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2 These results suggest a model in which both saprophytic and pathogenic growth of M. grisea is regula
4 f M. robertsii in the new range by enhancing saprophytic associations, and these benefits were mainta
5 eny with clusters of genes from a variety of saprophytic bacteria and phytobacteria, including Pseudo
6 ations, revealing that HrpZ is necessary for saprophytic bacteria carrying pHIR11 to elicit a typical
8 genes carried on cosmid pHIR11 that enables saprophytic bacteria like Escherichia coli and Pseudomon
12 is surprisingly more closely related to the saprophytic extremophile Bacillus haladurans and Bacillu
15 Infections follow traumatic implantation of saprophytic fungi and frequently require radical surgery
16 l America, follows traumatic implantation of saprophytic fungi and frequently requires radical surger
18 pha proteins MOD-D, MAGA, and CPG-2 from the saprophytic fungus Podospora anserina and the pathogenic
29 he culture supernatant of pathogenic but not saprophytic Leptospira inhibit the three complement path
31 e may be shaped by maintaining functions for saprophytic life stages while minimising opportunities f
32 ory plasmids thought to be necessary for the saprophytic lifestyle in soil show similar levels of gen
33 of the three quorum sensing circuits in the saprophytic lifestyle of B. thailandensis, and it provid
34 stances as nutrient sources) to maintain the saprophytic lifestyle rather than the virulence of the b
36 a genome: loss of genes advantageous for the saprophytic lifestyle; modulation of elements that its c
37 ine the gene-by-gene fitness of a generalist saprophytic marine bacterium (Vibrio sp. F13 9CS106) on
40 dimorphic" fungus, H. capsulatum exists as a saprophytic mold in soil and converts to the parasitic y
42 s completely on successful conversion of the saprophytic mycelial (mold) form of this fungus to a par
44 explore if this behaviour can be extended to saprophytic mycobacteria, whose more complex genomes enc
45 e the stringent response of a nonpathogenic, saprophytic mycobacterial species, Mycobacterium smegmat
50 rhizium robertsii is a versatile fungus with saprophytic, plant symbiotic and insect pathogenic lifes
51 pecies of Batrachochytrium to those of close saprophytic relatives reveals that pathogenicity is asso
53 ll wall-degrading enzymes synthesized by the saprophytic soil bacterium Cellvibrio japonicus, we sequ
56 (cryo-ET) was used to compare pathogenic and saprophytic species and examine the unique morphological
61 h in the fungus Arthrobotrys oligospora from saprophytic to nematode-predatory form; this predacious
62 gulation is critical for the transition from saprophytic to pathogenic growth and from vegetative to
63 ny orthologous gene families involved in the saprophytic trophic mode, while maintaining orthologs of
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