ライフサイエンスコーパス: morphotype

1 he parental mycolic acid profile and cording morphotype.

2 ched cocci (persister) form became the major morphotype.

3 ptibility testing of a single colony of each morphotype.

4 uch systems underwent rapid shifts to the WT morphotype.

5 read stabilizing selection upon their 'fish' morphotype.

6 ering host immune responses elicited by each morphotype.

7 the gingival phenotype, the thicker the bone morphotype.

8 tide polymorphisms associated with the mrdar morphotype.

9 cquire phosphate fail to adopt the seed cell morphotype.

10 iption factor as a determinant of an Azorean morphotype.

11 straints associated with the ancestral molar morphotype.

12 oupled from both queen head size and soldier morphotype.

13 ase HadABC complex, was constructed in the R morphotype.

14 lebs, as well an onset of a wrinkled surface morphotype.

15 morphology and assume at least four distinct morphotypes.

16 nd coexistence of "round" and "fuzzy" colony morphotypes.

17 P morphotypes and between clades with shared morphotypes.

18 tinct consequences for the growth of the two morphotypes.

19 itidis, for expression in yeast and mycelial morphotypes.

20 distributions overlapped broadly across all morphotypes.

21 icated into many subspecies with distinctive morphotypes.

22 immune system, by comparing river with cave morphotypes.

23 colony comprising cercariae of two distinct morphotypes.

24 icularly with a loss of detachable leaf gall morphotypes.

25 rence larger than 0.5, amounts to 15.4 of 68 morphotypes.

26 were examined to study their behavior across morphotypes.

27 ant taxa (n = 131), with 83 distinct foliage morphotypes.

28 a sequential differentiation of promastigote morphotypes.

29 n the supply of the three commonly occurring morphotypes.

30 that different diet groups exhibit distinct morphotypes.

31 from both surface-dwelling and cave-dwelling morphotypes.

32 hed species, as well as within saber-toothed morphotypes.

33 ization of hyperspectrally delineated plaque morphotypes.

34 roducers and higher producers; and phytolith morphotypes.

35 are self-righting potential of the two shell morphotypes.

36 ubclades of the IRLC with distinct bacteroid morphotypes.

37 g that OMTs may transition between these two morphotypes.

38 The detailed morphology of morphotype 1 and well-preserved, discrete segments of mo

39 Morphotype 1 consists of a structure that superficially

40 als that it comprises up to three successive morphotype 1 specimens organised in a linear fashion and

41 e 1 and well-preserved, discrete segments of morphotype 2 closely resemble the dorsal exoskeleton of

42 Morphotype 2 displays more elongated, tubular morphology

43 Here, we systematically sampled 3 coral morphotypes, 2 fish species, and planktonic communities

44 l component analysis (PCA) discriminated the morphotypes; 50 compounds out of 192 identified had the

45 ed probability of occurrence of 68 megafauna morphotypes, a seabed area extending over 62,000 km(2) w

46 Spores are dormant bacterial morphotypes able to withstand harsh environments for dec

47 Of these, the thick pilus morphotype, absent in a mutant disrupted for the pilin-e

48 investigated potential monthly variations in morphotype abundance and biomass composition of sargassu

49 S. fluitans III was the most abundant morphotype across the year.

50 first study to comprehensively compare body morphotype, adipokines, and cytokine responses between p

51 e colonies transitioned from smooth to rough morphotypes, again indicating the influence of different

52 Some other, but not all, fibril morphotypes also exhibit dense threads, implying that th

53 ed telencephalon-that is absent in the other morphotype and Coccocephalus.

54 growth and development, and therefore plant morphotype and fertility.

55 Our species-level comparative analyses of morphotype and head size evolution reveal that these key

56 tion of a genetic correlation between female morphotype and immunological condition.

57 sed after transition to the pathogenic yeast morphotype and is regulated by a mechanism for phase-spe

58 fossils, that they correspond to an extinct morphotype and it cautions about the common practice of

59 Moreover, similar morphotypes and 16S gene sequences were retrieved from s

60 We identified 12 spore morphotypes and 47 VTs across 5 families within Glomerom

61 of the genetic status of described discrete morphotypes and aid in delivery of conservation programs

62 ferences between nearly all recognized GSSCP morphotypes and between clades with shared morphotypes.

63 ing novel associations between computational morphotypes and disease.

64 on individual plant species, for both damage morphotypes and feeding groups.

65 predict aboveground biomass, using phytolith morphotypes and forest cover as predictor variables.

66 SIRV2 and STIV have fundamentally different morphotypes and genome sequences, it is surprising that

67 ica oleracea accessions representing various morphotypes and identified signals of selection at the m

68 ed against metabolically active A. fumigatus morphotypes and is stronger against membrane protein fra

69 rved ichnofossils including two burrow/trail morphotypes and microcoprolites that are attributed to a

70 ptomic analysis of fertilized eggs from both morphotypes and reciprocal F(1) hybrids showed a strong

71 aveled the complex interplay between Candida morphotypes and the gut bacterial microbiota and describ

72 variation in the relative abundance of three morphotypes and this could be traced to two distinct eas

73 52); or between those with Lactobacillus spp morphotypes and those without (70.48% vs 74.08%; pintera

74 with detected G vaginalis or Bacteroides spp morphotypes and those without these morphotypes (efficac

75 thought to be the important infectious cell morphotype, and after inoculation into a suitable host,

76 pathway was increased compared with the SmT morphotype, and inhibition of ERK resulted in decreased

77 mean head size across the three most common morphotypes, and head size distributions overlapped broa

78 hickness, keratinized tissue width, and bone morphotype are three important parameters used to catego

79 bly) abolishes cell motility, and both pilus morphotypes are absent.

80 entation in soil habitats, where filamentous morphotypes are highly prevalent and where environmental

81 Hyphal morphotypes are thus under both positive and negative se

82 rds, more than 35 million years before these morphotypes arose in the crown group.

83 systematic shifts in the distribution of 3D morphotypes as a function of cell type and seeding site,

84 o measure the degree of ramified vs. ameboid morphotypes as an indicator of activation state.

85 For immersion response, the morphotype associated with the low-shore-lengthened resp

86 A revealed a preference for hyphae, a fungal morphotype associated with virulence.

87 The results show that morphotype-based tumor sampling allows the detection of

88 rphotype bearing tricuspid teeth and a large morphotype bearing single-cusped teeth can be recognized

89 Among the Tanystropheus specimens, a small morphotype bearing tricuspid teeth and a large morphotyp

90 atistical analyses revealed three vestibular morphotypes, best explained by three locomotor categorie

91 ld be more effective than the current single-morphotype biopesticide, demonstrating that our synthesi

92 radiolabeled deacylated lipids from the SmT morphotype, by high-performance liquid chromatography an

93 that the formation of a small C. neoformans morphotype-called "seed" cells due to their colonizing a

94 driven by salinity and season, while the ECM morphotype community was determined by the soil fungal c

95 Within each coral morphotype, community composition is always determined b

96 y represented by six morphological patterns (morphotypes): complex tubular, desmoplastic, mucinous, p

97 In this study, we quantify the species and morphotype composition of Sargassum strandings in Barbad

98 In both WS and BrB, there were two ciliate morphotypes consistently represented in all disease lesi

99 Large morphotypes contained higher numbers of viable bacteria,

100 underscores the critical need to incorporate morphotype conversion into the prioritization of drug ta

101 otal fish fauna and that of the two dominant morphotypes (Coryphaenoides sp. 1 and C. profundicolus)

102 No particle morphotype could be unequivocally assigned to the sevent

103 Chemical profiles indicate each CP morphotype could trigger different immune response in pl

104 nstructions using a non-selective mixture of morphotypes could potentially be biased.

105 Most exhibited important morphotype-dependent variability within same tumor secti

106 Four of the eleven ciliate morphotypes detected contained coral algal symbionts, in

107 Across species, soldier morphotype determines entrance specialization and defens

108 In addition, morphotype did not predict mean head size across the thr

109 , we examine environmental influences on the morphotype distribution of Ewing Sarcoma, a pediatric ca

110 ells and decreased tissue specificity of the morphotype distribution.

111 The thin pilus morphotype does not appear to be altered in the pilA1 mu

112 We observe that SVs track morphotype domestication.

113 Our finding that the most heavily calcified morphotype dominates when conditions are most acidic is

114 ides spp morphotypes and those without these morphotypes (efficacy 68.62% vs 76.72%; pinteraction=0.6

115 state of mycobacteria into a soft mechanical morphotype, enhancing survival in macrophages.

116 ce in the PFG of two most prevalent parasite morphotypes, Filariopsis barretoi larvae and Strongyle-t

117 ving fungal form is defined by four distinct morphotypes: flagellated; zygomycetous; sac-bearing; and

118 titate the relative amounts of each distinct morphotype, followed by antibiotic susceptibility testin

119 ing competing hypotheses about the ancestral morphotype for crown catarrhines, early catarrhine phylo

120 ampla could be valuable in determining cyst morphotypes for other species in the lineage.

121 tty acids of each variety, a characteristic "morphotypes" for each oil variety was established.

122 n, experienced significant losses, but those morphotypes found on fast-swimming, pelagic sharks (e.g.

123 The morphotype frequency data are best explained by host-pat

124 a strong effect of Douglas-fir frequency on morphotype frequency that matches the data.

125 ion from a smooth (MAB(S)) to rough (MAB(R)) morphotype frequently occurs during chronic infection.

126 Moreover, it has a podoviral morphotype from the Caudoviricetes class with a 62.4 nm

127 Here, we report two distinct actinopterygian morphotypes from the latest Carboniferous-earliest Permi

128 collected beadlet anemones of two different morphotypes from three different shore heights.

129 cholerae O139, we show that cells with this morphotype gain a profound competitive advantage in colo

130 Compressed morphotypes had improved hydrodynamic stability (coastin

131 However, inflated morphotypes had improved maneuverability while rotating

132 diagnostic scales, the vast majority of cyst morphotypes have not been linked to specific species.

133 is limited because the vast majority of cyst morphotypes have not been linked to specific vegetative

134 scriptomes and chemical composition of three morphotypes, herein called RED, TAN, and BROWN.

135 Morphotypes historically given the name Acropora prolife

136 WT was the predominant morphotype in 26 (81%) of these samples and was absent i

137 nstructed to quantify the prevalence of each morphotype in ascending urinary tract infection.

138 two membranes, as well as vesicle chain-like morphotype in purified vesicle fraction.

139 ting fibrils and allowed us to identify this morphotype in STEM micrographs.

140 We identified more parasitic morphotypes in formalin-preserved samples but found no d

141 sotope and abundance measurements on the two morphotypes in sediment trap, core-top, and downcore sam

142 and distinguish between distinctly different morphotypes in the biomass, and these observations of di

143 ibodies and that sIgA influenced C. albicans morphotypes in the murine gut.

144 at 18 sites, we identified 23 oak gall wasp morphotypes in three guilds (leaf detachable, leaf integ

145 mplete but disarticulated skull of the large morphotype, including its endocast and inner ear, to rev

146 cal analyses disclosed bacteria with several morphotypes, including spiral-shaped, in the cytoplasm a

147 and we hypothesize that many of the "novel" morphotypes interpreted to occur among archosaurs later

148 They occur as four distinct morphotypes: irregular laminated convex plates that form

149 parent (SmT) or smooth opaque (SmO), the SmO morphotype is avirulent, whereas the SmT morphotype is v

150 A hypoxia-typic morphotype is generated through the expression of a subt

151 The newly discovered WT morphotype is multidrug resistant relative to other vari

152 vocal-sonic central pattern generator (CPG) morphotype is proposed for fishes and tetrapods that sha

153 quirements, the infectious and transmissible morphotype is the dormant spore.

154 SmO morphotype is avirulent, whereas the SmT morphotype is virulent.

155 The discontinuity between morphotypes is a consequence of extinction, indicating t

156 eatures indicate that one of these Brazilian morphotypes is more closely related to living actinopter

157 The clinical significance of the colonial morphotypes is unclear.

158 red to as Boreal, Pacific and Rocky Mountain morphotypes) is similar across the hybrid zones or wheth

159 notypes were identified only in B. anthracis morphotypes isolated from the letters, indicating that t

160 blocking the transition from yeast to hyphal morphotype, it has an immunomodulatory role on human den

161 Consequently, this morphotype leads to increased host inflammation, rapid d

162 ysiological differentiation among three crop morphotypes (leaf, turnip, and oilseed) and for correlat

163 stinal fungal commensalism by coating fungal morphotypes linked to virulence, thereby providing a pro

164 rmediate climate niches relative to parental morphotypes matches patterns for other plant and animal

165 These results suggest that territorial morphotypes may be more sensitive to changes in the spat

166 hybridization between more and less advanced morphotypes might have resulted in agricultural improvem

167 e that the transition from a smooth to rough morphotype not only impacts MAB's survival strategies bu

168 The third morphotype, not recognized in previous analyses, differs

169 The contrasting tail morphotypes observed between enantiornithines and early

170 Approximately half of the morphotypes occurred only on polymetallic nodules.

171 performed partial correlations of gall wasp morphotype occurrences on trees within regions).

172 To determine whether the WT morphotype occurs in humans, 32 MAI-positive clinical sa

173 address this, we have turned to the specific morphotype of Alphaproteobacterial stalks.

174 polyene metabolite causing the yellow colony morphotype of F. perrara.

175 The predominant morphotype of mycobacteriophage virions has a DNA-contai

176 ructions depend on assumptions regarding the morphotype of the Homo-Pan last common ancestor (LCA).

177 sm among an encapsulated and nonencapsulated morphotype of V. vulnificus.

178 geographic variation in the frequency of two morphotypes of a baculovirus that infects the Douglas-fi

179 research studies is enumeration of bacterial morphotypes of a Gram-stained vaginal smear (i.e., Nugen

180 mical composition and variability of various morphotypes of acorns from Quercus ilex have been determ

181 croscopy (SEM) to determine distribution and morphotypes of adhering microbes.

182 ntification of clinically important, similar morphotypes of Aspergillus spp. within the section Fumig

183 re, comparing the blind cave and the surface morphotypes of Astyanax mexicanus fish, we found heteroc

184 en the composition of the NCR family and the morphotypes of bacteroids.

185 dentified as well as several distinguishable morphotypes of each.

186 hat there is a pronounced seasonality in the morphotypes of Emiliania huxleyi, the most abundant cocc

187 ty of these properties of sun and shade leaf morphotypes of Ginkgo biloba trees under the present atm

188 Various morphotypes of large filamentous bacteria were isolated

189 ts were similar between the smooth and rough morphotypes of M. abscessus However, in cystic fibrosis

190 We also identify two morphotypes of maracuya that deviate from the core struc

191 Of the two common morphotypes of Mycobacterium avium, designated smooth tr

192 from genome assemblies of 16 representative morphotypes of neopolyploid Brassica napus accessions an

193 udies of life under boreholes found distinct morphotypes of perhaps >50 species.

194 butes between territorial and nonterritorial morphotypes of side-blotched lizards, Uta stansburiana,

195 microscopy, we were able to investigate the morphotypes of the bacteria in the urinary tract.

196 cing of 727 individuals representing diverse morphotypes of the Betta fish.

197 xygen tension on the macroscopic and biofilm morphotypes of the human fungal pathogen Aspergillus fum

198 d cryoelectron tomography to investigate the morphotypes of this double mutant.

199 rtebrate model, Astyanax mexicanus-different morphotypes of which survive in nutrient-rich surface an

200 previously healthy women with a slender body morphotype, often with scoliosis and/or pectus excavatum

201 The effects of climate and leaf morphotype on stomatal index were rather conserved (<1%)

202 n this paper, we revisit the topic of colony morphotype on the within-species scale and apply concept

203 ghlight the derived nature of the glyptodont morphotype, one aspect of which is a spectacular increas

204 investigate the spatial ecology of two coral morphotypes-"orange" and "pink" cup corals (likely Caryo

205 otype (sailors) enable motility, and smaller morphotype (passengers) presumably facilitate infection.

206 ssociated with >30 Gardnerella or Prevotella morphotypes per high-power field, as detected by Gram st

207 three morphotypes revealed that only the SmT morphotype possessed what appeared to be lipid component

208 ere has been considerable debate as to which morphotype predominates during urinary tract infection.

209 We conclude that, by far, the predominant morphotype present in the urinary tract during ascending

210 rsity of beak shapes paralleling many of the morphotypes present in extant passerine finches, thrushe

211 470 cranium from Kenya (Homo rudolfensis), a morphotype previously unrecognized at Olduvai.

212 ributed species in each ocean is composed of morphotypes previously described as separate species.

213 ysiological relevance of the distinct colony morphotypes produced by this bacterium.

214 ong the most diverse prokaryotic phyla, with morphotypes ranging from unicellular to multicellular fi

215 brook 7H10, however, revealed three distinct morphotypes representing smooth opaque (SmO), smooth tra

216 mb bone paleohistology reveal that the large morphotype represents a separate species (Tanystropheus

217 This reconstructed ancestral morphotype represents a testable hypothesis that can be

218 sion of the other to achieve the filamentous morphotype required for sexual development in Cryptococc

219 antigen; this antigen was not restricted to morphotypes resembling only cocci but was also present o

220 APK) pathway following infection with either morphotype revealed that all three members of the MAPK p

221 atographic analysis of lipids from the three morphotypes revealed that only the SmT morphotype posses

222 They are functionally specialized: larger morphotype (sailors) enable motility, and smaller morpho

223 21 marked a decade of holopelagic sargassum (morphotypes Sargassum natans I and VIII, and Sargassum f

224 work on the two principal white G. ruber (W) morphotypes, sensu stricto (ss) and sensu lato (sl), has

225 ifts in carbonate chemistry alone caused the morphotype shift.

226 Significantly, the more crownward morphotype shows a key neuroanatomical feature of extant

227 of M. avium presenting with all three colony morphotypes, SmO, SmT, and Rg.

228 Finally, H. capsulatum displays morphotype-specific expression of several genes, and a c

229 tumors) from 111 stage II-IV CRCs identified morphotype-specific gene expression profiles and molecul

230 lso highlights the importance of considering morphotype-specific genetic and functional adaptations w

231 prioritization of drug targets, as targeting morphotype-specific vulnerabilities could improve treatm

232 Skeletochronology of the small morphotype specimens indicates that they are skeletally

233 DNA extractions from pools of presorted and morphotyped specimens and using two levels of sample ind

234 We sought to show that a precise Af morphotype stage during spore swelling can trigger DCs t

235 2 ng/mL) than by the more virulent LR114 SmT morphotype strain (2.4 +/- 0.6 ng/mL; P < .05, paired t

236 ed rough-smooth, flat, and transparent (SmT) morphotype strain 86m2096 (26.8 +/- 5.2 ng/mL) than by t

237 Translucent and transparent morphotype strains were attenuated for virulence.

238 Both smooth and rough colony morphotype strains were initially present, but treatment

239 A "soft" mechanical morphotype switch enhances tolerance to intracellular ma

240 19;25:695-705.e5) reports that VRE undergo a morphotype switch in response to lithocholic acid (LCA)

241 This morphotype switch presents a potential non-bactericidal

242 was used to reveal a process of "mechanical morphotype switching" in mycobacteria exposed to host in

243 remodeling of fungal cell walls during their morphotype switching.

244 se cabbage and cabbage, with the non-heading morphotype Taicai as the control.

245 enting multiple ribotypes develop two colony morphotypes, termed rough and smooth, but the biological

246 xtensive cytoplasmic vacuolation, yielding a morphotype that is typical of necrosis.

247 kground yielded a nonreverting smooth-colony morphotype that produced no detectable EPS(ETr) and did

248 Here, we report a genus-specific starch morphotype that provides a means to identify chili peppe

249 sed reversible phase variation in the colony morphotype that was associated with extracellular polysa

250 stinctive part of the virosphere and display morphotypes that are not associated with the other two d

251 oformans' size variation represent inducible morphotypes that change host interactions to facilitate

252 e fitness and observation of distinct colony morphotypes that emerged.

253 We describe four distinct eggshell morphotypes that have been collected from this site and

254 e periodontal phenotype consists of the bone morphotype, the keratinized tissue (KT), and gingival th

255 versification into heading and tuber-forming morphotypes through convergent subgenome parallel select

256 Cell morphotypes/tissue components were compared between grou

257 ative cells that produced them, enabling the morphotype to be immediately linked to the synurophyte,

258 directly link three distinct pterosaur track morphotypes to specific pterodactyloid clades: ctenochas

259 viruses' distinctiveness extends from their morphotypes to their genome sequences and the structures

260 Oceanic mixing tends to blend the morphotypes together making it difficult to determine if

261 During this morphotype transition, the conidial cell wall undergoes

262 ofiling by microarrays of 202 tumor regions (morphotypes, tumor-adjacent normal tissue, supportive st

263 linked to the domestication of the tuberous morphotypes, turnip (B. rapa) and kohlrabi (B. oleracea)

264 ollowed by Nugent scoring based on bacterial morphotypes under the microscope is considered the gold

265 ained distinct reproductive castes including morphotypes unknown in solitary aculeate (stinging) wasp

266 nto a few ecologically meaningful functional morphotypes using field data from successive phases of t

267 s of retinal microglial cells as one of five morphotypes, using a support vector machine (SVM).

268 lates has concerned the effect of genetic or morphotype variation.

269 ed by PCR corresponded to specific bacterial morphotypes visible in vaginal fluid.

270 In summary, the white morphotype was common in humans and was favored in disea

271 The RT morphotype was heterogeneous with regard to infectivity.

272 escent protein in both swimming and swarming morphotypes, was constructed to quantify the prevalence

273 ly smaller build than the predominant modern morphotype were present in semi-arid southeastern Austra

274 Morphotypes were enumerated by dark-field microscopy.

275 All recovered morphotypes were identified and characterized according

276 All three morphotypes were identified as M. avium by standard bioc

277 The observed morphotypes were in remarkable agreement with the differ

278 Tissue and cell morphotypes were quantitated by 2 evaluators at 100 inte

279 Two small Paleodictyon morphotypes were recognized (average mesh size of 1.81 c

280 ed evolutionary gains and losses of the four morphotypes were reconstructed consistently across multi

281 ace in titan cells, a recently characterized morphotype where haploid 5-mum cells convert to highly p

282 quired for the biogenesis of the thick pilus morphotype which, in turn, is necessary for motility (he

283 PK) resulted in attenuated growth of the SmT morphotype, which correlated with reduced PGE(2) product

284 a albicans reveal that the pathogenic hyphal morphotype, which is specialized for adhesion and invasi

285 nia equina is linked to genetically distinct morphotypes, which are associated with different heights

286 can produce different pilus-dependent colony morphotypes, which have been previously shown to reflect

287 All denticle morphotypes, which reflect shark community composition,

288 chromatin features between surface and cave morphotypes, while retaining remarkably similar regulato

289 first genomic analysis of the Nostoc commune morphotype with a recent sample from the High Arctic and

290 Richness, estimated as the sum of morphotypes with a predicted probability of occurrence l

291 Cluster analysis identified five morphotypes with distinct spatial distributions, suggest

292 Morphotypes with dorsoventrally oblate headshields are h

293 For cabbage morphotypes with their typical leaf-heading trait, we id

294 might take on the parental or a non-parental morphotype, with both daughter cells showing robust expr

295 ments and accommodates the complete range of morphotypes within a single analytical framework.

296 We distinguished 170 morphotypes within the UK-1 contract area but species-ri

297 ts that a biopesticide made up of both viral morphotypes would be more effective than the current sin