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1 positive cultures included in the study (196 Gram-positive, 44 Gram-negative, 32 polymicrobial, and 2
5 with yeast cells and various strains of both Gram-positive and -negative bacteria revealed distinct b
6 ll fibrous platform effectively inhibit both gram-positive and -negative bacteria without inducting o
9 t anticancer activity, in addition to strong Gram-positive and Gram-negative antibiotic character.
10 e salt-functionalized filters quickly killed Gram-positive and Gram-negative bacteria aerosols in vit
11 ly, our data show that neutrophils recognize Gram-positive and Gram-negative bacteria by means of mul
12 esults show that DNA from various, unrelated gram-positive and gram-negative bacteria results in a mo
13 tivity exhibited by the extract against both Gram-positive and Gram-negative bacteria suggests the pr
15 mmatory responses that distinguished between Gram-positive and Gram-negative bacteria, both in vitro
16 trum antibiotics, with efficacy against both gram-positive and gram-negative bacteria, has the potent
17 hibits the growth of different rainbow trout Gram-positive and Gram-negative bacteria, namely Lactoco
18 nnocua and E. coli ATCC25922, as examples of Gram-positive and Gram-negative bacteria, respectively,
19 ng antibacterial activity against the tested Gram-positive and Gram-negative bacteria, with a large z
30 rs induce deformation and penetration of the Gram-positive and Gram-negative bacterial cell envelope,
31 lied to the analysis of intact proteins from Gram-positive and Gram-negative bacterial colonies sampl
32 11 displays antimicrobial activities against gram-positive and gram-negative bacterial pathogens, the
33 molecules, bacteriocins are produced by both gram-positive and gram-negative bacterial species and ar
34 hich is shown to be taken up in a variety of gram-positive and gram-negative bacterial strains in vit
36 trum sterilizing activity against a panel of gram-positive and gram-negative ESKAPE pathogens, and an
37 -deoxyglucosone (3-DG) were assessed against Gram-positive and Gram-negative pathogenic and food spoi
38 in reducing the intracellular burden of both Gram-positive and Gram-negative pathogenic bacteria.
39 Acute skin infections that involve mixed gram-positive and gram-negative pathogens must also be c
40 xacin is unique in being active against both gram-positive and gram-negative pathogens that cause ski
42 ition, and the antibacterial activity across Gram-positive and Gram-negative pathogens with N-linked
43 xhibited excellent efficacy against selected Gram-positive and Gram-negative pathogens, as well as cl
46 ve bactericidal drugs and a diverse range of Gram-positive and Gram-negative species (Escherichia col
47 madacycline displays potent activity against gram-positive and many gram-negative bacteria, including
50 were coagulase-negative staphylococci, other gram-positive, and gram-negative bacteria, respectively.
51 ts on a benzisoxazole scaffold with improved Gram-positive antibacterial activity relative to previou
54 he proposed EAST is successfully applied for Gram-positive Bacillus subtilis and Gram-negative Escher
58 Gram-negative (Pseudomonas fluorescens) and Gram-positive (Bacillus thuringiensis) bacterial species
59 DnaD protein is essential in low G+C content gram positive bacteria and is involved in replication in
63 ignaling', exists in other Gram-negative and Gram-positive bacteria and displays species-specificity.
65 on-classically secreted effector proteins in Gram-positive bacteria and further inspire the developme
66 ibiotic activity (MIC = 15.6 mug/mL) against Gram-positive bacteria and growth reduction of Gram-nega
68 on the biogenesis and functions of EVs from Gram-positive bacteria and identify key areas for future
69 of gut microbiota with reduced abundance of gram-positive bacteria and increased abundance of gram-n
70 ancomycin, an antibiotic that acts mainly on gram-positive bacteria and is restricted to the gut, pot
71 ins are related to class IIa bacteriocins of Gram-positive bacteria and kill members of the Bacteroid
72 lecular patterns including peptidoglycans of Gram-positive bacteria and lipopolysaccharides of Gram-n
73 rium spp. have demonstrated EV production in Gram-positive bacteria and shown the great importance EV
76 he serine-rich repeat (SRR) glycoproteins of Gram-positive bacteria are large, cell wall-anchored adh
78 A similar mechanism probably operates in the gram-positive bacteria as well, but these systems have b
79 nally, we discover aminoacyl-PGs not only in Gram-positive bacteria but also in Gram-negative C. jeju
80 none oxidoreductases (Sdh) are widespread in Gram-positive bacteria but little is known about the cat
81 bumin (ALA) and oleic acid and kills several Gram-positive bacteria by a mechanism that bears resembl
85 o differences in cell wall structure, EVs in Gram-positive bacteria have been disregarded for decades
88 ndant in the smokers at baseline and so were Gram-positive bacteria in the non-smokers (P <0.01).
89 has been widely used to treat infections of Gram-positive bacteria including Clostridium difficile a
91 -1'-enyl, 2-acyl phospholipids) in anaerobic Gram-positive bacteria led to studies on the physical ch
93 peptides when the flies were challenged with Gram-positive bacteria Micrococcus luteus In this settin
94 Pseudoalteromonas sp. strain CF6-2) can kill Gram-positive bacteria of diverse peptidoglycan (PG) che
98 for half a century but the possibility that Gram-positive bacteria secrete extracellular vesicles (E
101 found to specifically inhibit the growth of Gram-positive bacteria Staphylococcus aureus with MIC(50
103 ghput scRNA-seq method for Gram-negative and Gram-positive bacteria that can resolve heterogeneous tr
104 treptogramins(2), potent antibiotics against Gram-positive bacteria that inhibit the bacterial riboso
105 tein export systems in mycobacteria and many Gram-positive bacteria that mediate a broad range of fun
106 SCH-79797, that kills both Gram-negative and Gram-positive bacteria through a unique dual-targeting m
107 vation (up to 95%) against Gram-negative and Gram-positive bacteria was observed when curcumin-functi
108 tions in this study were caused by bacteria; Gram-positive bacteria were responsible for most cases.
109 en between structurally similar molecules in gram-positive bacteria while also demonstrating the powe
110 nductance and renders it ineffective against Gram-positive bacteria while nevertheless enhancing its
111 gle-cell transcriptomes of Gram-negative and Gram-positive bacteria with high purity and low bias, wi
112 e bacteria and lipoteichoic acids (LTA) from Gram-positive bacteria with host lipoprotein carriers in
113 ncubated with agonists of TLR2 (receptor for gram-positive bacteria), TLR4 (receptor for gram-negativ
114 gulase-negative staphylococci not included): Gram-positive bacteria, 58%; Gram-negative bacteria, 78%
116 isteria monocytogenes, as well as many other Gram-positive bacteria, and which highlights a more gene
117 a potent antibiotic against a broad range of Gram-positive bacteria, but its medical applications hav
118 nel to other methods of identification of 20 Gram-positive bacteria, four antimicrobial resistance ge
119 nd has broad-spectrum activity that includes gram-positive bacteria, gram-negative bacteria, anaerobe
120 cultures in patients with Gram-negative and Gram-positive bacteria, including 8/60 (13.3%) patients
122 robial agent; it performed well against many Gram-positive bacteria, including multidrug resistant st
124 hat rTCP96 aggregates both Gram-negative and Gram-positive bacteria, including Staphylococcus aureus
125 y used antibiotics against gram-negative and gram-positive bacteria, including Staphylococcus aureus,
126 loped to overcome the acquired resistance in Gram-positive bacteria, intrinsic resistance in Gram-neg
127 that modulates QS in both Gram-negative and Gram-positive bacteria, is phosphorylated by LsrK, and t
133 resistance seems to be universal across the Gram-positive bacteria, while the type of coselected tra
155 Pseudoalterin binds to the glycan strands of Gram positive bacterial PG and degrades the PG peptide c
162 a and shown the great importance EVs have in Gram-positive bacterial physiology and disease progressi
163 RgNanOx homologues across Gram-negative and Gram-positive bacterial species and co-occurrence with s
164 n fluorescence measurements on two different gram-positive bacterial species as the cells uptake memb
165 The model represents the first ME-model of a Gram-positive bacterium and captures all major central m
166 pp, all directly interact with XPRT from the Gram-positive bacterium Bacillus subtilis and inhibit XP
171 ibe the characterization of a MINPP from the Gram-positive bacterium Bifidobacterium longum (BlMINPP)
174 acterial GH161 gene sequence (PapP) from the Gram-positive bacterium Paenibacillus polymyxa ATCC 842
178 tance in the preeminent etiologic agent, the Gram-positive bacterium Staphylococcus aureus Bacterial
185 o damage caused by Listeria monocytogenes, a Gram-positive bacterium, BCV rupture by Gram-negative pa
188 enMark Dx ePlex Blood Culture Identification Gram-Positive (BCID-GP) Panel is a multiplex nucleic aci
189 lammatory response between Gram-negative and Gram-positive BK and to determine the diagnostic value o
190 RDT facilitated antibiotic optimization for Gram-positive BSIs but led to unnecessary escalation of
195 terial colonies (including Gram-negative and Gram-positive clinical isolates) grown on agar media by
196 than vancomycin against multidrug-resistant Gram-positive clinical isolates, including vancomycin- a
197 e separated states into bacteremia caused by Gram-positive cocci (GPC), susceptible Gram-negative bac
201 e separated states into bacteremia caused by gram-positive cocci, susceptible gram-negative bacilli (
203 e a highly effective approach for preventing gram-positive cocci-related, skin flora-related, or cent
204 ld be a highly effective approach to prevent gram-positive-cocci-, skin-flora-related, or central-lin
208 Gram-negative Escherichia coli (E. coli) and Gram-positive Enterococcus durans (E. durans) and Staphy
209 at-killed Gram-negative Escherichia coli and Gram-positive Enterococcus faecalis applied during the f
210 ed Gram-negative Escherichia coli Symbio and Gram-positive Enterococcus faecalis Symbio or placebo fr
211 ive uropathogenic Escherichia coli (UPEC) or Gram-positive Enterococcus faecalis, we used a mouse tra
213 embraned cells and the derived nature of the Gram-positive envelope following multiple OM losses.
216 teria have one pathway or the other, but the Gram-positive, facultative intracellular pathogen Lister
217 antibiotics that selectively suppress mainly gram-positive (fidaxomicin, streptomycin) or gram-negati
218 (WD) is a rare, chronic, infection caused by gram-positive filamentous aerobic actinobacterium Trophe
220 s largely due to an increase in abundance of Gram-positive Firmicutes and a concurrent decrease in Gr
221 d TNF-alpha proteins, gram-negative (GN) and gram-positive (GP) bacterial DNA, and the antibiotic-res
222 Virulent strains of Streptococcus pyogenes (gram-positive group A Streptococcus pyogenes [GAS]) recr
223 e virulent bacteria (gram-negative and other gram-positive groups) and presentation with light percep
224 reptococcus pneumoniae (Spn) is an important Gram-positive human pathogen that causes millions of inf
225 catechol species are important Fe sources in Gram-positive human pathogens, since PiuA functions in t
226 osporin with broad in vitro activity against gram-positive (including methicillin-resistant Staphyloc
227 tructure infections (ABSSSI), including both gram-positive (including methicillin-resistant Staphyloc
230 gainst clinically relevant Gram-negative and Gram-positive infections via enhanced leukocyte recruitm
234 tations, we show that encapsulating LsLAI in gram-positive Lactobacillus plantarum that is chemically
235 uated using osmotic stress management in the Gram-positive model bacterium Bacillus subtilis as proof
236 at RNAPs outpace pioneering ribosomes in the Gram-positive model bacterium Bacillus subtilis, and tha
242 tion of the gastrointestinal tract with this Gram-positive, obligate anaerobe can lead to potentially
244 Ryway was utilized to re-design Debio-1452-a Gram-positive-only antibiotic(8)-into versions that accu
245 nd a general blueprint for the conversion of Gram-positive-only compounds into broad-spectrum antibio
249 arative method to Gram stain for delineating gram-positive or gram-negative bacteria or fungi within
250 on between cell envelopes with one membrane (Gram-positive or monoderm) and those with two membranes
253 ns in the PCT arm for patients infected with gram-positive organisms or Escherichia coli and signific
259 key role in penicillin-induced lysis of the Gram-positive pathogen Streptococcus pneumoniae (Sp).
262 lecular methods for the identification of 20 Gram-positive pathogens and four antimicrobial resistanc
263 es inhibit the growth of multidrug-resistant Gram-positive pathogens by disrupting cell wall biosynth
265 e that BOFP binds the FtsZ proteins from the Gram-positive pathogens Staphylococcus aureus, Enterococ
267 he WalR-WalK pathway is conserved among many Gram-positive pathogens where it controls transcription
269 While horine was potent primarily against gram-positive pathogens, verine showed broad-spectrum an
270 n resistance methyltransferase found in many Gram-positive pathogens, whereas ErmE is found in the so
276 cuss recent advances in our understanding of Gram-positive, plant-associated bacteria and provide a f
278 its human homolog MRGPRX2 are receptors for Gram-positive QSMs, including competence-stimulating pep
279 nts, initial staining of liquid media showed Gram-positive rods or cocci, including some cocci in cha
280 treatments have the ability to inhibit both gram-positive (S. aureus) and gram-negative (E. coli) ba
281 on between influenza virus on the surface of Gram-positive, S. pneumoniae and S. aureus, and Gram-neg
282 ommonly used clinically for the treatment of Gram-positive skin and skin structure infections (SSSI),
283 of IL-10, whereas inflammatory responses to Gram-positive species were more sustained due to the abs
286 ioides (formerly Clostridium) difficile is a Gram-positive, spore-forming anaerobe and a leading caus
291 vitro infection model with heat-inactivated Gram-positive (Staphylococcus aureus) and Gram-negative
294 the outer cell wall of Lactococcus lactis, a Gram-positive surrogate that otherwise lacks adhesins to
296 obal biochemical and structural picture of a Gram-positive Tfp and have fundamental implications for
298 -17-mediated pathology in situations such as gram-positive toxic shock or Mycobacterium infection.
299 ctivity against both sensitive and resistant Gram positive (using 1500 ppm) as well as sensitive and
300 vity extends to a range of Gram-negative and Gram-positive wound pathogens in planktonic culture and,