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1 ts properties can limit the growth rate of a bacterial culture.
2 in with a yield of approximately 10 mg/liter bacterial culture.
3 les were subjected to HbA(1c) estimation and bacterial culture.
4 sensitivity and specificity and outperformed bacterial culture.
5 cted by the cryptococcal antigen test and/or bacterial culture.
6 t probe amplification assay and conventional bacterial culture.
7 the results of the accepted "gold standard," bacterial culture.
8  85.6 and 98.6%, respectively, compared with bacterial culture.
9 re compared to the "gold standard" method of bacterial culture.
10 nchoalveolar lavage (p = 0.011) quantitative bacterial culture.
11 odel biocatalyst without any optimization of bacterial culture.
12  to study the proliferation of mutators in a bacterial culture.
13 between a fungal blood culture and a routine bacterial culture.
14 ogen Panel, an in-house five-virus panel and bacterial culture.
15 een aptamer)) were readily obtained from 1 l bacterial culture.
16 f CO2 and O2 in situ in the headspace of the bacterial culture.
17 cally, and bacterial killing was assessed by bacterial culture.
18  C. trachomatis detection, and nonchlamydial bacterial culture.
19 resence of Mycobacterium tuberculosis in the bacterial culture.
20 the results with those obtained by classical bacterial culture.
21 mastitis, and are traditionally diagnosed by bacterial culture.
22 hat had more than one specimen submitted for bacterial culture.
23 ilic predominance (average 64%) and negative bacterial cultures.
24 in the mature toxin, MccE492m, isolated from bacterial cultures.
25 e biological processing of these analytes in bacterial cultures.
26 shown by light microscopy, and "clumping" of bacterial cultures.
27 ity of the Ni(II)-dependent enzyme urease in bacterial cultures.
28 e first report of CH(3)SeSSCH(3) produced by bacterial cultures.
29 ed fungi, 10 from fungal cultures and 8 from bacterial cultures.
30  The lungs were homogenized for quantitative bacterial cultures.
31 in proteins expressed in methionine-depleted bacterial cultures.
32  measurements of GFP fluorescence in growing bacterial cultures.
33 ient phenotypic conversion of drug-resistant bacterial cultures.
34 usly collected, had correspondingly positive bacterial cultures.
35 biochemical assays have been applied to bulk bacterial cultures.
36  from studies of nitrifying and denitrifying bacterial cultures.
37 were treated with cell-free supernatant from bacterial cultures.
38 S, similar to previous experiments with pure bacterial cultures.
39 ed reporter proteins and easily expressed in bacterial cultures.
40 patients, and 43 specimens were obtained for bacterial culture; 20 of the specimens (47 percent) were
41 method for screening of CDAD was as follows: bacterial culture, 95%; culture with cytotoxin assay of
42    Nine additional samples were prepared for bacterial culture, after initial irradiation with ultrav
43 cterial culture followed by cytotoxin assay, bacterial culture alone, latex agglutination assay, and
44 , resulting in an underdetection of fungi by bacterial culture alone.
45 results were compared to those with standard bacterial culture and biochemical identification with nu
46                          Diagnosis relies on bacterial culture and confirmation of toxin production,
47 cells were assessed by means of quantitative bacterial culture and expressed as colony-forming units
48             Comparison of Q-PCR results with bacterial culture and histopathological results from an
49                          Serial quantitative bacterial culture and noninvasive magnetic resonance ima
50 overed in yields of 5-7 mg x L-1 of starting bacterial culture and pure HemT at 10 mg x L-1 x HemA ha
51 n ages 6 to 36 months and included viral and bacterial culture and quantitative PCR for respiratory s
52 treatment of streptococcal pharyngitis since bacterial culture and rapid diagnostic tests are not fea
53                The addition of PCT levels to bacterial culture and viral detection results can assist
54 N, and V144N) interactions were expressed in bacterial culture and were studied with spectroscopy and
55 resistance from gDNA directly extracted from bacterial culture and without PCR amplification.
56       Detection of C. difficile by anaerobic bacterial culture and/or cytotoxicity assays has been la
57 in vanishingly small quantities (mug/L) from bacterial cultures and are believed to be unstable.
58 d levels of reactive oxygen species (ROS) in bacterial cultures and fecal microbiota using 2',7'-dich
59 properties of poly-L-lysine were measured in bacterial cultures and in whole CF sputum.
60    Examples include bioprocess monitoring of bacterial cultures and measurement of minute amounts of
61 itis grow well in media utilized for routine bacterial cultures and that cryptococcal antigen tests a
62 the low frequencies of persisters in growing bacterial cultures and the complex underlying molecular
63 l-wash specimens were obtained for viral and bacterial cultures and the detection of viral antigens.
64 of ethanol also induced the acidification of bacterial cultures and the production of indole-3-acetic
65 lutenin protein to relatively high levels in bacterial cultures and the protein exhibited the known a
66  of OMPs into serum was highest for immature bacterial cultures and was increased by antibiotics in v
67                          Blood was drawn for bacterial culturing and identification at 6 time points
68 solated in high yield (25-33 mg per liter of bacterial culture) and were shown to impart a high degre
69  often reach concentrations of 0.1-30 muM in bacterial cultures, and generally, LuxR-type receptors r
70 ctiveness was assessed by 3 criteria: death, bacterial cultures, and presumptive clinical cure score.
71 hirteen compounds were identified from these bacterial cultures, and the combination of these VOCs cr
72 lume of respiratory secretions; b) effect on bacterial cultures; and c) changes in the inflammatory c
73 ating kairomones, and using a combination of bacterial culturing approaches, bioassay-guided fraction
74 detection, nucleic acid probe detection, and bacterial culture are commonly used to confirm group A s
75     When both cryptococcal antigen tests and bacterial cultures are ordered routinely, eliminating fu
76  Traditional assays available for monitoring bacterial cultures are time-consuming and labor-intensiv
77         All results were compared to routine bacterial culture as the gold standard.
78 on assay (CCCNA), and to anaerobic toxigenic bacterial culture, as the "gold standard," for 285 clini
79         High vaginal swabs were obtained for bacterial culture before and after microbicide applicati
80                        Also, illumination of bacterial cultures before inoculation of pea roots incre
81                                              Bacterial culture broth extracts have been the starting
82 d in solution, membrane environments, and in bacterial culture by a combination of chiroptical and so
83 ction was monitored by clinical examination, bacterial culture, C. jejuni-specific PCR, gross patholo
84                                 Quantitative bacterial cultures, cell counts, chemokine, cytokine, pr
85 ple-to-result molecular test, to a toxigenic bacterial culture/cell cytotoxin neutralization assay (T
86 Conjunctival swab samples were collected for bacterial culture, Chlamydia trachomatis PCR, and RNA is
87 a bacterial culture or were recovered from a bacterial culture collected within 48 h.
88 mmunities and with their corresponding fecal bacterial culture collections.
89 uit yogurts were made from goat's milk using bacterial cultures comprising, Lactobacillus acidophilus
90 s and demonstrate that subtle differences in bacterial culture conditions may have important implicat
91  affected by shallow standing versus shaking bacterial culture conditions prior to macrophage infecti
92                                              Bacterial cultures detected anaerobes in 83% of lesions
93                                    Anaerobic bacterial culture determined the occurrence of potential
94         Fluctuations in the growth rate of a bacterial culture during unbalanced growth are generally
95  amount of SGP increased with the age of the bacterial culture, elevated temperature, or acidic pH.
96 cular techniques against comparator methods (bacterial culture, ELISA, and PCR) using 867 diarrhoeal
97               Spent liquid medium from 27/84 bacterial cultures enhanced iodide oxidation 2-10 fold i
98 ty acids (CFAs) are generally synthesized as bacterial cultures enter stationary phase.
99                                              Bacterial cultures, especially biofilms, produce a small
100                                    Anaerobic bacterial culture examination was performed on the poole
101                 The experiments consisted of bacterial cultures exposed to a nondisturbed nonaqueous
102                                    Lysate of bacterial cultures expressing the protein converted the
103 but are culture negative or in regions where bacterial culturing facilities are not available.
104 xin in stool by tissue culture, C. difficile bacterial culture followed by cytotoxin assay, bacterial
105 to all periprosthetic specimens received for bacterial culture from 198 revision arthroplasty procedu
106 cells/ml were obtained using genomic DNA and bacterial culture from M. capricolum subsp. capripneumon
107 tration in the lungs and liver, and positive bacterial cultures from internal organs.
108 ls also underwent necropsy with quantitative bacterial cultures from multiple organ tissue samples.
109           SLIP involves transferring arrayed bacterial cultures from multiwell plates onto large agar
110                 At 48 hrs, cardiac function, bacterial cultures from the septic focus, and inflammato
111                                              Bacterial culture grew aerobic bacteria from three cysts
112 arge filamentous aggregates in the medium of bacterial culture growing at 37 degrees C.
113 achieved biosynthetically through the use of bacterial cultures grown on isotopically enriched media,
114 Out of the 27 sequenced samples, only 20 had bacterial culture growth, while the microbiological and
115 nd suspected VAP, bilateral BAL quantitative bacterial cultures had significant growth on one side on
116 yranopterin monophosphate (1), isolated from bacterial culture, has previously been shown to be effec
117     Two novel compounds so far undetected in bacterial culture headspace, CH3Se2SCH3 and CH3SeSeSeCH3
118 roduces volatile organoselenium compounds in bacterial culture headspace.
119 ral PS-I due to its low expression levels in bacterial cultures, improved chemical synthesis protocol
120 ments (CLIA)-waived setting in comparison to bacterial culture in 481 children and adults.
121 pools performed throughout the growth of the bacterial culture in rich medium revealed a dramatic inc
122 rmining persistence versus extinction of the bacterial culture in the chemostat.
123 tails of these bacterium in JCP, we enforced bacterial culture in the nose and cytology in the nasal
124 e was evaluated by slit lamp examination and bacterial cultures in both a rabbit intrastromal model a
125 alveolar lavage, as the diagnostic source of bacterial cultures in cases of suspected aspiration pneu
126                                  Six hundred bacterial cultures, including M. avium subsp. paratuberc
127                               Even in clonal bacterial cultures, individual bacteria can show substan
128 m single colonies or from less than 1ml of a bacterial culture is possible.
129                                            A bacterial culture is vacuum-infiltrated into leaves, and
130 s formed from pyrene by two pyrene-degrading bacterial cultures known to be geographically widespread
131 of bacteria in these samples was assessed by bacterial culture, light microscopy, and 16S rRNA gene s
132                                 Quantitative bacterial cultures, measurement of C. difficile toxin ti
133 5'- cyclic adenosine monophosphate (cAMP) in bacterial culture media.
134 which we demonstrate through the analysis of bacterial culture media.
135 (yeast culture medium) broth, Luria-Bertani (bacterial culture medium) broth, and minimal essential m
136 onse to increased salt concentrations in the bacterial culture medium, and, concordant with the in vi
137 putum samples compared with that detected in bacterial culture medium, resulting in an underdetection
138 .1% of CIF-positive samples were detected in bacterial culture medium, whereas greater rates of detec
139 entrations of sodium chloride present in the bacterial culture medium.
140 ed for secretion of T3SS2 effectors into the bacterial culture medium; however, it is essential for t
141   Standard identification approaches include bacterial culturing method, which takes several days.
142 previous studies using conventional in vitro bacterial culture methods.
143 lmost interchangeably, impacting non-growing bacterial cultures more significantly than actively grow
144 cimens that were fungal culture positive but bacterial culture negative.
145                    In summary, we found that bacterial culture of BAL fluid is largely effective in d
146                     One week later, a liquid bacterial culture of Escherichia coli was injected into
147 rveyed by enzyme-linked immunosorbent assay; bacterial culture of liver, colon, and cecum; histology;
148 hat mice colonized for 2 months with a mixed bacterial culture of opportunistic pathogens showed an i
149  We retrospectively studied the quantitative bacterial cultures of 399 BAL sample pairs collected fro
150                                              Bacterial cultures of bronchoalveolar lavage fluid and l
151                                      Routine bacterial cultures of corneal scrapings from seven cats
152 ombined use of cryptococcal antigen test and bacterial cultures of CSF could replace routine fungal c
153 ermal colloid antibodies in a mixture of two bacterial cultures of different cell shape and size.
154                       Conditioned media from bacterial cultures of NU14 DeltaampG and NU14 DeltawaaL
155                                              Bacterial cultures of the recovered surgical material an
156 hea (n = 452) were similarly studied, except bacterial cultures of the stool were limited only to cas
157 r bacterial detection require time-consuming bacterial cultures on plates before the pathogens can be
158 was not observed on the surface of a drop of bacterial culture, on bacteria-free culture supernatant,
159 a show that pB15 invades static (nonshaking) bacterial cultures only at intermediate densities.
160 tional growth effect was performed either in bacterial culture or in an animal model of infection.
161 wo standard abutments were either exposed to bacterial culture or left sterile to serve as positive a
162  density values from the EIA with results of bacterial culture or skin test, the reference test, esta
163  had either been previously recovered from a bacterial culture or were recovered from a bacterial cul
164 se) B incubated with purified enzymes, whole bacterial cultures, or their separated components-cells
165 (92 and 77%, respectively, when adjusted for bacterial culture outcomes).
166  discordant cases were one specimen that was bacterial culture positive but fungal culture negative a
167                     Production steps involve bacterial culture, protein isolation, denaturation, puri
168                        Addition of hREG3A to bacterial cultures reduced levels of ROS and increased s
169 ed biochemically and by E. faecalis-specific bacterial cultures, respectively, in day 3 postburn rats
170       Macrophage crude cell lysates added to bacterial cultures resulted in the death of the SalY mut
171 .02, and 0.11mgkg(-1), respectively, and for bacterial culture samples were 1.32, 0.09, and 0.54mgkg(
172 tion of the target metabolites in cheese and bacterial culture samples.
173                                 Quantitative bacterial cultures showed a mean log10 C. difficile coun
174 sed to generate 50 different simulated mixed bacterial cultures similar to that done for an initial b
175  in the infected mouse lung, and in vitro in bacterial cultures subjected to gradual oxygen depletion
176 erase (LesA) that was abundantly secreted in bacterial culture supernatant and was characterized as a
177 by macrophages stimulated with gram-positive bacterial culture supernatants (GPCSs) after their LTA w
178                        PIF was purified from bacterial culture supernatants by anion/cation exchange
179 kine responses induced by partially purified bacterial culture supernatants containing a mixture of e
180                                  We screened bacterial culture supernatants for such activity using r
181       For the microtiter assay, either spent bacterial culture supernatants or extracts are added to
182                HPLC peptide fractionation of bacterial culture supernatants revealed several distinct
183          The Bartonella mitogen was found in bacterial culture supernatants, the soluble cell lysate
184 tudies examined legiobactin contained within bacterial culture supernatants.
185                                            A bacterial culture swab taken from the underlying granula
186      In five of these six recipients (83.3%) bacterial cultures taken from the explanted lungs contin
187 e capture by MR1 of 5-OP-RU and 5-OE-RU from bacterial cultures that activate MAIT cells, but not fro
188 d material was from 10 to 50 mg per liter of bacterial culture, the protein was soluble at concentrat
189 ollowing: conventional anaerobic and aerobic bacterial cultures; the Ibis T5000 universal biosensor (
190 ly optimized for the detection of toxin from bacterial cultures; the limit of detection was approxima
191 owth of S. enteritidis and S. typhimurium in bacterial cultures; this was the result of a decrease in
192 o show applicability to clinical samples and bacterial cultures, through extraction of PCR-amplifiabl
193                      For this study, we used bacterial culture to perform analyses not accurate with
194 zed by the ability of a subpopulation within bacterial cultures to survive exposure to antibiotics an
195  and WTC (n = 29) samples were collected for bacterial culturing to illustrate the relationship betwe
196                  This was confirmed when the bacterial culture, treated with chloramphenicol before t
197 ulture was attempted, five provided positive bacterial culture under both aerobic and anaerobic condi
198                     Importantly, compared to bacterial culture under planktonic conditions, the intra
199 shed on the health effects of yogurt and the bacterial cultures used in the production of yogurt.
200 h Corporation (SLRC), compared with standard bacterial culture using 966 clean-catch urine specimens
201       Of the nine experimental samples where bacterial culture was attempted, five provided positive
202                                              Bacterial culture was enforced symptomatic patients of J
203         The proportion of cases confirmed by bacterial culture was higher in the 1990s than in the 19
204                         A purified enzyme or bacterial culture was mixed with the BODIPY-alpha-casein
205                                    Toxigenic bacterial culture was performed as follows.
206 2,3-diol, and propane-1,3-diol in cheese and bacterial cultures was developed.
207 s very broad, from 0 to 1000mgkg(-1), and in bacterial cultures was from 0 to 5000mgkg(-1) with R(2)>
208 d on experiments in which the growth rate of bacterial cultures was observed to decrease as the osmol
209                                          For bacterial cultures we further demonstrate quantification
210 nization mass spectrometry (MALDI-MS), mixed bacterial cultures were analyzed in a double-blind fashi
211 ctive interleukin 8 (IL-8), and quantitative bacterial cultures were done in BALF from 54 CF (median
212                                              Bacterial cultures were grown, and protein synthesis was
213                                    Viral and bacterial cultures were obtained from ill students.
214                                              Bacterial cultures were performed on the sampling soluti
215                                              Bacterial cultures were positive in 64% of KPro eyes, 76
216 mination in pure cultures; analysis of mixed bacterial cultures, where examining one species in the p
217 cles can support the growth of heterotrophic bacterial cultures, which implicates these structures in
218  synthetic target, purified genomic DNA, and bacterial culture with a limit of detection (LoD) of 3.9
219 ll suited to multi-well imaging, analysis of bacterial cultures with high cell density (thousands of
220                                              Bacterial cultures with positive results were identified

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