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1 ing from food-borne illnesses to the bubonic plague.
2 the causative agent of bubonic and pneumonic plague.
3 antly attenuated in a mouse model of bubonic plague.
4 ouse and rat models of bubonic and pneumonic plague.
5 O92 in mouse models of bubonic and pneumonic plague.
6 However, they are susceptible to plague.
7 r in the lungs during experimental pneumonic plague.
8 for Yersinia pestis, the causative agent of plague.
9 t on the progression or outcome of pneumonic plague.
10 uses the fatal respiratory disease pneumonic plague.
11 otic infections, including enterocolitis and plague.
12 e invasive infection associated with bubonic plague.
13 s of Yersinia pestis, the causative agent of plague.
14 Yersinia pestis is the causative agent of plague.
15 d virulence and the emergence of the bubonic plague.
16 11 or 12 LD50 in a mouse model of pneumonic plague.
17 otential vaccine candidate against pneumonic plague.
18 otected from developing subsequent pneumonic plague.
19 N-gamma in protecting mice against pneumonic plague.
20 uction of bubonic, septicemic, and pneumonic plague.
21 the causative agent of bubonic and pneumonic plague.
22 r lysozyme resistance and the development of plague.
23 inst Yersinia pestis, the etiologic agent of plague.
24 tes to disease in the mouse model of bubonic plague.
25 m in Yersinia pestis, the causative agent of plague.
26 d pneumonic animal models (mouse and rat) of plague.
27 completely attenuated in an in vivo model of plague.
28 ice weakened T cell-mediated defense against plague.
29 ecules to slow down the rapid progression of plague.
30 nate immune response necessary for surviving plague.
31 important role in determining the outcome of plague.
32 e III secretion generated protection against plague.
33 or development of both bubonic and pneumonic plague.
34 important role in the progression of bubonic plague.
35 ic roles for these pathways during pneumonic plague.
36 y in murine models of systemic and pneumonic plague.
37 hromatosis who died from laboratory-acquired plague.
38 rium Yersinia pestis, the causative agent of plague.
39 iniosis, Far East scarlet-like fever and the plague.
40 significantly increased survival of bubonic plague.
41 Yersinia pestis results in primary pneumonic plague.
42 tibody therapy in the mouse model of bubonic plague.
43 and biological threats, such as anthrax and plague.
45 am-negative bacterium Yersinia pestis causes plague, a rapidly progressing and often fatal disease.
46 torical images labelled as depictions of the plague, although artistic and textual evidence shows tha
47 t numerous major public health problems have plagued American Indian communities for generations, Ame
49 study bacterial dissemination during bubonic plague and compare this model with an s.c. inoculations
50 d elsewhere that Mus spretus SEG mice resist plague and develop an immune response characterized by a
51 Yersinia pestis is the etiological agent of plague and has caused human pandemics with millions of d
52 s genus are A. astaci, the cause of crayfish plague and its close relative, A. invadans, which causes
53 is the impact of incidental setbacks such as plague and volcanism, which are seen to have compounded
54 7 contributed to the lethality of septicemic plague and was associated with the suppression of neutro
55 ffected by the Pla protease during pneumonic plague, and although A2AP participates in immune modulat
56 ally in protecting animals against pneumonic plague, and we have demonstrated an immunological basis
58 ypass a fundamental limitation that has long plagued applications of directed C-H activation in medic
60 ue in 1896 suggest that, only a decade after plague arrived, a heritable, plague-resistant phenotype
61 receptors for Yersinia pestis, the agent of plague, as shown by overexpression studies showing induc
62 screened them in a mouse model of pneumonic plague at a dose equivalent to 5 50% lethal doses (LD50)
68 of 2-component regulatory systems (2CSs) in plague because the latter are known to be key players in
69 t Y. pestis was capable of causing pneumonic plague before it evolved to optimally cause invasive inf
71 B resolves many of the issues that routinely plague biomedical researchers intending to work with dat
72 component of T cell-mediated defense against plague but can be dispensable for Ab-mediated defense.
73 ponent for the integrated management of both plagues, but local eradication successes have been limit
75 of all-solid-state rechargeable batteries is plagued by a large interfacial resistance between a soli
76 Nevertheless, such formulations have been plagued by a local acidic microenvironment and protein-p
79 tient population which tends to be older and plagued by comorbidities such as diabetes mellitus and h
80 daveric biologic mesh has been expensive and plagued by complications such as seroma, infection, and
82 We report that the current evidence base is plagued by considerable methodologic heterogeneity in al
83 increase cardiac output, their use has been plagued by excessive mortality due to increased tachycar
84 he computational and statistical methods are plagued by fundamental identifiability issues, instabili
86 of diffuse large B-cell lymphoma (DLBCL) is plagued by heterogeneous responses to standard therapy,
87 h comparative genomics has consistently been plagued by high false-positive rates and divergent predi
88 ever, the current Ag-NW thin films are often plagued by high NW-NW contact resistance and poor long-t
90 ired cell types using this approach is often plagued by inefficiency, slow conversion, and an inabili
98 ct DNA and RNA (collectively xNA) are easily plagued by noise, false positives, and false negatives,
100 applicable to several other material systems plagued by polydispersity, defects, and grain boundary r
102 ic vehicle operations, but their adoption is plagued by poor cycle life due to the structural and che
103 p polymeric alternatives, however, have been plagued by poor retention and off-target toxicity due to
104 d work has been reported on Mg/S system, all plagued by poor reversibility attributed to the formatio
105 wever, conventional transgenesis methods are plagued by position effects: the regulatory environment
106 he most important antibiotic classes but are plagued by problems of resistance, and the development o
107 use analyses based on observational data are plagued by problems of reverse causation and self-select
110 ailable for only half of all studies and are plagued by selective reporting of methods and results.
111 Doing so at the nanoscale has thus far been plagued by significant scalability problems, particularl
112 ct outcomes of mitral regurgitation (MR) are plagued by small size, inconsistent etiologies, and lack
116 The current status of CCS is that it is plagued by technical uncertainties, infrastructure, fina
118 quest for catalyst optimization in vitro is plagued by the elusive description of the active sites o
119 opment of a competitive magnesium battery is plagued by the existing notion of poor magnesium mobilit
120 ses in a field of inquiry that has been long plagued by the limited availability of research specimen
122 roteins in heterogeneous media are generally plagued by two distinct obstacles: lack of sensitivity d
123 ersion of one amide to another, is typically plagued by unfavourable kinetic and thermodynamic factor
127 nsequently, several pathogens, including the plague causing bacterium Yersinia pestis, avoid activati
133 the cost of quality control of manufacturing plague development of Li-ion rechargeable batteries that
136 biologically relevant i.d. model of bubonic plague differs significantly from the s.c. model in mult
137 mely high-prevalence outbreak (61%) of white-plague disease at 14 sites off southeastern Florida.
140 is causes bubonic, pneumonic, and septicemic plague, diseases that are rapidly lethal to most mammals
143 atical model coupling environmentally forced plague dynamics with evolutionary selection of rats, cap
145 climate fluctuations that preceded regional plague epidemics, based on a dataset of 7,711 georeferen
147 Yersinia pestis, the causative agent of plague, evolved from the gastrointestinal pathogen Yersi
148 Yersinia pestis, the causative agent of plague, expresses the plasminogen activator protease Pla
150 en due to either the presence of now-extinct plague foci in Europe itself, or successive disease intr
152 e of a previously uncharacterized historical plague focus that persisted for at least three centuries
153 we describe the characteristics of pneumonic plague, focusing on its disease progression and pathogen
154 Yersinia pestis, the cause of the disease plague, forms biofilms to enhance flea-to-mammal transmi
156 from Yersinia pestis, the causative agent of plague, from the closely related species Y. pseudotuberc
160 The debilitating choreic movements that plague HD patients have been attributed to striatal dege
161 es a fundamental problem that has previously plagued high-resolution Raman spectroscopy: fine spectra
162 verity, and difficulty of treating pneumonic plague highlight how differences in the route of disease
163 s essential for the development of pneumonic plague; however, the complete repertoire of substrates c
164 tolerable burden of malaria has for too long plagued humanity and the prospect of eradicating malaria
166 many of the practical limitations that have plagued hydrogen-bond donor catalysis and enables use of
167 in colonial India after the introduction of plague in 1896 suggest that, only a decade after plague
168 attenuated Y. pestis CO92 to evoke pneumonic plague in a mouse model while retaining the required imm
172 trade routes were to blame for the spread of plague in European history, yet this relationship has ne
173 Yersinia, including Y. pestis, the agent of plague in humans, and Y. pseudotuberculosis, the related
174 ght ill-prepared societies off-guard-Bubonic plague in medieval times, AIDS in the 1980s, and Ebola t
177 specimen and Yersinia pestis ("Black Death" plague) in a medieval tooth, which represented only minu
178 oted strains of Y. pestis to cause pneumonic plague, indicating that Y. pestis was primed to infect t
190 Yersinia pestis, the causative agent of plague, is able to suppress production of inflammatory c
192 sample-to-sample variability that typically plagues MALDI-TOF, and is the first method developed to
195 light on the practical limitations that have plagued many of the H-bond donor-catalyzed reactions dev
197 estis, H. influenzae, and Proteus that cause plague, meningitis, and severe wound infections, respect
200 tant was still fully virulent in a pneumonic plague model but had an approximately 90-fold increase i
201 p or DeltamsbB single mutant, in a pneumonic plague model were significantly protected against a subs
209 f this critical point and the "sign problem" plaguing numerical quantum Monte Carlo (QMC) methods, it
211 e that the Y pestis lineages that caused the Plague of Justinian and the Black Death 800 years later
212 it was responsible for three pandemics: the Plague of Justinian in the 6(th) century AD, which persi
218 esultant lack of biochemical specificity has plagued our understanding of how biological electrophile
222 a dataset of 7,711 georeferenced historical plague outbreaks and 15 annually resolved tree-ring reco
224 urthermore, the negative correlation between plague outbreaks and their distance from major trade por
226 hereby avoiding decomposition reactions that plague oxidations of neutral cerium(III) compounds.
227 This epidemic marked the start of the second plague pandemic, which lasted in Europe until the early
232 fection supports innate host defense against plague, perhaps by providing a nondiffusible spatial cue
233 ) to address mispriming issues that commonly plague poly(A) site (pA) identification, and we used the
235 ific insight into paleoviral infections that plagued primates deep in their evolutionary history.
237 sts, Yersinia pestis, the causative agent of plague, replicates as biofilm in the foregut of fleas th
242 lution based on experimental observations of plague resistance and reveal the buffering effect of suc
243 this study, we have further delineated this plague resistance locus to a region of less than 20 cM t
244 This programming plays a key role in the plague-resistance phenotype and may be similarly signifi
245 a decade after plague arrived, a heritable, plague-resistant phenotype had become prevalent among co
247 ale food-borne illnesses, dysentery, bubonic plague, secondary hospital infections, and sexually tran
249 racterized by severe epidemic events such as plague, smallpox, or influenza that shaped the immune sy
250 cing the genomes, we find that these ancient plague strains are basal to all known Yersinia pestis.
255 fundamental catalytic limitations that have plagued the electrochemical production of hydrogen for d
260 be achieved only if the systemic challenges plaguing the health system (poor coverage of early infan
262 e WT bacterium in a mouse model of pneumonic plague, the Deltalpp Deltaail double mutant and the Delt
263 dification is unnecessary to cause pneumonic plague, the substitution is instead needed to efficientl
265 addition to the risk of natural exposure to plague, there is also the threat of a bioterrorist act,
266 DA-CuCN avoids polymerization that otherwise plagues these alkylations and generates a reactive metal
267 The Yersinia-flea interactions that enable plague transmission cycles have had profound historical
269 on our findings, we propose the mechanism of plague transmission in historical Europe, which is imper
270 conducting on wildlife infectious diseases: plague transmission in prairie dogs and lyssavirus dynam
273 am-negative bacteria, including purveyors of plague, typhoid fever, whooping cough, sexually transmit
274 lored include tuberculosis, leprosy, bubonic plague, typhoid, syphilis, endemic and epidemic typhus,
275 hermal oxidation and corrosion problems that plague unprotected metal meshes, while also maintaining
277 Yersinia pestis, the causative agent of plague, uses a type III secretion system (T3SS) to injec
278 Yersinia pestis, the causative agent of plague, utilizes a type III secretion system (T3SS) to i
279 Mice delivered with a single dose of F1-V plague vaccine containing both gene and protein in the T
280 ar Typhi strain to create a bivalent mucosal plague vaccine that produces both the protective F1 caps
284 nce in mouse models of bubonic and pneumonic plague, we characterized an msbB in-frame deletion mutan
285 n providing the host with protection against plague, we developed a live-attenuated vaccine strain by
286 allergy, i.e., asthma and allergic rhinitis, plaguing westernized countries, with up to 8% of young c
290 traditional biochemical fractionation can be plagued with contaminants and loss of key components.
291 ratios, up to 30:1 (over-labeling), normally plagued with energy migration and background fluorescenc
292 try and single-cell RNA-seq (scRNA-seq), are plagued with systematic errors that may severely affect
294 LD50 when tested in a mouse model of bubonic plague, with infection by 10/20 of the aforementioned mu
295 c plague is the most severe manifestation of plague, with mortality rates approaching 100% in the abs
296 trol malaria, typhus, body lice, and bubonic plague worldwide, until countries began restricting its
300 ns such as the Yersinia pestis, which causes plague, Yersinia pseudotuberculosis, Yersinia enterocoli
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