ライフサイエンスコーパス: heat-stable

1 as the potato (Solanum tuberosum) tuber, are heat stable.

2 oxins, one of them heat labile and the other heat stable.

3 ing activity of this protein was found to be heat stable.

4 tivation energy of 69 kJ/mol), was extremely heat stable.

5 B has a molecular mass < 1 kDa and is heat-stable.

6 In contrast to mAC, sAC was heat-stable.

7 ncodes the phage excisionase and is a small, heat-stable 56-amino-acid protein that strongly stimulat

8 to other members of the LAP family: it is a heat-stable (70 degrees C; 20 min) hexameric ( approxima

9 heat-labile A-factor and about twofold less heat-stable A-factor than wild-type cells, suggesting th

10 genitors were divided based on expression of heat stable Ag (CD24) into a CD24- and a CD24+ subset, t

11 While the costimulatory molecules B7 and heat stable Ag (HSA) play a role in CTL response inducti

12 ntified a cell population with the phenotype heat stable Ag (HSA)low lin- CD43low that contained B ce

13 r from mature B cells in their expression of heat-stable Ag (CD24), B220 (CD45), and sIgD.

14 ntal blocks at the transition from immature (heat-stable Ag (HSA)(high)) to mature (HSA(low)) B cells

15 mocytes accumulate as quiescent cells with a heat-stable Ag (HSA)-positive CD25+ CD44- c-kit(low) phe

16 defined as cells that express high levels of heat-stable Ag and accumulate BrdU within 8 wk of labeli

17 IKO mice showed increased Qa-2 and decreased heat-stable Ag expression, suggesting an increased level

18 ells, and analysis of cytokine production by heat-stable Ag(low) thymocytes and peripheral NKT cells

19 umulation of mature single-positive CD3(high)heat-stable Ag(low) thymocytes.

20 ntrols this preselection population (CD4-CD8+heat-stable Ag+TCR-) is in a nonproliferative state, but

21 cell age was characterized by expression of heat-stable Ag, and B220 and B cell survival was studied

22 Expression of TCR, MHC class I, Qa-2, heat-stable Ag, and CD45RB among double-positive and CD4

23 y mAb or fusion proteins binding B7-1, B7-2, heat-stable Ag, or vascular cell adhesion molecule-1.

24 deleted nor anergic and are of an immature (heat-stable Aghigh) phenotype.

25 A-factor consists of a mixture of heat-stable amino acids and peptides, and at least two h

26 It is heat stable and glycine rich, lacks cysteine, is secrete

27 f the assay demonstrated that SCPA is highly heat stable and has optimal activity on the synthetic su

28 ia viruses have the added advantage of being heat stable and immunogenic after oral application, maki

29 This factor is relatively heat stable and is dissociable from the recombinant L pr

30 , we show that the CCR8-inducing factors are heat stable and protease resistant and include the vitam

31 The HR-eliciting activity was heat stable and protease sensitive.

32 st of at least two separable components, one heat stable and the other heat labile.

33 The complex is heat stable and unaffected by SDS or reducing conditions

34 ioned medium established that the factor was heat stable and was present in the <3 kDa and >10 kDa fr

35 All four alsotides are novel, heat-stable and enzyme-stable and contain 30 residues.

36 The allergen was heat-stable and had a robust capacity to inhibit IgE-bin

37 Sequence comparisons of heat-stable and heat-labile AGPases identified an N-term

38 A soluble heat-stable and protease-resistant factor was found to m

39 Quantitation was based on proteins for which heat-stable and species-specific peptide markers had bee

40 ken, and turkey meat, to select and identify heat-stable and species-specific peptide markers.

41 major cause of infectious diarrhea, produce heat-stable and/or heat-labile enterotoxins and at least

42 It is extremely hydrophilic, is heat stable, and behaves anomalously on SDS-PAGE with an

43 he inhibitor has a high molecular weight, is heat stable, and is resistant to trypsin.

44 romising platform to manufacture palatable, "heat" stable, and flexible pediatric granules for fixed-

45 te neuronal and endocrine cells, are acidic, heat-stable, and bind calcium.

46 Herring tissue is most heat-stable, and the mildest heat treatment for PUFA pre

47 new sources of antibiotics, including HSAF (Heat Stable Antifungal Factor), which was identified fro

48 Antifungal HSAF (heat-stable antifungal factor, dihydromaltophilin) is a

49 ns of pro-B/early pre-B cells expressing the heat stable antigen (HSA) were found in lower proportion

50 Upon reaching the mature heat stable antigen (HSA)low thymic developmental stage,

51 or surface IgM, but were positive for CD24 (heat stable antigen [HSA]) and CD43 (leukosialin), sugge

52 lymphomas were positive for Thy-1.2 (pan-T), heat stable antigen, and CD4 and CD8 markers, with no ma

53 es expressed AA4.1, CD43, B220, Sca-1, CD19, heat stable antigen, MHC class I, IL-7R, and FcyR, but d

54 arrying neomycin phosphotransferase or mouse heat stable antigen, replacing the HIV-1 sequences encod

55 Experiments performed with recombinant heat stable antigen-encoding HIV-1 indicated that the vi

56 sly that expression by the host cells of the heat-stable antigen (CD24), which was recently identifie

57 We report here that targeted mutation of the heat-stable antigen (HSA) abrogates development of EAE d

58 The heat-stable antigen (HSA) is a costimulatory molecule fo

59 Heterogeneous expression of L-selectin and heat-stable antigen (HSA) suggested that subsets emerge

60 n of green fluorescent protein (EGFP), mouse heat-stable antigen (HSA), and bacterial neomycin phosph

61 d mice with targeted mutations of either the heat-stable antigen (HSA), or both HSA and CD28.

62 class switches requires costimulation by the heat-stable antigen (HSA), we compared T helper cell ind

63 ometry for a virally encoded marker protein, heat-stable antigen (HSA).

64 n of the tolerance-susceptible population of heat-stable antigen (HSA)hiCD4+8- cells found in the med

65 ing the differentiation of DP TcRlow CD69low heat-stable antigen (HSA)high thymocytes to DP TcRhigh C

66 se, and a small murine cell surface antigen (heat-stable antigen [HSA]) as a selectable marker.

67 ctors were generated, one encoding the mouse heat-stable antigen gene and green fluorescent protein g

68 nt lengths that bear the cDNA for the murine heat-stable antigen in the vpr region of a CXCR4-tropic

69 V-1 reporter virus that expresses the murine heat-stable antigen on the surfaces of infected cells.

70 strain engineered to express the murine HSA heat-stable antigen surface marker, we explored the rela

71 osidase fusion protein), HSA (encoding mouse heat-stable antigen), or EGFP (encoding enhanced green f

72 reduced surface expression of CD23 and CD24 (heat-stable antigen).

73 tion of thymocytes with high TCR/CD3 and low heat-stable antigen-1 expression than controls, and an i

74 cells cultured with Flt3-ligand developed a heat-stable antigen-positive/Ly6C+ population comprised

75 lutination has been replaced by detection of heat-stable antigens by direct bacterial agglutination;

76 enterotoxins, one heat labile and the other heat stable, are known to cause diarrhea.

77 ation in either the heat-labile (alt) or the heat-stable (ast) cytotonic enterotoxin gene; three doub

78 tigen responsible for monokine induction are heat stable at 100 degree C but differ in sensitivity to

79 istant to pronase and trypsin digestion, was heat stable at 56 or 80 degrees C, and was not removed b

80 noglobulin G to whole bacterial cells and to heat-stable bacterial antigens of all seven prototypic P

81 This inhibition was mediated, in part, by a heat-stable bacterial component.

82 Maximal up-regulation is induced by heat-stable bacterial cytoplasmic proteins, whereas NTHi

83 The oligonucleotide-oligopeptide adducts are heat stable but are partially reversed by reducing treat

84 ecific to female germ cell chromatin and was heat stable but sensitive to DNase and protease treatmen

85 oplet surfaces can be made biocompatible and heat stable by merely exploiting binding interactions be

86 The T23 binding activity is heat stable, can be inhibited by poly(dA-dT).poly(dA-dT)

87 A small, heat stable chromophore extracted from mosquitoes has re

88 rate that the two proteins exist in a large, heat-stable complex that possesses single-strand endonuc

89 xplained by a more potent endotoxin or other heat-stable component.

90 The hypersensitivity was not associated with heat-stable covalent complexes, as was seen in another d

91 A heat-stable, detergent-extractable component from corn e

92 Glutaredoxins (Grxs) are ubiquitous small heat-stable disulfide oxidoreductases and members of the

93 This assay was also effective with a heat-stable DmrX analog from Methanocaldococcus jannasch

94 dium spp, enteropathogenic Escherichia coli, heat-stable enterotoxigenic E coli, rotavirus, Shigella

95 d Y. enterocolitica-like species, produces a heat-stable enterotoxin (designated YbST) which has biol

96 The effects of Escherichia coli heat-stable enterotoxin (ST) and uroguanylin were examin

97 lls and serves as the receptor for bacterial heat-stable enterotoxin (ST) peptides and the guanylin f

98 Oral delivery of the heat-stable enterotoxin (ST), an exogenous GUCY2C ligand

99 (GCC), the receptor for the Escherichia coli heat-stable enterotoxin (ST), exhibits multiple binding

100 (GCC), the receptor for the Escherichia coli heat-stable enterotoxin (ST), is inhibited by 2-substitu

101 Escherichia coli elaborate a peptide called heat-stable enterotoxin (ST), which binds to and activat

102 Diarrhea induced by Escherichia coli heat-stable enterotoxin (STa) is mediated by a receptor

103 in (D853A) of guanylyl cyclase-C (GC-C), the heat-stable enterotoxin (STa) receptor, rendered the enz

104 Heat-stable enterotoxin (STa), elaborated by enterotoxig

105 Enteroaggregative Escherichia coli (EAEC) heat-stable enterotoxin 1 (EAST1) was originally discove

106 organism produced enteroaggregative E. coli heat-stable enterotoxin 1 and contained the enteropathog

107 nst cholera toxin, and 35% effective against heat-stable enterotoxin [corrected].

108 lifying genes encoding K99 and F41 fimbriae, heat-stable enterotoxin a, intimin, and Shiga toxins 1 a

109 The Escherichia coli heat-stable enterotoxin analog, STa (5--18), is a 14--am

110 of STaR responsible for interacting with the heat-stable enterotoxin and other luminal intestinal pep

111 The role of Escherichia coli heat-stable enterotoxin B (STb) in neonatal porcine diar

112 Binding of Escherichia coli heat-stable enterotoxin B (STb) to the human intestinal

113 )(+) fimbriae, heat-labile enterotoxin (LT), heat-stable enterotoxin b (STb), and enteroaggregative E

114 The heat-stable enterotoxin binds to and activates guanylyl

115 plasmid of ETEC strain 27D that also encodes heat-stable enterotoxin Ib and colonization factor antig

116 the plasmids tested also contain the E. coli heat-stable enterotoxin II (STII) signal sequence for pr

117 rane-bound receptor for the Escherichia coli heat-stable enterotoxin in the intestine.

118 Some EAggEC produce a distinct heat-stable enterotoxin named EAST1.

119 stine after cAMP agonists, cholera toxin, or heat-stable enterotoxin of E. coli (STa toxin), with IC5

120 In contrast, intraluminal heat-stable enterotoxin of Escherichia coli (STa) increa

121 The heat-stable enterotoxin of Escherichia coli (STa) is a p

122 by its ligands guanylin, uroguanylin, or the heat-stable enterotoxin peptide (ST).

123 lonization factor antigen I; heat-labile and heat-stable enterotoxin positive) and that production of

124 lyl cyclase C (GC-C) is the receptor for the heat-stable enterotoxin produced by bacteria as well as

125 The heat-stable enterotoxin receptor, guanylyl cyclase C, ex

126 eted by the enterotoxigenic Escherichia coli heat-stable enterotoxin STa, which deregulates this path

127 The heat-stable enterotoxin suppressed proliferation by incr

128 Here, a bacterial heat-stable enterotoxin was demonstrated to suppress col

129 to Escherichia coli heat-labile enterotoxin, heat-stable enterotoxin, and Vibrio cholerae cholera tox

130 Prostaglandin E(2), Escherichia coli heat-stable enterotoxin, orexins, and carbonated beverag

131 , which shapes the amplitude and duration of heat-stable enterotoxin-dependent cyclic nucleotide accu

132 of GCC produces resistance in tumor cells to heat-stable enterotoxin-induced cytostasis.

133 ssociation with IKEPP significantly inhibits heat-stable enterotoxin-mediated activation of GCC.

134 ctor jejuni o C coli (around two times), and heat-stable enterotoxin-producing E coli ([ST-ETEC] arou

135 F, 25.8% [95% CI, 24.4%-26.7%]), followed by heat-stable enterotoxin-producing Escherichia coli (AF,

136 ose that express only the poorly immunogenic heat-stable enterotoxin.

137 Heat-stable-enterotoxin-producing enterotoxigenic E. col

138 including heat-labile enterotoxins (LT) and heat-stable enterotoxins (ST), are the key virulence fac

139 Heat-stable enterotoxins (STa), which cause an acute sec

140 Bacteria that produce heat-stable enterotoxins (STs), a leading cause of secre

141 (AID) episodes worldwide, often by producing heat-stable enterotoxins (STs), which are peptides struc

142 lar the plasmid-encoded heat-labile (LT) and heat-stable enterotoxins and the colonization factor ant

143 Bacterial diarrheagenic heat-stable enterotoxins induce colon cancer cell cytost

144 YbST has some properties in common with the heat-stable enterotoxins of Y. enterocolitica (YST I and

145 re a family of 17 major serological types of heat-stable enterotoxins that are one of the leading cau

146 cretory diarrhea may be caused by binding of heat-stable enterotoxins to the intestinal receptor guan

147 Because cGKII mediates the effects of heat-stable enterotoxins via the cystic fibrosis transme

148 e different from the natriuretic peptides or heat-stable enterotoxins.

149 (GC-C), an intestinal receptor for bacterial heat-stable enterotoxins.

150 s restores cancer cell cytostasis induced by heat-stable enterotoxins.

151 gate the post-hydrolytic events, we used two heat-stable enzyme-linked optical assays to measure the

152 ses identified an N-terminal motif unique to heat-stable enzymes.

153 g secretagogues, including cholera toxin and heat stable Escherichia coli enterotoxin STa.

154 on of many ETEC virulence factors, including heat-stable (estA) and heat-labile (eltA) enterotoxin ge

155 d that this effect is mediated by a soluble, heat-stable factor released by these bacteria in culture

156 ing activity of the hemolymph is caused by a heat-stable factor that can be extracted from the CNS an

157 U14 DeltaampG and NU14 DeltawaaL contained a heat-stable factor(s) which stimulated greater urothelia

158 e to Plasmodium infection through a secreted heat-stable factor.

159 ggested the presence of both heat-labile and heat-stable factors.

160 These structural changes led to more heat stable forms of PTT with a higher unfolding tempera

161 Both whole-cell sonicates and a heat-stable fraction were also coincubated with the cell

162 Saposins are small, heat-stable glycoprotein activators of lysosomal glycosp

163 The more heat stable grape proteins, i.e. those not contributing

164 Here, we characterize a small, heat-stable growth inhibitor secreted by a rat T lymphom

165 unization because of their potential to make heat-stable, heavy-chain-only antibodies.

166 h expression levels of type I procollagen as heat-stable heterotrimers in Saccharomyces.

167 ions and enhance formation of SDS-insoluble, heat-stable high molecular mass aggregates.

168 se from Caco-2 cells, apparently via a novel heat-stable, high-molecular-weight protein.

169 d (59.4 kDa) protein exists in solution as a heat-stable homotetramer, and enzymatic assays reveal th

170 e 74 C. jejuni strains belonging to the nine heat-stable (HS) serotypes most prevalent in human disea

171 Cleavage at most sites was greater and more heat-stable in the presence of the metabolites compared

172 We found that H. somnus LOS, which is heat stable, induced endothelial cell apoptosis in a tim

173 ing highly safe and efficacious, v2RVFH is a heat-stable, inexpensive, and easily administered vaccin

174 87 in vivo, whereas inhibition of PKA by its heat-stable inhibitor (PKI) induces dephosphorylation of

175 Interestingly, heat-stable inhibitor of cAMP-dependent protein kinase a

176 ansfection of an expression plasmid encoding heat-stable inhibitor of cAMP-dependent protein kinase,

177 s of oocyte maturation after addition of the heat-stable inhibitor of PKA, PKI.

178 can be reversed by a second injection of the heat-stable inhibitor of PKAc, PKI.

179 -fold enhanced, while in the presence of the heat-stable inhibitor protein of cAPK (PKI), there was a

180 family includes three genes encoding small, heat-stable inhibitors of the cyclic AMP-dependent kinas

181 This heat-stable inhibitory factor inhibits the classic pathw

182 The highest CFA frequency was observed among heat-stable isolates.

183 been disrupted with the htk gene encoding a heat-stable kanamycin adenyltransferase.

184 s) in media conditioned by A2:H-Ras cells is heat stable, larger than 3 kD, and sensitive to the non-

185 This heat-stable LpxC variant (the most divergent of all know

186 m a common precursor, prosaposin, are small, heat-stable lysosomal glycoproteins required for lysosom

187 e inactivation that is facilitated by small, heat-stable molecules.

188 Non-biotinylated Arc1p was more heat stable, more flexible in structure, and more effect

189 Studies with the heat-stable Nbp have now shown that it is present in E.

190 Advances are needed to develop single-dose, heat-stable, needle-free, and affordable formulations of

191 urthermore, lysate microbicidal activity was heat stable, neutralized by polyanionic filters or compo

192 The inhibitory activity was heat stable, not overcome by the addition of VEGF, and c

193 The binding sites from protein V mediate heat-stable nucleic acid associations, with some of the

194 The H-NS (heat-stable nucleoid structuring) protein affects both n

195 promoter and to compete for binding with the heat-stable nucleoid-structural protein (H-NS), a global

196 A comparative examination of the heat-stable (O) and heat-labile (HL) serogrouping result

197 Here we report that the PolX from the heat-stable organism Thermus thermophilus (TthPolX) inse

198 environment of LpxC from Aquifex aeolicus, a heat-stable orthologue that displays 32% sequence identi

199 doxins and thioredoxins are ubiquitous small heat-stable oxidoreductases that have proposed functions

200 nd thioredoxins are highly conserved, small, heat-stable oxidoreductases.

201 A set of 25 species and protein-specific heat stable peptide markers has been detected in process

202 23 heat stable peptide markers unique to species and muscle

203 CC), which binds the diarrheagenic bacterial heat-stable peptide enterotoxin ST.

204 Using nano-LC-QTOF-MS/MS, 20 new, heat-stable peptide markers unique to chicken, duck and

205 CRHSP-28 is a Ca(2+)-regulated heat-stable phosphoprotein, abundant in the apical cytop

206 an inhibitory domain similar to that of the heat-stable PKA inhibitor.

207 mIHF is a 105-residue heat-stable polypeptide that is not obviously related to

208 Studies using heat-stable preparations demonstrate that neither site a

209 The heat-stable protease Ser2 is secreted by the species Ser

210 The gidA* mutant releases a heat-stable, protease-resistant, small molecular weight

211 Multiple heat-stable, protease-sensitive peaks of calcium elevati

212 time that miR-155 targets calcium-regulated heat stable protein 1 (CARHSP1), which regulates the sta

213 ve Cd amounts in the biologically detoxified heat stable protein fraction were 35% higher in E. cyane

214 associated with the binding of MgATP and the heat stable protein kinase inhibitor (PKI) were probed b

215 inhibition assay, we have purified a small, heat stable protein that physically interacts with tubul

216 veloped in order to generate highly purified heat-stable protein (HPr).

217 nd carry out phosphotransfer to the acceptor heat-stable protein (HPr).

218 Higher-resolution fractionation of the heat-stable protein (HSP) fraction revealed further diff

219 Recently, calcium-regulated heat-stable protein 1 (CARHSP1) was identified as a biom

220 , which we have designated calcium-regulated heat-stable protein 28 (CRHSP-28).

221 n able to characterize the factor as being a heat-stable protein about 10 kDa in size.

222 Bovine brain contains a heat-stable protein factor that inhibits PLD2 activity i

223 A heat-stable protein has been detected in bovine liver th

224 rations of I1PP2A indicated that this potent heat-stable protein inhibitor of protein phosphatase 2A

225 mic peptide substrates as in the case of the heat-stable protein kinase inhibitor (PKI), or they may

226 The model also predicted that the endogenous heat-stable protein kinase inhibitor may enhance basal c

227 with a 20-residue peptide inhibitor from the heat-stable protein kinase inhibitor PKI(5-24) and adeno

228 f the catalytic subunit:ATP:PKI((5)(-)(24)) (heat-stable protein kinase inhibitor) ternary complex in

229 d is insensitive to PKI, the highly specific heat-stable protein kinase inhibitor.

230 ibitors, the regulatory (R) subunits and the heat-stable protein kinase inhibitors.

231 Two potent heat-stable protein phosphatase 2A (PP2A) inhibitor prot

232 A 38-kDa heat-stable protein stimulating the gastrin and IL-8 pro

233 depressant factor--specifically a 12-25 kDa heat-stable protein that is released into serum shortly

234 oprotein, termed CRHSP-24 (calcium-regulated heat-stable protein with a molecular mass of 24 kDa).

235 nitial characterization found that PIF was a heat-stable protein with a molecular mass of about 50 kD

236 PinA is a heat-stable protein with a subunit Mr of 18,800 and an i

237 the putative ptw effector(s) was a secreted, heat-stable protein(s) that caused plasmolysis of plant

238 ocardial depressant activity was found to be heat stable, proteinaceous, and of a molecular weight ra

239 Here we report that ETEC secretes a heat-stable, proteinaceous factor that blocks NF-kappaB

240 A heat-stable, proteinase K-resistant, low molecular weigh

241 died species is presented by the location of heat-stable proteins in the anodic range of the IEF gels

242 However, the concentrations of heat-stable proteins in the buffers were mostly similar.

243 Heat-stable proteins prepared from these bacterial sonic

244 Inhibitor-2 (I-2) is the most ancient of the heat-stable proteins specific for PP1.

245 for binding by many cellular factors such as heat-stable proteins, chaperones, and many small molecul

246 The active component is heat stable, reacts positively in the Limulus amebocyte

247 nent on F. nucleatum and a mannan-containing heat-stable receptor on the Candida species.

248 In addition, 7 of 54 ORFs examined yielded heat-stable recombinant proteins when they were expresse

249 Previously, we mapped the heat-stable resistance gene Mi-9 in Solanum arcanum acce

250 romised at 32 degrees C, indicating that the heat-stable resistance is mediated by a homolog of Mi-1.

251 Furthermore, we observed that Sll1130 is a heat-stable ribonuclease whose activity was inhibited by

252 ted with the TRV-Mi construct, Mi-9-mediated heat-stable root-knot nematode resistance was compromise

253 f being regenerated from its sulfite/sulfate heat stable salt, which enables the simultaneous absorpt

254 It mainly consists of MEA itself, ammonium, heat-stable salts (HSS), carbamate polymers, and water.

255 synthetic tau filaments with ONOO- generates heat-stable, SDS-insoluble aggregates with a significant

256 (3-NT) immunoreactivity and the formation of heat-stable, SDS-insoluble oligomers.

257 The xynA density factor is heat-stable, sensitive to proteases, and was partially p

258 s showed that replacement of WT SH2 with the heat-stable SH2HS33 enhanced interaction between the SH2

259 The major heat-stable shellfish allergen, tropomyosin, demonstrate

260 APF was determined to be an acidic, heat-stable sialoglycopeptide whose peptide chain has 10

261 HF-I is a small, heat-stable, site-specific RNA-binding protein originall

262 Previously, the presence of a heat-stable soluble factor in the cervicovaginal lavage

263 Although heat-stable (ST) and heat-labile (LT) enterotoxins produ

264 vel by the presence of genes that encode the heat-stable (ST) and/or heat-labile (LT) enterotoxins, a

265 li (ETEC) produces both heat-labile (LT) and heat-stable (ST) enterotoxins and is a major cause of di

266 enterotoxins, including heat-labile (LT) and heat-stable (STa) toxins, are the key virulence factors.

267 which was negative for heat-labile (LT) and heat-stable (STa, STb) ETEC toxins, was isolated only fr

268 in the appropriate bacterial host produce a heat-stable Sts phenotype (for survival of temperature s

269 oxacillin proved to be the less and the most heat-stable substance, with 78.3% and 9.6% degradation i

270 olic isoform, cMDH-S, was significantly more heat-stable than either the other cMDH (cMDH-L) or mMDH.

271 s point to the fact that CaD is not entirely heat-stable; the C-terminal CaM-binding regions and the

272 in (residues 1-292) as a thrombin-cleavable, heat-stable thioredoxin fusion.

273 ction of neutralizing antibodies against the heat-stable toxin (ST), a poor immunogenic peptide, is n

274 estine and producing heat-labile toxin (LT), heat-stable toxin (ST), or both LT and ST (LT+ST).

275 ETEC strains that express the heat-stable toxin (ST), with or without the heat-labile

276 , enterotoxigenic Escherichia coli producing heat-stable toxin (ST-ETEC; with or without co-expressio

277 Mucosally added Escherichia coli heat-stable toxin (STa, 55 ng ml-1) increased the nitrit

278 ether the ETEC heat-labile toxin (LT) or the heat-stable toxin (STa, also known as ST) potentiated EP

279 toxin b (STb), and enteroaggregative E. coli heat-stable toxin 1.

280 ich either or both ETEC enterotoxins (LT and heat-stable toxin [ST]) were detected.

281 hildren (44.2% heat-labile toxin [LT], 38.5% heat-stable toxin [ST], and 17.3% LT/ST) and asymptomati

282 of F4 fimbriae and the heat-labile toxin and heat-stable toxin B enterotoxins.

283 ria, but 11 strains were positive for EAggEc heat-stable toxin EAST/1.

284 eacts with LT and protects against LT and LT/heat-stable toxin ETEC disease in the field, was 6,741 E

285 monophosphate (db-cAMP), carbachol, and the heat-stable toxin of Escherichia coli (STa).

286 rs to these countries, is to protect against heat-stable toxin type Ib (STa or hSTa).

287 c necrotizing factor type 1 (CNF1) and CNF2, heat-stable toxin, and heat-labile toxin.

288 xigenic Escherichia coli strains produce the heat-stable toxin, STa, which, by activation of the inte

289 confirming the existence of nonagglutinable heat-stable toxin, we also identified the genes for a ty

290 0% increase in responsiveness to the E. coli heat-stable toxin.

291 , CRP positively regulates the expression of heat-stable toxin.

292 s orchestrated by heat-labile toxin (LT) and heat-stable toxins (STp and STh), acting in concert with

293 re selected and screened for heat-labile and heat-stable toxins by GM1 enzyme-linked immunosorbent as

294 helium and the elaboration of heat-labile or heat-stable toxins which induce a secretory diarrhea.

295 hrough the elaboration of heat-labile and/or heat-stable toxins.

296 However, bFGF also induced a heat-stable, transferable cytoplasmic factor in MCF-7 ce

297 ausing immediate contraction was found to be heat-stable, trypsin-sensitive, and resistant to extreme

298 ining either a U-A or a U-G base pair and is heat-stable up to 75 degrees C.

299 report the isolation and characterization of heat-stable variants of maize endosperm AGP.

300 The resuscitation factor was acid labile and heat stable, with a mass of less than 1,375 Da.