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1 serovar causing this disease is Typhimurium (Salmonella Typhimurium).
2  enterica serovar Typhimurium (also known as Salmonella typhimurium).
3 hia coli O157:H7, Pseudomonas aeruginosa and Salmonella typhimurium.
4 ptional regulation through sensing Mn(2+) in Salmonella typhimurium.
5 tion with herpes simplex virus-1 (HSV-1) and Salmonella typhimurium.
6  to increased susceptibility to infection by Salmonella typhimurium.
7 eome of the Gram-negative bacterial pathogen Salmonella Typhimurium.
8 wnregulated following infection of mice with Salmonella typhimurium.
9 istance to infection by the enteric pathogen Salmonella typhimurium.
10 s O-antigens from Salmonella Choleraesuis in Salmonella Typhimurium.
11 ate that 30 proteins are exported via Tat in Salmonella Typhimurium.
12 Salmonella genus: Salmonella enteritidis and Salmonella typhimurium.
13 n acquisition by the intracellular bacterium Salmonella typhimurium.
14 es their susceptibility to pathogens such as Salmonella typhimurium.
15 olog and ncRNA also associate with PNPase in Salmonella Typhimurium.
16 e housed in SPF conditions by infection with Salmonella typhimurium.
17 mensals and the invasive intestinal pathogen Salmonella Typhimurium.
18 ory ligand, rRL-6-CH2OH, previously found in Salmonella typhimurium.
19 d growth rate in the Gram-negative bacterium Salmonella typhimurium.
20 l specificity of Zur, ZntR, RcnR and FrmR in Salmonella Typhimurium.
21 ation of AI-2-based QS in Vibrio harveyi and Salmonella typhimurium.
22 nternalization of the Gram-negative pathogen Salmonella typhimurium.
23 hout orthologs in either Escherichia coli or Salmonella typhimurium.
24  macrophages with the intracellular pathogen Salmonella typhimurium.
25 se activity of AvrA, the YopJ homologue from Salmonella typhimurium.
26  SipC and accumulate at sites of invasion by Salmonella typhimurium.
27 e detection of type III protein secretion in Salmonella typhimurium.
28 NLRC4 both activate caspase-1 in response to Salmonella typhimurium.
29 for DNA condensation in Escherichia coli and Salmonella typhimurium.
30 nteric bacteria and had no known function in Salmonella Typhimurium.
31 n polymyxin-resistant strains of E. coli and Salmonella typhimurium.
32 n death after intraperitoneal inoculation of Salmonella typhimurium.
33 TD-(SH)(2)] and oxidized (NTD-S(2)) NTD from Salmonella typhimurium.
34 tivates transcription of the SlyA regulon in Salmonella typhimurium.
35 lla pneumophila, Pseudomonas aeruginosa, and Salmonella typhimurium.
36 been identified in both Escherichia coli and Salmonella typhimurium.
37  of the homologues from Escherichia coli and Salmonella typhimurium.
38              Here, we extend this concept to Salmonella typhimurium.
39 timicrobial peptides in Escherichia coli and Salmonella typhimurium.
40 xpression, including in the enteric pathogen Salmonella typhimurium.
41 pecially against the drug-resistant bacteria Salmonella typhimurium.
42 s biplex immunoassay of Escherichia coli and Salmonella typhimurium.
43 mmunomagnetic separation (IMS) for detecting Salmonella typhimurium.
44 osensor to know the concentration of serovar Salmonella typhimurium.
45 actamase-producing Klebsiella pneumoniae and Salmonella typhimurium.
46 acterial pathogens, Francisella novicida and Salmonella typhimurium.
47  Salmonella Enteritidis and 152 (43.3%) were Salmonella Typhimurium.
48  also shifted from Salmonella Enteritidis to Salmonella Typhimurium.
49  related AB5 toxin encoded by the broad-host Salmonella Typhimurium (15) .
50 tivity for other foodborne pathogens such as Salmonella Typhimurium, (7%) Listeria monocytogenes (3%)
51 er) were isolated at higher frequencies than Salmonella Typhimurium, a common cause of human illness.
52                         After infection with Salmonella typhimurium, a Gram-negative bacterium that e
53  NMR structure of the PrgI needle protein of Salmonella typhimurium, a human pathogen associated with
54 e have discovered additional SgrS targets in Salmonella Typhimurium, a pathogen related to E. coli th
55 e rapidly succumb to systemic infection with Salmonella Typhimurium, a pathogenic bacterium that mult
56                            Here we show that Salmonella Typhimurium activates the plant immune system
57 ncing in goblet cells increased or decreased Salmonella typhimurium adherence, respectively.
58                                              Salmonella typhimurium AhpC is a founding member of the
59    Here, we present such studies focusing on Salmonella typhimurium alkyl hydroperoxide reductase C c
60 tion system effector protein from broad-host Salmonella Typhimurium allowed Salmonella Typhi to survi
61 tive bacterial cancer therapy by engineering Salmonella typhimurium amino acid auxotrophs which grow
62 139 times (6.1%), of which 8017 (79.1%) were Salmonella Typhimurium and 1608 (15.8%) were Salmonella
63                 A majority (88/114 [77%]) of Salmonella Typhimurium and 30% (24/79) of Salmonella Ent
64 icrocystin LR and 10(0) and 10(1) cfu/mL for Salmonella typhimurium and Cronobacter sakazakii respect
65 as induced using 2 established mouse models (Salmonella typhimurium and dextran sodium sulfate) in PH
66 hesion, the type 1 fimbrial FimH adhesins of Salmonella Typhimurium and Escherichia coli share only 1
67 rs resistance to the antibiotic polymyxin in Salmonella typhimurium and Escherichia coli through the
68                                           In Salmonella typhimurium and Escherichia coli, the virulen
69  bacterial pathogens Listeria monocytogenes, Salmonella typhimurium and Escherichia coli.
70 ta and IL-18 in response to NLRC4 activators Salmonella Typhimurium and flagellin, canonical or non-c
71                                     Although Salmonella typhimurium and Legionella pneumophila normal
72 nd TLR5 ligands and the intestinal pathogens Salmonella typhimurium and Listeria monocytogenes to ind
73 in-resistant Staphylococcus aureus (MRSA) or Salmonella typhimurium and perish shortly after epicutan
74                                              Salmonella Typhimurium and Salmonella Enteritidis repres
75 ducted by testing Shigella, Salmonella spp., Salmonella typhimurium and Staphylococcus aureus on E. c
76 c4 phosphorylation by cytosolic flagellin of Salmonella Typhimurium and Yersinia enterocolitica.
77  genetically modified nonhalotolerant cells (Salmonella typhimurium) and dead vs. live differentiatio
78 ed in bottled water extracts using bacteria (Salmonella typhimurium) and human cell lines (HepG2 and
79  the flagellum acts as a 'wetness' sensor in Salmonella typhimurium, and as a mechanosensor in other
80 ative in vitro bioassays for mutagenicity in Salmonella typhimurium, and chronic cytotoxicity and acu
81  for the discrimination of Escherichia coli, Salmonella typhimurium, and Clostridium difficile genome
82  Roseburia intestinalis, Ruminococcus obeum, Salmonella typhimurium, and Clostridium difficile) to qu
83 pathogenic Escherichia coli (EHEC and UPEC), Salmonella typhimurium, and Francisella tularensis.
84 am-negative food-borne pathogens, especially Salmonella typhimurium, and it was, therefore, selected
85 eloped for the detection of E. coli O157:H7, Salmonella Typhimurium, and L. monocytogenes in food sam
86  tested pathogens (Escherichia coli O157:H7, Salmonella typhimurium, and Listeria monocytogenes) in b
87 Three bacterial pathogens (Escherichia coli, Salmonella typhimurium, and methicillin-resistant Staphy
88 ts, including latex beads, Escherichia coli, Salmonella typhimurium, and Mycobacterium tuberculosis i
89 ing Escherichia coli, Citrobacter rodentium, Salmonella typhimurium, and Shigella flexneri are sensed
90 eously detect viable Legionella pneumophila, Salmonella typhimurium, and Staphylococcus aureus in one
91 multiplex detection of model food pathogens, Salmonella typhimurium, and Staphylococcus aureus, in wh
92 d with anti-Escherichia coli O157:H7 or anti-Salmonella typhimurium antibodies that can specifically
93 s, and transcripts from Dickeya dadantii and Salmonella typhimurium are cleaved by RNase III when exp
94 Outer membrane vesicles (OMVs) isolated from Salmonella Typhimurium are potentially useful for develo
95 eneration in ethanolamine ammonia-lyase from Salmonella typhimurium at 234-248 K in a dimethylsulfoxi
96 tive also against the Gram negative bacteria Salmonella typhimurium ATCC 13311.
97 da KT2440, Enterococcus faecalis ATCC 29212, Salmonella Typhimurium ATCC 14028, and Escherichia coli
98 acterial species, Pseudomonas putida KT2440, Salmonella Typhimurium ATCC 14028, Staphylococcus epider
99  and two Gram negative (Escherichia coli and Salmonella typhimurium) bacterial strains.
100 -functional viral nanocontainer based on the Salmonella typhimurium bacteriophage P22 capsid, genetic
101 tremely susceptible to systemic infection by Salmonella Typhimurium because of loss-of-function mutat
102 and structural characterization of NirC from Salmonella typhimurium by lipid bilayer electrophysiolog
103 phils during infection with the gut pathogen Salmonella Typhimurium, calprotectin-mediated metal sequ
104  Nonvirulent, tumor-tropic bacteria, such as Salmonella typhimurium, can unmask a tumor by transformi
105          Cobyric acid synthetase (CbiP) from Salmonella typhimurium catalyzes the glutamine and ATP-d
106                                              Salmonella typhimurium causes a localized enteric infect
107                                              Salmonella Typhimurium causes a self-limiting gastroente
108 lmonella enterica serovar Typhimurium 12023 (Salmonella typhimurium) causes acute, fatal bacteremia w
109 and Salmonella enterica serovar Typhimurium (Salmonella typhimurium), cell lines expressing S100A8 in
110  The water samples were spiked with standard Salmonella typhimurium cells, and detection was done by
111                 The library was expressed in Salmonella typhimurium, clones with increased resistance
112                                              Salmonella Typhimurium combats phagocytic superoxide by
113 ible to the intracellular bacterial pathogen Salmonella typhimurium, consistent with reduced innate i
114  V. cholerae acfA-phoA reporter strain and a Salmonella typhimurium ctxAp-lacZ reporter strain.
115 luster was introduced into three constructed Salmonella Typhimurium Deltaasd mutants: SLT11 (Deltarfb
116 Ps against the multidrug-resistant bacterium Salmonella typhimurium DT 104.
117   The global epidemic of multidrug-resistant Salmonella Typhimurium DT104 provides an important examp
118 ometry, and inoculated Enterococcus spp. and Salmonella typhimurium during the drying of struvite und
119                                          The Salmonella typhimurium effector protein SifA regulates t
120                                              Salmonella typhimurium engineered to deliver cancer/test
121                     Expression of BpeGReg in Salmonella typhimurium enhances biofilm formation, while
122 cerevisiae OPRTase is similar to that of the Salmonella typhimurium enzyme, as judged by comparison o
123 t, base pairing-deficient SgrS homologs from Salmonella typhimurium, Erwinia carotovora and Klebsiell
124 domonas fluorescens, Salmonella Enteritidis, Salmonella Typhimurium, Escherichia coli).
125 st a mixture of related pathogens, including Salmonella typhimurium, Escherichia coli, Staphylococcus
126  Salmonella Enteritidis cases have risen and Salmonella Typhimurium fallen.
127                   We propose that unlike the Salmonella Typhimurium flagella-TLR5 driven pro-inflamma
128                               We find that a Salmonella typhimurium flagellin fragment comprising the
129   The chemoreceptors of Escherichia coli and Salmonella typhimurium form stable oligomers that associ
130 e; Salmonella Enteritidis from 1999 to 2002, Salmonella Typhimurium from 2002 to 2008, and Salmonella
131 re- and posttherapy MDR clinical isolates of Salmonella Typhimurium from a patient that failed antiba
132                                              Salmonella Typhimurium gene STM2215 (rtn) is conserved a
133 endent ethanolamine ammonia-lyase (EAL) from Salmonella typhimurium has been studied by using time-re
134 , by exploiting the host cellular machinery, Salmonella Typhimurium has evolved the capacity to broad
135 rmore, systemic administration of attenuated Salmonella typhimurium has little or no significant side
136 ate in ethanolamine ammonia-lyase (EAL) from Salmonella typhimurium have been measured by using time-
137 ermediate in ethanolamine ammonia-lyase from Salmonella typhimurium have been measured on timescales
138 endent ethanolamine ammonia-lyase (EAL) from Salmonella typhimurium have been studied by using pulsed
139 endent ethanolamine ammonia-lyase (EAL) from Salmonella typhimurium have been studied on the 10(-7)-1
140 tructures of a small heat shock protein from Salmonella typhimurium in a dimeric form and two higher
141 l matrix of immunoassay for the detection of Salmonella typhimurium in a sandwich ELISA format.
142 of the LysP-related transporter STM2200 from Salmonella typhimurium in Escherichia coli, its purifica
143 autophagy-mediated intracellular survival of Salmonella typhimurium in mammalian cells.
144 tal structure of the PhoQ sensor domain from Salmonella typhimurium in the Ca2+-bound state, which re
145 cterial autophagy induction and clearance of Salmonella typhimurium in the intestinal epithelial cell
146 l immunoassay device was developed to detect Salmonella typhimurium in the naturally occurring liquid
147   Here, we show that the intestinal pathogen Salmonella typhimurium increases its antibiotic toleranc
148 contrast, TLR4 and TRIF were dispensable for Salmonella typhimurium-induced caspase-1 activation.
149  an animal model of sepsis, we observed that Salmonella typhimurium-infected mice exhibited simultane
150                       Macrophages respond to Salmonella typhimurium infection by activating caspase 1
151                                              Salmonella typhimurium infection is reported to activate
152  that severity of disease induced by enteric Salmonella Typhimurium infection is strongly modulated b
153 r genome-wide association study (GWAS) using Salmonella typhimurium infection of human lymphoblastoid
154 de synthase 2 (NOS2) in macrophages and upon Salmonella typhimurium infection of mice was investigate
155                                   Similarly, Salmonella typhimurium infection of TLR-deficient mice i
156                           Here, we show that Salmonella Typhimurium infection was accompanied by dysb
157                                       During Salmonella Typhimurium infection, intestinal CX3CR1(+) c
158        Here, using a mouse model of systemic Salmonella Typhimurium infection, we determined that inf
159 emporally correlated with the restriction of Salmonella Typhimurium infection.
160 , anthrax lethal toxin, DNA transfection and Salmonella typhimurium infection.
161  on Salmonella enterica Serovar Typhimurium (Salmonella typhimurium) infection in 2 model organisms,
162 Here, we report that an intestinal pathogen, Salmonella Typhimurium, inhibits anorexia by manipulatin
163 e have inserted the D3 domain of FliCi (from Salmonella typhimurium) into the outer domain of EspA an
164  sub-ng/muL standard DNA and 10(1) copies of Salmonella typhimurium InvA gene sequences (cloned in E.
165                                              Salmonella typhimurium is a major cause of diarrhea and
166  of host cells, in which growth of cytosolic Salmonella Typhimurium is inhibited independently or pri
167            Although infection with wild-type Salmonella typhimurium is lethal to mice, we show here t
168 he tryptophan synthase bienzyme complex from Salmonella typhimurium is regulated by allosteric intera
169                                              Salmonella typhimurium is responsible for about a third
170                                              Salmonella Typhimurium isolate D23580 represents a recen
171 on structure of sub-Saharan African invasive Salmonella Typhimurium isolates and compared these to gl
172 y, the vast majority of sub-Saharan invasive Salmonella Typhimurium isolates fell within two closely
173 79.7% of Salmonella Enteritidis and 90.2% of Salmonella Typhimurium isolates) showed multidrug resist
174                                           Of Salmonella Typhimurium isolates, 42 of 43 were pathovar
175 zithromycin resistance was noted in 12.7% of Salmonella Typhimurium isolates, appearing in Bas-Congo
176 tryptophan synthase alpha2beta2 complex from Salmonella typhimurium led to the determination of the t
177 py by targeting viable tumor tissue by using Salmonella typhimurium leu-arg auxotrophs.
178  sub-Saharan Africa caused by highly related Salmonella Typhimurium lineages that may have occupied n
179 res of the RhamDs from both E. coli K-12 and Salmonella typhimurium LT2 (95% sequence identity) were
180 aracterization on the protein encoded by the Salmonella typhimurium LT2 genome (GI:16766982; STM3697)
181                      We recode 200 kb of the Salmonella typhimurium LT2 genome through a process we t
182 urli subunit homologs from Escherichia coli, Salmonella typhimurium LT2, and Citrobacter koseri were
183 show that IIA(Glc) directly binds to MelB of Salmonella typhimurium (MelB(St)) and Escherichia coli M
184                    The melibiose permease of Salmonella typhimurium (MelB(St)) catalyzes symport of m
185                         The MelB permease of Salmonella typhimurium (MelB-ST) catalyzes the coupled s
186  the three-dimensional crystal structures of Salmonella typhimurium MelBSt in two conformations, repr
187  increasingly constrained solution spaces of Salmonella Typhimurium metabolism during growth in both
188 ng Salmonella Enteritidis (n = 244 [35.5%]), Salmonella Typhimurium (n = 221 [32.2%]), I:4,[5],12:i:-
189 esized to investigate the impact of coupling Salmonella typhimurium O-antigen to different amino acid
190 firmed infection with the outbreak strain of Salmonella Typhimurium occurring between September 1, 20
191                        Autophagic capture of Salmonella Typhimurium occurs predominantly via generati
192 ng an E2 phage-coated ME biosensor to detect Salmonella typhimurium on tomato surfaces.
193                         The determination of Salmonella typhimurium, on screen-printed carbon electro
194 ptpn6 knockdown embryos were challenged with Salmonella typhimurium or Mycobacterium marinum at earli
195 uring intestinal infection with the pathogen Salmonella Typhimurium or pneumonic infection with Burkh
196 lly bound by IgY from chickens infected with Salmonella Typhimurium or S.
197                                              Salmonella typhimurium or Toxoplasma gondii were adminis
198 ates with NLRC4 in macrophages infected with Salmonella typhimurium or transfected with flagellin.
199 ens Mycobacterium tuberculosis, M bovis BCG, Salmonella typhimurium, or Toxoplasma gondii release fro
200 ophage P22, a podovirus infecting strains of Salmonella typhimurium, packages a 42-kbp genome using a
201 o be multidrug resistant, whereas a dominant Salmonella Typhimurium pathotype, ST313, was primarily a
202 n (MVC) site of the tryptophan synthase from Salmonella typhimurium plays essential roles in catalysi
203                                  In culture, Salmonella Typhimurium populations are bistable for the
204 murium isolates and compared these to global Salmonella Typhimurium populations.
205  In this study, we demonstrate that MVs from Salmonella typhimurium potently stimulated professional
206 minths induce IgG1, whereas Th1 Ags, such as Salmonella Typhimurium, predominantly induce IgG2a.
207 merging from the surface of bacteria such as Salmonella typhimurium propel the cells toward nutrient
208 To assess the roles of these residues in the Salmonella typhimurium QAPRTase reaction, they were indi
209 months (OR, 4.8; 95% CI, 1.1-21.1; P = .039).Salmonella Typhimurium represented 106 of 238 (44.5%) se
210  deletion mutants to identify novel genes of Salmonella Typhimurium required for survival during ente
211 d 28cfumL(-1) for Staphylococcus aureus, and Salmonella typhimurium, respectively.
212               The gastrointestinal pathogen, Salmonella Typhimurium, responds to acidic pH and CAMP t
213  infection of draining lymph nodes (DLNs) by Salmonella typhimurium results in the specific downregul
214  by independent exposures to flagellins from Salmonella typhimurium (S. typhimurium) and Bacillus sub
215                 The Gram-negative bacterium, Salmonella Typhimurium (S. Typhimurium) is a food borne
216 ing Escherichia coli, Klebsiella pneumoniae, Salmonella typhimurium, S. aureus, and Enterococcus faec
217 rmine the three-dimensional structure of the Salmonella typhimurium Saf pilus.
218 ity, Choi et al. (2013) demonstrate that the Salmonella Typhimurium-secreted protein tyrosine phospha
219 mpD surface antigen extraction was done from Salmonella typhimurium serovars, under the optimized gro
220 mic structure of the flagellar filament from Salmonella typhimurium serves as a model for all bacteri
221 egative bacteria including Escherichia coli, Salmonella typhimurium, Shigella flexneri, and Burkholde
222                  Flagellin isolated from the Salmonella Typhimurium SJW1660 strain, which differs by
223                                           In Salmonella typhimurium, some of these genes are controll
224 ive and sensitive immunosensor for detecting Salmonella typhimurium species.
225                                              Salmonella Typhimurium specifically targets antigen-samp
226 exemplified by a ubiquitin-binding domain in Salmonella Typhimurium SseL.
227 tegy incorporating delivery of the bacterium Salmonella typhimurium (ST), naturally tropic for the hy
228 nates (irrespective of HIV status), and with Salmonella Typhimurium ST313.
229                       The B cell response to Salmonella typhimurium (STm) occurs massively at extrafo
230                                              Salmonella Typhimurium (STm) remain a prominent cause of
231                       The first component is Salmonella typhimurium strain chi8937, with deletions of
232  in the Salmonella mutagenicity assay, using Salmonella typhimurium strain TA98 (with and without met
233                                              Salmonella typhimurium strain TA98 was used with and wit
234 able co-culture of metabolically competitive Salmonella typhimurium strains in microfluidic devices.
235 against sodium azide induced mutagenicity of Salmonella typhimurium strains TA 98 and TA 1531.
236 tivity of flavonoids, by the Ames test, with Salmonella typhimurium strains TA98, TA100 and TA102.
237 logical containment system using recombinant Salmonella Typhimurium strains that are attenuated yet c
238 nism that co-ordinates the expression of the Salmonella Typhimurium T3SS chaperone SicP and its cogna
239 ere, we show that human NAIP also senses the Salmonella Typhimurium T3SS inner rod protein PrgJ and t
240  revertants per nanomole of amine, log m, in Salmonella typhimurium TA 98 and TA 100 correlates with
241 ine-N-oxide (4-NQO), a direct mutagen toward Salmonella typhimurium TA 98 and TA 100.
242 ine-N-oxide (4-NQO), a direct mutagen toward Salmonella typhimurium TA 98 and TA 100.
243  benzo[a]pyrene, an indirect mutagen, toward Salmonella typhimurium TA 98 and TA 100.
244 ine-N-oxide (4-NQO), a direct mutagen toward Salmonella typhimurium TA 98 and TA 100.
245  exhibited maximum anti-mutagenicity against Salmonella typhimurium TA 98 and TA 1538, respectively a
246 monstrated both DNA adducts in target cells (Salmonella typhimurium TA100 and Chinese hamster V79) of
247 ed oxidant-induced mutagenicity (26%) in the Salmonella typhimurium TA102 strain, as determined by th
248 spectively, 69% and 64.8% in the presence of Salmonella typhimurium TA104, and 79.7% and 68.9% in the
249 showed mutagenic effect by Ames test against Salmonella typhimurium TA98 and TA100 strains.
250 Artocarpus heterophyllus Lam) extract, using Salmonella typhimurium tester strains TA98 and TA100 wit
251 luorescently labeled Escherichia coli HS and Salmonella typhimurium that passed through from the muco
252 bacterial cells (up to approximately 45% for Salmonella typhimurium) that is comparable to the widely
253 bacter aerogenes, Pseudomonas aeruginosa and Salmonella Typhimurium The geranylated residues are loca
254                                           In Salmonella typhimurium, the external needle is assembled
255 ely studied flagella of Escherichia coli and Salmonella typhimurium, the flagella of Campylobacter je
256 la While we tested for efficacy only against Salmonella Typhimurium, the modified Salmonella strain m
257  inhibitors of QS in both Vibrio harveyi and Salmonella typhimurium, the two organisms with defined A
258 nced cytokine expression during infection by Salmonella typhimurium This occurred in the first 3 d of
259 s citrate and iron from the enteric pathogen Salmonella Typhimurium to arrest growth and ameliorate t
260 n electrophysiological analysis of FocA from Salmonella typhimurium to characterize the channel prope
261         We used Escherichia coli 0157:H7 and Salmonella typhimurium to demonstrate that this design p
262            In order to assess the ability of Salmonella Typhimurium to replicate in human macrophages
263 estigated if the transcriptional response of Salmonella Typhimurium to temperature and acid variation
264                      We therefore screened a Salmonella Typhimurium transposon library to identify ba
265      Many intracellular pathogens, including Salmonella typhimurium, trigger autophagy in host cells,
266 nteractions regulate substrate channeling in Salmonella typhimurium tryptophan synthase.
267 onstrate the killing of Escherichia coli and Salmonella typhimurium, two common pathogens, at levels
268 hat the phosphoinositide phosphatase SopB, a Salmonella Typhimurium type III secreted effector protei
269 t a high-resolution in situ structure of the Salmonella Typhimurium type III secretion machine obtain
270        Here we report the engineering of the Salmonella Typhimurium type III secretion system in achr
271                           AhpC and AhpF from Salmonella typhimurium undergo a series of electron tran
272 -Dyer lipid extracts of Escherichia coli and Salmonella typhimurium using liquid chromatography/tande
273      The PhoQ sensor kinase is essential for Salmonella typhimurium virulence for animals, and a homo
274              Infection of DR3(-/-) mice with Salmonella typhimurium was associated with defective mic
275 tion from macrophages infected in vitro with Salmonella typhimurium was dependent on caspase 1 and Ip
276 e role of Irgm1 in controlling resistance to Salmonella typhimurium was explored to further define th
277                       The bacterial pathogen Salmonella typhimurium was grown aboard Space Shuttle mi
278                                              Salmonella Typhimurium was infrequent (2.3% pups; 4/175)
279 emonstrated and no significant adsorption of Salmonella typhimurium was observed.
280                        In contrast, although Salmonella typhimurium was proposed to induce the presen
281 ediators of PhoPQ-regulated OM remodeling in Salmonella Typhimurium, we identified PbgA, a periplasmi
282                            Here, by studying Salmonella Typhimurium, we show that the E3 ligase LUBAC
283         Highly specific DNA aptamers to live Salmonella typhimurium were selected via the cell-system
284 esponses and protection against infection by Salmonella typhimurium were spared.
285                   Listeria monocytogenes and Salmonella Typhimurium were used as negative controls.
286 ,6-trinitrobenzene sulfonic acid (TNBS), and Salmonella typhimurium were used to induce colitis in A(
287 intensively studied flagellar filament (from Salmonella typhimurium), which has approximately 5.5 sub
288                                       Motile Salmonella typhimurium, which are specifically attracted
289 -cell response to the intracellular pathogen Salmonella typhimurium, which can disrupt metabolism by
290 he bistable expression of virulence genes in Salmonella typhimurium, which leads to phenotypically vi
291  primarily been studied Escherichia coli and Salmonella typhimurium, which possess a single CheR invo
292                      Comparative genomics of Salmonella Typhimurium will provide insight into factors
293 eement with available experimental data from Salmonella typhimurium with only a single free parameter
294 ies of ethanolamine ammonia-lyase (EAL) from Salmonella typhimurium with site-directed mutations in a
295 ich allowed a direct label-free detection of Salmonella Typhimurium with the limit of detection (LOD)
296 chnique was used to capture a food pathogen, Salmonella typhimurium, with starting concentrations as
297                    Two isozymes are found in Salmonella typhimurium, with the A-isozyme expressed und
298                                  Survival of Salmonella typhimurium within a vacuole in host cells de
299     We show that the PilZ domain proteins of Salmonella Typhimurium, YcgR and BcsA, demonstrate a 43-
300 erived AMT databases (Shewanella oneidensis, Salmonella typhimurium, Yersinia pestis) for training an

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