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1 untingtin generated the most cell fragments (apoptotic bodies).
2 ompetent cell fragments (matrix vesicles and apoptotic bodies).
3 uring apoptosis to catalyze the formation of apoptotic body.
4 is, chromatin condensation, and formation of apoptotic bodies.
5 marker for assessing apoptosis or detecting apoptotic bodies.
6 ted with particles of a size consistent with apoptotic bodies.
7 RA on VSMCs and blocks phagocytic removal of apoptotic bodies.
8 contain abnormal microtubule arrangement and apoptotic bodies.
9 mmunogen expression before the generation of apoptotic bodies.
10 and increased the subsequent level of total apoptotic bodies.
11 d [3H]-membrane lipid release and release of apoptotic bodies.
12 pases arrested the maturation and release of apoptotic bodies.
13 functional properties of chondrocyte-derived apoptotic bodies.
14 f chromatin condensation, cell shrinkage and apoptotic bodies.
15 ntation, membrane blebbing, and formation of apoptotic bodies.
16 uclear DNA, and the subsequent appearance of apoptotic bodies.
17 the presence of cytoplasmic nucleosomes and apoptotic bodies.
18 udies demonstrate the ubiquitous presence of apoptotic bodies.
19 frequently sheared off the 'string' to form apoptotic bodies.
20 ts in the exclusion of nuclear contents from apoptotic bodies.
21 ation of 'beads-on-a-string' protrusions and apoptotic bodies.
22 teins that were specifically absent in HiBEC apoptotic bodies.
23 res were also obtained from intact cells and apoptotic bodies.
24 loid P component (SAP)-mediated clearance of apoptotic bodies.
25 rmation by constructing "blebbishields" from apoptotic bodies.
26 f its contents into membrane vesicles called apoptotic bodies.
27 These nucleosomal units are then included in apoptotic bodies.
28 phosphatidylserine exposed on the surface of apoptotic bodies.
29 present at the surface of apoptotic cells or apoptotic bodies.
30 de did not alter the rate of newly generated apoptotic bodies.
31 fragmentation, and the deposition of B cell apoptotic bodies.
32 rovesicles (MVs), but not exosomes (Exos) or apoptotic bodies (Abs), are the main type of EVs found i
33 normally surrounds the cells is degraded and apoptotic bodies accumulate within and in the vicinity o
35 ytosis is also required for the clearance of apoptotic bodies, an essential aspect of tissue homeosta
36 on, orally applied OTP reduced the number of apoptotic bodies and activated caspase-3-positive cells
37 o dehydration from that due to detachment of apoptotic bodies and can be used on samples where cell v
38 studies showing the formation and release of apoptotic bodies and cell death, and both processes are
39 ors have been implicated in the clearance of apoptotic bodies and could compensate for the TIM-4 defi
41 ectable at 24 h postinfection as revealed by apoptotic bodies and DNA fragmentation, indicating that
43 oside, WT or NRKvector exhibited significant apoptotic bodies and DNA laddering; in contrast, NRKproH
46 ed at the outer membrane surface to resemble apoptotic bodies and phosphatidic acid (PA) at the inner
47 with increased frequency of hepatocytes with apoptotic bodies and positivity for proliferating cell n
48 play an important role in the generation of apoptotic bodies and their recognition by phagocytosing
49 lar mechanisms followed by the generation of apoptotic bodies and their subsequent rapid elimination
50 eleased was proteinaceous in nature, free of apoptotic bodies, and had an apparent m.w. much larger t
51 ere detected in the cells with intracellular apoptotic bodies, and immunohistochemistry documented tr
53 atin condensation, PARP cleavage, release of apoptotic bodies, and release of labeled lipid, DEVD-tre
54 ion of microbial pathogens, senescent cells, apoptotic bodies, and retinal outer segment fragments.
56 el cell cleavage process in which developing apoptotic bodies are rescued by the virus and differenti
57 at encompasses microparticles, exosomes, and apoptotic bodies) are emerging as a novel mean of cell-t
58 lular vesicles (exosomes, microvesicles, and apoptotic bodies) are ubiquitous in human tissues, circu
59 mbrane and nuclear blebbing and formation of apoptotic bodies, are not observed in dying aleurone cel
60 ith a threefold increase in the frequency of apoptotic bodies as detected by terminal deoxynucleotidy
61 s and epithelial cells were found to contain apoptotic bodies at 3 times the rate of nonexpressing ce
62 erine macrophages resulting in a build up of apoptotic bodies at the uteroplacental interface that el
63 Several Kupffer cells were seen containing apoptotic bodies but did not show evidence of apoptosis.
64 ese cells show neither DNA fragmentation nor apoptotic bodies, but display lethal damage of the cell
65 re resistant to the Fas-induced formation of apoptotic bodies, but had an enhanced externalization of
68 r aim was to ascertain whether engulfment of apoptotic bodies by Kupffer cells promotes hepatic infla
71 e have previously shown that phagocytosis of apoptotic bodies by stellate cells induces procollagen a
72 ly we have demonstrated that phagocytosis of apoptotic bodies by stellate cells is profibrogenic.
74 drug delivery by phagocytosis of drug-loaded apoptotic bodies by the tumor cells and by increased dru
79 ents (a form of extracellular vesicle called apoptotic bodies) can facilitate removal of apoptotic de
81 r vesicles (EVs; exosomes, microvesicles and apoptotic bodies) containing proteins, lipids and RNAs i
83 optosis precedes VSMC calcification and that apoptotic bodies derived from VSMCs may act as nucleatin
84 uding cell shrinkage, rounding, formation of apoptotic bodies, detachment and nuclear condensation an
85 asma membrane blebbing, and the formation of apoptotic bodies do not occur when aleurone cells die.
87 ese results suggest that chondrocyte-derived apoptotic bodies express functional properties that may
88 ed (BDL) mice were phenotypically similar to apoptotic body-"fed" Kupffer cells with enhanced death l
89 levels [Ca(2+)](i), cell membrane integrity, apoptotic body formation and DNA fragmentation in cultur
91 vealed a block in chromatin condensation and apoptotic body formation when nuclei from HeLa cells exp
101 at macrophages have a function in scavenging apoptotic bodies from cells undergoing programmed cell d
102 ntation of the 19-kDa lipoprotein as well as apoptotic bodies from M. tuberculosis-infected cells.
104 ed murine Kupffer cells efficiently engulfed apoptotic bodies generated from UV-treated mouse hepatoc
107 s platform for proteomic characterization of apoptotic bodies in an effort to define the complex prot
108 significantly greater numbers of glomerular apoptotic bodies in C1q-deficient mice compared with con
110 ycotoxin induced cell death, DNA ladders, or apoptotic bodies in CV-1 cells expressing simian virus 4
111 of VP3 and a general lack of VP3-associated apoptotic bodies in infections of CIA-1 and chimeras con
116 MDMphis from PBC patients cultured with BEC apoptotic bodies in the presence of AMAs markedly increa
117 ages and B-1 cells do not efficiently engulf apoptotic bodies in vitro, or clear apoptotic bodies in
118 that TIM-4 is critical for the clearance of apoptotic bodies in vivo, and that lack of TIM-4 results
120 duced by lymphoid radiation, suggesting that apoptotic body ingestion by CD8(+) DCs initiates toleran
121 ther we demonstrate that the phagocytosis of apoptotic bodies inhibits both spontanous and UV-irradia
124 of TIM-4 results in aberrant persistence of apoptotic bodies leading to dysregulated lymphocyte acti
128 RECENT FINDINGS: Microvesicles, exosomes, apoptotic bodies, lipoproteins, and large microparticles
129 nfunctional, prothrombogenic, membrane-bound apoptotic bodies marked for rapid engulfment by macropha
130 ystem opsonin which binds nuclear debris and apoptotic bodies, may protect against autoimmunity.
132 extracellular vesicles (EVs), which include apoptotic bodies, microvesicles, and exosomes, have emer
133 mechanisms could include antigens present in apoptotic bodies, necrotic debris, exosomes or even rele
134 generated from CD14+ precursors, pulsed with apoptotic bodies of an allogeneic NSCLC cell line that o
135 cells as well as dendritic cells pulsed with apoptotic bodies of CLL cells to generate autologous and
136 re 11 proteins that localize specifically to apoptotic bodies of HiBEC and eight proteins that were s
137 wild-type mice affected either the number of apoptotic bodies or the number of live macrophages.
138 o exosomes, microvesicles/microparticles, or apoptotic bodies, originating from different subcellular
140 dular VSMCs was unaltered, but the number of apoptotic bodies per nodule increased approximately 3-fo
143 e a mechanistic link between phagocytosis of apoptotic bodies, production of oxidative radicals, and
144 iver injury where Kupffer cell engulfment of apoptotic bodies promotes inflammation and fibrogenesis.
146 sis of large extracellular particles such as apoptotic bodies requires delivery of the intracellular
148 ssion correlated with a dramatic increase in apoptotic bodies, suggesting that Xist-mediated X chromo
149 iruses encode caspases or form such modified apoptotic bodies, suggesting this caspase plays a direct
151 vesicles (EVs; exosomes, microvesicles, and apoptotic bodies) that differ in biogenesis, composition
152 response to the larger numbers of persistent apoptotic bodies, the number of live macrophages in thes
153 inflammatory sites it can bind bacteria and apoptotic bodies to trigger alternative pathway (AP) act
154 nsistent with these observations, binding of apoptotic bodies to VSMCs was decreased in the presence
157 HCC-derived cells, and the ultimate fate of apoptotic bodies was phagocytosis and degradation by nei
158 eutic HIV-1 vaccine based on DCs loaded with apoptotic bodies was safe and induced T-cell activation
159 hagocytosis model, engulfment of GFP-labeled apoptotic bodies was seen, and the expression of alpha-s
161 off of portions of cytoplasm and nucleus as "apoptotic bodies." We have combined our previously estab
166 of decreased calreticulin, CDKN2B-deficient apoptotic bodies were resistant to efferocytosis and not
167 ed) exhibited a high incidence of apoptosis (apoptotic bodies were seen in 55-75% of cells; 67-73% ha
168 ably, macrophages, which readily phagocytose apoptotic bodies, were very inefficient at acquiring lab
170 ng microvesicles (distinct from exosomes and apoptotic bodies), which induce proliferation in neighbo
171 Furthermore, incubation of VSMC-derived apoptotic bodies with (45)Ca demonstrated that, like mat
172 Confocal images confirm internalization of apoptotic bodies within KIM-1-expressing epithelial cell
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