戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1  parasite replicates within a membrane-bound parasitophorous vacuole.
2 n acidified (pH 4.5 to 5) phagolysosome-like parasitophorous vacuole.
3 nd TLR4 colocalized with the parasite in the parasitophorous vacuole.
4 asion as the parasite moves into the nascent parasitophorous vacuole.
5 rusion to accomplish cell entry and form the parasitophorous vacuole.
6  space, as well as secreted into the primary parasitophorous vacuole.
7 nvasion of host cells and establishment of a parasitophorous vacuole.
8 lication of C. burnetii and formation of the parasitophorous vacuole.
9  within the host cell cytosol and within the parasitophorous vacuole.
10 cretes a variety of proteins that modify the parasitophorous vacuole.
11 n serves as a source of membrane to form the parasitophorous vacuole.
12 rotein translocon within the membrane of the parasitophorous vacuole.
13 asite-derived compartment referred to as the parasitophorous vacuole.
14 ctor proteins that direct the formation of a parasitophorous vacuole.
15 e intracellular replication compartment, the parasitophorous vacuole.
16 oving junction and subsequent formation of a parasitophorous vacuole.
17  that replicates within an intraerythrocytic parasitophorous vacuole.
18 om within a phagosomal compartment to form a parasitophorous vacuole.
19 utside the parasites and is found within the parasitophorous vacuole.
20 lar protozoan parasite that resides inside a parasitophorous vacuole.
21 mic parasite residing in a host cell-derived parasitophorous vacuole.
22 the RBC and the coordinated induction of the parasitophorous vacuole.
23  junction formation and the induction of the parasitophorous vacuole.
24 ompartment of the host cell that is termed a parasitophorous vacuole.
25 ds, glucose being a limiting nutrient in the parasitophorous vacuole.
26 when CD40 was ligated after the formation of parasitophorous vacuoles.
27 ss program are revealed: (1) swelling of the parasitophorous vacuole accompanied by shrinkage of the
28 ted in culture supernatants but not into the parasitophorous vacuole after invasion.
29                                          The parasitophorous vacuole also failed to acquire any host
30 n network that connects parasites within the parasitophorous vacuole and allows vesicles to be exchan
31 rrangement persisted for the duration of the parasitophorous vacuole and contributed to the formation
32 oposed to be required for maintenance of the parasitophorous vacuole and host cell egress.
33                    The parasite modifies the parasitophorous vacuole and its host cell with numerous
34 nd b, the 452 aa Pfs230 is secreted into the parasitophorous vacuole and released as a soluble protei
35 arum infects an erythrocyte, it resides in a parasitophorous vacuole and remarkably exports proteins
36  1 clone (C9) formed morphologically unusual parasitophorous vacuoles and another (A2) was avirulent
37 a-activated macrophages results in collapsed parasitophorous vacuoles and increased host cell necrosi
38 nfected with T. gondii resulted in fusion of parasitophorous vacuoles and late endosomes/lysosomes.
39    Ligation of CD40 caused colocalization of parasitophorous vacuoles and LC3, a marker of autophagy,
40  a host cell, invasion, replication within a parasitophorous vacuole, and egress from the cell.
41 , inhibitory compounds must cross host cell, parasitophorous vacuole, and parasite membranes and cyst
42 mulation of LC3-containing vesicles near the parasitophorous vacuole, and to the relocalization towar
43 the rupture of infected erythrocytes but not parasitophorous vacuoles, and independently interfering
44 ndicating that formation of the junction and parasitophorous vacuole are molecularly distinct steps i
45 sion and survival of the parasite within the parasitophorous vacuole are required to induce and maint
46  are required for peptide degradation in the parasitophorous vacuole as the degradation of the marker
47  GRA6, a polymorphic protein secreted in the parasitophorous vacuole, as the source of the immunodomi
48  a unique intracellular but extracytoplasmic parasitophorous vacuole at the apical surface of infecte
49 rspectives for future research directions in parasitophorous vacuole biology.
50 the liver, invade hepatocytes, and develop a parasitophorous vacuole but do not significantly persist
51 otes, Toxoplasma propagates in intracellular parasitophorous vacuoles, but like nearly all other euka
52 s produced in the parasite mitochondrion and parasitophorous vacuole by decarboxylation of phosphatid
53 structure is produced by modification of the parasitophorous vacuole by the parasite and is important
54                                              Parasitophorous vacuoles contained sexual and asexual fo
55 e within tissue cysts, which are specialized parasitophorous vacuoles containing bradyzoites.
56 elin hydrolysis, is detected in newly formed parasitophorous vacuoles containing trypomastigotes but
57 lar pathogen that replicates in an acidified parasitophorous vacuole derived from host lysosomes.
58 f host protective responses, escape from the parasitophorous vacuole, differentiation, and other acti
59  revealed that the protein is present in the parasitophorous vacuole during growth and is later recru
60  the rhoptries are released into the nascent parasitophorous vacuole during invasion into the host ce
61       Toxoplasma gondii sporozoites form two parasitophorous vacuoles during development within host
62 pathways of host-parasite interaction at the parasitophorous vacuole employed by Toxoplasma and host,
63 lpB1), rhoptries (RON6), dense granules, and parasitophorous vacuole (EXP2, PTEX150, HSP101).
64  trafficking, leading to the biogenesis of a parasitophorous vacuole for intracellular replication.
65 hagosome for Mycobacterium tuberculosis or a parasitophorous vacuole for Toxoplasma gondii.
66                    The T4SS is essential for parasitophorous vacuole formation, intracellular replica
67 rectly into the host cells, participating in parasitophorous vacuole formation.
68  II molecules and FcR were excluded from the parasitophorous vacuole formed by active parasite invasi
69               Despite the segregation of the parasitophorous vacuole from the host endocytic network,
70 brane proteins are excluded from the forming parasitophorous vacuole hence conferring the resistance
71 unctional role for CT147 in establishing the parasitophorous vacuole in a nonfusogenic pathway.
72 in 1 was concentrated in the vicinity of the parasitophorous vacuole in infected cells.
73  that directs biogenesis of a lysosome-like, parasitophorous vacuole in mammalian cells.
74 ell, Toxoplasma forms a novel organelle, the parasitophorous vacuole, in which it resides during its
75 fore invading a hepatocyte by formation of a parasitophorous vacuole, in which they developed into th
76 atis elementary bodies and in the chlamydial parasitophorous vacuole (inclusion) membrane of infected
77 ranslation inhibits early trafficking of the parasitophorous vacuole (inclusion) to the microtubule-o
78 esicular bodies with the bacteria-containing parasitophorous vacuole ("inclusion").
79 -specific Ab, did not block formation of the parasitophorous vacuole, indicating that formation of th
80 granules--serves to establish and maintain a parasitophorous vacuole inside the host cell in which th
81 that Toxoplasma proteins can escape from the parasitophorous vacuole into the host cytoplasm and be p
82 y malaria merozoites involves formation of a parasitophorous vacuole into which the parasite moves.
83 st cellular attack physically disrupting the parasitophorous vacuole, involves autophagy to collect c
84                                          The parasitophorous vacuole is a unique replicative niche fo
85 se interaction of host mitochondria with the parasitophorous vacuole is connected to lipoate supply b
86                            The lysosome-like parasitophorous vacuole is subsequently disrupted, relea
87  syntaxin-5 in the development of Leishmania parasitophorous vacuoles (LPVs).
88  apical membranes overlying the parasite and parasitophorous vacuole may be the unsuspected major rou
89 es specific for proteins associated with the parasitophorous vacuole membrane (Pfs16 or Exp-1) or Mau
90 mma enhanced the recruitment of LC3 onto the parasitophorous vacuole membrane (PVM) and increased the
91 lasma-secreted protein that localizes to the parasitophorous vacuole membrane (PVM) and mediates pass
92 screte subcellular reservoirs and attack the parasitophorous vacuole membrane (PVM) as orchestrated,
93 ess and address the debate regarding how the parasitophorous vacuole membrane (PVM) is formed, we dev
94                                         This parasitophorous vacuole membrane (PVM) is often retained
95                             We show that the parasitophorous vacuole membrane (PVM) is permeabilized
96                                          The parasitophorous vacuole membrane (PVM) is the critical i
97        RNF213-mediated ubiquitination of the parasitophorous vacuole membrane (PVM) led to growth res
98 s a protein translocon (PTEX) complex at the parasitophorous vacuole membrane (PVM) of infected eryth
99 f phosphorylated IkappaB that is seen at the parasitophorous vacuole membrane (PVM) of T. gondii was
100                                          The parasitophorous vacuole membrane (PVM) surrounding T. go
101 ausative agent of malaria, wraps itself in a parasitophorous vacuole membrane (PVM), which constitute
102 thin a specialized vacuole surrounded by the parasitophorous vacuole membrane (PVM).
103 hepatocytes as liver stages, surrounded by a parasitophorous vacuole membrane (PVM).
104 ) either in the parasite cytoplasm or on the parasitophorous vacuole membrane (PVM).
105 th the parasite membranes, presumably at the parasitophorous vacuole membrane (PVM).
106  to an inability to rapidly permeabilize the parasitophorous vacuole membrane and host plasma membran
107 he export of hundreds of proteins across the parasitophorous vacuole membrane and into the human host
108 by Toxoplasma to overcome the barrier of the parasitophorous vacuole membrane and thereby allow the d
109 B1-deficient parasites failed to rupture the parasitophorous vacuole membrane and to egress from hepa
110  cells, but it is embraced by a double-layer parasitophorous vacuole membrane derived from host cell.
111 where it resides with little turnover in the parasitophorous vacuole membrane for most of the remaind
112 Additionally, the enrichment of TOM70 at the parasitophorous vacuole membrane interface suggests para
113 s reduced in uis4(-) parasites, which lack a parasitophorous vacuole membrane protein and arrest duri
114 s located on the gametocyte plasma membrane, parasitophorous vacuole membrane, and the membranes of c
115  for the disruption of the gamete-containing parasitophorous vacuole membrane, and thus for parasite
116 across its plasma membrane and a surrounding parasitophorous vacuole membrane, into its host erythroc
117 its parasite plasma membrane and surrounding parasitophorous vacuole membrane, most of which are like
118  by inhibiting the expansion of the encasing parasitophorous vacuole membrane.
119 rane domain connecting to two regions across parasitophorous vacuole membrane.
120 specific protein 16 (Pfs16) localized to the parasitophorous vacuole membrane.
121 cates with the host cell cytosol through the parasitophorous vacuole membrane.
122 ellular parasite infection by disrupting the parasitophorous vacuole membrane.
123      Based on these findings we propose that parasitophorous vacuoles not only offer protection but a
124 incorporation into the vacuole generates the parasitophorous vacuole occupied by TOXOPLASMA: The char
125 findings reveal the presence in the malarial parasitophorous vacuole of a regulated, PfSUB1-mediated
126         This network was also present in the parasitophorous vacuole of Encephalitozoon hellem.
127 ic environment of the sandfly gut and/or the parasitophorous vacuole of host macrophages.
128 form of DPAP1 was found to accumulate in the parasitophorous vacuole of mature parasites.
129 , molecular composition and functions of the parasitophorous vacuole of Plasmodium blood stages.
130 anules of T. gondii and is also found in the parasitophorous vacuole of replicating parasites.
131 ding protein family that is recruited to the parasitophorous vacuole of the intracellular parasite To
132 ichia coli beta-lactamase, secreted into the parasitophorous vacuole of transgenic tachyzoites was co
133 's membranous nanotubular network within the parasitophorous vacuole play a major role in determining
134                       We find the chlamydial parasitophorous vacuole protein CT135 triggers NLRP3 inf
135 ted bradyzoite stage, TgPL1 localizes to the parasitophorous vacuole (PV) and cyst wall.
136  0-12-h parasites is found released into the parasitophorous vacuole (PV) and in apposition with the
137  During infection, T. gondii replicates in a parasitophorous vacuole (PV) and modulates host function
138 rasite Plasmodium falciparum reside within a parasitophorous vacuole (PV) and set up unique "extrapar
139 ades a host erythrocyte, multiplies within a parasitophorous vacuole (PV) and then ruptures the PV an
140 tii generates a replication niche termed the parasitophorous vacuole (PV) by directing fusion with au
141 hat undergoes a biphasic life cycle within a parasitophorous vacuole (PV) called an inclusion.
142                           The formation of a parasitophorous vacuole (PV) establishes their intracell
143 lular bacterium that directs biogenesis of a parasitophorous vacuole (PV) for replication.
144 parasite proficiently adapted to thrive in a parasitophorous vacuole (PV) formed in the cytoplasm of
145 at replicates within an acidic lysosome-like parasitophorous vacuole (PV) in human macrophages.
146 es found that IGTP induces disruption of the parasitophorous vacuole (PV) in macrophages.
147 parasite Toxoplasma gondii develops within a parasitophorous vacuole (PV) in mammalian cells, where i
148 sisting the acidic pH of lysosomes to form a parasitophorous vacuole (PV) in which to replicate.
149 stem (T4SS) to generate a phagolysosome-like parasitophorous vacuole (PV) in which to replicate.
150 gosomes and lysosomes, establishing a unique parasitophorous vacuole (PV) in which to replicate.
151                      We demonstrate that the parasitophorous vacuole (PV) of T. gondii accumulates ma
152                       mGBP2 localizes at the parasitophorous vacuole (PV) of T. gondii; however, the
153 r macrophages in a unique phagolysosome-like parasitophorous vacuole (PV) required for survival.
154 en Coxiella burnetii directs biogenesis of a parasitophorous vacuole (PV) that acquires host endolyso
155 Liver stage Plasmodium parasites reside in a parasitophorous vacuole (PV) that associates with lysoso
156    Toxoplasma multiplies in a membrane-bound parasitophorous vacuole (PV) that interacts with mammali
157 omplexa that resides within an intracellular parasitophorous vacuole (PV) that is selectively permeab
158 ggers a pathway of lysosomal fusion with the parasitophorous vacuole (PV) to help clear Plasmodium.
159 ted biogenesis of a large, growth-permissive parasitophorous vacuole (PV) with phagolysosomal charact
160 i directs biogenesis of a phagolysosome-like parasitophorous vacuole (PV), in which it replicates.
161 king processes, particularly export from the parasitophorous vacuole (PV), is poorly understood and a
162 xoplasma gondii resides within a specialized parasitophorous vacuole (PV), isolated from host vesicul
163 a gondii resides within mammalian cells in a parasitophorous vacuole (PV), which closely contacts the
164 asmodium, replicates inside a membrane-bound parasitophorous vacuole (PV), which shields this intrace
165 throcyte (RBC) using a unique organelle, the parasitophorous vacuole (PV).
166 f the intravacuolar network (IVN) within the parasitophorous vacuole (PV).
167 parum replicates within an intraerythrocytic parasitophorous vacuole (PV).
168  formation of a specialized compartment, the parasitophorous vacuole (PV).
169 a unique membrane-bound vacuole known as the parasitophorous vacuole (PV).
170  within host cells by forming a nonfusogenic parasitophorous vacuole (PV).
171 te within a protective organelle, called the parasitophorous vacuole (PV).
172 D55, were also readily incorporated into the parasitophorous vacuole (PV).
173 pecialized membranous compartment termed the parasitophorous vacuole (PV).
174 ma gondii by inducing the destruction of the parasitophorous vacuole (PV).
175 alciparum replicates in an intraerythrocytic parasitophorous vacuole (PV).
176 ts own membrane-bound compartment, named the parasitophorous vacuole (PV).
177 asite replicates within an intraerythrocytic parasitophorous vacuole (PV).
178 icates in a modified acidic phagolysosome or parasitophorous vacuole (PV).
179 ts biogenesis of a vacuolar niche termed the parasitophorous vacuole (PV).
180 lysosomal trafficking pathways to form large parasitophorous vacuoles (PV) enabling parasite survival
181 thetase (iNOS) is highly enriched at GBP2(+) parasitophorous vacuoles (PV) in murine macrophages.
182  LBs were restricted to parasites inside the parasitophorous vacuoles (PV).
183 l fusions with parasite-containing vacuoles (parasitophorous vacuoles [PV]).
184  nitroblue tetrazolium, we found that 25% of parasitophorous vacuoles (PVs) that harbor promastigotes
185 d low pH, conditions found within macrophage parasitophorous vacuoles (PVs).
186 olesale transport of LDs into the lumen of a parasitophorous vacuole represents a unique mechanism of
187 ich are secreted via dense granules into the parasitophorous vacuole shortly after invasion, become p
188 rasite organelles (termed exonemes) into the parasitophorous vacuole space.
189 ocalized with a dense granule protein in the parasitophorous vacuole space.
190 r bacterium Chlamydia trachomatis occupies a parasitophorous vacuole termed an inclusion.
191 tracellular bacterium that develops within a parasitophorous vacuole termed an inclusion.
192 , Chlamydia trachomatis, replicates within a parasitophorous vacuole termed an inclusion.
193 d) inhibited formation of the mature (large) parasitophorous vacuole that is characteristic of C. bur
194 ides in a specialized compartment termed the parasitophorous vacuole that is derived from the host ce
195 ted/secreted antigen fraction as well as the parasitophorous vacuole that T. gondii occupies during i
196 esides within a specialized compartment, the parasitophorous vacuole, that sequesters the parasite an
197 es GBP1 and its ability to target Toxoplasma parasitophorous vacuoles through its GTPase activity and
198 s invade erythrocytes and replicate within a parasitophorous vacuole to form daughter cells that even
199  of host cell lysosomes, and escape from the parasitophorous vacuole to liberate amastigotes to multi
200 ufficient methionine is available within the parasitophorous vacuole to meet the needs of the parasit
201  results may suggest that TgPL1 moves to the parasitophorous vacuole to protect parasites from nitric
202 ts a trafficking route for DPAP1 through the parasitophorous vacuole to the food vacuole.
203 ved from HRPII and HRPI exports GFP from the parasitophorous vacuole to the host cytoplasm.
204 complex membrane network, which connects the parasitophorous vacuole to the host plasma membrane and
205 parasite divides within an intraerythrocytic parasitophorous vacuole until rupture of the vacuole and
206  filamentous network within the lumen of the parasitophorous vacuole was discovered.
207 ishes a replicative niche in a lysosome-like parasitophorous vacuole where it carries out a lengthy i
208 parasite that invades host cells, creating a parasitophorous vacuole where it communicates with the h
209  protease called SUB1 is discharged into the parasitophorous vacuole, where it proteolytically proces
210 nteractions between host cell organelles and parasitophorous vacuoles, which contain the developing p
211 intracellular pathogen, replicates within an parasitophorous vacuole with lysosomal characteristics.
212                         Thus, formation of a parasitophorous vacuole with lysosomal properties is ess
213  tachyzoites, host cells, tachyzoites inside parasitophorous vacuoles within host cells, extracellula

 
Page Top