ライフサイエンスコーパス: pathogenic bacterium

1 ate that can facilitate the maintenance of a pathogenic bacterium.

2 argely determine the virulence of this plant-pathogenic bacterium.

3 et sites explains evolutionary patterns in a pathogenic bacterium.

4 PLC) is a secreted virulence factor for this pathogenic bacterium.

5 first demonstration of a shared ATPase in a pathogenic bacterium.

6 these AMPs acted cooperatively against this pathogenic bacterium.

7 of pyomelanin-mediated ferric reduction by a pathogenic bacterium.

8 engineering is routinely performed with the pathogenic bacterium Agrobacterium tumefaciens and simil

9 Streptococcus pneumoniae (SP) is a pathogenic bacterium and a major cause of community-acqu

10 um perfringens is a ubiquitous and versatile pathogenic bacterium and is implicated in the etiology o

11 rst to be described in a Gram-positive plant pathogenic bacterium and is responsible for the emergenc

12 olecular basis for symbiosis between a human pathogenic bacterium and its arthropod vector and deline

13 he majority of cases interpreted as a single pathogenic bacterium and would have resulted in antibiot

14 Bartonella henselae is a recently recognized pathogenic bacterium associated with cat scratch disease

15 The pathogenic bacterium Bacillus anthracis has become the s

16 oteins is essential for the virulence of the pathogenic bacterium Bacillus anthracis.

17 phore-binding protein from the gram-positive pathogenic bacterium Bacillus cereus that binds multinuc

18 mum), a serine protease secreted by the non-pathogenic bacterium Bacillus subtilis, induces plasma c

19 Xylella fastidiosa, a xylem-colonizing plant pathogenic bacterium, block its interaction with various

20 iated T cell activation in resistance to the pathogenic bacterium Burkholderia pseudomallei.

21 mensal bacterium enhances the virulence of a pathogenic bacterium by modulating its spatial location

22 Xylella fastidiosa is a Gram-negative plant-pathogenic bacterium causing many economically important

23 The pathogenic bacterium Chlamydia replicates in a eukaryoti

24 We have purified recombinant HrcA from the pathogenic bacterium Chlamydia trachomatis and have show

25 In the pathogenic bacterium Chlamydia trachomatis, a transcript

26 ger RNA for a putative virulence gene in the pathogenic bacterium Clostridium difficile.

27 A full-length heme oxygenase gene from the pathogenic bacterium Corynebacterium diphtheriae has bee

28 The virulent phenotype of the pathogenic bacterium Corynebacterium diphtheriae is conf

29 ment of HmuO, a heme oxygenase (HO) from the pathogenic bacterium Corynebacterium diphtheriae, have b

30 ith Helicobacter hepaticus, an opportunistic pathogenic bacterium, developed granulomatous inflammati

31 smotic stress, or harpin (a protein from the pathogenic bacterium Erwinia amylovora).

32 pyoluteorin-mediated inhibition of the plant-pathogenic bacterium Erwinia amylovora.

33 ymes that degrade the plant cell wall by the pathogenic bacterium Erwinia carotovora.

34 ense to Pst DC3000 hrp mutants and the human pathogenic bacterium Escherichia coli O157:H7.

35 Since this is the first plant pathogenic bacterium for which a complete genome sequenc

36 chromosomal traits during the evolution of a pathogenic bacterium from an avirulent saprophyte.

37 The extracellular pathogenic bacterium group A Streptococcus (GAS) causes

38 In many countries, M1 strains of the human pathogenic bacterium group A Streptococcus are the most

39 The human pathogenic bacterium group A Streptococcus produces an e

40 The pathogenic bacterium Group A Streptococcus pyogenes prod

41 e susceptible to systemic infection with the pathogenic bacterium group B Streptococcus.

42 The human gastric pathogenic bacterium Helicobacter pylori lacks a MutSLH-

43 The pathogenic bacterium Helicobacter pylori utilizes two es

44 hifted toward inhibitory p53 isoforms by the pathogenic bacterium Helicobacter pylori, which is known

45 noglobulin-binding protein A (IbpA) from the pathogenic bacterium Histophilus somni adenylylates mamm

46 tective O-antigen of a human-disease-causing pathogenic bacterium is described.

47 I effectors in Pst DC3000 or any other plant pathogenic bacterium is not known.

48 on provides convincing evidence that a plant pathogenic bacterium is sexually transmitted from male t

49 nificantly increased the survival of the non-pathogenic bacterium Lactococcus lactis during a human w

50 During infection, the intracellular pathogenic bacterium Legionella pneumophila causes an ex

51 After the pathogenic bacterium Legionella pneumophila is phagocyto

52 During infection of macrophages, the pathogenic bacterium Legionella pneumophila secretes eff

53 s AnkX and DrrA/SidM, respectively, from the pathogenic bacterium Legionella pneumophila.

54 The pathogenic bacterium Listeria monocytogenes is capable o

55 filament assembly at the cell surface of the pathogenic bacterium Listeria monocytogenes requires the

56 similar to those behaviors displayed by the pathogenic bacterium Listeria monocytogenes.

57 for host cell invasion by the intracellular pathogenic bacterium Listeria monocytogenes.

58 Xylella fastidiosa, a xylem-colonizing plant pathogenic bacterium, mediated by a fatty acid Diffusibl

59 2) is an essential respiratory enzyme of the pathogenic bacterium Mycobacterium tuberculosis (Mtb) th

60 the X-ray crystal structure of MsrA from the pathogenic bacterium Mycobacterium tuberculosis refined

61 s method by applying it to the genome of the pathogenic bacterium Mycobacterium tuberculosis, assigni

62 Studies of these processes in the pathogenic bacterium Mycoplasma pneumoniae and its close

63 The terminal organelle of the cell wall-less pathogenic bacterium Mycoplasma pneumoniae is a complex

64 Heme oxygenase (HO), from the pathogenic bacterium N. meningitidis(NmHO), which secure

65 The HO from the pathogenic bacterium Neisseria meningitidis (NmHO) posse

66 crystal structure of heme oxygenase from the pathogenic bacterium Neisseria meningitidis at 1.5 A and

67 Heme oxygenase, HO, from the pathogenic bacterium Neisseria meningitidis catabolizes

68 The antigenic P64K protein from the pathogenic bacterium Neisseria meningitidis is found in

69 The HO from the pathogenic bacterium Neisseria meningitidis, NmHO, posse

70 phyrin IX (heme) have been described for the pathogenic bacterium Neisseria meningitidis.

71 Phenstatin (3b) inhibited growth of the pathogenic bacterium Neisseriagonorrhoeae and was a pote

72 mbrane lipoprotein P6 from the Gram-negative pathogenic bacterium nontypeable Haemophilus influenzae

73 first evidence of a super-integron in a non-pathogenic bacterium, one which is widely distributed in

74 f antibiotic resistant biofilms in the human pathogenic bacterium P. aeruginosa, which causes lethal

75 charide synthesis and virulence in the plant pathogenic bacterium Pantoea stewartii ssp. stewartii re

76 that are substituted when populations of the pathogenic bacterium Pseudomonas aeruginosa adapt to the

77 Alginate is secreted by the pathogenic bacterium Pseudomonas aeruginosa and is belie

78 The pathogenic bacterium Pseudomonas aeruginosa causes serio

79 ween cellular and secreted components by the pathogenic bacterium Pseudomonas aeruginosa during growt

80 average cost of rifampicin resistance in the pathogenic bacterium Pseudomonas aeruginosa is reduced b

81 During iron starvation the Gram-negative pathogenic bacterium Pseudomonas aeruginosa makes the no

82 In the pathogenic bacterium Pseudomonas aeruginosa PA14, antibi

83 The pathogenic bacterium Pseudomonas aeruginosa uses acyl-ho

84 The opportunistic pathogenic bacterium Pseudomonas aeruginosa uses quorum-

85 The pathogenic bacterium Pseudomonas aeruginosa utilizes the

86 d, triggering virulence in the opportunistic pathogenic bacterium Pseudomonas aeruginosa via an unkno

87 a molecule involved in quorum sensing in the pathogenic bacterium Pseudomonas aeruginosa, is describe

88 per-containing redox protein released by the pathogenic bacterium Pseudomonas aeruginosa, is highly c

89 e catabolic alanine racemase, DadX, from the pathogenic bacterium Pseudomonas aeruginosa, reported he

90 d-type to pyocyanin-dependent killing by the pathogenic bacterium Pseudomonas aeruginosa.

91 onstrated using disinfection assays with the pathogenic bacterium Pseudomonas aeruginosa.

92 tractable alternative for investigating the pathogenic bacterium Pseudomonas aeruginosa.

93 DUSP) that controls biofilm formation in the pathogenic bacterium Pseudomonas aeruginosa.

94 ALDI-TOF MS except for the opportunistically pathogenic bacterium Pseudomonas aeruginosa.

95 siderophores, iron-scavenging agents, in the pathogenic bacterium Pseudomonas aeruginosa.

96 The plant pathogenic bacterium Pseudomonas syringae is divided int

97 was able to protect Arabidopsis against the pathogenic bacterium Pseudomonas syringae pv tomato DC30

98 The plant-pathogenic bacterium Pseudomonas syringae, in which QS c

99 ne (COR), a phytotoxin produced by the plant-pathogenic bacterium Pseudomonas syringae.

100 experiments to address this question in the pathogenic bacterium, Pseudomonas aeruginosa Although pu

101 atory gene for the QS system of another rice pathogenic bacterium, Pseudomonas fuscovaginae.

102 he growth of Salmonella as well as the plant pathogenic bacterium, Pseudomonas syringae pv. tomato.

103 Agrobacterium tumefaciens is a unique plant pathogenic bacterium renowned for its ability to transfo

104 The co-option of mammalian LD function by a pathogenic bacterium represents a novel mechanism of euk

105 Activation of PARP-1 by a pathogenic bacterium represents a previously unrecognize

106 ter haemolyticus is an antibiotic resistant, pathogenic bacterium responsible for an increasing numbe

107 tanding the regulation of adhesins defines a pathogenic bacterium's interaction with the local enviro

108 The intracellular pathogenic bacterium Salmonella enterica serovar typhimu

109 The pathogenic bacterium Shigella flexneri uses a type III s

110 The pathogenic bacterium Staphylococcus aureus actively evad

111 structural component in many biofilms of the pathogenic bacterium Staphylococcus aureus, but its role

112 ing of protein A as well as virulence in the pathogenic bacterium Staphylococcus aureus.

113 e complex and heterogeneous cell wall of the pathogenic bacterium Streptococcus pneumoniae is compose

114 melittin efficiently inhibits growth of the pathogenic bacterium Streptococcus pyogenes as effective

115 Virtually all strains of the human pathogenic bacterium Streptococcus pyogenes express a hi

116 The pathogenic bacterium Streptococcus pyogenes has evolved

117 rotein expressed on the surface of the human pathogenic bacterium Streptococcus pyogenes, a common ag

118 In the human-pathogenic bacterium Streptococcus pyogenes, the tagatos

119 e expressed and characterized IMPDH from the pathogenic bacterium Streptococcus pyogenes.

120 rotein expressed on the surface of the human pathogenic bacterium, Streptococcus pyogenes, a common a

121 Escherichia coli is a commensal or pathogenic bacterium that can survive in diverse environ

122 Yersinia pseudotuberculosis is a foodborne pathogenic bacterium that causes acute gastrointestinal

123 Burkholderia pseudomallei, a highly pathogenic bacterium that causes melioidosis, is commonl

124 as campestris pv campestris (Xcc) is a plant pathogenic bacterium that controls the production of pat

125 mic infection with Salmonella Typhimurium, a pathogenic bacterium that multiplies within macrophages,

126 nsis, the causative agent of tularemia, is a pathogenic bacterium that replicates in the cytosol of m

127 Photorhabdus is a potent insect pathogenic bacterium that uses entomopathogenic nematode

128 ve Porphyromonas gingivalis, a Gram-negative pathogenic bacterium that uses TLR2 for innate immune si

129 rsatile devices that have evolved allowing a pathogenic bacterium to adjust to or counteract environm

130 Xylella fastidiosa is a xylem-limited plant-pathogenic bacterium transmitted by leafhopper vectors t

131 and insoluble ECM of a clinically important pathogenic bacterium--uropathogenic E. coli.

132 The pathogenic bacterium Vibrio cholerae is also shown to ha

133 In the pathogenic bacterium Vibrio cholerae, the alternate sigm

134 ic anhydrase (CA, EC 4.2.1.1) from the human pathogenic bacterium Vibrio cholerae, VchCA.

135 discovered as a virulence determinant in the pathogenic bacterium Vibrio cholerae.

136 he hemocytes and are increased at 24 h after pathogenic bacterium Vibrio harveyi challenge.

137 Francisella tularensis is a pathogenic bacterium whose virulence is linked to its ab

138 In this study, the effects of infection by pathogenic bacterium Xanthomonas oryzae pv. oryzae (Xoo)

139 The symbiotic pathogenic bacterium Xenorhabdus nematophila produces tw

140 swarm-cell differentiation in the symbiotic-pathogenic bacterium Xenorhabdus nematophila was examine

141 ort of several extracellular proteins in the pathogenic bacterium Yersinia enterocolitica.

142 nd an essential virulence determinant of the pathogenic bacterium Yersinia.