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1 llular concentration as compared with a wild-type strain.
2 produced less pyruvate and H2S than the wild-type strain.
3 increase BAFF at levels similar to the wild type strain.
4 allenge with the B. mallei lux (CSM001) wild-type strain.
5 pat mutant reaching the spleen than the wild type strain.
6 n were similar compared to those of the wild-type strain.
7 is type strain, and 83.8% to the S. ictaluri type strain.
8 r lipid production from phenol than the wild-type strain.
9 tly more biomass than those formed by a wild-type strain.
10 sor strains tested as compared with the wild-type strain.
11 ewer, smaller lesions compared with the wild-type strain.
12 ut strains and patients infected with a wild-type strain.
13 sease at a similar rate of onset as the wild type strain.
14 , and Tunisia, were sequenced along with the type strain.
15 es to a level comparable to that of the wild-type strain.
16 ility upon exposure to NO compared with wild-type strain.
17 initiate growth was comparable with the wild-type strain.
18 plasia on day 14 postinfection than the wild-type strain.
19 A moiety compared to that found in the wild-type strain.
20 red more efficiently, compared with the wild-type strain.
21 apsule production when expressed in the wild-type strain.
22 point is present and functional in the wild-type strain.
23 with the black spore suspension of the wild-type strain.
24 r when using the RARE strain versus the wild-type strain.
25 l sexual reproduction with the parental wild-type strain.
26 ows at a rate comparable to that of the wild-type strain.
27 oteins within the complex compared to a wild-type strain.
28 and performed competitions against the wild-type strain.
29 model of GAS invasive disease than the wild-type strain.
30 e to oxidative stress than the parental wild-type strain.
31 algZ mutant was 40% of the level of the wild-type strain.
32 howed a lower electro-activity than the wild-type strain.
33 ded protection against infection by the wild-type strain.
34 and biomass than those of the parental wild-type strain.
35 in the DeltaartA strain but not in the wild-type strain.
36 nt strain compared to expression in the wild-type strain.
37 e resistant to LpxC inhibitors than the wild-type strain.
38 old lower in the hfq mutant than in the wild-type strain.
39 tivity and cytotoxicity compared to the wild-type strain.
40 x ratio were comparable to those of the wild type strain.
41 erences between the yfiR mutant and the wild-type strain.
42 o infection than mice infected with the wild-type strain.
43 thral epithelial cells, relative to the wild-type strain.
44 ased in the ccpE mutant relative to the wild-type strain.
45 ics comparable to those observed in the wild-type strain.
46 ed carriage, exceeding even that of the wild-type strain.
47 tant S. exfoliatus ZD27 compared to the wild-type strain.
48 ytic activities similar to those of the wild-type strain.
49 ranscription response to FLs compared to the type strain.
50 ne resorption than the encapsulated W50 wild-type strain.
51 d ethanol levels in comparison with the wild-type strain.
52 reolysin (Aur) activity relative to the wild-type strain.
53 film on the implanted catheter than the wild-type strain.
54 tested compounds than does an isogenic wild-type strain.
55 longum subsp. infantis Bi-26 (Bi-26) and the type strain.
56 Sho1 strain was reduced compared to the wild-type strain.
57 nomic surveys and experiments using a single type strain.
58 o showed greater cooperativity than the wild-type strain.
59 eens during an acute infection than the wild-type strain.
60 low ribosome content, compared with the wild-type strain.
61 IN-1 both induced Ohr expression in the wild-type strain.
62 ions the mutant did not differ from the wild-type strain.
63 e and cold treatments than those of the wild-type strain.
64 hese matched the stress proteome of the wild type strain.
65 d on plastic surfaces compared with the wild-type strain.
66 ts associated with the pathogenicity of wild-type strains.
67 erize the latent infection of two HSV-1 wild-type strains.
68 of all currently recognized bifidobacterial type strains.
69 not accumulate in detectable amounts in wild-type strains.
70 mants were similar to the corresponding wild-type strains.
71 ungal susceptibility testing of clinical and type strains.
72 % (38-97) against single-antigen non-vaccine type strains.
73 % (47-88) against single-antigen non-vaccine type strains.
74 ival rates comparable to those found in wild-type strains.
75 ve cheats in vivo and cannot outcompete wild-type strains.
76 onization of BALB/cByJ mice compared to wild-type strains.
77 host cells compared with their isogenic wild-type strains.
78 sible to the steady-state phenotypes of wide-type strains.
79 more pyruvate in the growth medium than wild-type strains.
80 rhabditis elegans, whereas it is not in wild type strains.
81 oduction of new metabolites not seen in wild type strains.
82 s tolerant of deep ocean pressures than wild-type strains.
84 -essential ICP4 and ICP8 genes of HSV-1 wild-type strain 17syn+ were brought under the control of a d
86 s 70% (58-78) against single-antigen vaccine type strains, 37% (10-56) against partly heterotypic str
88 , 82% (70-89) against single-antigen vaccine type strains, 82% (70-89) against partly heterotypic str
89 gene was 98.8% similar to the S. halichoeri type strain, 84.6% to the S. canis type strain, and 83.8
92 ed by GII.R, while GII.Non-R and GII.NT (not typed) strains accounted for 6 (5.5%) and 9 (8.3%) norov
93 usceptible to early host clearance than wild-type strains after intravenous infection, but impaired i
94 mif(-/-) L. major, when compared to the wild-type strain, also showed a 3-fold reduction in parasite
96 f two Caenorhabditis elegans strains, a wild-type strain and a strain containing two complex rearrang
97 tome-sequencing (RNA-seq) analysis of a wild-type strain and an isogenic fabT deletion mutant strain
98 d strain grows at a similar rate to the wild-type strain and does not exhibit any major growth defect
100 red expression compared to the isogenic wild-type strain and included transcriptional regulators, tra
101 n (CDT) were evaluated first by using a wild-type strain and its corresponding cdtB isogenic mutant a
103 provement in FA titer compared with the wild-type strain and the strain carrying the uncontrolled met
104 These genomes double the number of existing type strains and expand their overall phylogenetic diver
106 uteoviolacea and Pseudoalteromonas phenolica type strains and show clear evidence of gene and gene cl
107 kin 8 expression was evaluated by using wild-type strains and their corresponding CdtB isogenic mutan
109 alichoeri type strain, 84.6% to the S. canis type strain, and 83.8% to the S. ictaluri type strain.
110 bactericidal activity than against the wild-type strain, and the IgG1 MAbs had similar or greater ac
111 for the T2SS mutant than it was for the wild-type strain, and the mutant's defect was maintained over
112 ed biofilm architecture relative to the wild-type strain, and these phenotypes were partially complem
113 ation of macrophages, compared with the wild-type strain, and with delayed inflammatory stimuli as co
116 embrane proteins, TraK and TraB, in the wild-type strain as well as in overexpression strains and in
117 iculation phenotype of DeltanlpA in the wild-type strain as well as in the degP deletion strain was f
118 biomass productivity than the parental wild-type strains as well as near wild-type ability to carry
119 ly attenuated virulence relative to the wild-type strain, as manifested by prolonged survival, reduce
120 t compared with those infected with the wild-type strain, as well as significantly greater expression
121 ch differs by a point mutation from the wild-type strain, assembles into straight filaments in which
123 ely measure toxin production by C. difficile type strain ATCC 9689 under 768 culture conditions.
124 ecular mechanisms of HMO utilization for the type strain B. longum subsp. infantis ATCC 15697 (type s
128 attenuated virulence as compared to the wild-type strain but did not significantly affect bacterial g
129 ficantly up-regulated in the irradiated wild-type strain but not in the irradiated wdpks1 mutant, imp
130 nts were not attenuated compared to the wild-type strain, but multiple plc mutants showed reduced vir
131 pressing PR1 enhanced resistance to the wild-type strain, but not to the Sscp1 knockout strain of S.
133 ns were more sensitive to acid than the wild-type strain, but the Deltahyc strains were like the viru
134 Removal of GPI-anchored proteins in the wild-type strain by hydrofluoric acid (HF) pyridine treatment
135 te mitochondrion, even outcrossing with wild-type strains cannot facilitate spread of resistance.
136 Pulmonary spore challenge with the wild-type strain caused high mortality, intra-alveolar hemorr
137 formed a de novo assembly of the C. glabrata type strain CBS138 using long single-molecule real-time
138 both classes of promoters, peak KOA in wild-type strains coincided late in the circadian cycle near
140 first episodes of infections due to vaccine-type strains, community-acquired pneumonia occurred in 4
141 re immune-stimulatory than the parental wild-type strains, consistent with an immune-suppressive role
142 d its isogenic choline-treated parental wild-type strain D39 degrade extracellular DNA readily, sugge
147 rt, we demonstrate that the majority of wild-type (strain EGDe) and mouse-adapted (InlA(m)-expressing
148 and bactericidal assays using the infecting-type strain, emm cluster-related strains, and nonrelated
149 inal metaplasia in subjects infected with i2-type strains, even in a vacA s1, cagA(+) background.
150 sequence of the field strain ILRI181 and the type strain F38 and that was further evidenced in 10 fie
151 act that the dislocation, besides the phonon-type strain field analogous to dislocations in ordinary
152 acking all three genes behaved like the wild-type strain for all phenotypes mentioned above, but all
155 ed four strains of Bacillus subtilis and the type strains for two closely related species, Bacillus v
160 nts in defined competitions against the wild-type strain identified nine mutants that exhibited a rep
163 ct of the Deltatkt strain compared with wild-type strain in early intracellular proliferation and in
165 bp) showed ~89.5% similarity to the nearest type strain in EzTaxon database and may be considered no
168 Rapid differentiation of vaccine from wild-type strains in suspect measles cases is a valuable epid
169 in exflagellation EC50 relative to the wild-type strains in the presence of compound 1294, providing
170 ind fibronectin relative to that of the wild-type strain; in situ reconstitution of fnm in the deleti
171 inoculation of an SPI-1 mutant with the wild-type strain increased the number of mutant organisms in
172 tress, and in response to H(2)O(2), the wild-type strain increases superoxide radical production to a
173 omes of an rppH deletion mutant and the wild-type strain incubated at 20 degrees C and 30 degrees C.
174 ccumbed to infection with a more recent wild-type strain, indicating that immune responses to the mor
175 cells exposed to the isogenic S. aureus wild-type strain, indicating that PSMs inhibit the production
176 hly induced under oxidative stress in a wild-type strain, indicating the critical role of Cys-25 in r
177 djustment (MOMA) from the corresponding wild-type strains instead of having maximal growth rates afte
180 olates were phenotypically distinct from the type strain isolated from a seal; comparative whole-geno
183 nges are reduced in comparison with the wild type strain, likely due to ineffective translation of tr
185 orcine lungs and was outcompeted by the wild-type strain (median competitive index of 2 x 10(-5)).
186 not detected in cell-free extracts from wild-type strain methanol- and lanthanum-grown cultures.
189 ion was also noticed in an M. smegmatis wild-type strain (MSWt) induced with cumene hydroperoxide (CH
190 Here we present the genomic background of type strain NRRL Y-12632 and its transcriptomic response
193 ta indicate that murine death caused by wild-type strains occurs by a mechanism different from that b
194 were purified and used to show that the wild-type strain of Cba. tepidum can grow on biogenic S(0) gl
195 Archaea by sequencing, where available, the type strain of each species with a validly published nam
196 ipt in host macrophages infected with a wild-type strain of M. tuberculosis or an attenuated mutant s
197 ng were performed on the human isolates, the type strain of S. halichoeri, and type strains of closel
198 These two complete genome sequences of the type strain of S. pyogenes will effectively serve as val
199 cal isolates that most closely resembled the type strain of Streptococcus halichoeri isolated from a
203 s strains NCTC 8198(T) and CCUG 4207(T), the type strain of the type species of the genus Streptococc
205 lopment of reverse genetics systems for wild-type strains of CDV and the use of the resulting recombi
210 nidia (asexual spores) of two different wild-type strains of N. fumigata and three different ergot al
211 V13) in preventing first episodes of vaccine-type strains of pneumococcal community-acquired pneumoni
212 a mechanistic explanation for how different types (strains) of rhinoviruses may elicit different cel
213 umber of disease lesions incited by the wild-type strain on bean was also significantly higher than t
214 l inoculation with the encapsulated W50 wild-type strain or isogenic non-encapsulated DeltaPG0116-PG0
215 d higher rates of survival than the S. mitis type strain or the capsule-switching mutant, except in t
216 th the fully virulent B. anthracis Ames wild-type strain or the isogenic toxin-deficient mutants Delt
217 uited to the site of infection with the wild-type strain or the mutant strain complemented with lipA
221 its greater genetic diversification than the type strain PA01, despite its lower per base mutation ra
223 that OMVs generated from P. aeruginosa wild-type strain PAO1 were more cytotoxic to alveolar epithel
224 s significantly reduced compared to the wild-type strain PH-1, while 10 Group 2 mutants grew normally
225 n model, 1 week following infection the wild-type strain produced significantly more widespread lesio
226 of 239 samples (M. gallisepticum vaccine and type strains, pure cultures, and clinical samples) origi
227 ic map derived from a cross between the drug-type strain Purple Kush and the hemp variety "Finola." T
228 nuated in the mouse and equine, whereas wild-type strain RacL11 induces severe inflammation of the lu
229 ore, impairment of the Sec pathway in a wild-type strain reduced Ag43 production but did not signific
230 Cse4, transient induction of PSH1 in a wild-type strain resulted in phenotypes similar to a pat1 str
231 ficient S. aureus and the corresponding wild-type strain reveal that activation of acid sphingomyelin
232 omic comparisons between one isolate and the type strain revealed an average nucleotide identity of 9
233 The average genome configuration of the wild-type strain revealed strong intra- and inter-chromosomal
234 a leaky Escherichia coli strain and the wild-type strain reveals the contribution of the formidable o
236 ium salmoniphilum and Mycobacterium chelonae type strains, seven M. salmoniphilum isolates, and five
238 e accurate diagnosis among other prevalent B-type strains, simultaneous detections of four conserved
239 rved in domesticated and undomesticated wild-type strains sporulating in liquid and on solid media.
240 efficiency equal to that seen with the wild-type strain, suggesting that competing commensal organis
241 her of these cell lines relative to the wild type strain, suggesting that it is attenuated in virulen
242 as still less virulent in vivo than the wild-type strain, suggesting that SecA2 function was still re
243 n adhesion level similar to that of the wild-type strain, suggesting that the gene does not direct at
244 t spread in tomato stems as well as the wild-type strain, suggesting that these exDNases facilitate b
245 d for stable colonization relative to a wild-type strain, suggesting the presence of genotoxic stress
246 revealed numerous clades that do not contain type strains, suggesting considerable species level dive
251 l1951 strain was similar to that of the wild-type strain, the viability of the Deltasll1951 strain wa
252 uring amino acid stress, whereas in the wild-type strain these levels declined under the same growth
254 nd characterization of Nanosynbacter lyticus type strain TM7x (HMT_952)-the first Saccharibacteria st
255 e generated through seeds by crossing a wild-type strain to a transgenic strain with altered centrome
256 ta mutant was less susceptible than the wild-type strain to noniron metalloporphyrins, further indica
257 with altered biofilm formation and the wild-type strain to predict drug targets against P. aeruginos
259 gnotobiotic mice together with 11 other wild-type strains to generate a 15-member artificial human gu
260 molecular clock for VP1 of circulating wild-type strains to infer that the mean time from the initia
261 comparative genome sequence analysis of wild-type strain TX82 and TX6051 and found a single mutation,
262 ing medium and grew slower than did the wild-type strain under aerobic and anaerobic conditions, at l
266 lted in the inability to compete with a wild-type strain under selective conditions that required spo
269 ed on the V-nitrogenase on acetate, the wild-type strain uses exclusively the Mo-nitrogenase on both
272 oid tissues and reveals the protective (wild-type strain) versus harmful (yopP-deficient strain) cons
273 NA-mRNA interactions between Drosophila wild-type strain W(1118) and a mutant of the key circadian tr
275 e to tolerate 100 mM serine whereas the wild type strain was already inhibited by 1 mM of the amino a
276 iet did not affect the outcome that the wild-type strain was better able to persist and colonize.
277 n static conditions, the fitness of the wild-type strain was higher under fluctuating humidity condit
278 d-Kah) element isolated from the Kahuku wild-type strain was highly degenerate and appeared to have a
281 tions, a pair of congenic a and alpha mating type strains was generated by a series of 11 backcrosses
282 dependent growth arrest, and unlike the wild-type strain, was susceptible to fatty acid synthesis inh
283 from five single gene knockouts and the wild type strain, we decrease the mean squared error of predi
285 Edmonston vaccine/laboratory and IC323 wild-type strains were equally affected by the inhibitors.
288 is Tn library, and in various C. jejuni wild type strains, were compared and correlated to detect gen
289 tant was the same as that of the parent wild-type strain when cultured in nutrient-rich media with or
291 substantial fraction of isoleucine in a wild-type strain when propionate is available in the medium.
292 vel in the DeltaytoI strain than in the wild-type strain, whereas two genes (lmo1917 and lmo2103) dem
294 P as well as stimulates swarming in the wild-type strain, while overexpression of MotA from a plasmid
296 tivity of M. pulcherrima, we compared a wild-type strain with a spontaneously occurring, pigmentless,
297 larly, bombardment of a morphologically wild-type strain with the Cas9 plasmid and sgRNA plasmids tar
299 more-severe pulmonary infection by the wild-type strain (with a 30-fold increase in the number of co
300 using a virulent C. perfringens type D wild-type strain (WT), an isogenic ETX null mutant (etx mutan