ライフサイエンスコーパス: lysis

1 which subsequently inhibits NK-cell-mediated lysis.

2 e old pole of M. tuberculosis, with eventual lysis.

3 ome of this carbon during infection and cell lysis.

4 e artifact of cytosine deamination upon cell lysis.

5 e the inner and outer membranes during phage lysis.

6 ed for both virulence and host cell membrane lysis.

7 g also induced T cell mediated leukemia cell lysis.

8 ic events are denser and less susceptible to lysis.

9 nt C3b deposition and, thus, autoimmune cell lysis.

10 spore gene expression and frequently undergo lysis.

11 rotected TLF-1-treated T. brucei brucei from lysis.

12 r induction of caspase-1-mediated macrophage lysis.

13 ARE concentrations fused without concomitant lysis.

14 0(Glued) in CTLs also inhibited CTL-mediated lysis.

15 interleukin-2) pathway was susceptible to NK lysis.

16 ucei became rapidly susceptible to hypotonic lysis.

17 to be a source of free radicals during TLF-1 lysis.

18 plex that mediates complement-dependent cell lysis.

19 rozoites protection from complement-mediated lysis.

20 rucei brucei to oxidation-stimulated osmotic lysis.

21 the loss of HLA can trigger NK cell-mediated lysis.

22 the Hpr-Hb complex was not involved in TLF-1 lysis.

23 AP to fibrin and consequently prolonged clot lysis.

24 ing cells without the need for suspension or lysis.

25 NG-stimulated Pro(2+) influx and pyroptotic lysis.

26 idual Chaetoceros affinis diatoms undergoing lysis.

27 cytosolic lipid peroxidases prevented TLF-1 lysis.

28 c change in red blood cells, leading to cell lysis.

29 d extracellular polymeric substance and cell lysis.

30 the phagosome, which can result in host cell lysis.

31 l transduction and induce apoptosis and cell lysis.

32 dding and, for some variants, virus membrane lysis.

33 s, and Ab-dependent complement-mediated cell lysis.

34 lls (GBM-SC), inducing their strong targeted lysis.

35 arrel-like pore structures that lead to cell lysis.

36 f the lytic activity to prevent overall cell lysis.

37 er rates, facile oxygen binding and O-O bond lysis.

38 ed in surrounding regions to protect against lysis.

39 he peptidoglycan that ultimately led to cell lysis.

40 tures is essential as in our case of splenic lysis.

41 the hybrid protein causes sheep erythrocyte lysis.

42 ntil the membrane undergoes scission through lysis.

43 cell's plasma membrane area to prevent cell lysis.

44 DNA damage occurs, triggering viral-mediated lysis.

45 les its conditional inactivation during cell lysis.

46 erial invasion attempts leading to host cell lysis.

47 tion and IL-1beta cleavage occur before cell lysis.

48 ptibility, misplaced division septa and cell lysis.

49 o understand the mechanism of ESX-1-mediated lysis.

50 rapidly with the onset of antibiotic-induced lysis.

51 arasite from complement-mediated and osmotic lysis.

52 released and remain active following vesicle lysis.

53 emia due to protein instability and red cell lysis.

54 mydia bacteria, such as those resulting from lysis.

55 f trabeculectomy eyes underwent laser suture lysis.

56 antibodies and are resistant to NK-mediated lysis.

57 Following quorum lysis, a small number of surviving bacteria reseed the g

58 Efficacy was correlated to in vitro lysis ability by the infecting phage and the level of vi

59 2) Substantial lysis accompanies reconstituted fusion.

60 esist antibody-dependent complement-mediated lysis (ADCML).

61 (NCR) peptide that acts to promote bacterial lysis after differentiation.

62 The molecule inhibited clot lysis, alluding to its promise as an allosteric regulato

63 sis increased with MC-containing treatments, lysis always appeared more severe in the liver of female

64 ed Hill coefficients of 0.69 for target cell lysis and 0.68 in interferon secretion.

65 mechanistic basis for GC cells to escape NK lysis and a promising prospect of NK immunotherapy for G

66 hin competing bacteria, induce P. aeruginosa lysis and activate PARA, thus providing a mechanism for

67 ophagy, which is required for efficient cell lysis and adenoviral spread.

68 Further, cell lysis and biofilm formation were governed by the SrrAB t

69 or each stage of the method, comprising cell lysis and bisulfite (BS) conversion, preamplification an

70 CR with purified DNA, demonstrating that the lysis and capture steps effectively bind DNA and suffici

71 competitor for FH and measuring erythrocyte lysis and deposition of complement C3b and C5b-9 on endo

72 T), a virulence factor that causes host cell lysis and elicits inflammasome-mediated IL-1beta secreti

73 sufficient to promote the efficient vacuole lysis and escape of the modified bacteria into the cytos

74 cells through two equally active mechanisms: lysis and extrusion.

75 richment techniques including red blood cell lysis and immunomagnetic purification.

76 ive IL-1beta release secondary to pyroptotic lysis and in nonlytic/nonclassical IL-1beta export.

77 could explain how protamine instigates clot lysis and increases bleeding after surgery.

78 Although cell lysis and outer-membrane vesicle extrusion are possible

79 ost survival with lysogen formation, or host lysis and phage production.

80 er external mechanical vibration caused cell lysis and released DNA in the supernatant.

81 viral environments or following cell/virion lysis and removal of proteins.

82 Following cell lysis and sampling crude cell lysate for analysis, the s

83 histone-induced increases in red blood cell lysis and splenic clearance may be a significant factor

84 ut the bacterial determinants of nascent SCV lysis and subsequent survival and replication of Salmone

85 The absence of laser suture lysis and surgeon are factors potentially associated wit

86 e pattern of MurA mutations that block Qbeta lysis and the conformational changes of MurA that facili

87 ion of Triton X-100 and CoQ10 causes the MLs lysis and the cresyl violet oxidation, obtaining a decre

88 evice to detect an intact cell just prior to lysis and the injected lysate 2, 5, 10, or 15 mm downstr

89 ipermeable membrane, enabling efficient cell lysis and transcript capture.

90 s is prone to artifacts associated with cell lysis and whole-genome amplification.

91 ead, purified ApoL1 was sufficient to induce lysis, and ApoL1 lysis was inhibited by the antioxidant

92 -inflammatory signaling, prevents neutrophil lysis, and dampens immune responses.

93 o infection, as evidenced by apoptosis, cell lysis, and phagocytosis of infected cells.

94 Necroptotic cell lysis, and resultant release of proinflammatory mediator

95 ogenization, compete among each other during lysis, and that confusion between the two pathways occas

96 association with O. tauri debris after viral lysis, and unlike other allomers were not observed befor

97 degradation of the zona pellucida and embryo lysis, and wild-type embryos transferred into cKO oviduc

98 Effective cell lysis approaches that completely release intracellular m

99 Fibrin clot structure and clot lysis are crucially involved in development of cardiovas

100 K-562 using both live-cell and in-situ cell lysis assay formats, with special focus on metalloprotei

101 platelet aggregometry, platelet-rich thrombi lysis assays, thromboelastography (ROTEM), and high-shea

102 on microscopy, confocal microscopy, and clot lysis assays, we confirm that UHRA does not incorporate

103 apping, IFA and inhibition of the complement lysis assays.

104 Piggyback-the-Winner model of reduced phage lysis at higher host densities.

105 including cell elongation, cell swelling, or lysis, at 90 min.

106 eps required for efficient host and bacteria lysis, barcoding of samples, technical advances in sampl

107 microfluidic cell enrichment with a saponin lysis before MRR detection can overcome these challenges

108 le B cells into emulsion droplets containing lysis buffer and magnetic beads for mRNA capture; subseq

109 for conducting sample heating with chemical lysis buffer and silica microbeads are employed for DNA

110 ity to capture the nucleoprotein directly in lysis buffer used for releasing this viral protein, whic

111 action from fresh and fixed samples required lysis buffer with high concentrations of Tris-HCl and so

112 ology and removal of detergent from the cell lysis buffer.

113 ent at 4 degrees : C decreased HMBPP-induced lysis but did not reduce lysis induced by bis (pivaloylo

114 ne profoundly suppressed NG and TcdB-induced lysis but not Pro(2+) influx.

115 tion of Ostreococcus tauri often causes cell lysis, but two spontaneously arising resistance mechanis

116 acterial cells are fortified against osmotic lysis by a cell wall made of peptidoglycan (PG).

117 CD55-blocking Ab inhibited erythrocyte lysis by conditioned medium, suggesting that CD55/sCD55

118 olecules, but leaves the cells vulnerable to lysis by natural killer (NK) cells.

119 tibility of normal articular chondrocytes to lysis by NK cells is modulated by NKR-P1A/LLT1 interacti

120 Normal cartilage cells are susceptible to lysis by NK cells.

121 uptake and, subsequently, susceptibility to lysis by PR1-specific cytotoxic T cells.

122 arget cells is required for BTN3A1-dependent lysis by Vgamma9Vdelta2 effector T cells.

123 [ADCC]) or complement (complement-dependent lysis [CDL]).

124 ead ChIA-PET that includes cell fixation and lysis, chromatin fragmentation by sonication, ChIP, prox

125 on were less susceptible to NK cell-mediated lysis compared with normoxic cells expressing a moderate

126 sion rates or growth arrest, persistence, or lysis, concomitant with ICE excision, and likely, ICE lo

127 t alleles that restored plaque formation for lysis-defective mutants of Rz and Rz1 were selected.

128 ubdominant TCD8 responses by relieving their lysis-dependent suppression by immunodominant TCD8 To ou

129 port, we demonstrate a microfluidic electric lysis device that is effective for mRNA extraction from

130 pathogen Listeria monocytogenes show severe lysis, division and growth defects due to distortions of

131 ga7Delta result in defective septum and cell lysis during cytokinesis.

132 ng invasion and to host cell plasma membrane lysis during egress.

133 it yield than previous methods by optimizing lysis, elution, sample clean-up and detection of interac

134 ative to chlorophyll-a) just after the major lysis event.

135 h second-site suppressor mutations supported lysis events that were preceded by spherical cell format

136 y in which viral replication induces nuclear lysis followed by cell cleavage, yielding numerous large

137 r from all other viruses by inducing nuclear lysis followed by cleavage of host cells into numerous a

138 Lysis follows the uptake of APOL1 into acidic endosomes

139 ation-optimizing beneficial mutations during lysis from sequence diversification during lysogeny, all

140 specimens were processed by investigational lysis/heating (i.e., manual) and by chromatography/centr

141 , 0.83-0.94; Pinteraction=0.0027), or recent lysis (HR, 0.63; 95% CI, 0.40-1.01; Pinteraction=0.0001)

142 MII oocyte microinjection reduced lysis, improved blastocyst rate, increased the number of

143 ven when considering the fastest phage (cell lysis in 9 minutes), the concentrations of phage-induced

144 at histones induce erythrocyte fragility and lysis in a concentration-dependent manner.

145 V particles, potentially protecting HCV from lysis in circulation.

146 ound that mAb 2E8 caused complement-mediated lysis in DENV-infected cells.

147 The final step of lysis in phage lambda infections of Escherichia coli is

148 ing agents were also sensitized to hypotonic lysis in the absence of TLF-1.

149 c antibody efficiently induces targeted cell lysis in the presence of effector cells at as low as sub

150 formation and prevented complement-mediated lysis in vitro.

151 .7% of that for conventional detergent-based lysis in yielding detectable protein.

152 Although hepatocyte lysis increased with MC-containing treatments, lysis alw

153 eased HMBPP-induced lysis but did not reduce lysis induced by bis (pivaloyloxymethyl) (E)-4-hydroxy-3

154 umolysin, which is released during bacterial lysis, induces DNA double strand breaks (DSBs), as indic

155 ultistep process including direct tumor cell lysis, induction of cytotoxic or apoptosis-sensitizing c

156 lytes from cells stochastically entering the lysis intersection could be determined for the first tim

157 nflammation by transducing cell swelling and lysis into proinflammatory eicosanoid signaling.

158 ESX-1-mediated lysis is also morphologically distinct from the contact-

159 port here that ESX-1-dependent cell membrane lysis is contact dependent and accompanied by gross memb

160 ross bacterial species, we show that vacuole lysis is not a common feature of T3SA, as an effectorles

161 We show DNA released via cell lysis is readily available for HGT and may be partially

162 The timing of lysis is regulated and is thought to involve the activat

163 To sensitively detect the lysis, low conductive growth media have been developed.

164 g of individual phage infections affects the lysis-lysogeny decision of bacteriophage lambda despite

165 a novel, low-field-enabled electromechanical lysis mechanism of bacterial cells using electroconvecti

166 We examined lysis mediated by human Vgamma9Vdelta2 effector T cells

167 Using a rapid bacterial lysis method, the Check MDR CT103 and CT103 XL microarra

168 nto rapidly expanding pores causing membrane lysis (minutes).

169 itions support a unified model that membrane lysis occurs at or above a critical P:L ratio, which is

170 tants in vivo Unlike the wild type, in which lysis occurs while the cells retain a rod shape, reverta

171 The spontaneous lysis of a coronary thrombus is a natural protective mec

172 Laparoscopic lysis of adhesions for adhesive SBO (aSBO) is becoming m

173 Surgeons should approach laparoscopic lysis of adhesions with a higher level of awareness and

174 s in bacteriophage [Formula: see text] Here, lysis of an infected bacterial cell is orchestrated by t

175 that intravenous NAC administration promotes lysis of arterial thrombi that are resistant to conventi

176 We found that lysis of articular chondrocytes by PBMC or polyclonal NK

177 d the receptive synergid, culminating in the lysis of both interaction partners.

178 opidium iodide influx assay demonstrated the lysis of C. albicans cells by carvacrol and its 2,3-unsa

179 ling of cells into microwells; (ii) chemical lysis of cells in each microwell; (iii) PAGE of each sin

180 rophoresis after concurrent in situ chemical lysis of each isolated cell.

181 imaging demonstrated that replication in and lysis of endothelial cells precedes invasion of the cent

182 ier disruption develops by protease-mediated lysis of epithelial tight junctions, leading to accelera

183 We also observed recognition and lysis of healthy BOB1-expressing B cells.

184 ited by an increased risk of bleeding due to lysis of hemostatic clots that prevent hemorrhage in dam

185 ing additional membrane strain that leads to lysis of highly curved membranes.

186 1V2 domain induce up to 60% NK cell mediated lysis of HIV-1 infected PBMCs in a physiologically relev

187 eport that polymeric C4BP strongly inhibited lysis of human erythrocytes incubated with monomeric IAP

188 viously reported that necrostatin-1 inhibits lysis of human neutrophils fed CA-MRSA and attributed th

189 suggest that in addition to neutralization, lysis of infected cells by Abs can effectively participa

190 Ultimately, cyanophage-induced lysis of infected cells results in the release of fixed

191 nd DNAM-1 playing a role in NK cell-mediated lysis of infected cells.

192 ing cell division induced by immune-mediated lysis of infected hepatocytes will be critical for the f

193 Lysis of intact fibrin is initiated by t-PA, and uPA act

194 ntinuous, efficient and food-grade enzymatic lysis of lactic bacteria (Oenococcus oeni) in white and

195 Electrical lysis of mammalian cells has been a preferred method in

196 he kinase RIPK3 is essential for IAV-induced lysis of mammalian fibroblasts and lung epithelial cells

197 ing the molecular pathways that culminate in lysis of neutrophils during CA-MRSA infection may serve

198 Lysis of neutrophils fed CA-MRSA was independent of tumo

199 ogically distinct from the contact-dependent lysis of other bacterial secretion systems.

200 Interestingly, ex vivo lysis of patient thrombi was more successful when adding

201 perative management of peptic ulcer disease, lysis of peritoneal adhesions, appendectomy, and laparot

202 Lysis of plasma clots from TM-AC cases was significantly

203 We demonstrate that lysis of Pseudomonas aeruginosa cells triggers a program

204 cherichia coli and found to potently inhibit lysis of rabbit erythrocytes in assays of the alternativ

205 moderate to good selectivity with respect to lysis of red blood cells.

206 lular DNA was targeted by performing ex vivo lysis of retrieved thrombi with DNase 1 and t-PA.

207 ion using flour-rich waste (FRW) streams and lysis of Rhodosporidium toruloides yeast cells.

208 P. aeruginosa LasA endopeptidase potentiates lysis of S. aureus by vancomycin, rhamnolipids facilitat

209 p-by-step instructions for the isolation and lysis of single cells; the physical separation of polyA(

210 production of antiviral cytokines and direct lysis of target cells.

211 In general, phages cause lysis of the bacterial host to effect release of the pro

212 ation, can occur very efficiently even after lysis of the cells, if the lysate is not protected from

213 he NK cell results in NK cell activation and lysis of the HSV1-infected cell in the absence of HSV1-s

214 o influenza virus-infected cells and mediate lysis of the infected cells by natural killer (NK) cells

215 None of the mutants were affected for lysis of the nascent SCV or vacuolar replication in epit

216 Viral infection led to mass cell lysis of the O. tauri cells within 48 h.

217 proteinosome population by protease-induced lysis of the protein-polymer membrane.

218 Conversely, lysis of TLF-1-treated T. brucei brucei was increased by

219 Overexpression of bsrE causes cell lysis on agar plates.

220 The vortex-assisted lysis only requires a field strength of approximately 10

221 d mechanism is independent of explosive cell lysis or cell death, and the release of DNA is confined

222 iofilms while showing minimal red blood cell lysis or cytotoxicity against HeLa cells.

223 arbon analyses suggest that products of cell lysis or microbial products released under starvation st

224 Death by lysis or other means can be harmful, while PCD can evolv

225 plasmic water content, resulting in cellular lysis or plasmolysis.

226 ther allomers were not observed before viral lysis, or during cell death due to growth limitation.

227 We suggest that activation of the Alp cell lysis pathway is a disease-enhancing response to bacteri

228 n of mum-scale holes by the phage holin, the lysis pathway is seen to require dramatic dynamics on th

229 paired respiration elicits a programmed cell lysis (PCL) phenomenon in S. aureus leading to the relea

230 ce, delayed epiboly progression and an early lysis phenotype during gastrula stages.

231 To estimate this diversity, we used lysis plaque assays to detect viruses that infect the wi

232 structure, fibrin susceptibility to plasmin-lysis, plasma redox status, leukocyte oxidative stress m

233 dds (OR = 7.24, P = .0125), and argon suture lysis procedure was associated with decreased odds (OR =

234 is introduced at the clot or thrombus edge, lysis proceeds as a front.

235 n protein, A2, has an additional role as the lysis protein, by its ability to bind and inhibit MurA,

236 ated the mechanism of action of an unrelated lysis protein, Lys(M), of the Escherichia coli levivirus

237 Phage lysis proteins that overcome this barrier can point the

238 ubes were tested with a new erythrocyte bulk-lysis protocol allowing acquisition of high cell numbers

239 ll using a microfluidic chip and a two-stage lysis protocol.

240 cations of all components and elucidates how lysis rates are determined by the interplay between the

241 rived CTCs, a biophysical CTC phenotype more lysis-resistant than breast cancer cell lines, a capacit

242 However, cell lysis revealed a viscoplastic response of the underlying

243 h suppressed PM pore activity and pyroptotic lysis, robust IL-1beta release was observed in lanthanid

244 be an inevitable consequence of how osmotic lysis ruptures the plasma membrane, and may also apply t

245 ughput and cost-effective assay, the Saponin-lysis Sexual Stage Assay (SaLSSA), for identifying small

246 pe and specifically eliminates, through cell lysis, sporulating cells that assemble the envelope inco

247 que assay, whereas phageFISH identified cell lysis starting at < 5 h and lasting to 11 h, but for onl

248 After a thermal lysis step, the released viral N1 gene was exponentially

249 e by species and require an additional viral lysis step.

250 andard therapies, we orally administered the lysis strain alone or in combination with a clinical che

251 uidic devices to characterize the engineered lysis strain and we demonstrate its potential as a drug

252 The lysis strain exhibits pulsatile population dynamics in v

253 in intact normal neurons, but not after cell lysis, suggesting a dynamic equilibrium.

254 limiting fatty acid synthesis leads to cell lysis, supporting a role for ppGpp as a linchpin linking

255 of sutures in the scleral flap, laser suture lysis, surgeon, and laterality of surgery.

256 the dose-escalation schedule, clinical tumor lysis syndrome did not occur in any of the 60 patients i

257 mencing venetoclax at 20 mg, clinical tumour lysis syndrome did not occur.

258 Clinical tumor lysis syndrome occurred in 3 of 56 patients in the dose-

259 Clinical tumour lysis syndrome occurred in two patients (resulting in on

260 After enhancing tumour lysis syndrome prophylaxis measures and commencing venet

261 e was not observed, whereas laboratory tumor lysis syndrome was documented in three patients.

262 Clinical tumor lysis syndrome was not observed, whereas laboratory tumo

263 nalysis of few single cells, a one-step cell lysis, target labelling and hybridisation approach as we

264 We conclude that our electric lysis technique is an effective approach for mRNA releas

265 oportionally greater lowering of the vesicle lysis tension and hydration repulsive pressure that comb

266 ation (vesicle leakage, hemolysis, bacterial lysis) than their linear counterparts.

267 These data are consistent with a model of lysis that involves endocytic recycling of APOL1 and the

268 ibrinolytic degradation (+25% prolonged clot lysis time [CLT]) and a 5% slower rate of increase in D-

269 ent experimental observations of single-cell lysis times in bacteriophage [Formula: see text] Here, l

270 pounds caused serious damage and significant lysis to M. aeruginosa cells.

271 ty buffer expedites the transition from cell lysis to protein electrophoresis.

272 er metabolites, likely released through cell lysis, to supplement metabolic pathways.

273 erapeutic combination of tumor-specific cell lysis together with immune stimulation, therefore acting

274 However, bacterial lysis typically requires at least a 10-fold higher elect

275 G-mediated tumor cell resistance to specific lysis under hypoxia.

276 n of viruses, once they are released by cell lysis, undergo fast decomposition.

277 NA phages (the leviviruses) that effect host lysis using a single non-enzymatic protein (2) .

278 tolytica trophozoites and accelerated amebic lysis via activation of the classical complement cascade

279 of the complement cascade induces tumor cell lysis via complement-dependent cytotoxicity (CDC) and at

280 Impaired respiration led to increased cell lysis via divergent regulation of two processes: increas

281 arget cell conjugation, and K562 target cell lysis was compared between mutant- and wild-type-transdu

282 ed, the efficiency of SAW-induced mechanical lysis was determined to be 12.9% +/- 0.7% of that for co

283 L1 was sufficient to induce lysis, and ApoL1 lysis was inhibited by the antioxidant DPPD.

284 e competing soil bacteria species, P. putida lysis was less critical in mitigating interspecies compe

285 or differences in baseline IOP, laser suture lysis was negatively correlated with low IOP after trabe

286 es incubated with monomeric IAPP, whereas no lysis was observed after incubation with preformed IAPP

287 Consequently, bacterial lysis was observed at 37 degrees C, whilst growth was ma

288 ells, a 12- and 7-fold increased erythrocyte lysis was observed with the IgG1 and IgG3, respectively,

289 rinking water; (2) subsequent phage-mediated lysis was used to release endemic beta-galactosidase (be

290 prevention of macrophage activation and cell lysis, we suggest that the molecular environment surroun

291 and fibrin susceptibility to plasmin-induced lysis were significantly impaired in BD patients (P<0.00

292 This suggests suppressed lysis where established models predict lytic dynamics ar

293 her PEf1 propagation was offset by P. putida lysis, which decreased stress from interspecies competit

294 are released primarily by virus-induced cell lysis, while in insect cells they bud from the plasma me

295 efore, we believe that the electromechanical lysis will not only facilitate microfluidic bacterial se

296 fected, produce infectious virus and undergo lysis within 48 h after exposure to low titers (multipli

297 expressed in a single cell, and released by lysis within a droplet.

298 ficient bacterial invasion and rapid vacuole lysis within select host cell types, indicating roles fo

299 o(2+) influx and markedly delayed pyroptotic lysis without limiting upstream inflammasome assembly an

300 at LtnA1 and LtnA2 can induce rapid membrane lysis without the need for lipid II binding.