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1 bacterium bovis, Mycobacterium ulcerans, and Mycobacterium marinum.
2 ram-positive bacterium Bacillus subtilis, or Mycobacterium marinum.
3 ents of lipooligosaccharide IV (LOS-IV) from Mycobacterium marinum.
4 r for the analysis of culture filtrates from Mycobacterium marinum.
5 m tuberculosis, Mycobacterium bovis BCG, and Mycobacterium marinum.
6 complexity, the secreted protein fraction of Mycobacterium marinum.
7 istinct patterns of innate susceptibility to Mycobacterium marinum.
8 nd mel2, that affect macrophage infection by Mycobacterium marinum.
9 urally susceptible to tuberculosis caused by Mycobacterium marinum.
10 acterium tuberculosis, and 85.9% homology to Mycobacterium marinum.
11 urA-katG loci in the nontuberculous pathogen Mycobacterium marinum.
12 alyse the initial response of neutrophils to Mycobacterium marinum, a close genetic relative of M. tu
13 generated a mutation in the erp homologue of Mycobacterium marinum, a close genetic relative of M. tu
14 urally susceptible to tuberculosis caused by Mycobacterium marinum, a close genetic relative of the c
16 ographic structure determination of NAT from Mycobacterium marinum, a close relative of the pathogeni
21 Ts required for lytic activity, we leveraged Mycobacterium marinum, a nontubercular pathogen and a mo
22 ulosis, the cause of human tuberculosis, and Mycobacterium marinum, a nontubercular pathogen with a b
23 X-1 substrates in secretion and virulence in Mycobacterium marinum, a pathogen of humans and animals.
25 We infected murine RAW264.7 macrophages with Mycobacterium marinum, a surrogate model organism for M.
28 of the ESX-1 substrate pair EsxB_1/EsxA_1 in Mycobacterium marinum Although this substrate pair was h
31 poson mutants of the closely related species Mycobacterium marinum and Mycobacterium avium harboring
32 collaborated to characterize an outbreak of Mycobacterium marinum and other nontuberculous mycobacte
33 ycolyl-diarabino-glycerol, was purified from Mycobacterium marinum and subsequently identified as a 5
34 sterase) in the opportunistic human pathogen Mycobacterium marinum and the characterization of this m
35 or studying mycobacterial pathogenesis using Mycobacterium marinum and the goldfish, Carassius auratu
36 andii, is closely related to M. ulcerans and Mycobacterium marinum, and as further evidence is gather
39 re challenged with Salmonella typhimurium or Mycobacterium marinum at earlier stages of development,
41 is essential for ESX-5-mediated secretion in Mycobacterium marinum, but for which the role in secreti
42 duction was isolated from the photochromogen Mycobacterium marinum by heterologous complementation of
43 network that results in iniBAC induction in Mycobacterium marinum By transposon mutagenesis, we iden
44 In zebrafish, we find that susceptibility to Mycobacterium marinum can result from either inadequate
52 rafish with natural fish pathogens including Mycobacterium marinum has significantly advanced our und
53 eria, such as Mycobacterium tuberculosis and Mycobacterium marinum, have up to five of these systems,
54 screen for determinants of susceptibility to Mycobacterium marinum identified a hypersusceptible muta
56 Mtmr4-specific siRNA were more resistant to Mycobacterium marinum-induced phagosome arrest, associat
62 es host immune responses in vivo, we studied Mycobacterium marinum infection in two different hosts:
64 f the tuberculous granuloma in the zebrafish-Mycobacterium marinum infection model, which is characte
65 restricting mycobacteria growth, we examined Mycobacterium marinum infection of Drosophila S2 cells.
67 et al., (2016) using the zebrafish model of Mycobacterium marinum infection provides new insights in
68 wed TriSLas to protect zebrafish larvae from Mycobacterium marinum infection, suggesting a vulnerabil
69 rison of intravenous and hindbrain routes of Mycobacterium marinum infection, which are indistinguish
71 erculosis, and its close pathogenic relative Mycobacterium marinum, initially infect, evade, and expl
77 ation to conclude that the MMAR_0039 gene in Mycobacterium marinum is required to promote Esx-1 expor
81 We recently identified inhibitors targeting Mycobacterium marinum MelF (Rv1936) by in silico analysi
82 antimicrobial activity was assessed against Mycobacterium marinum (Mm) (a model for Mtb), Pseudomona
84 to mycobacteria in vivo, we used a zebrafish Mycobacterium marinum (Mm) infection tuberculosis model.
92 compartments disrupted after infection with Mycobacterium marinum or after sterile damage caused by
95 erculosis, and its close pathogenic relative Mycobacterium marinum, preferentially recruit and infect
96 crimination of wild type and DeltaRD1 mutant Mycobacterium marinum strains in a zebrafish embryo mode
97 We conducted a genetic screen to identify Mycobacterium marinum strains which failed to lyse amoeb
99 However, work in zebrafish infected with Mycobacterium marinum suggests that granulomas contribut
100 We analyzed the gene expression profile of Mycobacterium marinum, the cause of fish and amphibian t
101 several genes preferentially expressed when Mycobacterium marinum, the cause of fish and amphibian t
102 cobacterium liflandii, and the fish pathogen Mycobacterium marinum; the structural diversity in the m
103 cobacterium bovis Bacille Calmette-Guerin or Mycobacterium marinum to thiacetazone, a second line ant
105 ecent studies have shown that superinfecting Mycobacterium marinum traffic rapidly to established fis
107 e secretion of PE_PGRS proteins by screening Mycobacterium marinum transposon mutants for secretion d
108 Finally, we show that flies infected with Mycobacterium marinum undergo a process like wasting: Th
111 we determined for the intracellular pathogen Mycobacterium marinum whether it uses conserved strategi
112 regulating the levels of ESX-1 substrates in Mycobacterium marinum WhiB6 is a transcription factor th
113 gravis developed a cutaneous infection with Mycobacterium marinum, which apparently resolved followi