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1 SDA gives rise to an increase in the spatial dispersion
2 SDA requires only 200 s per sample with inductively coup
3 SDA specificity in the M. tuberculosis-negative specimen
4 SDA specificity ranged from 90% (PT = 2.4 M. tuberculosi
5 SDA was adapted for quantitative RNA amplification (QRT-
6 SDA was found in significant amounts in Echium plantagin
7 SDA-enriched soybean oil increased the omega-3 index by
8 SDA-enriched soybean oil is a land-based n-3 fatty acid
11 n for the synthesis of zeolite ZSM-5 using a SDA that contains a cyclic ketal group that is removed f
12 proach, specimens initially positive by AC2, SDA, or PCR were retested by different NAATs (SDA, PCR,
13 id (ALA), 0.73 g/100 mL of stearidonic acid (SDA) and 0.65 g/100mL of plant sterol esters (PSE) were
15 nic acid (GLA, 18:3n6) and stearidonic acid (SDA, 18:4n3) of several Sardinian Boraginaceae species.
22 mold agar (IMA) and Sabouraud dextrose agar (SDA), were compared with respect to recovery of fungi.
24 on of the organic structure-directing agent (SDA) inside the channel system of a zeolite be determine
27 ons, imidazolium structure-directing agents (SDA(+)), and crystalline silicate frameworks for as-synt
28 eling studies of structure-directing agents (SDA) for MTT-type zeolites, a large number of amines or
30 ormance of these structure directing agents (SDAs) in fluoride media vs hydroxide media (the more con
31 creating organic structure-directing agents (SDAs) that can be disassembled within the zeolite pore s
35 were trained on spatial delayed alternation (SDA) in a T-maze after ip administration of 0.06 mg/kg M
36 instead of rigid and large quaternary amine SDAs, and (iii) careful temperature control, with the pr
38 rmance of strand displacement amplification (SDA) and transcription-mediated amplification (TMA) to d
42 We found strand displacement amplification (SDA) to be ideal for use in our microelectronic chip sys
46 ProbeTec (strand displacement amplification [SDA]) (Becton Dickinson Co., Sparks, MD), and Amplicor (
48 lysis and structural decomposition analysis (SDA) were applied to investigate the driving forces behi
49 Using structural decomposition analysis (SDA), the change in water withdrawals for the economy fr
51 ids (NSCs) and sparse discriminant analysis (SDA) with k-nearest neighbors for imputation for varying
54 ns swab: N. gonorrhoeae detection by AC2 and SDA (method 1) had the best performance (sensitivities,
56 low-risk or asymptomatic patients by AC2 and SDA, and we would not recommend their use on the basis o
57 rrhoeae, all swabs were evaluated by AC2 and SDA, FCU was tested by AC2, and the clinician-collected
64 and only partially compatible framework and SDA symmetries, which can lead to indecipherable electro
65 olates recovered, 69.3% grew on both IMA and SDA; 24.9% grew only on IMA; and 5.8% grew only on SDA,
66 provide the energies of the six SDA-ITW and SDA-TON zeolites, and their relative stabilities fully a
67 data, the results are compared with NSC and SDA models with four different types of imputation, all
70 of core components of subdistal appendages (SDAs) and of recycling endosomes, which may be associate
71 nd beta-carotene in sulfured dried apricots (SDAs) were investigated during storage at 4, 20 and 30 d
73 and to the sexually dimorphic preoptic area (SDA), but those projections involve less than 20% of the
74 son strand displacement amplification assay (SDA) with the BDProbeTec ET instrument and then to evalu
75 ET amplified DNA strand displacement assay (SDA), and the Roche Cobas Amplicor PCR was defined by us
76 T System C. trachomatis amplified-DNA assay (SDA; Becton Dickinson Diagnostic Systems) were retested
77 for 326 (74%) of the yeasts cultured on BBL SDA versus only 214 (49%) of yeasts grown on Remel SDA (
78 t quality control conditions, the BDProbeTec-SDA assay is a sensitive, specific, and efficient method
79 lacement amplification assay (the BDProbeTec-SDA assay) in detecting Neisseria gonorrhoeae in urine s
81 approach 2, specimens initially positive by SDA and the Hybrid Capture 2 CT-ID DNA Test (HC2; Digene
82 found that 89 to 96% of samples positive by SDA, PCR, and AC2 were confirmed by repeat testing and t
83 . trachomatis, 41% and 44%, respectively, by SDA and 82% and 71%, respectively, by AC2; for N. gonorr
86 ecimens (one tested by AC2 and one tested by SDA), or a positive result for a single glans specimen c
88 tion of N. gonorrhoeae and C. trachomatis by SDA with respect to sensitivity, one in four vaginal swa
92 We found that compared with Sham controls, SDA rats consistently displayed reduced innate anxiety-l
93 l of subdiaphragmatic vagal deafferentation (SDA), the most complete and selective vagal deafferentat
95 oscillate in phase) or spatially discordant (SDA, cells in different regions oscillate out of phase).
96 yr); patients with asthma of short duration (SDA; n = 37) had asthma for < 26 yr (median = 9 yr).
99 n product that rises in concentration during SDA and the single- to double strand conversion is monit
103 aximization sparse discriminant analysis (EM-SDA), produces a sparse LDA model for datasets with and
106 100% and 100% for AC2 and 76.2% and 100% for SDA, respectively, while culture was only 23.8% sensitiv
113 ing Sabouraud dextrose agar with gentamicin (SDA), inhibitory mold agar (IMA), and brain heart infusi
116 hydrophobic alkyl ligands on the imidazolium SDA(+) species under otherwise identical zeolite synthes
118 ngi were found in IMA (65.8%; P < 0.001), in SDA (at 30 degrees C, 64.7%; P = 0.005), and in BHI agar
124 SA (13.9-31.8g/kgdw) was the major OA in SDAs containing SO2 at lower than 1594mgSO2/kg, while MA
125 ncapsulated soybean oil/d plus 14.7 g liquid SDA-enriched soybean oil/d, providing 4.2 g SDA (SDA gro
127 cells in the lateral MeApd, PdPN, and medial SDA do not participate in any projection studied, sugges
128 the sexually dimorphic preoptic area (medial SDA), and the parvicellular part of the subparafascicula
129 ections from the lateral MeApd to the medial SDA and PdPN, and from the medial SDA to the lateral MeA
130 the medial SDA and PdPN, and from the medial SDA to the lateral MeApd, were also activated with matin
134 DA, or PCR were retested by different NAATs (SDA, PCR, AC2, and Aptima Neisseria gonorrhoeae assay [A
135 ene Corp.) were retested by different NAATs (SDA, PCR, AC2, and the APTIMA assay for C. trachomatis [
137 rmed by repeat testing and that 85 to 98% of SDA, PCR, and AC2 results were confirmed by using differ
138 irmed by a repeat test and that 89 to 99% of SDA and AC2 and 93% of HC2 positive results were confirm
139 The objective was to evaluate the ability of SDA-containing soybean oil to increase the omega-3 index
141 hat 2 mechanisms underlie the development of SDA in the heart, leading to 2 distinct behaviors of nod
143 ition discrimination learning, impairment of SDA by MK-801 likely reflects disruption of spatial work
148 BHI, 30 days; sediment from Isolator tube on SDA, 30 days; and sediment from Isolator tube in a BACTE
149 re fed for two weeks on diets rich in ALA or SDA derived from linseed or Echium plantagineum, respect
151 antially less specific than culture, TMA, or SDA and should not be used for the detection of pharynge
152 eolite synthesis-the location of the organic SDA in the channel system and of the positions adopted b
154 y available NAATs (Becton-Dickinson ProbeTec SDA, Gen-Probe Aptima Combo2 TMA, and Roche Amplicor PCR
156 pted for quantitative RNA amplification (QRT-SDA) of an HIV gag sequence by including AMV reverse tra
159 nalytical demonstration of the technique, RT-SDA was quantitative to within twofold over a range of 5
161 calculations provide the energies of the six SDA-ITW and SDA-TON zeolites, and their relative stabili
164 of C18 precursors for LC-PUFA - stearidonic (SDA) and gamma-linolenic acid (GLA) - from Echium planta
165 e, we suggest using 1594mgSO2/kg and storing SDAs at 4 degrees C to protect OAs and beta-carotene.
166 l isomer, which is shown to be the strongest SDA for ITW and, at the same time, is the more hydrophil
167 ctional photoactivatable cross-linker, sulfo-SDA (diazirine), has yielded high-density data that faci
168 nd a strand displacement amplification test (SDA; ProbeTec; Becton Dickinson Co.) in MSM seen at the
171 nlike prokaryotic cysteine desulfurases, the SDA structure adopts an unexpected architecture in which
173 ieve reliable experimental positions for the SDA by using a combination of simulated annealing (globa
175 cyclic ketal group that is removed from the SDA while it is inside the zeolite without destruction o
176 c and electron microscopic structures of the SDA complex coupled to enzyme kinetic and cell-based stu
177 ISD11 subunits form the dimeric core of the SDA complex, which clarifies the critical role of ISD11
179 Z-59, and SSZ-60), where the location of the SDA had only been simulated using molecular modeling tec
180 threshold (PT) value, above which 95% of the SDA results were judged to be M. tuberculosis positive (
183 vents to a single source and event, with the SDA identified as the emission source and flood transpor
191 on is common and that the AC2 is superior to SDA for the detection of C. trachomatis and N. gonorrhoe
193 esting did not confirm 11% of C. trachomatis SDA positive results that could be confirmed by more ext
194 associated with short-term memory underlies SDA formation in the heart, in addition to steep CV rest
199 gher in subjects with LDA than in those with SDA (142.9 +/- 5.6 versus 124.1 +/- 4.4, respectively, p
200 lower FEV(1)% predicted than did those with SDA (59.5 +/- 2.6% versus 73.8 +/- 3.1% [mean +/- SEM],
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