ライフサイエンスコーパス: tetracycline

1 sistant to negamycin and hypersusceptible to tetracycline.

2 oth sulfonamides, three aminoglycosides, and tetracycline.

3 Honey samples were also tested for tetracycline.

4 d in adult animals by oral administration of tetracycline.

5 th a limit of detection as low as 266 pM for tetracycline.

6 genes to aminoglycosides, beta-lactams, and tetracycline.

7 he ribosome, negamycin was shown to displace tetracycline.

8 detectable output, which can be tuned using tetracycline.

9 f tamoxifen and SPDEF upon administration of tetracycline.

10 isoniazid, chloramphenicol, erythromycin and tetracycline.

11 -limiting genetic trait that is repressed by tetracycline.

12 -5) for amoxicillin, and 4% (95% CI 2-5) for tetracycline.

13 al difference in the absence and presence of tetracycline.

14 s means that AgNPs first form a complex with tetracycline.

15 ally effective 100-200 mg/day dose for these tetracyclines.

16 ugh to the present day examples, such as the tetracyclines.

17 , alkaloids, prostaglandins, macrolides, and tetracyclines.

18 ng/mL for beta-lactams, 0.04-0.98 ng/mL for tetracyclines, 0.08-2.0 ng/mL for quinolones, and 0.1-3.

19 ce across the different farming systems was: tetracycline (10.61; 95%CI: 7.40-13.82), ampicillin (6.0

20 ood isolates were most commonly resistant to tetracycline (19%), and more likely resistant to a first

21 own to influence the relative ratio of 1 and tetracycline 2.

22 The commercial antibiotics tetracycline (3), minocycline (4), chlortetracycline (5)

23 cosides exhibited intermediate (33.8-43.6%), tetracycline (30.4%) and trimethoprim (22.6%) intermedia

24 e net effect of colloids on the transport of tetracycline (~50% sorbed on colloids) could be facilita

25 exhibited substantial in vitro resistance to tetracycline (53.2% resistant), erythromycin (80.8% resi

26 ethod covers the analytes from the groups of tetracyclines (6), fluoroquinolones (11), sulphonamides

27 Tetracyclines, a class of antibiotics that target bacter

28 validated by the observation of reduction in tetracycline accumulation in an E. coli strain expressin

29 and was significantly more active than other tetracyclines against Burkholderia cepacia, Escherichia

30 otics (i.e., ciprofloxacin, ceftriaxone, and tetracycline) against Escherichia coli W1485 as a model

31 The tetracycline-AgNPs complex interacts more strongly with

32 A series of novel hexacyclic tetracycline analogues ("hexacyclines") was designed, sy

33 onship between treatment dose and signal for tetracycline and ampicillin, two clinically used antibac

34 hylococcus aureus that confers resistance to tetracycline and certain unsaturated fatty acids.

35 methodologies as previously employed, using tetracycline and chloramphenicol resistance cassettes, a

36 Tetracycline and doxycycline MICs and disk diffusion zon

37 Tetracycline and doxycycline MICs and zones were compare

38 species viridans group with the exception of tetracycline and erythromycin.

39 ipts and an 8-fold increase in resistance to tetracycline and fatty acids.

40 t38 efflux transporter confers resistance to tetracycline and fitness in abscesses, but its natural s

41 y to be multidrug resistant and resistant to tetracycline and gentamicin than clinical isolates.

42 ndomized to treatment with the furazolidone, tetracycline and lansoprazole regimen, twice a day for 7

43 gative element ICE-emm12, encoding genes for tetracycline and macrolide resistance, and prophage PhiH

44 gh precision, to 6.33 and 9.22 ng mL(-1) for tetracycline and pristinamycin, respectively.

45 of two commonly employed antibiotic classes tetracycline and streptogramin.

46 design strategy by applying the approach to tetracycline and streptomycin aptamers.

47 minocycline has greater activity than other tetracyclines and glycylcyclines against various MDR pat

48 ics (ampicillin, cefalexin, chloramphenicol, tetracycline) and their combinations on Escherichia coli

49 c systems especially reduced aminoglycoside, tetracycline, and beta-lactam ARG levels relative to ana

50 e positive and were resistant to penicillin, tetracycline, and ciprofloxacin.

51 d with nonsusceptibility to chloramphenicol, tetracycline, and co-trimoxazole.

52 by steatotic drugs (valproate, doxycycline, tetracycline, and cyclosporin A) in cultured hepatic cel

53 otics from nature: penicillin, streptomycin, tetracycline, and erythromycin, among others.

54 biotics including ciprofloxacin, tobramycin, tetracycline, and gentamicin.

55 es to penicillin, erythromycin, clindamycin, tetracycline, and other antimicrobial agents.

56 nslation inhibitors such as chloramphenicol, tetracycline, and streptomycin gather predominantly at t

57 suggests that extended-spectrum penicillins, tetracycline, and trimethoprim-sulfamethoxazole are good

58 ses such as new quinolones, aminoglycosides, tetracyclines, and beta-lactams have been designed to ev

59 synthesized, and evaluated against panels of tetracycline- and multidrug-resistant Gram-positive and

60 e of EGFR-induced lung adenocarcinomas using tetracycline- and tamoxifen-inducible transgenic mouse m

61 Intriguingly, the tetracycline antibiotic minocycline, which has been in c

62 synthetic strategies toward this intriguing tetracycline antibiotic resulted in the development of k

63 Minocycline is a tetracycline antibiotic with immune-modulatory propertie

64 Tetracycline antibiotics (TCs) are frequently detected m

65 multiplexed determination of sulfonamide and tetracycline antibiotics residues in milk is reported in

66 hts that could inform the development of new tetracycline antibiotics resistant to enzymatic degradat

67 Furthermore, genes encoding resistance to tetracycline antibiotics were significantly more abundan

68 Upon addition of tetracycline, Apt leaves CSs, resulting in disassembly o

69 inert tetracycline repressible promoter with tetracycline aptamer and constitutive target protein des

70 In the presence of tetracycline, aptamer binds to its target, signal transd

71 Oral tetracyclines are commonly used for acne and other condi

72 Using tetracycline as example substance, we ultimately evaluat

73 r sensitive, selective and fast detection of tetracycline based on triple-helix molecular switch (THM

74 or ultrasensitive and selective detection of tetracyclines, based on M-shape structure of aptamer (Ap

75 The use of newly developed tetracycline-based systems that are more sensitive could

76 he U1052G mutant ribosome possesses a second tetracycline binding site that correlates with its hyper

77 p of loop III is located directly within the tetracycline binding site where it interacts with nucleo

78 e to negamycin are in close proximity of the tetracycline binding site within helix 34 of the small s

79 In contrast to clarithromycin, tetracycline binding to humic acid increased in the pres

80 Thus, the switching functionality of the tetracycline-binding aptamer appears to include both a c

81 e folding kinetics and thermodynamics of the tetracycline-binding aptamer, which can be employed as s

82 li populations with the same total amount of tetracycline but administered in different temporal patt

83 tection proteins (RPPs) confer resistance to tetracycline by binding to the ribosome and chasing the

84 tracycline complexes which reduced uptake of tetracycline by E. coli hence diminishing the biorespons

85 ctrostatic interaction of positively charged tetracycline-Ca complexes with humic acid rather than du

86 xperimental data was achieved by considering tetracycline cation interaction with both low and high p

87 lin, methicillin, erythromycin, clindamycin, tetracycline, ciprofloxacin, vancomycin, trimethoprim, g

88 ly synthetic fluorocycline antibiotic of the tetracycline class with in vitro activity against clinic

89 ummarized some of the characteristics of the tetracycline class, and quantified the minocycline activ

90 ondary pseudotumor cerebri syndrome included tetracycline-class antibiotics (n = 11), chronic kidney

91 However, in contrast to tetracycline-class antibiotics, which serve to prevent c

92 upies a site that partially overlaps that of tetracycline-class antibiotics.

93 ions (e.g., Ca(2+) and Mg(2+)) to form metal-tetracycline complexes in water.

94 h Mg(2+) and Ca(2+) in solution formed metal-tetracycline complexes which reduced uptake of tetracycl

95 reporter responded linearly to intracellular tetracycline concentration.

96 Tetracycline contains ionizable functional groups that m

97 pe using an adenovirus-based system based on tetracycline-controlled expression of the SacI restricti

98 pression may sensitize cells to the intended tetracycline-controlled loss or gain of function, thereb

99 s expressed under the control of the reverse tetracycline-controlled transactivator and the tetracycl

100 line to Clara cell secretory protein-reverse tetracycline-controlled transactivator/tetracycline oper

101 apid insertion and conditional expression of tetracycline-controlled transgenes, including fluorescen

102 is indicative of an unexpected potential for tetracycline "degradation" (i.e., antibiotic resistance)

103 nce-based transgenic mouse model that allows tetracycline-dependent regulation of PTEN in a time- and

104 netic states of various target genes using a tetracycline-dependent transcription factor.

105 Minocycline is a semisynthetic tetracycline derivative with activity against this patho

106 Indeed, treatment with doxycycline-a tetracycline derivative-disturbs mitochondrial proteosta

107 oduced only females when raised on a limited tetracycline diet.

108 Minocycline, a synthetic tetracycline, displays antitumor activity.

109 gative organisms when compared directly with tetracycline, doxycycline, and other broad-spectrum anti

110 Here, we show that expression of the tetracycline/doxycycline-controlled Tet-transactivator,

111 a simple, method to screen and discriminate tetracycline drugs, in aquaculture, being a promising to

112 ic toxic effect which can be counteracted by tetracyclines, drugs able to hinder the formation of lar

113 The presence of tetracycline enhances the binding of Ag to Salmonella by

114 Less tetracycline entered E. coli cells at solution pH of 8.0

115 clean-up of tetracyclines (oxytetracycline, tetracycline, epi-chlorotetracycline, chlorotetracycline

116 uperantigens SSA and SpeC, and resistance to tetracycline, erythromycin and clindamycin.

117 Resistance to tetracycline, erythromycin, and clindamycin was seen in

118 Tetracycline, erythromycin, clindamycin, and metronidazo

119 taminophen, diclofenac, codeine, ampicillin, tetracycline, erythromycin-H2O, and gemfibrozil have sig

120 ype IV isolates (89%) were clonally related, tetracycline-, erythromycin-, and clindamycin-resistant

121 solates belonged to sequence type (ST)459, a tetracycline-, erythromycin-, and clindamycin-resistant

122 Tetracycline exposure for 7 days effectively silenced TR

123 as a surrogate for the susceptibility other tetracyclines fails to detect minocycline-susceptible is

124 A follow-up of antibiotics (tetracyclines, fluoroquinolones, cephalosporins, penicil

125 n modulate the selective pressure exerted by tetracycline for development and enrichment of antibioti

126 hich could be explained by the common use of tetracyclines for control of sheep abortions in the Unit

127 Thus, we propose that the use of tetracycline from 1948 onwards led in humans to the comp

128 Y506/Y507, to directly dislodge and release tetracycline from the ribosome.

129 carbon nanotubes (RACNTs) in the analysis of tetracyclines from milk samples, in a multidimensional l

130 therapy fails a second-line treatment using tetracycline, furazolidone and proton-pump inhibitors ha

131 The C-8 position of the tetracyclines has been largely underexplored because of

132 The use of tetracyclines has declined because of the appearance of

133 In vitro susceptibility testing using tetracycline HCL as a surrogate for the susceptibility o

134 doxycycline (MIC(50/90): 2/>8 microg/mL) and tetracycline hydrochloride (HCL) (only 30.2% susceptible

135 loped to fabricate aligned-fiber antibiotic (tetracycline hydrochloride, TE-HCL) patches using polyca

136 ndicate that the same total concentration of tetracycline in ambient solution can evoke very differen

137 oxacin, colistin, gentamicin, meropenem, and tetracycline in comparison to the results obtained with

138 or was effectively used for the detection of tetracycline in milk and serum samples with LODs of 740

139 ptasensor was successfully applied to detect tetracycline in serum and milk.

140 ptasensors were applied for determination of tetracycline in some real samples such as drug, milk, ho

141 m homeostasis, we caution against the use of tetracyclines in experimental approaches.

142 techniques for detection and quantitation of tetracyclines in food products are greatly in demand.

143 has been evaluated for the determination of tetracyclines in infant foods based on meat and vegetabl

144 ntibiotics (sulfamethoxazole, ciprofloxacin, tetracycline) in pilot- and full-scale biological treatm

145 ication of 14 antimicrobials (quinolones and tetracyclines) in fish.

146 At physiological magnesium concentrations, tetracycline induces a significant conformational shift

147 1 in keratinocyte responses to IL-17 using a tetracycline inducible short hairpin RNA targeting TRAF3

148 e stably transduced keratinocytes expressing tetracycline-inducible AREG-targeted shRNA with lentivir

149 Tetracycline-inducible Bcl-2 and Bcl-xL dual knockdown s

150 MITF expression in the tetracycline-inducible C32 melanoma model caused a marke

151 understand the function of Ctcfl, we created tetracycline-inducible Ctcfl transgenic mice.

152 In this issue of Blood, Schulze et al use a tetracycline-inducible Dnmt3b knock-in mouse model to in

153 By using tetracycline-inducible down-regulation of gene expressio

154 rified proteins from HeLa cells containing a tetracycline-inducible GFP-S peptide-NFkappaB expression

155 gh and physiological methylation levels in a tetracycline-inducible knock-in mouse model.

156 In this study, we generated novel tetracycline-inducible Madin-Darby canine kidney type I

157 When expressed in a tetracycline-inducible manner, the ectopically expressed

158 Previous studies with a tetracycline-inducible mutant demonstrated that I2-defic

159 xpression of CXCL1 is under the control of a tetracycline-inducible promoter active within glial fibr

160 ressing this fragment under the control of a tetracycline-inducible promoter and examined functional

161 in SPT fusion protein under the control of a tetracycline-inducible promoter in stably transfected ce

162 expressed in HEK293 cells under control of a tetracycline-inducible promoter, allowing controlled and

163 ch the lambda Cro gene is transcribed from a tetracycline-inducible promoter, and a "memory element"

164 VACV promoter and IFN-gamma under engineered tetracycline-inducible promoters.

165 sAC knockdown by tetracycline-inducible short hairpin RNA also prevented

166 nomic safe harbors combined with an improved tetracycline-inducible system and CRISPR/Cas9 technology

167 n on/off- and tissue-specific manner using a tetracycline-inducible system.

168 However, such tetracycline-inducible systems carry a risk.

169 were established by using two dose-dependent tetracycline-inducible systems in four hepatoma cell lin

170 A tetracycline-inducible transgenic mouse model expressing

171 on of nude mouse xenograft tumors carrying a tetracycline-inducible vector system was observed with t

172 M gene overexpression, a lentivirus-mediated tetracycline-inducible vector system, and human papillom

173 Using a tetracycline-inducible Zap70 transgene (TetZap70), thymi

174 lopment of Zap70-deficient thymocytes with a tetracycline-inducible Zap70 transgene to allow temporal

175 The translation inhibitors negamycin and tetracycline interfere with tRNA binding to the aminoacy

176 In this paper, the detection of tetracycline is compared using CPE/OA/anti-TET and MBCPE

177 cterial ribosome from binding the antibiotic tetracycline, is a translational GTPase with significant

178 is available for topical metronidazole, oral tetracycline, laser and light-based therapy, and topical

179 xins, which belong to a rare class of fungal tetracycline-like mycotoxins, were subjected to comprehe

180 Significantly, the fungal-derived tetracycline-like viridicatumtoxins are resistant to fun

181 e linked to the acquisition of resistance to tetracycline, macrolides, and lincosamides.

182 unique to the United States, and the use of tetracyclines may have facilitated selection of this hig

183 n embryonic kidney cells (T-REx-293) using a tetracycline-mediated (Tet-On) system.

184 g-based transcriptome analysis revealed that tetracycline-mediated AREG silencing significantly alter

185 d as ABC efflux pumps, RND efflux pumps, and tetracycline MFS efflux pumps.

186 and analysis indicated that the present CLSI tetracycline MIC and disk breakpoints did not fit the su

187 M was detected in >/= 90% of isolates having tetracycline MICs of >/= 4 mug/ml and in >/= 90% with do

188 Scattergrams of tetracycline MICs versus corresponding zone diameters an

189 ed the potential therapeutic efficacy of two tetracyclines, minocycline and the newer generation tige

190 clinical use, and in contrast to most older tetracyclines, minocycline has high activity against Aci

191 High levels of tetracycline, multidrug, erythromycin, and aminoglycosid

192 Tetracycline, multidrug, macrolide-lincosamide-streptogr

193 Antibiotics, such as tetracyclines, needed for the treatment of murine typhus

194 Moreover, drug resistance to tetracycline, norfloxacylin, ceftriaxone and ciprofloxac

195 lied to detect the effects of ampicillin and tetracycline on sensitive and resistant strains of E.col

196 r different beta-lactams, ciprofloxacin, and tetracyclines on multiple occasions.

197 tracycline-controlled transactivator and the tetracycline operator minimal promoter.

198 verse tetracycline-controlled transactivator/tetracycline operator-VEGF-C double-transgenic mice duri

199 nd that deactivating microglia in utero with tetracyclines or eliminating microglia from the fetal ce

200 for the selective isolation and clean-up of tetracyclines (oxytetracycline, tetracycline, epi-chloro

201 ad, ampicillin, dicloxacillin, enrofloxacin, tetracycline, oxytetracycline, erythromycin, spinosad, c

202 ple therapy (PPI + bismuth + metronidazole + tetracycline [PBMT]).

203 Tetracycline possesses multiple ionizable moieties and f

204 nifested in dramatic differences in altering tetracycline potency when coadministered with that antib

205 Here we find that sub-inhibitory levels of tetracyclines potentiate selection for or against tetrac

206 Here we take advantage of the leaky tetracycline promoter system in the Tat-transgenic mouse

207 nalysis, the cut-off values of beta-lactams, tetracyclines, quinolones and sulfonamides were determin

208 four families of antibiotics (beta-lactams, tetracyclines, quinolones and sulfonamides) in milk with

209 l of breast cancer, Pten suppression using a tetracycline-regulatable short hairpin (sh)RNA cooperate

210 Using a tetracycline-regulated pulse-chase system, we measured p

211 (reference), -G1, and -G2 (variants) using a tetracycline-regulated system in HEK293 cells.

212 cells proliferate by virtue of a transduced tetracycline-regulated v-myc oncogene.

213 discovered a novel regulator of tet38, named tetracycline regulator 21 (TetR21), that bound specifica

214 nas aeruginosa both in vitro and in vivo for tetracyclines reported to date.

215 ing the combination of a metabolically inert tetracycline repressible promoter with tetracycline apta

216 ed a murine model that harbors Mll-AF9 and a tetracycline-repressible, activated NRAS (NRAS(G12V)).

217 cycline) vectors are designed to express the tetracycline repressor under a constitutive VACV promote

218 ne-inducible promoter system (comprised of a tetracycline repressor, several promoter constructs, and

219 Tetracycline repressors (TetRs) modulate multidrug efflu

220 The honey samples were free from tetracycline residue and form coarse granules slowly.

221 Overall, we observed a high rate of tetracycline resistance (89%) among colonizing GBS isola

222 egrative and conjugative elements conferring tetracycline resistance (TcR).

223 cyclines potentiate selection for or against tetracycline resistance around localized sources of almo

224 se in ceftiofur resistance and a decrease in tetracycline resistance elements were observed among the

225 led to rapid expansion of both ceftiofur and tetracycline resistance gene copies/gram of feces.

226 ains ampicillin resistance gene blaTEM-1 and tetracycline resistance gene tetA, with UV254 doses up t

227 gene of P. aeruginosa was replaced with the tetracycline resistance gene via allelic exchange.

228 The highest relative abundance was tetracycline resistance genes (manures) and multidrug re

229 ment regimens on quantities of ceftiofur and tetracycline resistance genes in feedlot cattle.

230 Beta-lactamase and tetracycline resistance genes were the most prevalent (2

231 including a deletion that is associated with tetracycline resistance in Helicobacter pylori.

232 d sequences found in all samples belonged to tetracycline resistance mechanisms.

233 promoters that provided E. coli with higher tetracycline resistance over the native promoter when pl

234 Tetracycline resistance protein Tet(O), which protects t

235 RCDI patients, although donors primarily had tetracycline resistance.

236 ne residue result in loss of Tet(O)-mediated tetracycline resistance.

237 ineered with a stochastic switch controlling tetracycline resistance.

238 olecules to regulate conjugative transfer of tetracycline-resistance plasmid pCF10 in E. faecalis.

239 The tetracycline-resistance plasmid pCF10 represents a parad

240 RNA accommodation and prevents rescue by the tetracycline-resistance protein TetM.

241 nt in the early U.S. isolates, it was not as tetracycline resistant (19% versus 100%) or predominant

242 among our MRSA CC398 strains; MRSA CC398 was tetracycline resistant and carried no phi3 bacteriophage

243 ections, but since 2003 a highly pathogenic, tetracycline-resistant C. jejuni clone (named SA) has be

244 e function in the human gut microbiome, with tetracycline-resistant ribosomal protection proteins and

245 eus, methicillin-resistant S. aureus (MRSA), tetracycline-resistant S. aureus (TRSA), multidrug-resis

246 Macrolide- and tetracycline-resistant Streptococcus pyogenes emm12 isol

247 iduals, livestock-associated MRSA and MDRSA (tetracycline-resistant, CC398, scn-negative) were only p

248 e isolates were resistant to clindamycin and tetracycline, respectively.

249 The resulting tetracycline riboswitches exhibit robust regulatory prop

250 Enoxacin, kanamycin, neomycin, and tetracycline show synergistic growth inhibition against

251 ween histidine and the nano optical samarium tetracycline [Sm-(TC)2](+) complex doped in sol-gel matr

252 We suggest that tetracycline speciation analysis should be incorporated

253 Among the various tetracycline species present in solution, including both

254 mulation in an E. coli strain expressing the tetracycline-specific efflux pump (TetA) compared to the

255 the 6-day vermicomposting process, including tetracyclines, sulfonamides, and fluoroquinolones.

256 ome that explain its divergent negamycin and tetracycline susceptibility profiles.

257 th was measured over a 17-month period using tetracycline tagging of the calcareous feeding lanterns.

258 d for treatment of aqueous antibiotics using tetracycline (TC) as a model compound.

259 e binding sites between silane molecules and tetracycline (TC) as well as TC analogues.

260 fabricated as a portable tool for monitoring tetracycline (TC) in bovine milk.

261 e and visual detection of streptomycin (SM), tetracycline (TC), and penicillin G (PC-G) in milk.

262 , 0.994 and 0.998 for oxytetracycline (OXI), tetracycline (TC), chlortetracycline (CTC) and doxycycli

263 ncluding carbapenem-resistant bla OXA-23 and tetracycline (tet) resistance islands, but the genome st

264 the NEG site of action overlaps with that of tetracycline (TET), the two antibiotics exhibit differen

265 Synthetic regulatory proteins such as tetracycline (tet)-controlled transcription factors are

266 ed this IRF-3 threshold idea by generating a tetracycline (Tet)-inducible cell line for IRF-3 express

267 otent mutagenic capabilities, we generated a tetracycline (tet)-regulated ORFeus element harboring a

268 In the absence of tetracycline, the M-shape structure, which acts as a gat

269 In the absence of tetracycline, the tetracycline transactivator (tTAV) acc

270 adjusted IRR, 2.03 [95% CI, 1.67-2.48]), and tetracycline therapy appeared to reduce the risk of Park

271 In the absence of tetracycline, THMS is stable, leading to the aggregation

272 of migration of dissolved and colloid-bound tetracycline to the change in solution ionic strength.

273 e TSS as tTA can be repressed by addition of tetracycline to the diet at larval and/or adult stages.

274 nolone-induced DNA damage and the ability of tetracyclines to traverse the outer membrane.

275 ns (viz., the antibiotics clarithromycin and tetracycline) to dissolved humic acid in the absence and

276 e (kanamycin and neomycin), and polykeptide (tetracycline) to explore their synergistic mechanism whe

277 l epithelial cell (PEC)-specific PEC-reverse-tetracycline transactivator (rtTA) transgenic mouse also

278 active in embryos to drive expression of the tetracycline transactivator (tTA), the transcription fac

279 In the absence of tetracycline, the tetracycline transactivator (tTAV) accumulates, resultin

280 ositive epicardial cells were higher in hSCF/tetracycline transactivator compared with wild-type mice

281 ntly higher in the peri-infarct area of hSCF/tetracycline transactivator mice compared with wild-type

282 Amyloid precursor protein/tetracycline transactivator mice underwent behavioral te

283 cible cardiac-specific hSCF transgenic (hSCF/tetracycline transactivator) mice were subjected to MI.

284 ifferent animal models of NAFLD: iatrogenic (tetracycline-treated rats), genetic (glycine N-methyltra

285 linezolid, meropenem, penicillin, rifampin, tetracycline, trimethoprim-sulfamethoxazole, and vancomy

286 showed that the complexation of Fe(II) with tetracycline (TTC), oxytetracycline (OTC), or chlorotetr

287 0/pTGM whole-cell bioreporter to investigate tetracycline uptake from solution under varying conditio

288 prior systemic antibiotic use, and systemic tetracycline use.

289 s pneumoniae and to reassess breakpoints for tetracycline using the requirements defined in Clinical

290 afety mechanism assisted by the repressor of tetracycline) vectors are designed to express the tetrac

291 nd free (noncomplexed) species, zwitterionic tetracycline was identified as the predominant species t

292 Limits of quantitation of examined tetracyclines were from 14.5 to 56.6mug/kg significantly

293 d antimicrobials, including sulfonamides and tetracyclines, were measured using liquid chromatography

294 nolones, and moderate susceptibility to most tetracyclines, whereas other contemporary isolates had h

295 form 5'-RNA aptamers that bind to the added tetracycline, which represses translation of aptamer-con

296 f bovine urine revealed frequent presence of tetracyclines, which was related with animal's age.

297 ptible to most tested antibiotics, including tetracycline, while the late U.S. isolates were universa

298 release by 26% in comparison to that without tetracycline, while the presence of penicillin does not

299 ical assay indicated high selectivity toward tetracycline with a limit of detection (LOD) as low as 4

300 ed aptasensor showed high selectivity toward tetracyclines with a limit of detection as low as 266 pM