戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 0C of Streptomyces coelicolor and SmAA10A of Serratia marcescens.
2  system on intrinsic multidrug resistance in Serratia marcescens.
3 ative bacteria, including the human pathogen Serratia marcescens.
4 monas aeruginosa, Staphylococcus aureus, and Serratia marcescens.
5 between closely related clinical isolates of Serratia marcescens.
6       One example is serratin, isolated from Serratia marcescens.
7  study of the processive chitinase ChiA from Serratia marcescens.
8 ypocrea jecorina and the chitinase ChiA from Serratia marcescens.
9 ost resistance test using the live bacterium Serratia marcescens.
10  controls, including Clostridium species and Serratia marcescens.
11  T6SS from the opportunistic human pathogen, Serratia marcescens.
12 y 18 nonprocessive endochitinase, ChiC, from Serratia marcescens.
13  display a TagJ homologue as shown here with Serratia marcescens.
14 nce to infection with the bacterial pathogen Serratia marcescens.
15 infection by a Gram-negative entomopathogen, Serratia marcescens.
16 acter freundii group, Enterobacter spp., and Serratia marcescens.
17 em receptors from Pseudomonas aeruginosa and Serratia marcescens.
18 bacter species (3%), Proteus mirabilis (2%), Serratia marcescens (0.6%), and Pseudomonas aeruginosa (
19 abilis (9), Pseudomonas aeruginosa (10), and Serratia marcescens (1), were included; and 123 (98.4%)
20 plex (42%), Klebsiella pneumoniae (18%), and Serratia marcescens (12%).
21 umoniae, 21 Enterobacter cloacae complex, 18 Serratia marcescens, 12 Proteus mirabilis, 10 Citrobacte
22  the clearance of a bacterial infection with Serratia marcescens, 3 Acps significantly reduced the ba
23 r cloacae (9.1%), Acinetobacter spp. (6.2%), Serratia marcescens (5.5%), Enterobacter aerogenes (4.4%
24                       Secretomes from 95% of Serratia marcescens, 71% of Pseudomonas aeruginosa, 29%
25                                              Serratia marcescens, a member of the carbapenem-resistan
26                                              Serratia marcescens, a member of the Enterobacteriaceae
27 structure of anthranilate synthase (AS) from Serratia marcescens, a mesophilic bacterium, has been so
28 luding yeast histone acetyltransferase 1 and Serratia marcescens aminoglycoside 3-N-acetyltransferase
29 cal GCN5-related N-acetyltransferase (GNAT), Serratia marcescens aminoglycoside 3-N-acetyltransferase
30 east histone acetyltransferase 1) and SmAAT (Serratia marcescens aminoglycoside 3-N-acetyltransferase
31 sin, a microbial pigment, was produced using Serratia marcescens and encapsulated with beta-cyclodext
32 neumoniae, Acinetobacter baumannii, E. coli, Serratia marcescens and Enterobacter cloacae complex.
33  sequences of the cheA loci from isolates of Serratia marcescens and Enterobacter cloacae, demonstrat
34 the aspartate transcarbamoylases (ATCase) of Serratia marcescens and Escherichia coli differ in both
35 the aspartate transcarbamoylases (ATCase) of Serratia marcescens and Escherichia coli have distinct a
36 entical to the natural product isolated from Serratia marcescens and from overexpression of the biosy
37  sfu and hit operons previously reported for Serratia marcescens and Haemophilus influenzae, respecti
38 ence time of TLM on the ecFabB homologues in Serratia marcescens and Klebsiella pneumonia is an impor
39 obacter hormaechei, Acinetobacter baumannii, Serratia marcescens and Leclercia adecarboxylata are dom
40                        The rare gut bacteria Serratia marcescens and Pseudomonas protegens contribute
41 rval stages and in the ants of two bacteria, Serratia marcescens and S. entomophila, which are involv
42 Ds accumulate in midgut cells in response to Serratia marcescens and Sindbis virus or when the native
43 ditis elegans against the bacterial parasite Serratia marcescens and tested for a correlation between
44 nces were noted among Acinetobacter spp. and Serratia marcescens and, to a lesser extent, with Strept
45 e, Proteus spp., Pseudomonas aeruginosa, and Serratia marcescens) and 6 antimicrobial resistance dete
46  colonization by a focal non-core bacterium (Serratia marcescens) and its consequences for bee health
47 roPhenoloxidase activity, resistance against Serratia marcescens), and for the life history traits, a
48 ntoea agglomerance., Microbacterium sp., and Serratia marcescens), and their nine mixture treatments
49  no known homologues, a homologue of OmpF of Serratia marcescens, and a locus (designated rscBAC) wit
50 terobacter roggenkampii, Klebsiella oxytoca, Serratia marcescens, and Citrobacter farmeri.
51 revealed eradication of Pseudomonas species, Serratia marcescens, and Enterobacter aerogenes in most
52 odegradation including Citrobacter freundii, Serratia marcescens, and Klebsiella aerogenes.
53 trobacter freundii, Yersinia enterocolitica, Serratia marcescens, and Morganella morganii) and two no
54 (Neisseria gonorrhoeae and N. meningitidis), Serratia marcescens, and other gram-negative bacteria ut
55 ve gram-negative bacteria (Escherichia coli, Serratia marcescens, and Pseudomonas aeruginosa).
56 rium tumefaciens, Agrobacterium radiobacter, Serratia marcescens, and Pseudomonas aureofaciens) and f
57 st similar to biotin synthases from E. coli, Serratia marcescens, and Saccharomyces cerevisiae (about
58 inst Burkholderia cepacia, Escherichia coli, Serratia marcescens, and Stenotrophomonas maltophilia is
59  in antibiotic-treated mosquitoes identified Serratia marcescens as a commensal bacterium critical fo
60                                        Using Serratia marcescens as a model organism, we identify her
61  we identify a common fecal enterobacterium, Serratia marcescens, as the causal agent of white pox.
62 l intensive care unit of a hospital acquired Serratia marcescens bacteremia.
63 ybrid microswimmer system driven by multiple Serratia marcescens bacteria, we quantify the chemotacti
64                      Experiments showed that Serratia marcescens better colonizes the gut when bees a
65                               In March 2011, Serratia marcescens bloodstream infections (BSIs) were i
66 idguts after they fed on the insect pathogen Serratia marcescens but not after feeding on the Leishma
67  resistant species like B. thailandensis and Serratia marcescens, but also a majority of Gram-negativ
68 ngs were observed with another CGD pathogen, Serratia marcescens, but not with Escherichia coli.
69                                              Serratia marcescens can cause a range of severe infectio
70 functional antibiotic resistance enzyme from Serratia marcescens catalyzes adenylation and acetylatio
71 egative bacterium and opportunistic pathogen Serratia marcescens causes ocular infections in healthy
72 of an alpha + beta domain similar to that of Serratia marcescens chitinases A and B.
73                                              Serratia marcescens culture filtrates have been reported
74 , sensitive detection of Escherichia coli or Serratia marcescens cultures from 1 to 10(3) CFU mL(-1).
75              The hemophore protein HasA from Serratia marcescens cycles between two states as follows
76 re-forming effectors, exemplified by Ssp4 of Serratia marcescens Db10.
77                                              Serratia marcescens, E. cloacae, and Enterobacter kobei
78  the enteric bacteria Klebsiella pneumoniae, Serratia marcescens, Erwinia carotovora, and Proteus vul
79 of the enterobacteria Klebsiella pneumoniae, Serratia marcescens, Erwinia carotovora, and Proteus vul
80 nt algorithms, especially in differentiating Serratia marcescens, Escherichia coli, and Yersinia ente
81                                          The Serratia marcescens extracellular nuclease gene, nucA, i
82       A family of mutants overexpressing the Serratia marcescens extracellular nuclease has been know
83                                          The Serratia marcescens extracellular nuclease is a secreted
84 phore secreted by the Gram-negative bacteria Serratia marcescens, extracts heme from host hemoprotein
85 Klebsiella pneumoniae, Escherichia coli, and Serratia marcescens, for which the trend is >= 30% and t
86                              Hemophores from Serratia marcescens (HasA(sm)) and Pseudomonas aeruginos
87 ns of well-known chitinases and an LPMO from Serratia marcescens Importantly, comparison of the chiti
88        After initial developmental work with Serratia marcescens in water, Salmonella Typhimurium ATC
89 Klebsiella pneumoniae, Escherichia coli, and Serratia marcescens, in a further nine of 11 (81%) cases
90 alf-site pairs of the trpEDCBA operator from Serratia marcescens indicated an obligate hierarchy of s
91 eudo-outbreaks of Pseudomonas aeruginosa and Serratia marcescens infections associated with bronchosc
92 a California hospital acquired postoperative Serratia marcescens infections, and 1 died.
93 ucts generated by the opportunistic pathogen Serratia marcescens involved in activation of autophagy.
94                                              Serratia marcescens is a bacterium frequently found in t
95                                              Serratia marcescens is a chitinolytic bacterium that can
96                      Chitinase B (ChiB) from Serratia marcescens is a family 18 exo-chitinase whose c
97                                              Serratia marcescens is a Gram-negative bacterium of the
98                                              Serratia marcescens is a gram-negative environmental bac
99                                              Serratia marcescens is a red pigment (prodigiosin)-produ
100                                              Serratia marcescens is a soil- and water-derived bacteri
101                                              Serratia marcescens is a well-known cause of nosocomial
102                                              Serratia marcescens is an extremely rare cause of necrot
103                                              Serratia marcescens is an opportunistic AmpC beta-lactam
104                                              Serratia marcescens is an opportunistic bacterium that i
105                                              Serratia marcescens is an opportunistic human pathogen i
106                                              Serratia marcescens is an opportunistic human pathogen t
107                        The enteric bacterium Serratia marcescens is an opportunistic human pathogen.
108                                              Serratia marcescens is an opportunistic pathogen associa
109                                              Serratia marcescens is frequently isolated from lenses o
110                The extracellular nuclease of Serratia marcescens is one of a wide variety of enzymes
111 ered by a T6SS of the opportunistic pathogen Serratia marcescens, is a toxin that forms ion-selective
112                                            A Serratia marcescens isolate was particularly efficient i
113 olates, 6 Pseudomonas aeruginosa isolates, 1 Serratia marcescens isolate, 1 Aeromonas hydrophila isol
114                      Three bla(SME)-carrying Serratia marcescens isolates and one bla(NDM-1) carrying
115 to 0.5 nM alpha-thrombin by only 10% whereas Serratia marcescens metalloprotease reduced the Ca2+ res
116 film formation in the opportunistic pathogen Serratia marcescens, mutations in an oxyR homolog and pr
117  was the main cause of neonatal sepsis, with Serratia marcescens (n = 151), Klebsiella michiganensis
118 loacae (n = 23), Klebsiella oxytoca (n = 8), Serratia marcescens (n = 6), Citrobacter freundii (n = 4
119 domonas aeruginosa (n = 2 and n = 5), two of Serratia marcescens (n = 9 and n = 7), five of Staphyloc
120 ion of extracellular nuclease (Nuc) from the Serratia marcescens nucA chromosomal locus is inhibited
121                                          The Serratia marcescens NucC protein is structurally and fun
122                   Extracellular secretion of Serratia marcescens nuclease occurs as a two-step proces
123 , a natural secondary metabolite produced by Serratia marcescens, on HSV infection.
124 immune priming during infections with either Serratia marcescens or with Escherichia coli.
125  that contained group B Streptococcus (GBS), Serratia marcescens, or Escherichia coli before their se
126 is (20%, 3 of 15), and Enterobacter cloacae, Serratia marcescens, Pneumocystis carinii pneumonia, and
127 monas aeruginosa PAO1, Proteus mirabilis and Serratia marcescens, possibly by interfering with their
128 e that is located upstream of NucC-dependent Serratia marcescens promoters and the late promoters of
129 gens (Escherichia coli, Salmonella muenchen, Serratia marcescens, Proteus mirabilis, and Proteus vulg
130 sented here in complex with chitinase B from Serratia marcescens provide further insight into the mec
131 gations, we discover that the E2 enzyme from Serratia marcescens regulates cGAS by imitating the ubiq
132  that coevolution with a bacterial pathogen (Serratia marcescens) resulted in significantly more outc
133                            R-flagellins from Serratia marcescens (S. marcescens) and Salmonella muenc
134  increased host survival in a mouse model of Serratia marcescens sepsis.
135 li, Salmonella enterica serovar Typhimurium, Serratia marcescens, Shigella flexneri, Enterobacter aer
136  and hhdB, which, based on their homology to Serratia marcescens shlA and shlB genes, are believed to
137 ins using a targeted protease, Enhancin from Serratia marcescens (SmE), with ultraviolet photodissoci
138 ebsiella pneumoniae, Pseudomonas aeruginosa, Serratia marcescens, Staphylococcus aureus, and Stenotro
139 ith exogenous bacteria (Enterobacter sp. and Serratia marcescens strain Db11) and parasitic African t
140  the RNA-binding protein, RsmA, in Ecc71 and Serratia marcescens strain SM274.
141               The VME was found for a single Serratia marcescens strain.
142 ed to the chromosome of carbapenem-resistant Serratia marcescens strains.
143  caused by ingesting the pathogenic bacteria Serratia marcescens, suggesting that subdued has novel f
144 d the same set of D. melanogaster lines with Serratia marcescens, the bacterium used in the previous
145 nsect pathogens (the gram-negative bacterium Serratia marcescens, the gram-positive bacterium Bacillu
146 rate that Rhs1 effectors from two strains of Serratia marcescens, the model strain Db10 and clinical
147 ing medium on prodigiosin (PG) production by Serratia marcescens TKU011 is examined.
148                 We adsorbed swarmer cells of Serratia marcescens to polydimethylsiloxane or polystyre
149 lated data and experimental Tn-Seq data from Serratia marcescens transposon mutant library used to id
150 instance, the chitinase secretion pathway of Serratia marcescens uses an endopeptidase to facilitate
151 coli, Pseudomonas spp., Salmonella enterica, Serratia marcescens, Vibrio vulnificus and Enterobacter
152 ce of infection with Burkholderia cepacia or Serratia marcescens was caused by a new strain in 9 of 1
153 ely 10,000 nM), and Enterobacter cloacae and Serratia marcescens were highly resistant (IC(50), >10,0
154  to consume the virulent bacterial parasite, Serratia marcescens, when given a choice between the par
155 t the lipases produced by P. fluorescens and Serratia marcescens, which comprise a second sequence fa
156 e describe the structure of chitinase B from Serratia marcescens, which consists of a catalytic domai
157 FLP analysis except for Escherichia coli and Serratia marcescens, which could not be interdifferentia
158 ana, we isolated the Gram-negative bacterium Serratia marcescens, which is a potent entomopathogen th

 
Page Top