ライフサイエンスコーパス: biotype

1 ) and those in which it was not (i.e., thick biotype).

2 in biotype; group 2 = 50 patients with thick biotype).

3 zed gingiva (WKG) and assessment of gingival biotype.

4 otype in nine sites that had an initial thin biotype.

5 atinized gingiva, and assessment of gingival biotype.

6 on in individuals with a thick-flat gingival biotype.

7 see-accessed, glyphosate-resistant horseweed biotype.

8 ing phages for the Vibrio cholerae O1 El Tor biotype.

9 but not within those of a whitefly nonvector biotype.

10 ing certain characteristics of the classical biotype.

11 onization by V. cholerae O1 of the classical biotype.

12 seem to be influenced by the adjacent teeth biotype.

13 uces CT expression in the V. cholerae El Tor biotype.

14 by Vibrio cholerae O1 strains of the El Tor biotype.

15 at a fivefold higher level in the classical biotype.

16 s higher in the classical than in the El Tor biotype.

17 peptides, and iron was higher in the El Tor biotype.

18 e virulence gene expression in the classical biotype.

19 e genes were regulated by VieA in the El Tor biotype.

20 type are controlled by VieA in the classical biotype.

21 te-resistant' and a 'glyphosate-susceptible' biotype.

22 k peri-implant biotype as compared to a thin biotype.

23 5-fold higher IC(50)(glyphosate) for the (R) biotype.

24 by Vibrio cholerae serogroup, serotype, and biotype.

25 ins expressing the mature EPSPS from the (S) biotype.

26 usceptible biotype compared to the resistant biotype.

27 e to which is used as a marker of the El Tor biotype.

28 hat only functions in the V. cholerae El Tor biotype.

29 Tor that is not functional in the classical biotype.

30 specific activity compared to the classical biotype.

31 s nearly silent in V. cholerae of the El Tor biotype.

32 mechanism of glyphosate resistance in parent biotype.

33 ility in Vibrio cholerae O1 of the classical biotype.

34 biotype in 9 sites which had an initial thin biotype.

35 inized tissue, and thickness of the gingival biotype.

36 tinized tissue and thickness of the gingival biotype.

37 s NTHI strains using PCR capsule typing, and biotyped.

38 ed with glyphosate-resistant or -susceptible biotypes.

39 CYDV-RPV was determined in all genotypes and biotypes.

40 lly independent, field-collected S. graminum biotypes.

41 nt increase in CT and TCP expression in both biotypes.

42 clustering based on IS1016, hmw or hia, and biotypes.

43 ype A) and sexually transmitted (serotype D) biotypes.

44 inically to distinguish classical and El Tor biotypes.

45 ic, low-pathogenicity, and highly pathogenic biotypes.

46 nd to be differentially expressed in the two biotypes.

47 in carbohydrate metabolism between these two biotypes.

48 expressed at similar levels in both cholera biotypes.

49 ty (GMD) as an independent validator for the Biotypes.

50 erated just a small consensus of significant biotypes.

51 phosate-resistant and glyphosate-susceptible biotypes.

52 ipolar psychosis); this was not the case for biotypes.

53 rties of Rosalia, Montero and Leiva 1 lucuma biotypes.

54 he divergence between host plant specialized biotypes.

55 omain structure distinct from that of either biotype 1 or biotype 2.

56 e that encodes MARTX(Vv) in 40 V. vulnificus Biotype 1 strains and found four distinct variants of rt

57 Biotype 1 strains of V. vulnificus are most commonly ass

58 We examined 69 V. vulnificus biotype 1 strains that were genotyped by several methods

59 spect to pathogenicity, i.e., nonpathogenic (biotype 1A), low pathogenicity (biotypes 2 to 5), and hi

60 However, seven other biotype 1B strains sequenced did possess the domain.

61 ty (biotypes 2 to 5), and highly pathogenic (biotype 1B).

62 re distinct from that of either biotype 1 or biotype 2.

63 npathogenic (biotype 1A), low pathogenicity (biotypes 2 to 5), and highly pathogenic (biotype 1B).

64 d analysis of the MARTX toxin and found that biotype 3 MARTX toxin has an effector domain structure d

65 This is the first demonstration that the biotype 3 MARTX toxin is essential for virulence and tha

66 nctional autoprocessing RTX (MARTX) toxin of biotype 3 strains was shown to be an essential virulence

67 cognized variant of V. vulnificus designated biotype 3.

68 y regulates gene expression in the classical biotype; 401 genes (10.3% of the genome), including thos

69 ter rodentium (formally Citrobacter freundii biotype 4280) is a highly infectious pathogen that cause

70 Clostridium perfringens biotype A strains are the causative agents of gas-gangre

71 ed with vinifera-based rootstocks, known as "biotype A".

72 We carried out mutant screens of both biotypes, aiming to identify classical V. cholerae mutan

73 cataloguing the profiles based on the known biotypes, all the employed RNA-Seq methods generated jus

74 from assembling the unmapped reads pooled by biotype allowed us to recover some divergent genomic reg

75 als and evaluate potential correlations with biotype, along with other clinical parameters.

76 ontrast brain anatomy characteristics across Biotypes alongside conventional diagnoses, examining gra

77 The gingival biotype also showed a thick biotype in 9 sites which had

78 The gingival biotype also showed a thick biotype in nine sites that h

79 Both classical and El Tor biotypes alternated and persisted between 1966 and 1988;

80 tient and site characteristics, e.g., tissue biotype and buccal plate thickness.

81 and a greater methylation compared to the G1 biotype and healthy controls.

82 and in PBMCs by V. cholerae varies with the biotype and is mediated by both NLRP3-dependent and -ind

83 bolites and functional properties related to biotype and ripeness stage.

84 e factors that drove emergence of the El Tor biotype and the displacement of the classical biotype ar

85 relatives, and healthy subjects organized by Biotype and then by DSM-IV-TR diagnosis (n = 1409) using

86 IIP in thick biotype and with immediate provisionalization had less M

87 alue in seed total flavanols compared to all biotypes and cultivars.

88 We show that XRNAX captures all RNA biotypes and use this to characterize the sub-proteomes

89 s in which the probe was visible (i.e., thin biotype) and those in which it was not (i.e., thick biot

90 are colonized on average with five commensal biotypes, and it is widely thought that the commensals s

91 expressed in the classical versus the El Tor biotype are controlled by VieA in the classical biotype.

92 s, we conclude that the strains of classical biotype are likely defective compared to those of El Tor

93 iotype and the displacement of the classical biotype are unknown.

94 iation in pathogenesis and whether different biotypes are associated with specific nonhuman hosts are

95 oted in the presence of a thick peri-implant biotype as compared to a thin biotype.

96 uccal plate thickness between thick and thin biotypes as determined by probe visibility.

97 Most genogroups had consistent biotypes (as determined with the RapID ANA II system); h

98 ype were significantly greater than the thin biotype at MT, MI, and DT (P<0.05).

99 Here, we sampled seeds from one plant (= biotype) at 24 sites in Ohio and 20 in Iowa, screened th

100 iated with only AXR#1 rootstock, defined as "biotype B", and another group associated with vinifera-b

101 roteins differentially expressed between the biotypes before and after glyphosate treatment.

102 or biotype compared to that of the classical biotype both as a global cause of cholera and as an envi

103 sequently displaced strains of the classical biotype both in the environment and as a cause of choler

104 , gender, jaw, craniofacial growth, gingival biotype, buccal bone dehiscence after extraction, space

105 old standard to discriminate thick from thin biotype but is prone to subjective interpretation.

106 ior foregut or cibarium of a whitefly vector biotype but not within those of a whitefly nonvector bio

107 olera pandemics were caused by the classical biotype, but El Tor has subsequently spread globally and

108 slightly less in IIP with thick versus thin biotypes, but not statistically significantly different

109 We determined the VieA regulon in both biotypes by transcriptome comparison of wild-type and vi

110 Biotyping by MALDI-TOF-MS will prove effective in situat

111 orption ionization (MALDI) mass spectrometry biotyping can be used for measurement of cellular potenc

112 These biotypes cannot be differentiated solely on the basis of

113 However, the evolution of new soybean aphid biotypes capable of defeating host-plant resistance conf

114 Although strains of the El Tor biotype caused sporadic infections and cholera epidemics

115 th whole live M. mycoides subsp. mycoides SC biotype cells, indicating cellular proliferation.

116 A and motility to the pathogenesis of El Tor biotype cholera.

117 s, whereas a previous pandemic strain of the biotype Classical is polymyxin-sensitive.

118 In Vibrio cholerae, two natural epidemic biotypes, classical and El Tor, exhibit distinct phenoty

119 rae strains of the O1 serogroup exist as two biotypes, classical and El Tor.

120 arrheal disease cholera, is divided into two biotypes: classical and El Tor.

121 olutionary fitness of the V. cholerae El Tor biotype compared to that of the classical biotype both a

122 ed production were higher in the susceptible biotype compared to the resistant biotype.

123 nique brain structure characteristics within Biotypes, consistent with their cognitive and sensorimot

124 rine substitution at position 106 in the (R) biotype, corresponds to a substitution previously identi

125 We hypothesized that commensal biotypes could exert colonization resistance by consumin

126 lthough some differences were detected among biotypes, data indicate that biotype does not play a fun

127 ided into four neurophysiological subtypes ('biotypes') defined by distinct patterns of dysfunctional

128 Analysis of a defined mutation in the El Tor biotype demonstrated that msbB is required for resistanc

129 One gene from the resistant biotype, designated PPX2L, contained a codon deletion th

130 Bone width and soft-tissue biotype did not influence the incidence of gingival papi

131 egion near the N terminus (L8P) in both BVDV biotypes did not antagonize IFN-alpha/beta production, c

132 rsisted between 1966 and 1988; the classical biotype disappeared by 1988, and the O139 serogroup firs

133 ize the variants, including an assessment of biotype-distinguishing characteristics.

134 s similar to that in human in terms of size, biotype distribution, and family composition (e.g. with

135 can be concluded that bone width and tissue biotype do not have an effect on the incidence and heigh

136 detected among biotypes, data indicate that biotype does not play a fundamental role in influencing

137 Current pandemic O1 Vibrio cholerae biotype El Tor is resistant to polymyxins, whereas a pre

138 solates are closely related to serogroup O1, biotype El Tor V. cholerae, and comprise a single sublin

139 pandemic V. cholerae serogroups O1 and O139 biotype El Tor(2-4).

140 rt, cases of V. cholerae O1 (serotype Ogawa, biotype El Tor) were confirmed in all 10 administrative

141 rly as 1910, it was not until 1961 that this biotype emerged to cause the 7th pandemic, eventually re

142 Toxigenic strains of the El Tor biotype emerged to cause the seventh pandemic of cholera

143 ressing the mature EPSPS enzyme from the (R) biotype exhibited an approximately 3-fold increase in gl

144 'Liatiko' and its biotypes exhibited different polyphenolic profiles betwe

145 sites in Ohio and 20 in Iowa, screened these biotypes for levels of resistance, and sequenced their D

146 ntification of two novel distinct epigenetic biotypes for PTSD may have future utility in understandi

147 avian-adapted S. enterica serovar Gallinarum biotypes Gallinarum and Pullorum, and the most frequent,

148 quenced the genome of a UK clinical isolate (biotype gravis strain NCTC13129), representative of the

149 ed the strain as nontoxigenic C. diphtheriae biotype Gravis.

150 ional study (group 1 = 50 patients with thin biotype; group 2 = 50 patients with thick biotype).

151 In V. cholerae strains of the classical biotype, H-NS has been reported to silence virulence gen

152 Tissue biotypes have been linked to the outcomes of periodontal

153 In both biotypes, herbicide effectiveness was reduced when plant

154 Periodontal biotype, horizontal and vertical peri-implant bone defec

155 y on plants previously attacked by the other biotype, however, on their respective noninfested contro

156 ins were more often biotype V (P < 0.001) or biotype I (P = 0.04) than IS1016-negative NTHI strains,

157 Two of the S. bovis biotype I cases were associated with colon cancer.

158 nt of a PCR test which can identify S. bovis biotype I strains among S. bovis clinical isolates.

159 We describe here the isolation of biotype I-specific DNA sequences and the development of

160 s variant (sometimes referred to as S. bovis biotypes I and II, respectively) are phenotypically simi

161 The majority of IS1016-positive NTHi were biotypes I and V and showed some genetic relatedness by

162 S. bovis is divided into two biotypes: I and II.

163 negative NTHI strains, which were most often biotype II.

164 nus, previously known as Streptococcus bovis biotype II.2, is an uncommon pathogen in neonates.

165 nus, previously known as Streptococcus bovis biotype II.2, is known to cause multiple infectious comp

166 ingitis caused by S. bovis variant (S. bovis biotype II/2) and review the literature.

167 enotypically reported as Streptococcus bovis biotype II/2, 16S rRNA sequencing revealed S. gallolytic

168 was identified as nontypeable H. influenzae, biotype III.

169 ing analysis of weedy rice (Oryza sativa L.) biotypes illuminates distinct evolutionary paths and out

170 The gingival biotype also showed a thick biotype in 9 sites which had an initial thin biotype.

171 the emerging concept of a lithium-responsive biotype in BD.

172 the enhanced survival capacity of the El Tor biotype in environmental reservoirs.

173 The gingival biotype also showed a thick biotype in nine sites that had an initial thin biotype.

174 y spread globally and replaced the classical biotype in the current pandemic.

175 ak calling to simultaneously profile all RNA biotypes in apheresis-prepared human plasma pooled from

176 ssical (O395) and El Tor (C6706) V. cholerae biotypes in growth and biochemical assays.

177 The commensal biotypes included E. coli HS, which is known to successf

178 ntial against M. mycoides subsp. mycoides SC biotype-induced mycoplasmemia.

179 y of recession during tooth movement in thin biotype is high to justify gingival augmentation when th

180 The classical biotype is susceptible to CAMPs, but current pandemic El

181 sate-resistant horseweed (Conyza canadensis) biotypes is an example of how unrelenting use of a singl

182 ptible to CAMPs, but current pandemic El Tor biotype isolates gain CAMP resistance by altering the ne

183 Haemophilus biotype IV strains belonging to the recently recognized

184 isolates in serogroup O1 (consisting of two biotypes known as 'classical' and 'El Tor') and the deri

185 We sequenced two isolates from the remaining biotype, LGV, a long-term laboratory passaged strain and

186 both alleles were present prior to pea aphid biotype lineage diversification, we estimated that the i

187 Thirty healthy patients with thin gingival biotype (<1 mm) and history of periodontal disease recei

188 and better PH maintenance in IIP with thick biotype (MFR: MD -0.478, P <0.001; cumulative PH: MD -0.

189 allow viticulturists to select the varieties/biotypes most appropriate for obtaining higher quality p

190 s to mitigate occurrence of the inflammatory biotype of depression.

191 mediators of resistance against an avirulent biotype of Hyaloperonospora parasitica.

192 characterized genome, and RNAi in the sexual biotype of the planarian Schmidtea mediterranea to test

193 artite system, which is restricted to EI Tor biotype of Vibrio cholerae O1.

194 Tissue biotypes of 22 fresh cadaver heads were assessed clinica

195 ip performed best, correctly classifying the biotypes of 371 of 380 (97.6%) different challenge strai

196 sequences of this bacterium from the B and Q biotypes of B. tabaci.

197 city of: (a) five obscure cultivars; (b) Six biotypes of cultivar 'Liatiko'; (c) Five prominent culti

198 Various biotypes of endogenous small RNAs (sRNAs) have been dete

199 The biotypes of Haemophilus influenzae and Haemophilus parai

200 The El Tor and classical biotypes of O1 V. cholerae show striking differences in

201 iations between disease states and different biotypes of S. bovis are apparent.

202 The two biotypes of V. cholerae O1 capable of causing cholera, c

203 Historically, the O1 El Tor and classical biotypes of Vibrio cholerae have been differentiated by

204 on patterns between the classical and El Tor biotypes of Vibrio cholerae O1 were determined under con

205 lence genes be-tween the two disease-causing biotypes of Vibrio cholerae, classical and El Tor, is pr

206 is being posed by the inexorable increase in biotypes of weeds that are resistant to herbicides.

207 potential long-term influence of periodontal biotype on the volume maintenance of block grafts.

208 rference confers immunity to all Hessian fly biotypes on normally susceptible wheat genotypes.

209 had less MFR and better PH than IIP in thin biotype or with delayed restoration.

210 ce of neonatal infection caused by different biotypes or newer species of S. bovis.

211 one dehiscence (P = 0.052) and thin gingival biotype (P = 0.054).

212 eSAB promoter by H-NS and HapR in the El Tor biotype prior to the cessation of exponential growth res

213 Both the classical and El Tor biotypes produce inactive ToxT protein when they are cul

214 Both biotypes produce the major virulence factors toxin-coreg

215 same species, and same susceptible-resistant biotype profile during any 7-day period) and uncontrolle

216 same species, and same susceptible-resistant biotype profile during any 7-day period) and uncontrolle

217 TG)-inducible M. mycoides subsp. mycoides SC biotype protein with a 28-kDa apparent molecular mass, i

218 enes from the M. mycoides subsp. mycoides SC biotype pyruvate dehydrogenase region, and two IPTG-inde

219 be significantly correlated with periodontal biotype (r = 0.325, P = 0.000) and post-suturing flap po

220 .2%) with thick-scalloped and thin-scalloped biotypes, respectively, had APE.

221 nificant anti-M. mycoides subsp. mycoides SC biotype responses were observed in mice vaccinated with

222 clinical isolate belonging to the O1 El Tor biotype responsible for the current cholera pandemic.

223 with same sensitivity-resistance profile and biotype results during any 7-day period) and uncontrolle

224 of a PPO-inhibitor-resistant A. tuberculatus biotype revealed that resistance was a (incompletely) do

225 red from the resistant (R) and sensitive (S) biotypes revealed an approximately 5-fold higher IC(50)(

226 PSPS mature protein coding regions from both biotypes revealed four single-nucleotide differences, tw

227 plasma mycoides subsp. mycoides small colony biotype (SC) is the high-consequence animal pathogen cau

228 and M. mycoides subsp. mycoides small colony biotype (SC), (ii) antibodies to specific peptide determ

229 iotypes scored as S, R1, or R2, while all 25 biotypes scored as R3 or R4 had the same proline-to-seri

230 The p106 mutation was not found in the19 biotypes scored as S, R1, or R2, while all 25 biotypes s

231 All 'Liatiko' biotypes scored the highest concentrations in seed total

232 All isolates were biotyped, serotyped by slide agglutination serotyping (S

233 istance to polymyxin B. msbB mutants of both biotypes showed decreased colonization of infant mice, w

234 Biotypes showed stronger between-group separation based

235 coli is a single species consisting of many biotypes, some of which are commensal colonizers of mamm

236 NA gene sequence analysis and recorded their biotypes, sources, and disease associations.

237 ion of HA/protease and motility in an El Tor biotype strain by constructing a Deltahns mutant.

238 This O1 biotype strain has 95 to 97% similarity with the classic

239 However, growth of El Tor biotype strain N16961 was enhanced due to its ability to

240 lting in the global elimination of classical biotype strains as a cause of disease.

241 genotypic and phenotypic differences, El Tor biotype strains displaying classical biotype traits have

242 In contrast, El Tor biotype strains expressed negligible LeuO under identica

243 en grown with added carbohydrates, classical biotype strains generated a sharp decrease in medium pH,

244 El Tor biotype strains induced release of IL-1beta dependent on

245 e ToxRS-dependent expression of CT in El Tor biotype strains is related to the differences between cl

246 ion was observed in the classical and El Tor biotype strains of serogroup O1 that is most frequently

247 In El Tor biotype strains of toxigenic Vibrio cholerae, the CTXvar

248 wed the same defect in growth that classical biotype strains show in media rich in carbohydrates.

249 Classical biotype strains, which do not produce either hemolysin o

250 ctxAB only on the large chromosome of El Tor biotype strains.

251 of CT, including levels typical of classical biotype strains.

252 regulator HapR, which is absent in classical biotype strains.

253 2) keratinized tissue width (KT); 3) tissue biotype (TB); and 4) plaque level.

254 onger discrimination for biologically driven biotypes than symptom-based diagnoses.

255 ts on adjacent teeth and in a thicker-tissue biotype that would be amenable to partial-thickness diss

256 d three neurobiologically distinct psychosis biotypes that did not respect clinical diagnosis boundar

257 S29 isoform was present in all genotypes or biotypes that efficiently transmit CYDV-RPV and more spe

258 Building on experimental constructs-Biotypes-that were previously developed from cognitive a

259 Even when adjacent teeth had a thin biotype, the transplanted sites maintained statistically

260 nses of the El Tor and classical V. cholerae biotypes to increased c-di-GMP concentrations were deter

261 e of Flight Mass Spectrometry (MALDI-TOF-MS) biotyping to deliver rapid and accurate strain separatio

262 om phenotypic analysis, such as serology and biotypes, to much-more-robust molecular genetic approach

263 MALDI should be accepted as a biotyping tool to complement and enhance standard molecu

264 holera toxin, lipopolysaccharide, and El Tor biotype traits can be confirmed.

265 El Tor biotype strains displaying classical biotype traits have been reported and subsequently were

266 a major regulator of genes in the classical biotype under virulence gene-inducing conditions.

267 red several properties with R2866: they were biotype V (indole and ornithine decarboxylase positive,

268 IS1016-positive NTHI strains were more often biotype V (P < 0.001) or biotype I (P = 0.04) than IS101

269 Multilocus sequence typing showed that most biotype V isolates belonged to the same phylogenetic clu

270 Restoring HapR expression in classical biotype V. cholerae repressed vieSAB transcription by bi

271 hapA) single and double mutants of an El Tor biotype V. cholerae strain.

272 in a ToxT-independent manner in a classical biotype V. cholerae, and that this activation requires t

273 We show that in classical biotype V. cholerae, LeuO cooperates with the nucleoid-a

274 A significant association of IS1016 with biotypes V and I and the presence of hia adhesins was fo

275 The V. cholerae classical biotype (V. cholerae(Cl)), which caused previous cholera

276 Probands grouped by Biotype versus healthy controls showed a stepwise patter

277 have constructed a relaxed mutant of El Tor biotype Vibrio cholerae strain C7258 by disruption of th

278 In El Tor biotype vibrios, transcription of vieSAB is repressed by

279 The influence of the peri-implant biotype was also examined.

280 The G2 biotype was associated with an increased PTSD risk and h

281 a mycoides subsp. mycoides small colony (SC) biotype was cloned into lambda ZAP Express, and two stro

282 One biotype was common to several genogroups, with all of th

283 Biotype was determined by probe visibility through the t

284 In addition, the peri-implant biotype was evaluated and categorized as thick or thin.

285 e resequencing of seven additional horseweed biotypes was performed.

286 wed that lipid A of the msbB mutant for both biotypes was underacylated compared to lipid A of the wi

287 lants (horizontal distance), and soft-tissue biotype were assessed in 29 interimplant areas in the up

288 /=3 mm from the osseous crest and thick-flat biotype were associated with greater tissue rebound.

289 hermore, 34 (75.6%) patients with thick-flat biotype were diagnosed with APE, whereas 30 (31.3%) and

290 mensions of peri-implant mucosa in the thick biotype were significantly greater than the thin biotype

291 oppositely dysregulated, suggesting that the biotypes were not simply a function of a dimensional rel

292 EB and GABA-PKC-CREB signaling pathways, the biotypes were oppositely dysregulated, suggesting that t

293 significant differences were detected among biotypes, whereas: 1) TT, 2) age, and 3) smoking habit w

294 of APE, clinical crown length, and gingival biotype, which was divided into three categories: thin-s

295 , and 4 = overfill), marginal tissue levels, biotype, width of keratinized tissue, and soft tissue th

296 yphenol amounts, and the differences between biotypes, will allow viticulturists to select the variet

297 Intraoral examination revealed a thick biotype with an adequate band of keratinized gingiva, Mi

298 xposure rapidly selected for Amaranthus spp. biotypes with reduced herbicide sensitivity over two gen

299 mba spray drift could select Amaranthus spp. biotypes with reduced herbicide sensitivity.

300 interacted with the vieSAB promoter of both biotypes with similar affinities and protected overlappi

301 hylation (DNAm) profiles identified two PTSD biotypes within the PTSD+ group, G1 and G2, associated w