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 anoxia is greater than 3 kDa in size and is heat-stable.

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

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

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

9 We targeted heat-stable 6PGDH to endosperm amyloplasts by fusing the

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

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

12 d that cytosolic PGD1 and PGD2 isozymes have heat-stable activity, while amyloplast-localized PGD3 ac

13 The alpha-Lactalbumin was relatively heat stable after drying and predominated the powder sur

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

99 ae, E. coli common pilus, flagellin and EAEC heat-stable enterotoxin 1.

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

101 exposed to enterotoxigenic Escherichia coli heat-stable enterotoxin A (ST) and evaluated under condi

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

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

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

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

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

107 The heat-stable enterotoxin binds to and activates guanylyl

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

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

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

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

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

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

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

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

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

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

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

119 The heat-stable enterotoxin suppressed proliferation by incr

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

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

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

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

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

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

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

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

128 sporidium (in 27.8% and 8.2%, respectively), heat-stable enterotoxin-producing Escherichia coli (in 2

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

158 ss spectrometry was employed to identify new heat-stable guinea-fowl-specific peptide markers that ca

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

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

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

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

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

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

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

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

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

168 87 in vivo, whereas inhibition of PKA by its heat-stable inhibitor (PKI) induces dephosphorylation of

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

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

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

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

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

174 This heat-stable inhibitory factor inhibits the classic pathw

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

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

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

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

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

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

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

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

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

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

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

186 The heat-stable nucleoid structuring (H-NS, also referred to

187 on, where it overcomes gene silencing by the heat-stable nucleoid structuring protein H-NS, enhancing

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

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

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

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

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

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

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

195 Heat-stable peptidases released in refrigerated raw milk

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

197 23 heat stable peptide markers unique to species and muscle

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

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

200 Of the 49 heat-stable peptides detected in pure cooked rabbit meat

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

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

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

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

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

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

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

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

209 ignaling down-regulated the Ca(2+)-regulated heat stable protein 1 that stabilizes Tnf-alpha mRNA via

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

236 Heat-stable proteins prepared from these bacterial sonic

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

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

239 use an increase in the relative abundance of heat-stable Rca1beta.

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

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

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

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

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

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

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

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

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

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

250 (3-NT) immunoreactivity and the formation of heat-stable, SDS-insoluble oligomers.

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

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

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

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

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

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

257 We identified 49 heat-stable specific peptides.

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

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

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

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

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

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

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

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

266 tment with CSF from progressive patients was heat stable, thereby prompting us to conduct an unbiased

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

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

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

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

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

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

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

274 p, enterotoxigenic Escherichia coli encoding heat-stable toxin (with or without genes encoding heat-l

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

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

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

278 Enterotoxigenic E coli producing heat-stable toxin among children aged 12-23 months also

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

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

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

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

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

284 months); for enterotoxigenic E coli encoding heat-stable toxin was 4.2 versus 0.1 (0-11 months), 5.2

285 igella spp, enterotoxigenic E coli producing heat-stable toxin, and Cryptosporidium spp might substan

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

287 richia coli, enterotoxigenic E coli encoding heat-stable toxin, enteroaggregative E coli, Shigella sp

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.