However, systems-level E/I patterns, at spatial scales larger than single neuro

164 By examining replisomes in live E. coli with fluorescence microscopy, we found that the

165 ransitions from the conduction band to lower E- and upper E+ valence subbands has been observed at ro

166 n North African Y chromosome markers (E-M81, E-M78, and J-M267) and mitochondrial lineages such as U6

167 d common North African Y chromosome markers (E-M81, E-M78, and J-M267) and mitochondrial lineages suc

168 1,3-diol, 3-monochloropropane-1,2-diol (MCPD-E), and glycidol (G-E).

169 as screening methods for estimating the MCPD-E and G-E contents in the fish products.

170 C II or the nonclassical MHC I molecule, MHC-E.

171 retained a preference for the 5caC modified E-box.

172 EcoCyc now supports running and modifying E. coli metabolic models directly on the EcoCyc website.

173 g nests are more related where there is more E. umbellata.

174 ernal perturbation in a dense bath of motile E. coli bacteria.

175 helial cell adhesion molecule [EpCAM](+)MPs, E-cadherin(+)MPs), platelet MPs (CD31(+)CD41(+)MPs), eos

176 In experiments on nonmotile E. coli exposed to polymyxin B, cell-generated frequency

177 The current study identified a novel E. chaffeensis ubiquitin ligase and revealed an importan

178 calcium signaling, transformation, and novel E-cadherin-RalBP1 interaction.

179 ntly lower for the R-E group than for the NR-E group (treatment main effect: F1,68 = 5.4, P = .02, d

180 Conservation of putative NusB/E binding sites upstream of Nus factor genes suggests th

181 flavivirus particle structure, definition of E dimers as the key antigenic target, and deep understan

182 investigated the quantitative destruction of E.

183 ensitive and 99.3% specific for detection of E. coli serotype O:157.

184 mal cellular architecture and development of E. muelleri.

185 d provide a framework for the development of E/I balance at the cellular level.

186 or 1 (HIF-1), followed the downregulation of E-cadherin, and produced heterogeneous cell subsets whos

187 cholera toxin, or heat-stable enterotoxin of E. coli (STa toxin), with IC50 down to approximately 5 n

188 ores (1.193 to 1.624), with the exception of E. lecanii-corni and E. lavatrina, for which there was c

189 educed in Nlrp3(-/-) mice, and expression of E-cadherin was reestablished.

190 the BMP9/BMP10-induced surface expression of E-selectin, and both ALK1 and ALK2 in the up-regulation

191 The transmissive form of E. histolytica is the cyst, with a single infected indiv

192 es and suggest routes for the improvement of E "mimicry" by E1 by increasing its recognition of the F

193 tic enterocytes promote divisions by loss of E-cadherin, which releases cadherin-associated beta-cate

194 t of reactive oxygen species induces loss of E-cadherin-mediated cell contact, followed by a regenera

195 esource for future computational modeling of E. coli gene regulation, transcription, and translation.

196 tion, without affecting host phagocytosis of E. coli RA101295 treatment reduced plasma LPS content in

197 amate residue in the transmembrane region of E. coli TatC, which when modified by DCCD interferes wit

198 FPR2 ligands resulted in down-regulation of E-cadherin and up-regulation of vimentin, which were rev

199 (2) The retention of E. coli O157:H7 was 3.3 fold higher than that of E. coli

200 on and pointing to particular sensitivity of E. verrucosus to persisting low-level toxicant pressure.

201 ycline on sensitive and resistant strains of E.coli, as well as effects of amphotericin-B and miconaz

202 oli O157:H7 was 3.3 fold higher than that of E. coli K12 in all biochar-amended sand columns.

203 size (10- to 50-fold lower fresh weights of E. cyaneus) and cellular stress response (CSR) capacity,

204 Thus, a main effect of Ca(2+) on E-Syt1 is to reverse an autoinhibited state and to coupl

205 te the antibacterial effect of gentamicin on E. coli growth.

206 hanced tethering and rolling interactions on E-selectin-bearing endothelium under flow conditions in

207 ntial efficiency of spiders as a predator on E. vitis.

208 When exposed to Cd at LC1 over 4 weeks, only E. verrucosus continuously showed 15-36% reduced oxygen

209 cillators (M cells) and evening oscillators (E cells)-are largely responsible for these activity burs

210 t, in animals colonized at P2 but not at P9, E. coli K1 bacteria gain access to the enterocyte surfac

211 te almost completely retained the pathogenic E. coli in the subsurface, suggesting that utilizing san

212 Mechanisms that allow for a persistent E. coli infection are not fully understood.

213 metabolization in the presence of polymyxin E (PE) and PB via pH-induced color change.

214 e of the chlorine formal reduction potential E degrees (Cl(*/-)) = 1.87 V vs NHE that is at least 300

215 Furthermore, the formal potential (E(0)') and heterogeneous rate constant (k0) for CO2 redu

216 The ability to prepare E. gracilis of uniform shape at high purities has signif

217 as well as a cell line expressing ZIKV C-prM-E proteins for RVP production.

218 cell line expressing high levels of ZIKV prM-E proteins that constitutively produce VLPs as well as a

219 tion with a commensal, potentially probiotic E. coli bacteriuria strain.

220 Inhibiting COX-2 or microsomal prostaglandin E synthase-1 suppressed the 6-OHDA-triggered PGE2 produc

221 d 1-month were significantly lower for the R-E group than for the NR-E group (treatment main effect:

222 e impressive findings by examining whether R-E training could attenuate smoking-related craving and b

223 In vitro studies of reconstituted E. coli replisomes have attributed this remarkable proce

224 016 and 7 previously determined PB-resistant E. cloacae isolates from JMI Laboratories.

225 Supporting these results, E-Syt1 constructs defective in Ca(2+) binding in either

226 RNase E/enolase distribution changes from membrane-associated

227 /stromal cells reduce the severity of rodent E. coli-induced acute respiratory distress syndrome.

228 t Zn(2+) in opposing directions across the S(E)R membrane in cardiomyocytes and that changes in their

229 hin the activation loop signature sequence S-E-G.

230 on of a core quaternary protein complex (SCL:E-protein:LMO1/2 [LIM domain only 1 or 2]:LDB1 [LIM doma

231 c and tangible change to patients.-Scolnick, E.

232 utilizing inertial microfluidics to separate E. gracilis by a key shape parameter-cell aspect ratio (

233 retained for all serogroups except serogroup E which has a synthetic requirement for UDP-GalNAc.

234 ony-forming units per mL of vaccine-serotype E coli was noted in the vaccine compared with the placeb

235 uitment between dimeric and monomeric Siglec-E expressed on HEK293A cells.

236 SBU showed the smallest E% and BF showed a significantly smaller D% than other g

237 iate in a monomer-trimer equilibrium (Smith, E.

238 oin products from the corresponding starting E- or Z-N'-alkenyl urea, each of which may be formed fro

239 urally occurring cytotoxic (+)-subincanadine E was also accomplished from (S)-acetoxysuccinimide via

240 nd recombinant HIV-1 gp120 subtype B/subtype E (B/E) proteins demonstrated 31% vaccine efficacy.

241 f1 was 20-fold more effective in suppressing E. coli under simulated multispecies biofilm conditions

242 ty of ranibizumab 0.5 mg treat-and-extend (T&E) versus monthly regimens in patients with neovascular

243 ns were required in patients receiving the T&E (8.7) versus monthly (11.1) regimen, with mean number

244 with adult T+E but not in rats given adult T+E alone.

245 ats given neonatal low-dose BPA with adult T+E but not in rats given adult T+E alone.

246 At both doses tested, E-OIT had an acceptable safety profile and was highly su

247 by purely electric field means (rather than E-field induced strain) remains unexplored thus far.

248 ple genetic strategies, we demonstrated that E proteins E2A and HEB acted in synergy in the thymus to

249 Importantly, it is also demonstrated that E. coli bacteremia initiated from translocation across t

250 This indicates that E- and P-cadherin expression patterns evolved differentl

251 The E coli O-antigen is a promising vaccine target.

252 The E/Z isomerization process of a uracil-azobenzene derivat

253 of H2O2 in the leaves of plants 3h after the E. cloacae inoculation, according to a mechanism involvi

254 ting classical DC (cDC) is controlled by the E protein transcription factor TCF4 (E2-2).

255 ey method to stereoselectively establish the E,Z-diene part, an ester-tethered ring-closing metathesi

256 k, providing the molecular basis for how the E. coli replisome can maintain high processivity and yet

257 as 12 genera were uniquely identified in the E. faecalis group on d 14 and 28.

258 ich may underlie its role in maintaining the E/I ratio.

259 experiments show that the acidic tip of the E. coli Hfq CTD transiently binds the basic Sm core resi

260 In the excited state of the E:THF:NADPH product release complex, the reduced nicotin

261 Glutamate E153 on the E-loop and arginine R210 on the adjacent subunit's backb

262 RA101295 reduced the E. coli-induced "oxidative burst," as well as leukocyte

263 Paneth cells population and reinstating the E-cadherin and N-Cadherin expression.

264 alkene shift affords stereospecifically the E or Z isomer of the 5-alkenyl-4-iminohydantoin products

265 , a model of Fragile-X Syndrome, to test the E/I imbalance theory.

266 ings in L2/3 of awake mice revealed that the E/I ratio systematically declines with increasing stimul

267 iggered transcriptional pathway, through the E-box binding Myc protein, that promotes the expression

268 Theaphenon E treatment significantly decreased gamma-OHPdG levels i

269 Snail binds to three E-boxes present in the human 4E-BP1 promoter to repress

270 Classification of Retinoblastoma group C to E.

271 However, yield prediction in response to E-[CO2] varied significantly among the rice models.

272 an oxidoreductase, in the responsiveness to E-2-hexenal.

273 lyzed by trace copper salts and that a Z- to E-hydrazone isomerization occurs through an enehydrazine

274 erinsulinemic clamp after SGLT2-I treatment, E-Rd increased by normalizing glucose effectiveness to s

275 rcation (P), contiguous extrahepatic tumour (E), multifocal tumour (F), and spontaneous rupture (R).

276 and Ultra Definition Mass Spectrometry (UDMS(E)) label-free quantitative approach.

277 om the conduction band to lower E- and upper E+ valence subbands has been observed at room temperatur

278 Specifically, we have used E-AB sensors to perform the multihour, real-time measure

279 culating lymphocytes, which exhibit variable E-selectin binding among CD4(+) and CD8(+) T cells but n

280 ion has the potential to allow the versatile E. coli system to be employed as an exciting new carbon

281 to OMCCs from the A. tumefaciens VirB/VirD4, E. coli R388 Trw, and Bordetella pertussis Ptl systems s

282 fold remarkably similar to the dengue virus E glycoprotein and related class II viral fusogens.

283 s, total dietary fiber, minerals and vitamin E.

284 tudy evaluated the effect of dietary vitamin E supplementation (1000mg of DL-alpha-tocopheryl acetate

285 tive method for the determination of vitamin E, being comparable to reversed-phase high performance l

286 e randomized to vitamin E, selenium, vitamin E and selenium, or placebo.

287 tial of tocotrienol, a member of the vitamin E family of compounds with potent in vitro anti-cancer p

288 Participants were randomized to vitamin E, selenium, vitamin E and selenium, or placebo.

289 acterized defensive compounds, the volatile (E)-alpha-bergamotene and trypsin proteinase inhibitors (

290 concentrations in P. ruminicola 23, whereas E. coli and Salmonella spp. responses to excess nitrogen

291 ing S. aureus and B. anthracis compared with E. coli Alveolar macrophages and CD14(+) cells were over

292 tates migration primarily via crosstalk with E-cadherin and ZEB1.

293 markedly greater adhesive interactions with E-selectin than do circulating lymphocytes, which exhibi

294 eta-hydroxywithanolide (17-BHW), withanolide E (1), as a promising lead.

295 nted in the cross-linked motifs found within E. coli.

296 d from the Genomes to Fields (G2F) Maize G x E project to assess the effect of selection on G x E var

297 ect to assess the effect of selection on G x E variation and characterize polymorphisms associated wi

298 defined the sequence of the NDSM as Psi-K-x-E/D-x1-x2-(x3/E/D)-(x4/E/D)-xn and determined that K74 a

299 equence of the NDSM as Psi-K-x-E/D-x1-x2-(x3/E/D)-(x4/E/D)-xn and determined that K74 and K76 were cr

300 f the NDSM as Psi-K-x-E/D-x1-x2-(x3/E/D)-(x4/E/D)-xn and determined that K74 and K76 were critical Ub