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1  not with a polysaccharide A (PSA) deficient isogenic strain.
2  yeast strain at 90% the rate of a wild-type isogenic strain.
3 ed fungal traits, relative to the virus-free isogenic strain.
4 milarly to the profile that was observed for isogenic strains.
5 d laboratory parasites as well as across non-isogenic strains.
6 the underlying genetic lesions, and generate isogenic strains.
7 strain tested, including identically reared, isogenic strains.
8  inhibited by HGA secreted from neighboring, isogenic strains.
9  an experimental population composed from 20 isogenic strains.
10 f an IS6110-mediated deletion event in truly isogenic strains.
11 ed replication rate in amoebae compared with isogenic strains.
12 ated in piglets and mice using GGT-deficient isogenic strains.
13 set of conditionally growth-defective/lethal isogenic strains.
14 unctions-within the population of individual isogenic strains, along single misshaped cells, and even
15                            Reconstruction of isogenic strains also showed that the IS150 insertions i
16            Previous data generated using non-isogenic strains and transfection models suggest that va
17                             Variation within isogenic strains appears to be generated mainly by devel
18                                           An isogenic strain bearing a kanamycin insertion in mtaR wa
19 estored the fucosylation program, whereas an isogenic strain carrying a transposon insertion that dis
20 pendent on CorA for Mg(2+) uptake but not of isogenic strains carrying a second Mg(2+) uptake system.
21                                              Isogenic strains carrying either no plasmid, wild-type p
22                                              Isogenic strains carrying in-frame deletions in genes re
23                               We showed that isogenic strains carrying mutations in luxS(Hp), cysK(Hp
24                    Importantly, the repaired isogenic strain colonized the mouse oropharynx with sign
25  an average 6-fold decreased GAS recovery in isogenic strain competition assays.
26  variants from the IC-I and IC-II groups and isogenic strains complemented with IC-I or IC-II pilA, t
27                  Engineered polymorphisms in isogenic strains confirmed an interaction between the ma
28 ch precolonized strain nearly eliminated its isogenic strain, confirming that colonization resistance
29                          A recent study with isogenic strains constructed by recombinant DNA strategi
30                            The corresponding isogenic strain containing ccaR:gfp in the chromosome pr
31          Although the levels of virulence of isogenic strains containing either nt 5 A or nt 5 G did
32                                              Isogenic strains containing either the complete phoB pro
33 n vivo activities of all eight pheromones on isogenic strains containing four different ComP receptor
34                                              Isogenic strains containing specifically disrupted flaAl
35 ow levels of these self-poisoning enzymes in isogenic strains defective for the Rad9 DNA damage check
36                                  Two sets of isogenic strains deficient in SpeB cysteine protease act
37                                  Using three isogenic strains derived from PRV263, each expressing a
38                               Y. pestis psaA isogenic strains did not show any significant difference
39 tect against mixed infections with otherwise isogenic strains differing in promoter sequence.
40 -toxin in experimental endocarditis by using isogenic strains differing in the capacity to produce fu
41 nd respiratory tract infection in mice using isogenic strains differing only in SpyCEP expression.
42 expressed during starvation in two otherwise-isogenic strains differing only in their H1s.
43 tly increased compared to that of cells from isogenic strains expressing active PBP 5.
44 h the hemolysin structural gene deleted, and isogenic strains expressing different amounts of hemolyt
45                                        Using isogenic strains expressing either meningococcal fHbp or
46         However, in murine infection models, isogenic strains expressing the two delta-toxin variants
47 survival defect more pronounced than that of isogenic strains harbouring single mutations.
48                       Infection studies with isogenic strains having defined toxin deletions have est
49           We found that virulence among near-isogenic strains in a murine model of cryptococcosis cor
50  with 0.5% rifampin- and isoniazid-resistant isogenic strains in some experiments.
51                              In contrast, an isogenic strain lacking Shiga toxin induced similar but
52 ntext of the live bacterium by generating an isogenic strain lacking the scl-1 gene.
53 ype T. thermophilus outcompetes an otherwise isogenic strain lacking TtAgo.
54            In contrast to wild-type UPEC, an isogenic strain lacking ybcL expression (UTI89 DeltaybcL
55 omatin organization and transcription, using isogenic strains lacking all combinations of these enzym
56 atory strains carrying pMB2 grew faster than isogenic strains lacking the plasmid in both rich and mi
57 ased PNAG and biofilm production relative to isogenic strains lacking the plasmid.
58 e (NSR) of wild type S. meliloti Rm1021, and isogenic strains missing both PII proteins, GlnB and Gln
59 ential growth without cell lysis, whereas an isogenic strain mutated in a peptidoglycan hydrolase gen
60 y to disruption of ompCD by constructing the isogenic strain O35E.CD1.
61 ed a high fat/sugar water-induced animal (an isogenic strain of C57BL/6 J:129S1/SvImJ mice) model of
62 e report transmission of an azole-resistant, isogenic strain of Candida albicans in a human immunodef
63        In contrast, in mice infected with an isogenic strain of pneumococci lacking PspA, significant
64 A/J lacking T and NK cells), and SK(-/-) (an isogenic strain of strain C57BL6/J lacking SK1), to inve
65 L6/J (both immunocompetent), Tgepsilon26 (an isogenic strain of strain CBA/J lacking T and NK cells),
66          Taking advantage of a highly inbred isogenic strain of the species, we rapidly identified th
67                       Our aim was to use two isogenic strains of a neurotropic virus (pseudorabies, B
68 he amount of serotype 1 or 5a CP produced by isogenic strains of A. pleuropneumoniae correlated with
69                                              Isogenic strains of Agrobacterium tumefaciens carrying p
70  catalase in CGD directly, we have generated isogenic strains of Aspergillus nidulans in which one or
71 xtracellular proteomes (secretomes) of three isogenic strains of B. anthracis that differed solely in
72 h inactivated HWP1 genes, whereas mice given isogenic strains of C. albicans that had a single copy o
73 e cantilever tip and confluent monolayers of isogenic strains of Escherichia coli mutants exhibiting
74        We tested this hypothesis by creating isogenic strains of gliotoxin-producing and nonproducing
75 lets from six litters were given one of four isogenic strains of H. pylon orally.
76  expression in three selected lines, and six isogenic strains of mice known to differ markedly in vol
77 orsal lateral geniculate nucleus (LGN) in 58 isogenic strains of mice.
78                  Construction of genetically isogenic strains of mycobacteria is complicated by poor
79 oach was applied to Tn-Seq libraries made in isogenic strains of Mycobacterium tuberculosis lacking t
80 ry of structurally diverse compounds in four isogenic strains of P. aeruginosa with varied permeabili
81                                              Isogenic strains of PAO1 that lacked surface adhesins we
82                For this purpose, recombinant isogenic strains of PRV were injected into these respira
83 uronal viral retrograde tract tracing, using isogenic strains of pseudorabies virus (PRV) with distin
84 e transneuronal transport of two recombinant isogenic strains of pseudorabies virus.
85 ssions from seven species of Lycopersicon to isogenic strains of Pst differing in the presence of avr
86  memory CD8 T cells were coinfected with two isogenic strains of recombinant Listeria monocytogenes t
87 ptic arthritis by comparing the virulence of isogenic strains of S. aureus expressing (1) wild-type C
88                     Mice were gavaged with 2 isogenic strains of S. typhimurium after administration
89 H1, MLH2, MSH2, MSH3, MSH6, but not PMS1) in isogenic strains of Saccharomyces cerevisiae led to incr
90 f each gene in virus-infected and uninfected isogenic strains of the fungus by using nuclear run-on a
91  transcriptional profiling of infection with isogenic strains offered a detailed molecular picture of
92 alent inhibitory effects of SAL on a pair of isogenic strains, one of which was a polysaccharide/adhe
93  one of two strategies: pairwise crossing of isogenic strains or simple mixing of strains in equal pr
94 -1beta) in mice, similar to what occurs with isogenic strain P4 (DeltactxAB), but is less virulent an
95                             We created three isogenic strain pairs (serotypes 3, 4, and 24) that diff
96 type 2 S. pneumoniae strain D39, or with the isogenic strain PLN, which does not express pneumolysin.
97  nasopharyngeal isolates express pili, while isogenic strains recovered from the middle ear are often
98  shape bacterial behavior, we generated near-isogenic strains representing each configuration in Agro
99  comparison between CpMV1-free and -infected isogenic strains revealed no overt effects of the virus.
100 ative analysis of proteins isolated from the isogenic strains revealed that growth phase-associated r
101 Fluorescent protein-based differentiation of isogenic strains revealed that priority of gut colonizat
102  Candq1 and its candidate genes to create an isogenic strain set with large differences in collateral
103                                  Assays with isogenic strains show that a single copy of rtxA is asso
104         Notably, our results differ from non-isogenic strain studies, thus highlighting the importanc
105                      Our data obtained using isogenic strains suggest that the liaS(R135G) mutation i
106 do display enhanced resistance to a virulent isogenic strain that lacks the avirulence gene.
107                    Furthermore, we generated isogenic strains that allowed us to establish that Exigu
108                                        Using isogenic strains that carry a temperature sensitivity al
109  a field experiment comparing the fitness of isogenic strains that differ in the presence or absence
110                                    Comparing isogenic strains that differ only in their ability to in
111 f the organisms compared to the virulence of isogenic strains that do not overexpress SrrAB.
112 ss this discordance, we constructed a set of isogenic strains that enabled us to inhibit selectively
113     While the adhesive abilities of Opa-Pil+ isogenic strains that express LOS molecules lacking the
114 omoter by a variety of phenolic compounds in isogenic strains that express or lack virH1 and virH2.
115   We report the construction and use of four isogenic strains that lack nitrate reductase Z and the p
116             In competition experiments using isogenic strains, the strain with the insertional allele
117 s (FnBPs); the capacity of an FnBP-deficient isogenic strain to invade HCEC was reduced by more than
118 s, thus highlighting the importance of using isogenic strains to study the role of CagA toxin polymor
119                                      We used isogenic strains to test the hypothesis that a single am
120                               The "repaired" isogenic strain was significantly more virulent than the
121 ment (P[lArB]) insertional mutagenesis of an isogenic strain was used to identify autosomal loci affe
122           The colony-forming potential of 10 isogenic strains was defined as a function of time spent
123          The results indicated that all K88+ isogenic strains were able to colonize the small intesti
124 nsertion of an Omega kanamycin cassette, and isogenic strains were constructed.
125                                          The isogenic strains were found to be equally capable of blo
126  of CovRS in the virulence of AP53, two AP53 isogenic strains were generated, one in which the natura
127                          Coinoculation of an isogenic strain which produced the endogenous HHL signal
128 growth rate by up to 100-fold relative to an isogenic strain with normal editing function.
129        Compared with naturally occurring and isogenic strains with a wild-type GAS-like PBP2X, strain
130 derived macrophages as well as did otherwise isogenic strains with a wild-type rpoS allele.
131                            The capacities of isogenic strains with an insertion mutation in emm49; wi
132 er-assisted estimations of CO frequencies to isogenic strains with and without transgenically inserte
133 onditions that led to germ tube formation in isogenic strains with CAP1.
134           In vitro treatment of clinical and isogenic strains with ciprofloxacin increased the produc
135                                      Several isogenic strains with defects in recombination/repair ge
136 A uptake to rapidly generate greater than 30 isogenic strains with deletions of genes encoding BB120
137                                          Two isogenic strains with identical growth kinetics at 35 de
138                                              Isogenic strains with mutations in ftpA or losB bound as
139                             Here we compared isogenic strains with naturally occurring mtrR locus mut
140         In comparison to a wild-type strain, isogenic strains with null mutations in either HP0165 or
141 c E. coli was examined by comparing adherent isogenic strains with or without STb.
142 id A-modifying genes into 18-323 to generate isogenic strains with varying penta-acyl lipid A structu

 
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