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1 floxacin-resistant Escherichia coli (CipREc) colonization.
2 ion and subsequent BRP production to promote colonization.
3 Enterococcus faecium gastrointestinal tract colonization.
4 te care hospitals (ACHs) as risk factors for colonization.
5 ely 3 months after experimental pneumococcal colonization.
6 of the most abundant habitats for microbiota colonization.
7 were attenuated in persisting during vaginal colonization.
8 ing and community diversity on plant species colonization.
9 xylate antiporter DcuABC in early murine gut colonization.
10 ed moderate gastric inflammation and many HP colonization.
11 y in patients who later acquire C. difficile colonization.
12 group developed an S aureus infection before colonization.
13 th key functions within the plant to promote colonization.
14 illance cultures assessed prevalence of MRSA colonization.
15 sequent bottlenecks consistent with European colonization.
16 or a causal role of IL10 in supporting liver colonization.
17 fects of host genetic programs and microbial colonization.
18 vents trigger susceptibility to C. difficile colonization.
19 dissemination, and the degree of metastatic colonization.
20 he plasmid significantly improved chlamydial colonization.
21 een distinct CSC subtypes and organ-specific colonization.
22 hain in Rag-deficient mice did rescue mutant colonization.
23 r signaling to limit or facilitate microbial colonization.
24 suggest a genomic signature for neonatal gut colonization.
25 consume sialic acids was impaired in vaginal colonization.
26 e NCR1-deficient mice still inhibited mutant colonization.
27 decrease in multidrug-resistant pneumococcal colonization.
28 ty protect mice from long-term C. auris skin colonization.
29 system modification associated with European colonization.
30 g gene (Rag) failed to show rescue of mutant colonization.
31 omic signatures in organ-specific metastatic colonization.
32 nted IFN-gamma production and rescued mutant colonization.
33 %) of 31 detainees with care at clinic A had colonization.
34 and candidate pathways associated with host colonization.
35 ce could potentially target gastrointestinal colonization.
36 by tumor cell clusters supporting metastatic colonization.
37 0 days and continue to resist Staphylococcus colonization.
38 acid levels in the gut and promotes pathogen colonization.
39 e, but their presence was restored by gut re-colonization.
40 ore intranasal challenge in a mouse model of colonization.
43 catheter-related bloodstream infections and colonization according to the insertion type (femoral vs
45 ce of vancomycin-resistant Enterococci (VRE) colonization after receiving OVP, adverse effects, and c
46 I glycan extensions affect (i) mouse vaginal colonization and (ii) efficacy in vitro and in vivo of a
48 t to characterize S aureus and S epidermidis colonization and biofilm propensity and determine their
49 ts for insight into how VREfm adapted during colonization and bloodstream infection within each patie
50 man gut microbiome, we detected C. difficile colonization and blooms in people recovering from food p
51 ns of VacA as an important determinant of Hp colonization and chronic infection remain poorly underst
52 tudy, we describe the early events of tissue colonization and compartmentalization as well as the rol
53 Bacteroidetes protect against K. pneumoniae colonization and contagion, providing insight into how t
54 ensal from the same family) can prevent NTHi colonization and disease in vivo using a murine NTHi oti
55 pe distribution associated with pneumococcal colonization and disease is essential for evaluating and
56 ivate expression of traits required for host colonization and disease; however, the importance of Eut
58 ve diapause was a key trait that facilitated colonization and eventual radiation into savannahs in th
59 Metapopulation dynamics - patch occupancy, colonization and extinction - are the result of complex
60 ynamics of ecosystem assembly, where species colonization and extinction depends on the constraints i
61 e features of the metapopulation dynamics of colonization and extinction, and their expected trends w
63 ur study indicates that beech capacities for colonization and gene flow were sufficient to preserve g
64 stainable probiotics on Campylobacter jejuni colonization and gut microbiome composition was evaluate
67 ly related human commensal, can inhibit NTHi colonization and infection of human respiratory epitheli
68 stem cell transplantation are vulnerable to colonization and infection with multidrug-resistant orga
69 ucture and morphology, nutrient acquisition, colonization and invasion, and protection against extern
70 effects of this introduction on pneumococcal colonization and invasive disease in children aged <5 ye
75 iated signaling to promote cellular adhesion/colonization and organoid formation by controlling the p
79 nificantly delay tumor growth and metastatic colonization and reverse neuroendocrine features in Trop
81 bed ways that VREfm evolve during intestinal colonization and subsequent bloodstream infection in imm
83 results reveal the complex nature of vaginal colonization and suggest that multiple factors contribut
84 responses and reprogram plant metabolism for colonization and survival in planta Kiwellin (KWL) prote
86 data suggests bosR may have a role in heart colonization and the induction of dbpBA indicates a RpoS
87 del for C. auris to dissect risk factors for colonization and to test interventions that might protec
89 dapted an infant mouse model of pneumococcal colonization and transmission to investigate factors tha
93 s, chronic necrotizing aspergillosis, fungal colonization, and allergic bronchopulmonary aspergillosi
96 apocarotenoids during arbuscular mycorrhizal colonization, and the associated maintenance of caroteno
98 ium-salivary flow and adhesion, shedding and colonization-and by interactions among and between micro
99 environments - abscess formation; epithelial colonization; and cigarette smoke toxin exposure; as wel
101 ed for enabling bacterial outgrowth and host colonization, as in the case of Clostridioides difficile
102 ansposon sequencing analysis and competitive colonization assays to describe how aspartate/malate can
103 ts that were underrepresented during vaginal colonization at 1, 5, and 8 days postinoculation compare
104 I, 33-83%) protection against PCV13-serotype colonization at ages 13-24 months and 25-59 months, resp
107 a common pathway in the early stages of fly colonization but apparently use different mechanisms to
108 he primary end point was concordant S aureus colonization by 90 days, defined as neonatal acquisition
110 rily, the susceptibility of Halomicrobium to colonization by Ca Nanohalobium can be interpreted as a
114 f resident C4 grasses were more resistant to colonization by legume, nonlegume forb and C3 grass colo
115 d diabetes, known to have abnormal sleep and colonization by Odoribacter, treatment with antibiotics
117 otherwise indigestible plant matter, resist colonization by pathogens, and train the developing immu
118 The initiation of intracellular host cell colonization by symbiotic rhizobia in Medicago truncatul
121 ne protease has been implicated in bacterial colonization by virtue of its mucinolytic activity.
123 ition, metabolic crossfeeding and stochastic colonization - can qualitatively reproduce patterns foun
125 The multiple fires that followed European colonization caused near total mortality of A. selaginoi
127 terial strains observed across the different colonization conditions indicated that later-phase strai
131 M. muris pretreatment decreased the median colonization density of NTHi from 6 x 10(5) CFU/ml to 9
134 mechanism for B. thetaiotaomicron to sustain colonization during inflammation and suggests a mechanis
136 onditions and mechanisms supporting pathogen colonization during vaginal dysbiosis remain obscure.
137 climate change-related population extinction-colonization dynamics within species that explains obser
142 face topography is known to affect bacterial colonization, how multiple individual settlers develop i
143 eath in CRSwNP was associated with bacterial colonization, however, neutrophils were less prone to un
148 , hydrogen peroxide sensitivity, and chicken colonization in C. jejuni Inactivation of the CjNC110 nc
149 LC(+mcra) was found to reduce C. jejuni colonization in cecum, ileum and jejunum, by more than o
151 veal the impact of the plasmid on chlamydial colonization in distinct regions of gastrointestinal tra
152 ger initial Salmonella Typhimurium gut-lumen colonization in mice, providing insight into the signifi
153 estinal stem cell lineages and gut microbial colonization in single animals, revealing spatiotemporal
155 and intestinal effectors and (ii) chlamydial colonization in small intestine was highly dependent on
158 al induction of hydrosalpinx with chlamydial colonization in the gastrointestinal tract than in the g
159 lpinx in the genital tract also reduce their colonization in the gastrointestinal tract, leading to a
160 PUS by investigating the effect of microbial colonization in the mouse digestive system, through anal
161 in regulating tumor formation and metastatic colonization in various solid tumors, including those of
162 cal cells in vitro but did not contribute to colonization in vivo Thus, we screened a low-complexity
164 having higher rates of local extinction and colonization, in more forested landscapes during extreme
165 herpesviruses during the early phase of host colonization indicates that highly specialized strategie
166 espiratory tract is the primary site for GAS colonization, infection, and transmission, but the host-
167 tic (M) support of nematode reproduction and colonization initiation in the infective juvenile (IJ) s
168 root ganglia nociceptors protect against STm colonization, invasion, and dissemination from the gut.
169 This improved understanding of S. aureus colonization is an important first step toward the devel
172 Our results indicate that the likelihood of colonization is highest in the days immediately followin
174 mals colonized, indicating that QS-dependent colonization is responsive to the intrinsic conditions w
175 ncomycin-resistant enterococcal infection or colonization is significantly associated with oral vanco
178 ysis suggests that the observed reduction in colonization may be caused, in part, by altered transcri
180 tasis (MMTV-PyMT), a syngeneic melanoma lung colonization model (B16F10), and orthotopic injection of
181 We modified an established mouse vaginal colonization model to explore E. faecalis vaginal carria
183 d reduced fitness in a gastrointestinal (GI) colonization model, yet induced greater damage to epithe
188 , relative to low- or no-Lrp expressors, for colonization of additional nematode stages: juvenile, ad
189 dle Miocene, accelerated diversification and colonization of adjacent regions were likely driven join
190 e host and microbiota to initiate intestinal colonization of avian and animal hosts for commensalism
191 mportant for infection of humans and optimal colonization of avian hosts, senses butyrate likely by i
192 secondary metabolites is triggered by local colonization of bacteria affiliated with the genus Bacil
193 ce sensing in bacteria is a precursor to the colonization of biotic and abiotic surfaces, and an impo
194 les, (c) demonstration of relatively heavier colonization of C. auris in nares than in the axilla/gro
195 C(+mcra) as sustainable approach to decrease colonization of C. jejuni and S. enterica in poultry gut
196 s, the evolution of terrestrial system, e.g. colonization of continents by vascular land plants in la
200 ochemical stressors and whether the repeated colonization of extreme environments is facilitated by p
201 the neuronal transcription factor cFos, and colonization of germ-free mice with bacteria that produc
204 organisms between hosts on resilience to the colonization of invaders after antibiotic-induced dysbio
207 endophytic or a pathogenic lifestyle during colonization of maize (Zea mays) and soybean (Glycine ma
208 relevant materials research, since microbial colonization of medical implants and devices is a ubiqui
212 can serve many functions, from facilitating colonization of naive habitats to maintaining bacterial
213 of the chicken gut and competitively reduce colonization of natural and challenged C. jejuni and nat
214 uggest diversification was largely driven by colonization of novel geographic areas and subsequent ev
221 riven population genetic models suggests the colonization of the Atlantic has occurred in two distinc
222 vascular interactions facilitate microglial colonization of the brain to later regulate neural circu
223 penetration of the mucus layer and increased colonization of the colonic epithelium by Wild-type EAEC
225 tle is known about the mechanisms of ectopic colonization of the gut by oral bacteria, we also discus
226 these data indicate that neonatal microbial colonization of the gut elicits concomitant effects on t
227 we show that interleukin (IL)-22, induced by colonization of the gut microbiota, is crucial for the p
230 equired for optimal virulence regulation and colonization of the host intestinal tract during infecti
232 CCR6, showed full rescue of the long-lasting colonization of the mutant, indicating a role for group
237 life, thymopoiesis depends on the continuous colonization of the thymus by bone-marrow-derived hemato
238 actors are known to contribute to persistent colonization of this niche, and many are important in mu
240 serotype, we investigated the effect of Spn colonization on lung cells.Methods: We collected BAL fro
243 f the 3D EEC model revealed species-specific colonization patterns and alterations of ultracellular s
244 isinfection is key to infection control, the colonization patterns and resistomes of hospital-environ
245 tivity to redox-active compounds and reduced colonization persistence in a murine model of relapse C.
246 robial infection with Pseudomonas aeruginosa Colonization, persistence, and virulence of S. maltophil
249 uisition, we assessed the kinetics of GBS GI colonization, progression to invasive disease, and the r
250 nterobacteriaceae family, was sufficient for colonization resistance after treatment with antibiotics
251 ole of the commensal microbiota in mediating colonization resistance against C. difficile have associ
254 ry to secondary bile acids, and facilitating colonization resistance against intestinal pathogens.
258 bi-colonized gnotobiotic mice abolished the colonization-resistance capacity of K. michiganensis aga
259 hniques do not mitigate against detection of colonization, resulting in false positive catheter-assoc
262 e outgrowth in mature IJs, the advantage for colonization shifted to low-Lrp expressors: fixed low-Lr
266 relevant phenotypes such as virulence, host colonization, sporulation, biofilm formation, among othe
268 n due to competitive interactions limits the colonization success of spores that relocate to new site
269 functions, including facilitating bacterial colonization, suppression of callose deposition, and tar
272 in knock-down cells have impaired metastatic colonization to distant sites including liver, lung, kid
273 in vitro functional assays, and gnotobiotic colonizations to define the microbial composition and fu
274 requirements demonstrated that geographical colonization tracked spatial expansion of permissive env
275 re, transposon sequencing analysis along the colonization trajectory of S. Typhimurium implicates the
276 microorganisms that protect against pathogen colonization; treatment with antibiotics disrupts the mi
278 pproaches can help dissect the physiology of colonization versus infection, suggesting that the molec
283 the impact of diarrhoea on susceptibility to colonization, we developed a mouse model of variable dis
284 To define the impact of IFNs on S. aureus colonization, we examined the effects of type I and type
286 ation, and fecal shedding as a marker for GI colonization, we showed that K. pneumoniae can asymptoma
287 this pathogen leads to decreased intestinal colonization, which suggests that T3SS1 repression is re
288 olled human infection model to achieve nasal colonization with 6B serotype, we investigated the effec
289 germ-free (GF) neonatal mice is restored by colonization with a human commensal, Bacteroides fragili
291 8 of 16 (50%) patients developed intestinal colonization with Blastocystis, with identical ST sequen
292 orresponding prospectively collected data on colonization with C. difficile are largely unavailable.
293 d alpha-synuclein (alphaSyn), we reveal that colonization with curli-producing Escherichia coli promo
299 lusions: Our findings demonstrate that nasal colonization with pneumococcus and microaspiration prime