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1 uch systems underwent rapid shifts to the WT morphotype.
2 ase HadABC complex, was constructed in the R morphotype.
3 lebs, as well an onset of a wrinkled surface morphotype.
4 he parental mycolic acid profile and cording morphotype.
5 ched cocci (persister) form became the major morphotype.
6 ptibility testing of a single colony of each morphotype.
7 itidis, for expression in yeast and mycelial morphotypes.
8 g that OMTs may transition between these two morphotypes.
9 are self-righting potential of the two shell morphotypes.
10 morphology and assume at least four distinct morphotypes.
11 nd coexistence of "round" and "fuzzy" colony morphotypes.
12 ubclades of the IRLC with distinct bacteroid morphotypes.
13 tinct consequences for the growth of the two morphotypes.
16 first study to comprehensively compare body morphotype, adipokines, and cytokine responses between p
20 sed after transition to the pathogenic yeast morphotype and is regulated by a mechanism for phase-spe
23 SIRV2 and STIV have fundamentally different morphotypes and genome sequences, it is surprising that
24 ica oleracea accessions representing various morphotypes and identified signals of selection at the m
25 ed against metabolically active A. fumigatus morphotypes and is stronger against membrane protein fra
26 52); or between those with Lactobacillus spp morphotypes and those without (70.48% vs 74.08%; pintera
27 with detected G vaginalis or Bacteroides spp morphotypes and those without these morphotypes (efficac
28 thought to be the important infectious cell morphotype, and after inoculation into a suitable host,
29 pathway was increased compared with the SmT morphotype, and inhibition of ERK resulted in decreased
31 radiolabeled deacylated lipids from the SmT morphotype, by high-performance liquid chromatography an
32 In both WS and BrB, there were two ciliate morphotypes consistently represented in all disease lesi
34 otal fish fauna and that of the two dominant morphotypes (Coryphaenoides sp. 1 and C. profundicolus)
38 Our finding that the most heavily calcified morphotype dominates when conditions are most acidic is
39 ides spp morphotypes and those without these morphotypes (efficacy 68.62% vs 76.72%; pinteraction=0.6
40 titate the relative amounts of each distinct morphotype, followed by antibiotic susceptibility testin
41 ing competing hypotheses about the ancestral morphotype for crown catarrhines, early catarrhine phylo
48 sotope and abundance measurements on the two morphotypes in sediment trap, core-top, and downcore sam
49 cal analyses disclosed bacteria with several morphotypes, including spiral-shaped, in the cytoplasm a
50 and we hypothesize that many of the "novel" morphotypes interpreted to occur among archosaurs later
52 parent (SmT) or smooth opaque (SmO), the SmO morphotype is avirulent, whereas the SmT morphotype is v
54 vocal-sonic central pattern generator (CPG) morphotype is proposed for fishes and tetrapods that sha
58 notypes were identified only in B. anthracis morphotypes isolated from the letters, indicating that t
59 ysiological differentiation among three crop morphotypes (leaf, turnip, and oilseed) and for correlat
61 hybridization between more and less advanced morphotypes might have resulted in agricultural improvem
66 ructions depend on assumptions regarding the morphotype of the Homo-Pan last common ancestor (LCA).
68 research studies is enumeration of bacterial morphotypes of a Gram-stained vaginal smear (i.e., Nugen
70 ntification of clinically important, similar morphotypes of Aspergillus spp. within the section Fumig
72 hat there is a pronounced seasonality in the morphotypes of Emiliania huxleyi, the most abundant cocc
73 ty of these properties of sun and shade leaf morphotypes of Ginkgo biloba trees under the present atm
75 butes between territorial and nonterritorial morphotypes of side-blotched lizards, Uta stansburiana,
78 previously healthy women with a slender body morphotype, often with scoliosis and/or pectus excavatum
80 ghlight the derived nature of the glyptodont morphotype, one aspect of which is a spectacular increas
81 ssociated with >30 Gardnerella or Prevotella morphotypes per high-power field, as detected by Gram st
82 three morphotypes revealed that only the SmT morphotype possessed what appeared to be lipid component
83 ere has been considerable debate as to which morphotype predominates during urinary tract infection.
84 We conclude that, by far, the predominant morphotype present in the urinary tract during ascending
86 ributed species in each ocean is composed of morphotypes previously described as separate species.
87 ong the most diverse prokaryotic phyla, with morphotypes ranging from unicellular to multicellular fi
88 brook 7H10, however, revealed three distinct morphotypes representing smooth opaque (SmO), smooth tra
89 sion of the other to achieve the filamentous morphotype required for sexual development in Cryptococc
90 antigen; this antigen was not restricted to morphotypes resembling only cocci but was also present o
91 APK) pathway following infection with either morphotype revealed that all three members of the MAPK p
92 atographic analysis of lipids from the three morphotypes revealed that only the SmT morphotype posses
93 work on the two principal white G. ruber (W) morphotypes, sensu stricto (ss) and sensu lato (sl), has
97 2 ng/mL) than by the more virulent LR114 SmT morphotype strain (2.4 +/- 0.6 ng/mL; P < .05, paired t
98 ed rough-smooth, flat, and transparent (SmT) morphotype strain 86m2096 (26.8 +/- 5.2 ng/mL) than by t
101 kground yielded a nonreverting smooth-colony morphotype that produced no detectable EPS(ETr) and did
102 Here, we report a genus-specific starch morphotype that provides a means to identify chili peppe
103 sed reversible phase variation in the colony morphotype that was associated with extracellular polysa
104 stinctive part of the virosphere and display morphotypes that are not associated with the other two d
106 versification into heading and tuber-forming morphotypes through convergent subgenome parallel select
108 viruses' distinctiveness extends from their morphotypes to their genome sequences and the structures
109 linked to the domestication of the tuberous morphotypes, turnip (B. rapa) and kohlrabi (B. oleracea)
110 ained distinct reproductive castes including morphotypes unknown in solitary aculeate (stinging) wasp
115 escent protein in both swimming and swarming morphotypes, was constructed to quantify the prevalence
120 quired for the biogenesis of the thick pilus morphotype which, in turn, is necessary for motility (he
121 PK) resulted in attenuated growth of the SmT morphotype, which correlated with reduced PGE(2) product
122 can produce different pilus-dependent colony morphotypes, which have been previously shown to reflect
124 might take on the parental or a non-parental morphotype, with both daughter cells showing robust expr
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