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1 ntibodies, and MCs in host defense against a pathogenic bacterium.
2 ate that can facilitate the maintenance of a pathogenic bacterium.
3 argely determine the virulence of this plant-pathogenic bacterium.
4  and independent activities of CcpA in a key pathogenic bacterium.
5 et sites explains evolutionary patterns in a pathogenic bacterium.
6 PLC) is a secreted virulence factor for this pathogenic bacterium.
7  first demonstration of a shared ATPase in a pathogenic bacterium.
8  these AMPs acted cooperatively against this pathogenic bacterium.
9 of pyomelanin-mediated ferric reduction by a pathogenic bacterium.
10  engineering is routinely performed with the pathogenic bacterium Agrobacterium tumefaciens and simil
11                Clostridioides difficile is a pathogenic bacterium and a leading cause of antibiotic-a
12           Streptococcus pneumoniae (SP) is a pathogenic bacterium and a major cause of community-acqu
13 Clostridioides difficile is a Gram-positive, pathogenic bacterium and a prominent cause of hospital-a
14 um perfringens is a ubiquitous and versatile pathogenic bacterium and is implicated in the etiology o
15 rst to be described in a Gram-positive plant pathogenic bacterium and is responsible for the emergenc
16 olecular basis for symbiosis between a human pathogenic bacterium and its arthropod vector and deline
17 he majority of cases interpreted as a single pathogenic bacterium and would have resulted in antibiot
18 Bartonella henselae is a recently recognized pathogenic bacterium associated with cat scratch disease
19                                          The pathogenic bacterium Bacillus anthracis has become the s
20 oteins is essential for the virulence of the pathogenic bacterium Bacillus anthracis.
21 phore-binding protein from the gram-positive pathogenic bacterium Bacillus cereus that binds multinuc
22  mum), a serine protease secreted by the non-pathogenic bacterium Bacillus subtilis, induces plasma c
23 Xylella fastidiosa, a xylem-colonizing plant pathogenic bacterium, block its interaction with various
24 vo murine model of infection with the highly pathogenic bacterium Burkholderia pseudomallei, indicati
25 iated T cell activation in resistance to the pathogenic bacterium Burkholderia pseudomallei.
26 mensal bacterium enhances the virulence of a pathogenic bacterium by modulating its spatial location
27         Evidence that learned avoidance of a pathogenic bacterium can be transmitted to future genera
28  Xylella fastidiosa is a Gram-negative plant-pathogenic bacterium causing many economically important
29                                          The pathogenic bacterium Chlamydia replicates in a eukaryoti
30   We have purified recombinant HrcA from the pathogenic bacterium Chlamydia trachomatis and have show
31                                       In the pathogenic bacterium Chlamydia trachomatis, a transcript
32 ion model involving controlled spread of the pathogenic bacterium Citrobacter rodentium from infected
33 ger RNA for a putative virulence gene in the pathogenic bacterium Clostridium difficile.
34                                    The human pathogenic bacterium Clostridium perfringens secretes an
35   A full-length heme oxygenase gene from the pathogenic bacterium Corynebacterium diphtheriae has bee
36                The virulent phenotype of the pathogenic bacterium Corynebacterium diphtheriae is conf
37 ment of HmuO, a heme oxygenase (HO) from the pathogenic bacterium Corynebacterium diphtheriae, have b
38 ith Helicobacter hepaticus, an opportunistic pathogenic bacterium, developed granulomatous inflammati
39 inuous reactor hosting a strain of the plant pathogenic bacterium Dickeya dadantii and in which the d
40 dings elucidate a novel mechanism by which a pathogenic bacterium employs tRNA mimicry to hijack a ri
41  threat of hydrogen peroxide produced by the pathogenic bacterium Enterococcus faecium.
42 smotic stress, or harpin (a protein from the pathogenic bacterium Erwinia amylovora).
43 pyoluteorin-mediated inhibition of the plant-pathogenic bacterium Erwinia amylovora.
44 ymes that degrade the plant cell wall by the pathogenic bacterium Erwinia carotovora.
45 ense to Pst DC3000 hrp mutants and the human pathogenic bacterium Escherichia coli O157:H7.
46                                         This pathogenic bacterium exploits a sophisticated protein ma
47                Since this is the first plant pathogenic bacterium for which a complete genome sequenc
48 chromosomal traits during the evolution of a pathogenic bacterium from an avirulent saprophyte.
49                            The extracellular pathogenic bacterium group A Streptococcus (GAS) causes
50   In many countries, M1 strains of the human pathogenic bacterium group A Streptococcus are the most
51                                    The human pathogenic bacterium group A Streptococcus produces an e
52                                          The pathogenic bacterium Group A Streptococcus pyogenes prod
53 e susceptible to systemic infection with the pathogenic bacterium group B Streptococcus.
54                            The human gastric pathogenic bacterium Helicobacter pylori lacks a MutSLH-
55                                          The pathogenic bacterium Helicobacter pylori utilizes two es
56 hifted toward inhibitory p53 isoforms by the pathogenic bacterium Helicobacter pylori, which is known
57 noglobulin-binding protein A (IbpA) from the pathogenic bacterium Histophilus somni adenylylates mamm
58 duced by Tenacibaculum maritimum, a relevant pathogenic bacterium in fish aquaculture.
59 tective O-antigen of a human-disease-causing pathogenic bacterium is described.
60 I effectors in Pst DC3000 or any other plant pathogenic bacterium is not known.
61 on provides convincing evidence that a plant pathogenic bacterium is sexually transmitted from male t
62                     Salmonella enterica is a pathogenic bacterium known for causing severe typhoid fe
63 Vibrio natriegens is the fastest-growing non-pathogenic bacterium known to date and is gaining more a
64 nificantly increased the survival of the non-pathogenic bacterium Lactococcus lactis during a human w
65          During infection, the intracellular pathogenic bacterium Legionella pneumophila causes an ex
66                                    After the pathogenic bacterium Legionella pneumophila is phagocyto
67         During infection of macrophages, the pathogenic bacterium Legionella pneumophila secretes eff
68 s AnkX and DrrA/SidM, respectively, from the pathogenic bacterium Legionella pneumophila.
69 LRC4 inflammasome detects flagellin from the pathogenic bacterium, Legionella pneumophila.
70                                          The pathogenic bacterium Listeria monocytogenes is capable o
71 filament assembly at the cell surface of the pathogenic bacterium Listeria monocytogenes requires the
72  similar to those behaviors displayed by the pathogenic bacterium Listeria monocytogenes.
73  for host cell invasion by the intracellular pathogenic bacterium Listeria monocytogenes.
74 Xylella fastidiosa, a xylem-colonizing plant pathogenic bacterium, mediated by a fatty acid Diffusibl
75 in, we tested the ability of CF from the non-pathogenic bacterium Mycobacterium smegmatis (Msm) to st
76                Tuberculosis is caused by the pathogenic bacterium Mycobacterium tuberculosis (Mtb) an
77 2) is an essential respiratory enzyme of the pathogenic bacterium Mycobacterium tuberculosis (Mtb) th
78 the X-ray crystal structure of MsrA from the pathogenic bacterium Mycobacterium tuberculosis refined
79 s method by applying it to the genome of the pathogenic bacterium Mycobacterium tuberculosis, assigni
80            Studies of these processes in the pathogenic bacterium Mycoplasma pneumoniae and its close
81 The terminal organelle of the cell wall-less pathogenic bacterium Mycoplasma pneumoniae is a complex
82                Heme oxygenase (HO), from the pathogenic bacterium N. meningitidis(NmHO), which secure
83 e multidrug efflux pump operon mtrCDE in the pathogenic bacterium Neisseria gonorrhoeae.
84                              The HO from the pathogenic bacterium Neisseria meningitidis (NmHO) posse
85 crystal structure of heme oxygenase from the pathogenic bacterium Neisseria meningitidis at 1.5 A and
86                 Heme oxygenase, HO, from the pathogenic bacterium Neisseria meningitidis catabolizes
87          The antigenic P64K protein from the pathogenic bacterium Neisseria meningitidis is found in
88                              The HO from the pathogenic bacterium Neisseria meningitidis, NmHO, posse
89 phyrin IX (heme) have been described for the pathogenic bacterium Neisseria meningitidis.
90 iotic ampicillin and the porin PorB from the pathogenic bacterium Neisseria meningitidis.
91      Phenstatin (3b) inhibited growth of the pathogenic bacterium Neisseriagonorrhoeae and was a pote
92 mbrane lipoprotein P6 from the Gram-negative pathogenic bacterium nontypeable Haemophilus influenzae
93  first evidence of a super-integron in a non-pathogenic bacterium, one which is widely distributed in
94 ) domain in the OtDUB protein encoded by the pathogenic bacterium Orientia tsutsugamushi A proteomics
95 f antibiotic resistant biofilms in the human pathogenic bacterium P. aeruginosa, which causes lethal
96 charide synthesis and virulence in the plant pathogenic bacterium Pantoea stewartii ssp. stewartii re
97 c strain with an adhesion protein from a non-pathogenic bacterium provides a new paradigm to exclude
98 that are substituted when populations of the pathogenic bacterium Pseudomonas aeruginosa adapt to the
99 d the microanatomy of biofilms formed by the pathogenic bacterium Pseudomonas aeruginosa and discover
100                  Alginate is secreted by the pathogenic bacterium Pseudomonas aeruginosa and is belie
101                                          The pathogenic bacterium Pseudomonas aeruginosa causes serio
102 s the survival of the wild-type worms on the pathogenic bacterium Pseudomonas aeruginosa despite dimi
103 ween cellular and secreted components by the pathogenic bacterium Pseudomonas aeruginosa during growt
104 average cost of rifampicin resistance in the pathogenic bacterium Pseudomonas aeruginosa is reduced b
105     During iron starvation the Gram-negative pathogenic bacterium Pseudomonas aeruginosa makes the no
106                                       In the pathogenic bacterium Pseudomonas aeruginosa PA14, antibi
107                                          The pathogenic bacterium Pseudomonas aeruginosa produces pig
108                                          The pathogenic bacterium Pseudomonas aeruginosa uses acyl-ho
109                            The opportunistic pathogenic bacterium Pseudomonas aeruginosa uses quorum-
110                                          The pathogenic bacterium Pseudomonas aeruginosa utilizes the
111 d, triggering virulence in the opportunistic pathogenic bacterium Pseudomonas aeruginosa via an unkno
112                       A common Gram-negative pathogenic bacterium Pseudomonas aeruginosa wild-type PA
113 a molecule involved in quorum sensing in the pathogenic bacterium Pseudomonas aeruginosa, is describe
114 per-containing redox protein released by the pathogenic bacterium Pseudomonas aeruginosa, is highly c
115 e catabolic alanine racemase, DadX, from the pathogenic bacterium Pseudomonas aeruginosa, reported he
116 siderophores, iron-scavenging agents, in the pathogenic bacterium Pseudomonas aeruginosa.
117 d-type to pyocyanin-dependent killing by the pathogenic bacterium Pseudomonas aeruginosa.
118  tractable alternative for investigating the pathogenic bacterium Pseudomonas aeruginosa.
119 een the motile and biofilm lifestyles in the pathogenic bacterium Pseudomonas aeruginosa.
120 onstrated using disinfection assays with the pathogenic bacterium Pseudomonas aeruginosa.
121 DUSP) that controls biofilm formation in the pathogenic bacterium Pseudomonas aeruginosa.
122 ALDI-TOF MS except for the opportunistically pathogenic bacterium Pseudomonas aeruginosa.
123                                    The plant pathogenic bacterium Pseudomonas syringae is divided int
124  was able to protect Arabidopsis against the pathogenic bacterium Pseudomonas syringae pv tomato DC30
125                                    The plant pathogenic bacterium Pseudomonas syringae pv. tomato DC3
126                                    The plant-pathogenic bacterium Pseudomonas syringae, in which QS c
127 ne (COR), a phytotoxin produced by the plant-pathogenic bacterium Pseudomonas syringae.
128  experiments to address this question in the pathogenic bacterium, Pseudomonas aeruginosa Although pu
129 atory gene for the QS system of another rice pathogenic bacterium, Pseudomonas fuscovaginae.
130 he growth of Salmonella as well as the plant pathogenic bacterium, Pseudomonas syringae pv. tomato.
131 al communities predict invasion by the plant-pathogenic bacterium Ralstonia solanacearum.
132  Agrobacterium tumefaciens is a unique plant pathogenic bacterium renowned for its ability to transfo
133  The co-option of mammalian LD function by a pathogenic bacterium represents a novel mechanism of euk
134                    Activation of PARP-1 by a pathogenic bacterium represents a previously unrecognize
135 ter haemolyticus is an antibiotic resistant, pathogenic bacterium responsible for an increasing numbe
136 tanding the regulation of adhesins defines a pathogenic bacterium's interaction with the local enviro
137                            The intracellular pathogenic bacterium Salmonella enterica serovar typhimu
138                                          The pathogenic bacterium Shigella flexneri uses a type III s
139                    The addition of AUDA to a pathogenic bacterium significantly increased bacterial p
140                                          The pathogenic bacterium Staphylococcus aureus actively evad
141  different metal specificity produced by the pathogenic bacterium Staphylococcus aureus identifies tw
142 structural component in many biofilms of the pathogenic bacterium Staphylococcus aureus, but its role
143 ing of protein A as well as virulence in the pathogenic bacterium Staphylococcus aureus.
144                  In the oral microbiome, the pathogenic bacterium Streptococcus mutans uses quorum-se
145 e complex and heterogeneous cell wall of the pathogenic bacterium Streptococcus pneumoniae is compose
146  melittin efficiently inhibits growth of the pathogenic bacterium Streptococcus pyogenes as effective
147           Virtually all strains of the human pathogenic bacterium Streptococcus pyogenes express a hi
148                                          The pathogenic bacterium Streptococcus pyogenes has evolved
149 rotein expressed on the surface of the human pathogenic bacterium Streptococcus pyogenes, a common ag
150                                 In the human-pathogenic bacterium Streptococcus pyogenes, the tagatos
151 e expressed and characterized IMPDH from the pathogenic bacterium Streptococcus pyogenes.
152 rotein expressed on the surface of the human pathogenic bacterium, Streptococcus pyogenes, a common a
153           Escherichia coli is a commensal or pathogenic bacterium that can survive in diverse environ
154   Yersinia pseudotuberculosis is a foodborne pathogenic bacterium that causes acute gastrointestinal
155          Burkholderia pseudomallei, a highly pathogenic bacterium that causes melioidosis, is commonl
156 as campestris pv campestris (Xcc) is a plant pathogenic bacterium that controls the production of pat
157 mic infection with Salmonella Typhimurium, a pathogenic bacterium that multiplies within macrophages,
158 nsis, the causative agent of tularemia, is a pathogenic bacterium that replicates in the cytosol of m
159              Photorhabdus is a potent insect pathogenic bacterium that uses entomopathogenic nematode
160 ve Porphyromonas gingivalis, a Gram-negative pathogenic bacterium that uses TLR2 for innate immune si
161 rsatile devices that have evolved allowing a pathogenic bacterium to adjust to or counteract environm
162  Xylella fastidiosa is a xylem-limited plant-pathogenic bacterium transmitted by leafhopper vectors t
163  and insoluble ECM of a clinically important pathogenic bacterium--uropathogenic E. coli.
164                   Our findings reveal that a pathogenic bacterium utilizes an effector to manipulate
165                                          The pathogenic bacterium Vibrio cholerae is also shown to ha
166                                       In the pathogenic bacterium Vibrio cholerae, the alternate sigm
167 ic anhydrase (CA, EC 4.2.1.1) from the human pathogenic bacterium Vibrio cholerae, VchCA.
168 discovered as a virulence determinant in the pathogenic bacterium Vibrio cholerae.
169 he hemocytes and are increased at 24 h after pathogenic bacterium Vibrio harveyi challenge.
170   Pseudomonas aeruginosa is an opportunistic pathogenic bacterium whose type III secretion system (T3
171                  Francisella tularensis is a pathogenic bacterium whose virulence is linked to its ab
172   In this study, the effects of infection by pathogenic bacterium Xanthomonas oryzae pv. oryzae (Xoo)
173                                The symbiotic pathogenic bacterium Xenorhabdus nematophila produces tw
174  swarm-cell differentiation in the symbiotic-pathogenic bacterium Xenorhabdus nematophila was examine
175 dellinae) are important vectors of the plant pathogenic bacterium Xylella fastidiosa Wells et al. (Xa
176 e (LPS) MAMP isolated from the xylem-limited pathogenic bacterium, Xylella fastidiosa, acts as a prim
177 ort of several extracellular proteins in the pathogenic bacterium Yersinia enterocolitica.
178 nd an essential virulence determinant of the pathogenic bacterium Yersinia.

 
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