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1 luding siderophores, exotoxin, proteases and haemolysin.
2  multiple drug resistance efflux pumps and a haemolysin.
3 nduces the expression of an otherwise latent haemolysin.
4 ne receptor orthologue compatible with gamma-haemolysin.
5 or the failure to translate alpha- and delta-haemolysins.
6 ory gene functions, especially including the haemolysins.
7 eatly reduced, while the expression of alpha-haemolysin, a sae target with high affinity for phosphor
8                                        gamma-haemolysin AB and CB (HlgAB, HlgCB) are bicomponent pore
9  reduce the toxicity of staphylococcal alpha-haemolysin (alpha-toxin) and thus improve the survival r
10 ls and early production of lipase, protease, haemolysin and antibiotic activity.
11              Protein nanopores such as alpha-haemolysin and Mycobacterium smegmatis porin A (MspA) ca
12  activation (maturation) of Escherichia coli haemolysin and related toxins is further clarified by in
13 nctions in export (e.g. diverse xenobiotics, haemolysin) and as an attachment site for phage and coli
14 lved in intestinal adhesion, a plasmid-borne haemolysin, and phage-encoded Shiga toxins.
15 lts in failure to translate alpha- and delta-haemolysins, and hence, in a non-haemolytic phenotype.
16              NHE is a non-redundant toxin to haemolysin BL (HBL) despite having a similar mechanism o
17  we identified a multicomponent enterotoxin, haemolysin BL (HBL), that engages activation of the infl
18 organic molecules can be procured from alpha-haemolysin by equipping the channel with an internal, no
19 nent of the type VI secretion system (T6SS), haemolysin co-regulated protein (Hcp), binds directly to
20 nsporters of secreted proteins, specifically haemolysin co-regulated protein and an RTX toxin-like me
21 uperfamily and the founding substrate of the haemolysin co-regulated protein secretion island II T6SS
22     Our laboratory has demonstrated that the haemolysin co-regulated secretion island I (HSI-I)-encod
23 monas aeruginosa encodes three distinct T6SS haemolysin coregulated protein (Hcp) secretion islands (
24                               We report that haemolysin coregulated protein (Hcp), a ring-shaped hexa
25 regulates transcription of a cytotoxin, beta-haemolysin/cytolysin (beta-H/C) that is critical for sur
26 lence factors including the pluripotent beta-haemolysin/cytolysin (beta-H/C).
27 ion of a genetic locus encoding the GBS beta-haemolysin/cytolysin activity.
28 eported genetic locus (cyl) required for GBS haemolysin/cytolysin activity.
29    Group B streptococci (GBS) express a beta-haemolysin/cytolysin that contributes to disease pathoge
30 y represents the structural gene for the GBS haemolysin/cytolysin, a novel bacterial toxin.
31 sin in virulence, we constructed an isogenic haemolysin-deficient mutant of H. ducreyi strain 35000 T
32   We evaluated the accuracy of combined anti-haemolysin E and anti-lipopolysaccharide IgA readings us
33                                              Haemolysin E is a cytolytic pore-forming toxin found in
34 haemolytic determinant revealed two borrelia haemolysin genes, blyA and blyB, that are part of a pred
35  of the bacterial pore-forming protein alpha-haemolysin have been used to identify and quantify dival
36    All S. aureus isolates harbored both beta-haemolysin (hlb) and leucotoxin (lukMF) genes, while 44.
37                               phiNM3, a beta-haemolysin (hlb) converting phage, encodes modulators of
38 sly for activation of the homologous E. coli haemolysin (HlyA).
39                                          The haemolysin, however, is not responsible for the activity
40 he requirement of group G streptococcus beta-haemolysin in producing necrotising infection was examin
41           In order to assess the role of the haemolysin in virulence, we constructed an isogenic haem
42 functionality was assessed relative to alpha-Haemolysin into microfluidic DIBs using the same Cl(-) f
43   These results indicate that the H. ducreyi haemolysin is responsible for the previously observed cy
44 osomal membrane is initiated by the secreted haemolysin listeriolysin O (LLO), which is essential for
45 chieved by DNA polymerases held at the alpha-haemolysin nanopore orifice.
46                                          The haemolysin of Haemophilus ducreyi is the newest member o
47 t may contribute to pathogenicity--including haemolysins, phospholipases and iron acquisition functio
48                    The Enterococcus faecalis haemolysin plasmid pAD1 (60 kb) confers a conjugative ma
49 te thioredoxin, when pulled through an alpha-haemolysin pore, differ markedly depending on whether th
50 ratus, eliminated lipase but not protease or haemolysin production indicating these enzymes are secre
51                                      Lack of haemolysin production therefore generally represents a d
52 ow that a nanopore sensor based on the alpha-haemolysin protein can selectively detect microRNAs at t
53  cysteine residues 6 A apart within an alpha-haemolysin protein pore that acts as the nanoreactor.
54 , through covalent modification of the alpha-haemolysin protein pore with arylazopyrazole photoswitch
55                                  The 110 kDa haemolysin protoxin (proHlyA) is activated in the Escher
56 e linked with an increased expression of the haemolysin S-associated gene sagA.
57 A streptococcus sag operon encoding the beta-haemolysin streptolysin S (SLS).
58 t in expression of the secreted pore-forming haemolysin, streptolysin O (SLO).
59 expressing an unrelated second streptococcal haemolysin, streptolysin S, during infection of keratino
60     Here, we report that thermostable direct haemolysin (TDH), an exotoxin of the food-borne pathogen
61  directing synthesis and export of the toxin haemolysin, the lipopolysaccharide core, and the F-facto
62 ed peptides and the pore-forming toxin alpha-haemolysin, through distinct mechanisms.
63 encoding synthesis, maturation and export of haemolysin toxin was strongly dependent upon a 35 bp DNA
64 , exopolysaccharide, F conjugation pilus and haemolysin toxin.
65 oated nanoparticles and staphylococcal alpha-haemolysin, we demonstrate effective virulence neutraliz