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1 od of plasma membrane permeabilization using streptolysin O.
2 ng secreted toxins NAD(+)-glycohydrolase and streptolysin O.
3 i) reversible membrane permeabilization with streptolysin O.
4 tory effect of an unrelated cytolytic toxin, streptolysin O.
5 equired expression of the pore-forming toxin streptolysin O.
6 ing enhanced by the effects of M protein and streptolysin O.
7 e Dynasore also protected HeLa cells against streptolysin O.
8 sed for the homologous member of the family, streptolysin O.
9 ludes listeriolysin O, perfringolysin O, and streptolysin O.
10 ed wild-type amounts of type 3 M protein and streptolysin O.
11 ly permeabilised with the pore-forming toxin streptolysin O.
12 y permeabilized with the pore-forming toxin, streptolysin-O.
13 mmalian cells has been achieved by employing Streptolysin O, a bacterial enzyme which forms temporary
15 lored various methods including TAT peptide, Streptolysin O and microporation for delivering NeutrAvi
16 kidney (PK-15) cells were permeabilized with streptolysin-O and incubated with a library of 125I-labe
17 and permeabilization of cultured acini with streptolysin-O and insertion of GDP beta S or antibodies
19 was similar to mga, i.e., slo (which encodes streptolysin O) and plr (encoding the plasmin receptor/g
20 hils, that this activity was attributable to streptolysin O, and that platelet/neutrophil complex for
21 by collagenase digestion, permeablized with streptolysin O, and the release of Ca2+ from internal st
22 ced into the cells via permeabilization with streptolysin-O, and cellular uptake was confirmed by flu
23 requires NF-kappaB and the virulence factor streptolysin O, but proceeds independently of P2X7R and
25 ion of toxic shock syndrome toxin-1, whereas streptolysin O directly damages the mucosa to allow for
26 e pores are produced by perfringolysin O and streptolysin O during insertion (and not small pores tha
27 alpha-toxin and the streptococcal cytolysin streptolysin O enhanced penetration of toxic shock syndr
28 While reports have linked sloR function to streptolysin O expression, transport experiments with ra
31 alpha-hemolysin from Staphylococcus aureus, streptolysin O from Streptococcus pyogenes, and anthroly
33 ization of plasma membranes by detergents or streptolysin-O in hepatocytes, thymocytes, and P19, Jurk
34 tion of antibodies to HlpA and antibodies to streptolysin O, indicating that the histone-like protein
38 omosomal region encoding secreted NADase and streptolysin O, is the key driver of increased toxin pro
39 efect was preserved by permeabilization with streptolysin-O, it was determined that Lec35p is not dir
41 e genes encoding streptokinase, CAMP factor, streptolysin O, M protein (more abundant in the CvfA(-)
43 or) but did not affect transcription of slo (streptolysin O), mga (multiple gene regulator of GAS), e
46 an antagonist of Gq/11, was introduced into streptolysin-O permeabilized acini to bypass the plasma
48 concentration ([Ca2+]i) from both intact and streptolysin-O permeabilized isolated nerve endings of t
50 We have developed a novel assay system using Streptolysin-O permeabilized neutrophils that recapitula
51 ify this, we measured resting Ca2+ sparks in streptolysin-O permeabilized ventricular myocytes from w
52 in or addition of Ca2+-containing buffers to streptolysin O-permeabilized cells induced exocytosis of
53 um) of isolated microsomes, Ca2+ uptake into streptolysin O-permeabilized cells, and analysis of SERC
55 t vastly different transport capabilities in streptolysin O-permeabilized cells, in accordance with t
56 secretion when introduced after docking into streptolysin O-permeabilized cells; so does a Rab3A-22A
58 bility of inducers to elicit exocytosis when streptolysin O-permeabilized human sperm were loaded wit
61 tron microscopy and proteolytic digestion of streptolysin O-permeabilized parasitized erythrocytes.
63 d in alpha-granule secretion, we developed a streptolysin O-permeabilized platelet model of alpha-gra
72 ant CRHSP-28 (rCRHSP-28) was introduced into streptolysin-O-permeabilized acinar cells, and amylase s
75 2+) uptake into the endoplasmic reticulum of streptolysin-O-permeabilized cells by sarco/endoplasmic
76 tion of function-blocking Sec8 antibodies to streptolysin-O-permeabilized cells revealed exocyst requ
84 by TLR2 and TLR4 ligands in the presence of streptolysin O required Myd88/Trif, whereas that induced
85 ided that cells are first permeabilized with Streptolysin-O (SL-O), and (2) chimeric methylphosphonod
86 ith CLI reduced extracellular DNase Sda1 and streptolysin O (SLO) activity in vivo, whereas subinhibi
87 articipate in CMT, the pore-forming molecule streptolysin O (SLO) and an effector protein with the ch
92 tudies identified the pore-forming cytolysin streptolysin O (SLO) as necessary and sufficient for the
93 including the SpeB cysteine protease and the streptolysin O (SLO) cytolysin, but not SIC, a protein t
94 rearrangement in the upstream region of the streptolysin O (slo) gene of Streptococcus pyogenes whic
95 ssumes that the NAD-glycohydrolase (nga) and streptolysin O (slo) genes that code for these products
97 cell lines using cationic lipid systems and streptolysin O (SLO) is used to effect their delivery.
98 duction of the cholesterol-binding cytotoxin streptolysin O (SLO) prevented internalization of GAS in
99 ed the abundance of streptolysin S (SLS) and streptolysin O (SLO) production between clinically domin
100 er permeabilization with the bacterial toxin streptolysin O (SLO) requires endocytosis via a novel pa
101 utilizes the cholesterol-dependent cytolysin Streptolysin O (SLO) to translocate the NAD(+) -glycohyd
102 utilizes the cholesterol-dependent cytolysin Streptolysin O (SLO) to translocate the NAD(+) glycohydr
103 athogen Streptococcus pyogenes that utilizes streptolysin O (SLO), a cholesterol-dependent cytolysin.
104 rulence factor that is present among most is streptolysin O (Slo), a protein with well-characterized
105 f the archetypical member of the CDC family, streptolysin O (SLO), a virulence factor from Streptococ
106 bronectin-binding proteins (sfbI and fbp54), streptolysin O (slo), hyaluronic acid capsule (hasA), st
107 rol-binding CDCs, perfringolysin O (PFO) and streptolysin O (SLO), were found to exhibit strikingly d
108 easuring the properties of Ca2+ signaling in streptolysin O (SLO)-permeabilized cells were used to st
114 using either cells gently permeabilized with streptolysin-O (SLO) or microsomes from homogenized cell
115 her streptococcal cell wall antigen (SCW) or streptolysin-O (SLO) to augment lung injury in rats.
117 g the immunity factor IFS and the cytolysin (streptolysin O [SLO]), were more abundant in the mutant
118 between patient groups with nonfilarial Ag (streptolysin O)-stimulated supernatant (LP = 0.160 relat
119 dies recognizing specific domains of apoB in streptolysin-O (STP-O)- and saponin-permeabilized HepG2
120 n of other extracellular products, including streptolysin O, streptokinase, and DNase, was not affect
122 were used in cultured acini permeabilized by streptolysin-O to determine the role of the G proteins i
124 A when delivered into P815 target cells with streptolysin O, whereas transfection of target cells wit
125 Examples include the pore-forming cytotoxin streptolysin O, which oligomerises to form large pores i
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