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1 amino acid 614-681 (p6 plus part of p7) was nonviable.
2 9Delta taf14Delta sas5Delta triple mutant is nonviable.
3 t with the microorganisms and rendering them nonviable.
4 GT1(-/-) cells were determined to be nonviable.
5 th at 37 degrees C, but the E285D mutant was nonviable.
6 wild-type, but a pbpA pbpH double mutant was nonviable.
7 ely ceased consuming oxygen, and most became nonviable.
8 30 to 75 min, at which time the cells became nonviable.
9 mas declined in numbers or became completely nonviable.
10 ltinucleated syncytia that eventually became nonviable.
11 rdium as stunned, hibernating, remodeled and nonviable.
12 32 min(-1) (P<.0001) and 98% of samples were nonviable.
13 Yeast with a null mutation in scRUVBL1 was nonviable.
14 e remain as spores, while most cells are now nonviable.
15 deletion mutant lacking codons 2 to 230 was nonviable.
16 eletion mutant lacking codons 190 to 261 was nonviable.
17 ter which nearly all ova were observed to be nonviable.
18 ive-amino-acid insertions in the linker were nonviable.
19 However, produced white eggs were nonviable.
20 riod and regional dispersal make eradication nonviable.
21 tent, indeterminate state that is ultimately nonviable.
22 ed endocardial/endothelial lineages and were nonviable.
23 albicans could not acquire inositol and was nonviable.
24 The last three mutants were nonviable.
25 lanine and alanine (3F4A), respectively, was nonviable.
26 ther group of VP1 mutants rendered the virus nonviable.
27 and Fancg(-/-)Atm(-/-) mice were found to be nonviable.
28 oth viable (0.48+/-0.15; n = 8 patients) and nonviable (0.45+/-0.14; n = 8 patients) regions (post-CA
30 58 samples from no-reflow regions, 97% were nonviable after 5 minutes of reperfusion (k3=0.096 +/- 0
32 ich affect one probable interchain bond were nonviable and could not be propagated in either canine o
33 nificant proportion of mmdh1mmdh2 seeds were nonviable and developed only to torpedo-shaped embryos,
35 rapidly detect and distinguish viable versus nonviable and pathogenic versus nonpathogenic captured o
36 bility to render highly pathogenic organisms nonviable and safe for handling in a biosafety level 2 l
41 BC1 Spd/+ progeny, 23.9% are estimated to be nonviable, and 32.1% are nonpenetrant for the white bell
42 utants with altered active-site residues are nonviable, and depletion of CtpA yields chains of cells
43 d that nearly one half of CUL-4A+/- mice are nonviable, and in this report, we show that the viable h
44 cing His(704) with alanine renders the phage nonviable, and no DNA synthesis is observed in vivo.
49 %) and retention (41% +/- 13%) of Q12 in the nonviable as compared to the viable segments (p < 0.001)
50 can characterize the myocardium as viable or nonviable, automatically track the endocardium throughou
51 ts and secreted proteins than coculture with nonviable B. burgdorferi in RPMI, which corresponded wit
52 mice, a mixed T-helper-cell-like response to nonviable B. mallei is obtained, as demonstrated by a Th
54 n more rapid water uptake by both viable and nonviable (boiled) seeds, but did not affect semipermeab
55 Accordingly, all substitutions for G61 are nonviable but mutant proteins differ vis-a-vis recessive
56 midis that specifically bound and coated the nonviable, but not the viable, spermatozoa within the ep
57 impair protein function and can render seeds nonviable, but PROTEIN ISOASPARTYL METHYLTRANSFERASE (PI
58 ant DHFR proteins aggregated, rendering them nonviable, but, intriguingly, the majority exhibited fit
59 However, of the 78 segments confirmed to be nonviable by 18FDG PET, 57 (73%) were nonviable by 18FDG
63 enhancement also occurred in segments judged nonviable by dobutamine echocardiography (P</=0.03).
65 tion of viable myocardium in tissue declared nonviable by thallium (to 88% of the sensitivity achieva
67 t occur to turn a BRCA-deficient cell from a nonviable cell into a tumor cell capable of endless grow
78 factor displayed an increased proportion of nonviable cells in the presence of TSP2, but the additio
79 demonstrate the immobilization of viable and nonviable cells in the vicinity of each other along the
80 ence of TUNEL-positive cells, the numbers of nonviable cells increased with exposure duration and as
81 ace is composed mainly of viable cells, with nonviable cells making up a small percentage of the whol
82 ties of polystyrene microspheres, viable and nonviable cells of the budding yeast Saccharomyces cerev
84 viability of cells, most methods to exclude nonviable cells require the use of density gradient cent
85 refore, the separation and immobilization of nonviable cells separately or in the vicinity of viable
87 and then irradiated (480 nm), the number of nonviable cells was increased, whereas the latter was de
89 NEL-positive viable cells and TUNEL-positive nonviable cells were observed, indicating that apoptosis
91 ness was validated as a sorting parameter as nonviable cells were substantially stiffer than live cel
92 d subsequent postanalysis of both viable and nonviable cells with and without the presence of each ot
93 and separation, as well as the formation of nonviable cells with multiple, fragmented micronuclei, a
94 try revealed a relatively high percentage of nonviable cells, implying that soluble antigen promotes
101 ur findings also reveal MVs are a functional nonviable complex vaccine for Salmonella by their abilit
102 ses that were severely impaired in growth or nonviable, confirming that combination therapy may be ad
106 neus) was viable during 1987-1999 but became nonviable during 2000-2006 in association with an abrupt
109 tions, only inhibit macrophage activation by nonviable E. coli In total, this study shows that cathel
111 days 0, 7, and 14, as well as percentage of nonviable endothelial cells by vital dye staining on day
114 underrepresented synonymous codon pairs) are nonviable except for P2(Min), a variant temperature-sens
116 he question: "was evidence of HCC (viable or nonviable) found in the explant?" in patients with T2 ME
117 upon surface conductance as well as sorting nonviable from viable cells of the budding yeast Sacchar
118 es within an inversion interval will lead to nonviable gametes, while gametes generated from recombin
122 e system can discriminate between viable and nonviable Gram-negative bacteria to tune the immune resp
123 modified mouse inoculation protocol whereby nonviable H. pylori is first inoculated into mice, follo
125 hepatocytes (13 cells/high-power field), and nonviable hepatocytes increased slightly to approximatel
126 of viable diplococci, as well as viable and nonviable host cells, attached to a fibrous matrix that
127 ifference between EHMs containing viable and nonviable human cardiomyocytes in this chronic xenotrans
129 r1Delta/P(MET3)::ITR1 strain was found to be nonviable in medium containing methionine and cysteine (
135 DNA topoisomerases I and III are found to be nonviable, indicating that the two type IA enzymes share
136 dangerous for a virus because it results in nonviable individuals, it has been hypothesized that hig
138 defined as the involuntary termination of a nonviable intrauterine pregnancy before 28 completed wee
139 uman islets could prevent transplantation of nonviable islets and facilitate the optimization of isle
140 e the prevalence of serotypes between viable/nonviable isolates and culture-negative clinical specime
143 radermal injection with fluorescent-labeled, nonviable larvae from the helminth parasite nonviable Ni
144 Suppression of only PG growth resulted in nonviable larvae, but larvae with enlarged PGs produced
146 he experimental animals were euthanized with nonviable lungs soon after the postoperative day 50 biop
147 for the label-free separation of viable and nonviable mammalian cells within a microfluidic device.
149 differential determination of viable versus nonviable microbes is critical for formulation of an app
151 s mutants were studied: the entry-defective, nonviable mutant 4028T.G and the viable mutants 4028T.S
153 equent comparative molecular analysis of two nonviable mutants impaired in chloroplast translation, o
154 of two host range-restricted mutants and two nonviable mutants replicated to wild-type levels in both
155 tion of >20 sequence variants, including the nonviable mutations and several resistance mutations.
156 patients with dysfunctional viable than with nonviable myocardium (48% vs. 77% survival, p = 0.02).
157 tamine would discriminate between viable and nonviable myocardium in patients with ischemic cardiomyo
158 differentiate between viable but stunned and nonviable myocardium within the postischemic injured myo
159 gnetic resonance imaging (MRI) to viable and nonviable myocardium within the region at risk throughou
160 t thallium differentiates between viable and nonviable myocardium, in some patients with chronic isch
169 nonviable larvae from the helminth parasite nonviable Nippostrongylus brasiliensis L3 larvae (Nb), a
176 We have shown that appropriately prepared nonviable organisms are as effective as viable organisms
178 sitivity, it may potentially detect DNA from nonviable organisms following effective therapy, leading
179 n some treated patients is slow clearance of nonviable organisms that may lead to prolonged inflammat
181 exal hemorrhagic content was associated with nonviable ovaries in seven of 10 patients (70%) and with
182 The successful recovery of replication of a nonviable P/L (A(5)C) mutant replicon with an artificial
185 t that mutations that have repeatedly led to nonviable phenotypes would be introduced less frequently
186 or near either zinc-binding finger generated nonviable phenotypes, demonstrating that both domains ar
187 h aHUS resulted in a significant increase of nonviable PIGA-deficient TF-1 cells compared with serum
188 efects in gametophyte development, including nonviable pollen and embryo sacs with unfused polar nucl
189 T-DNA mutants were not recoverable, and 50% nonviable pollen was detected in heterozygous ssspta mut
190 -enhanced region encompasses both viable and nonviable portions of the ischemically injured myocardiu
191 cardium is frequently composed of viable and nonviable portions, a method to discriminate the two is
192 ic heterodimer, the chimeric virus is almost nonviable, producing about 10(-7) as much virus as SIN a
195 ment by MRI distinguishes between viable and nonviable regions within the myocardium at risk througho
196 ecies have a defective LEC1 gene and produce nonviable seed, whereas species that produce plantlets o
199 retention (24 +/- 12%) of tetrofosmin in the nonviable segments compared with the viable segments.
200 variable regression analysis, the number of nonviable segments was independently associated with IS
201 ent compelling evidence that the residues of nonviable spirochetes can persist in cartilaginous tissu
203 o-acid insertions in individual linkers were nonviable, suggesting the critical roles these linkers p
204 al-time molecular imaging in both living and nonviable systems at the microscale can be achieved.
205 y of biological processes in both living and nonviable systems at the molecular level and has a high
207 spectroscopy showed that [Na+] was higher in nonviable than viable myocardium (isolated, 99 +/- 4 ver
208 terne) and rendered their germinating spores nonviable, they also inactivated the enzymatic activity
209 ish dysfunctional but viable myocardium from nonviable tissue has important prognostic implications a
212 tention of Q12 was significantly less in the nonviable tissue when compared to the initial uptake (p
213 nosis, primarily because of its success with nonviable tissue, and is especially valuable in analyses
216 netic resonance [MR] imaging), and amount of nonviable tumor determined as decreased echogenicity at
218 liovirus infectivity, all 2195H mutants were nonviable upon introduction of the mutant genomes into H
219 ces a high rate of mutation that generates a nonviable viral phenotype and that lethal mutagenesis is
221 phosphomimetic aspartate (Asp) resulted in a nonviable virus which could only be recovered with an ad
222 s in a microliter) and distinguish them from nonviable viruses in a label-free electrochemical assay
225 43, Leu245, or both to glutamate were nearly nonviable, whereas those with Vp3 alterations reduced, b
227 ange the dielectrophoretic (DEP) response of nonviable yeast cells by treating them with low concentr
228 the sorting and immobilization of viable and nonviable yeast cells, along consecutive microelectrode
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