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1 macrophages within the granuloma, which they phagocytose.
2  they neither die at the injury site nor are phagocytosed.
3 ke of L. tropica by MCs, L. donovani was not phagocytosed.
4 are degraded while host cells are killed and phagocytosed.
5 nce at the cell body, bacteria could then be phagocytosed.
6 n-expressing recombinant of E. coli K-12 was phagocytosed.
7 tuberculosis survival and its ability to get phagocytosed.
8 hology when microbes were small enough to be phagocytosed.
9 aid in the recruitment of neutrophils, which phagocytose Ab- and complement-opsonized bacteria via Fc
10 y, adult microglia had diminished ability to phagocytose Abeta fibrils.
11          Microglia can be neuroprotective by phagocytosing Abeta; however, this comes at the cost of
12 rly also function when mammalian macrophages phagocytose aerosolized bacteria, and infection of human
13 display 1) significantly reduced capacity to phagocytose Ags via macropinocytosis and endocytosis as
14                        Cross-presentation of phagocytosed Ags by MHC class I (MHC-I) molecules is tho
15          Microglia may be neuroprotective by phagocytosing amyloid-beta (Abeta), but their activation
16 nd Fc receptors, suggesting that neutrophils phagocytose and clear antibody-opsonized bacteria via Fc
17                             Their ability to phagocytose and clear microorganisms has been well docum
18  Abeta plaques but are unable to efficiently phagocytose and clear plaques from the brain.
19 es from Cftr-/- mice retained the ability to phagocytose and generate an oxidative burst, but exhibit
20 ntation donors and compared their ability to phagocytose and inhibit A. fumigatus conidia.
21      Dendritic cells (DC) have been shown to phagocytose and kill Cryptococcus neoformans in vitro an
22 ice lacking TNF have a diminished ability to phagocytose and kill NTHi, and this defect is partially
23 lipoprotein enhanced the capacity of pDCs to phagocytose and prime antigen-specific T cell responses.
24  cell populations respond to immune stimuli, phagocytose and process Ag, and migrate from the injecti
25               This capacity of mast cells to phagocytose and retain whole and antigenically intact al
26 in blood cells affects the flies' ability to phagocytose and survive after an infection.
27 s were severely impaired in their ability to phagocytose and to generate reactive oxygen species in v
28 se of IL-33, whereas cleaved chitin could be phagocytosed and could induce the activation of caspase-
29          Primary cultures of human RPE cells phagocytosed and digested ROSs with kinetics comparable
30        First-responding resident macrophages phagocytosed and eradicated infecting mycobacteria, sugg
31 25 years ago demonstrating that antigens are phagocytosed and processed by antigen-presenting cells a
32                             Hemocyanins were phagocytosed and slowly processed.
33 n all influence whether B. pertussis will be phagocytosed and ultimately killed by neutrophils.
34  microglia are believed to be ineffective at phagocytosing and clearing amyloid-beta (Abeta), a major
35 s of tissue damage, to contract and possibly phagocytose, and to synthesize ECM components to promote
36 und by an unknown extracellular receptor, is phagocytosed, and traffics to lysosomes, where it is deg
37 re phagocytes that can acquire peptides from phagocytosed antigen to elicit cytotoxic immune response
38 preciation for the regulated presentation of phagocytosed antigens by MHC class II molecules as a dir
39 ) DCs was the processing and presentation of phagocytosed antigens containing Toll-like receptor stim
40 r machinery of macroautophagy, and maintains phagocytosed antigens for prolonged presentation on majo
41 ctional evidence for processing that allowed phagocytosed antigens to load into class I MHC was not d
42 g from phagosomes stimulates presentation of phagocytosed antigens, the mechanisms underlying this en
43  capacity of poorly phagocytic Mph1 cells to phagocytose apoptotic cells by a mechanism that was inde
44 he inability of Btk-deficient macrophages to phagocytose apoptotic cells efficiently, indicating the
45 ients with mild-moderate asthma were able to phagocytose apoptotic cells in response to LPS, resultin
46       SPM and LPM differ in their ability to phagocytose apoptotic cells, as well as in the productio
47 with significant decreases in the ability to phagocytose apoptotic host cells were produced.
48 iculin increased E. histolytica's ability to phagocytose apoptotic lymphocytes and calcium ionophore-
49  transfected with Megf10 gain the ability to phagocytose apoptotic neurons and that Megf10 binds with
50 rophages, but not peritoneal macrophages, to phagocytose apoptotic neutrophils.
51          Moreover, the CD31(+)F4/80(+) cells phagocytosed apoptotic cells as functionally matured mac
52 IM-4- or TIM-1-transfected cells efficiently phagocytosed apoptotic cells, and phagocytosis could be
53 ls expressing mouse or human TIM-3 bound and phagocytosed apoptotic cells, with the BALB/c allelic va
54 istolytica, the cause of invasive amebiasis, phagocytoses apoptotic host cells during tissue invasion
55 ly the MHC II(lo) population is effective at phagocytosing apoptotic cells in vivo and only the MHC I
56 tion by pruning synapses during development, phagocytosing apoptotic newborn neurons, and regulating
57  alveolar macrophages limited germination of phagocytosed Aspergillus fumigatus spores.
58  surface rodlet layer, wild-type spores were phagocytosed at similar rates as DeltalaeA spores.
59                           B. burgdorferi was phagocytosed avidly by monocytes, while T. pallidum was
60 the primary olfactory nerve and are known to phagocytose axon debris in the adult and postnatal anima
61 lpha increased the ability of neutrophils to phagocytose B. pertussis, suggesting that elevated CR3 e
62 sites of mycobacterial infection, where they phagocytose bacilli.
63 t trafficking of mycobacterial proteins from phagocytosed bacilli to exosomes was dependent on protei
64        Although both populations efficiently phagocytose bacteria in vivo, only the MHC II(lo) popula
65 acrophages fail to spread, transmigrate, and phagocytose bacteria, and SRF-deficient neutrophils show
66 exhibited a remarkable deficiency to spread, phagocytose bacteria, and synthesize cytokines in respon
67     Further, 24p3(-/-) neutrophils failed to phagocytose bacteria, which may account for the enhanced
68 tant and wild-type S. iniae and were able to phagocytose bacteria.
69 agents and are deficient in their ability to phagocytose bacteria.
70  produce superoxide or undergo chemotaxis or phagocytose bacteria.
71  not polymorphonuclear leukocytes (PMNs), to phagocytose bacteria.
72                                    Hemocytes phagocytosed bacteria after injection, and antimicrobial
73 cence; fluorescence microscopy revealed that phagocytosed bacteria were completely quenched but that
74 when they were pretreated with AHLs, rapidly phagocytosed bacteria, whereas untreated cells phagocyto
75 d greater antimicrobial activity against the phagocytosed bacteria.
76 e capabilities of killing and containment of phagocytosed bacteria.
77 ysfunction affect neutrophil chlorination of phagocytosed bacteria.
78 sis, in contrast to neutrophils that had not phagocytosed bacteria.
79 matory sites and by enhancing the killing of phagocytosed bacterial pathogens.
80 mber of phagocytosing macrophages (-12%) and phagocytosed beads within macrophages (-15%) in CX3CR1(G
81 ed macrophages from multiple tissues as they phagocytosed blood-borne cellular material.
82                                              Phagocytosed Borrelia burgdorferi (Bb) induces inflammat
83         We have previously demonstrated that phagocytosed Borrelia burgdorferi induces activation pro
84 ively sample the tissue microenvironment and phagocytose both microbial and host apoptotic cells.
85               We found that supporting cells phagocytose both type I and II hair cells.
86 diates (wbbL2 and MMAR_2331) and efficiently phagocytosed but less than class I mutants; class III, l
87                 ACT mutants were efficiently phagocytosed, but wild-type B. pertussis or ACT mutants
88 nd that IgE-bound particulate allergens were phagocytosed by activated mast cells in a lipid raft-dep
89 ythrocytes from anti-C5-treated patients are phagocytosed by activated monocytes in vitro.
90 nt beads in vitro and the number of bacteria phagocytosed by alveolar macrophages in vivo was decreas
91      We found that C. neoformans spores were phagocytosed by alveolar macrophages via interactions be
92 causative agent of Legionnaires' disease, is phagocytosed by alveolar macrophages, it delivers a larg
93 oposes that airborne bacilli are inhaled and phagocytosed by alveolar macrophages, resulting in the f
94            Once inside the host, conidia are phagocytosed by alveolar macrophages.
95 tion back to the bone marrow, where they are phagocytosed by bone marrow macrophages.
96  and shown that in vivo, they are ultimately phagocytosed by bone marrow stromal macrophages.
97 les, which are rich in arachidonic acid, are phagocytosed by CACs.
98 ge number of apoptotic neurons generated are phagocytosed by glial precursor cells.
99  bacterial genes after the pathogen had been phagocytosed by host cells.
100 l-induced hepatocyte apoptotic bodies can be phagocytosed by HSCs and Kupffer cells and result in inc
101 ined its intrabacterial pH and survived when phagocytosed by IFN-gamma-activated macrophages.
102 rensis, the causative agent of tularemia, is phagocytosed by immune cells such as monocytes and macro
103 umoral immune system alone, but many must be phagocytosed by individual hemocytes or encapsulated by
104  rodent hippocampus, with interneuron debris phagocytosed by infiltrating microglia.
105 evealed that at 42 h 38% of JG752 cells were phagocytosed by leech macrophage-like cells compared wit
106 tissues, where they become apoptotic and are phagocytosed by macrophages and dendritic cells.
107                             F. tularensis is phagocytosed by macrophages followed by escape from phag
108 d exosomes released by capsaicin are readily phagocytosed by macrophages in which an increase in miR-
109                     Bacteria are efficiently phagocytosed by macrophages strategically located undern
110           spxB mutants were less efficiently phagocytosed by macrophages than wild-type bacteria, whi
111 onized pathogens, particles, or proteins are phagocytosed by macrophages through Fcgamma receptors (F
112                            C. albicans cells phagocytosed by macrophages undergo a dramatic change in
113 lliptical disk-shaped particles that are not phagocytosed by macrophages were made to internalize thr
114 at apoptotic nanoparticle-labeled hMSCs were phagocytosed by macrophages while viable nanoparticle-la
115                  Apoptotic cells are rapidly phagocytosed by macrophages, a process that represents a
116 erved in vitro that all 3 nanoparticles were phagocytosed by macrophages, while alphavbeta3-integrin-
117                 On infection, it is actively phagocytosed by macrophages; it then escapes from the ph
118              These cells were preferentially phagocytosed by monocyte-derived macrophages, thus linki
119 sing Cd47 were less frequently contacted and phagocytosed by murine RAW264.7 macrophages in vitro tha
120    FHA mutants failed to attach and were not phagocytosed by neutrophils.
121 g85A-infected ALDC and containing Ag85A were phagocytosed by noninfected migrating ALDC expressing SI
122                  Fibrillar Abeta was rapidly phagocytosed by postnatal microglia and both oligomeric
123 nosome-rich packages, which subsequently are phagocytosed by the keratinocyte.
124 eptors daily shed their distal OS, which are phagocytosed by the RPE cells.
125                        Dendritic cells (DCs) phagocytose C. neoformans following inhalation.
126                    Dendritic cells (DCs) can phagocytose C. neoformans, present cryptococcal antigen,
127  By confocal microscopy, a greater number of phagocytosed C. neoformans cells in wild-type mice than
128 rphi) and the ability of these cells to kill/phagocytose Candida albicans or Escherichia coli cells b
129 t the efficiency of presenting antigens from phagocytosed cargo is dependent on the presence of TLR l
130  which results in optimal degradation of the phagocytosed cargo.
131 as where nonhematopoietic cells express CD47 phagocytose CD47(null) cells, whereas those in the chime
132 ges recognize CD47 as a marker of "self" and phagocytose CD47(null) hematopoietic cells.
133 D47-deficient mice, whose macrophages do not phagocytose CD47-/- mouse cells, showed markedly delayed
134 D-1 on, and apoptosis of, CD8(+) T cells and phagocytosed CD8(+) T cells.
135  exist with regard to the ability of pDCs to phagocytose cell-derived particulate Ags and cross-prese
136       Here we demonstrate that rigidity of a phagocytosed cell also hyperactivates myosin-II, which l
137 ICANCE STATEMENT The roles of microglia, the phagocytosing cells of the CNS, and invading macrophages
138 papA4), devoid of LOS and highly efficiently phagocytosed; class II, accumulating only early LOS inte
139 and undergo calcium transients, and robustly phagocytose CNS substrates.
140            Both monocyte subsets efficiently phagocytose conidia, but only CD14(+)CD16(-) monocytes i
141                                              Phagocytosed cryptococcal cells exhibited less viability
142      We show that macrophages preferentially phagocytose cryptococci with smaller polysaccharide caps
143 onstrated that DC in the lung are capable of phagocytosing Cryptococcus in vivo and presenting antige
144 tor expressed on microglia and is thought to phagocytose damaged brain cells.
145  major role in the early response to SCI, by phagocytosing damaged and degenerating tissue, processin
146 mmatory responses, degrade lipoproteins, and phagocytose dead cells.
147 use, the CD8alpha+ subset of dendritic cells phagocytoses dead cell remnants and cross-primes CD8+ T
148 analysis to confirm that the radial glia had phagocytosed debris from olfactory axons.
149 lia has been in brain infection and disease, phagocytosing debris and secreting factors to modify dis
150                            These macrophages phagocytose degenerating OSNs and secrete chemokines, wh
151                  CpG-loaded tumor cells were phagocytosed, delivering both tumor antigen(s) and the i
152 ough comparable inflammatory disease because phagocytosed DNA from apoptotic cells cannot be adequate
153 ivery of Yops into cells that were unable to phagocytose due to the presence of cytochalasin D.
154                      Activated microglia can phagocytose dying, stressed, or excess neurons and synap
155 e that the host cells expressing DC-SIGN can phagocytose E. coli in part by interacting with the comp
156 ased proteolysis and killing of subsequently phagocytosed E. coli compared to naive macrophages.
157 ro studies have suggested that RPE cells can phagocytose emulsified oil droplets, this report represe
158 acrophages were IFNgamma treated and contain phagocytosed erythrocytes, a model for haemophagocytosis
159           Mast cells retained the ability to phagocytose Escherichia coli particles and respond to TL
160 ent copper transport is required for killing phagocytosed Escherichia coli in a cultured macrophage c
161                         HMs are able to kill phagocytosed Escherichia coli, produce reactive nitrogen
162    We show that macrophages are incapable of phagocytosing Exserohilum Despite a lack of phagocytosis
163           Here we show that both soluble and phagocytosed extracellular Ags accessed the cytosol via
164 agocytosed bacteria, whereas untreated cells phagocytosed fewer bacteria.
165  ANE significantly impaired their ability to phagocytose fluorescent beads.
166 It also inhibited perinuclear aggregation of phagocytosed fluorescent microspheres and reduced mean c
167 cytose fungal cells, PBMCs did not appear to phagocytose fungal cells in biofilms.
168 MCs with planktonic C. albicans, where PBMCs phagocytose fungal cells, PBMCs did not appear to phagoc
169  of peritoneal macrophages from C3(-/-) mice phagocytosed GPs, and this percentage was further reduce
170 demonstrated that human dendritic cells (DC) phagocytose H. capsulatum yeasts and, unlike human macro
171             The ability of E. histolytica to phagocytose host cells correlates with virulence in vivo
172 e-silenced strains with a reduced ability to phagocytose host cells validates the previously publishe
173 , this effect was independent of whether the phagocytosed Huh7.5.1 cells were infected with HCVcc.
174 man blood, porcine Kupffer cells bind to and phagocytose human erythrocytes causing the hematocrit to
175 9 cells maintained in this medium could also phagocytose human photoreceptor outer segments (POS).
176 orcine livers also have shown the ability to phagocytose human platelets in the absence of immune-med
177 ur data suggest that primary pig KC bind and phagocytose human platelets with involvement of CD18.
178 way are decreased with ageing in both myelin-phagocytosing human monocytes and mouse macrophages usin
179  in pH determined the rate of degradation of phagocytosed ICs.
180 g these blocks reduces the cell's ability to phagocytose IgG-opsonized bioparticles by decreasing Fc
181 like receptor 3 (TLR3) pathway detects dsRNA phagocytosed in endosomes; the helicases retinoic acid-i
182 arriving macrophages to efficiently find and phagocytose infected macrophages undergoing apoptosis, l
183 hat trophoblast giant cells of aborting mice phagocytosed infected red blood cells and hemozoin.
184 cell niche for M. tuberculosis, are not only phagocytose inhaled microbes and particulate matter but
185 acellular transport, we examined latex beads phagocytosed into living mammalian macrophages.
186 thogenic bacterium Legionella pneumophila is phagocytosed, it injects more than 250 different protein
187                  We investigated whether DCs phagocytosing killed lymphoma cells coated with tumor-sp
188 or-specific T cells by dendritic cells (DCs) phagocytosing killed tumor cells can be augmented in the
189 ne of defense of the innate immune system by phagocytosing, killing, and digesting bacteria and fungi
190 myeloperoxidase, are less capable of killing phagocytosed L. monocytogenes, and have decreased oxidat
191  fly transmission or needle inoculation, but phagocytosed L.m. remained viable and infected neutrophi
192  histochemical and ultrastructural analyses, phagocytose-labeled bacterial preparations in vivo, and
193                        Dendritic cells (DCs) phagocytose large particles like bacteria at sites of in
194 -alpha) production; and in vitro capacity to phagocytose latex beads and to migrate toward the chemok
195 litates phagolysosomal fusion for killing of phagocytosed Listeria.
196 tion activity was observed in DCs containing phagocytosed live or dead parasites.
197  to examine the response of individual cells phagocytosing living parasites.
198 f alveolar macrophages from diabetic mice to phagocytose M. tuberculosis ex vivo and promote T-cell a
199 res, iron was preferentially taken up by non-phagocytosing, M1-polarized macrophages and induced M1 (
200 aging in MS patients: iron is present in non-phagocytosing, M1-polarized microglia/macrophages at the
201 onuclear leukocytes (PMN) influx followed by phagocytosing macrophage (Mphis) that clear injurious st
202 s at 3 (+89%) but not 1 d, reduced number of phagocytosing macrophages (-12%) and phagocytosed beads
203 t low-grade secondary inflammation involving phagocytosing macrophages amplifies demyelination, Schwa
204 low-grade secondary inflammation implicating phagocytosing macrophages amplifies demyelination, Schwa
205 e, genetically null for CLIC4, the number of phagocytosing macrophages stimulated by LPS is reduced.
206 d in MS tissue sections predominantly in non-phagocytosing macrophages/microglia at the edge of estab
207 stinguish between cell-membrane adherent and phagocytosed magnetic particles.
208  functions include secretion, trafficking of phagocytosed material, replication and egress of viral p
209 d in the perinuclear-directed aggregation of phagocytosed melanosomes.
210 ited to sites of infection, to recognize and phagocytose microbes, and then to kill pathogens through
211  cross-presentation of peptides derived from phagocytosed microbes, infected cells, or tumor cells to
212 sional wounds, but are able to recognise and phagocytose microbial antigens.
213 ng cell and formyl peptide receptor 2 on the phagocytosing microglia.
214  as a defense mechanism for the clearance of phagocytosed microorganisms.
215 is study demonstrates that human macrophages phagocytose more Francisella than monocytes with contrib
216 nocytes were shown to be more aggressive and phagocytose more particles.
217 he absence of complement, these mutants were phagocytosed more efficiently by macrophages than wild-t
218 cytes opsonized with serum or human C1q were phagocytosed more efficiently than control cells, an eff
219 h C1q, MBL, or purified collectin tails were phagocytosed more efficiently than control particles.
220 ease of FHA from the bacterial surface, were phagocytosed more efficiently than wild-type bacteria.
221                                              Phagocytosed Mtb did not replicate within MSCs, thus sug
222                                MDSCs readily phagocytosed Mtb, and released proinflammatory (IL-6, IL
223                For example, when macrophages phagocytose Mucor yeast, subsequent phagosomal maturatio
224                          We report that MSCs phagocytose Mycobacterium tuberculosis (Mtb) through two
225 icroglial cells some of these inclusions are phagocytosed myelin.
226 ular activity, but the exact cell types that phagocytose nanoparticles in vivo and how phagocytic act
227 (-/-) resident peritoneal macrophages (rPMs) phagocytose necrotic cells and other opsonized targets n
228                                          SCs phagocytose nerve terminals contacting the muscle fiber.
229 olonize the cortical proliferative zones and phagocytose neural precursor cells as neurogenesis nears
230  limit the production of cortical neurons by phagocytosing neural precursor cells.
231       In the first study, the mean number of phagocytosing neutrophils was statistically significantl
232 acrophages to be PMA-primed, untreated cells phagocytose nonopsonized silica and latex.
233                       Syt VII-/- macrophages phagocytose normally at low particle/cell ratios but sho
234                              Epidermal cells phagocytosed not only somatosensory axon debris but also
235 rted TAP dependence of cross-presentation of phagocytosed OVA may principally reflect a requirement f
236                          The presentation of phagocytosed OVA-ICs to CD4(+) T cells was considerably
237 thase and reactive oxygen intermediates, and phagocytose P chabaudi parasites in vitro, and in a prop
238 sed ability of cav1-deficient neutrophils to phagocytose P. aeruginosa.
239  isolated from embryos on day 7 of gestation phagocytosed P. chabaudi AS-infected red blood cells and
240 inacous products (encapsulated sporocysts or phagocytosed parasite components) and processing/degrada
241 of invasion-competent or invasion-inhibited (phagocytosed) parasites with IL-12p40 (YET40) reporter m
242 ted data suggests that gammadeltaT cells can phagocytose particles and act as professional antigen-pr
243                                              Phagocytosed particles are delivered via a complex route
244 ways-on" signals which compromise discerning phagocytosed particles from adherent particles.
245  In the phagosome-to-cytosol pathway, Ags in phagocytosed particles must become freely soluble before
246 omplex-II (MHC-II) antigen presentation from phagocytosed particles requires phagosome-intrinsic Toll
247 , a cysteine proteinase involved in lysis of phagocytosed particles; metabolic enzymes such as ornith
248 C populations retain the ability to actively phagocytose particulate Ags.
249 in activated DC populations, presentation of phagocytosed particulate Ags is dependent on the nature
250                                  Fibroblasts phagocytosed particulate wear debris and responded to cy
251 , as one of the antimicrobial agents to kill phagocytosed pathogens within phagolysosomes.
252 nt and required function is that the iPS-RPE phagocytose photoreceptor outer segments (POS).
253            Likewise, the autofluorescence of phagocytosed photoreceptor outer segments increased by l
254 ctants, but not their negative counterparts, phagocytosed PLA-expressing Y. pestis and Escherichia co
255 -deficient mice showed decreased capacity to phagocytose platelet-derived microvesicles.
256 of circulating PMPs but may serve to locally phagocytose PMPs generated at sites of platelet activati
257 e found that both endothelial cell types can phagocytose PMPs, and by using TAM-blocking antibodies o
258 n increased ability of these immune cells to phagocytose pneumococci independent of capsule.
259 nexin A2 recruitment to endosomes containing phagocytosed polyethylene particles.
260                Highly differentiated iPS-RPE phagocytose POS more efficiently than hfRPE.
261 etate enhanced the ability of macrophages to phagocytose preformed fibrillar amyloid-beta1-42 (P < 0.
262                  Newly recruited macrophages phagocytose previously infected apoptotic macrophages to
263                        Dendritic cells (DCs) phagocytose, process, and present bacterial antigens to
264 nction with hydrolysis pattern assessment of phagocytosed proteins, we demonstrated that NOX2 activit
265 ages with the chaperone isofagomine restored phagocytosed RBC clearance only partially, regardless of
266 hages had a defect in their ability to clear phagocytosed RBC, a phenotype of tissue-infiltrating GD
267 ly restored when macrophages were allowed to phagocytose red blood cells prior to infection.
268 and other pathogens that are too large to be phagocytosed remain unknown.
269  proteomic, and phosphoproteomic analysis of phagocytosing RPE cells, utilizing three different exper
270 creased capacity of CD36(-/-) macrophages to phagocytose S. pneumoniae, minor effects on mortality oc
271                    Macrophages recognize and phagocytose senescent or damaged erythrocytes.
272 , microglia pretreated with the TLR2 agonist phagocytosed significantly more bacteria than unstimulat
273  LOS-IV (losA, MMAR_2319, and MMAR_2321) and phagocytosed similarly to the control strain.
274 ines also display macrophage functions: They phagocytose small particles and bacteria, mount a partia
275 ytes, but we have found that epidermal cells phagocytose somatosensory axon debris in zebrafish.
276 injected but lack the parasite, or that have phagocytosed T. gondii.
277            B. thailandensis was more readily phagocytosed than B. pseudomallei, but both displayed si
278 amaged and apoptotic sperm were more rapidly phagocytosed than healthy ones, suggesting that depositi
279 n vitro, budding particles were more readily phagocytosed than smooth particles and induced more lipi
280 thin the deeper layers of the olfactory bulb phagocytose the axonal debris.
281 otein (PGRP) SC1a and impairs the ability to phagocytose the bacteria Staphylococcus aureus, but not
282 ic cell (DC) and macrophage populations that phagocytose the parasite or are infected can express IL-
283 lm) C. glabrata, human neutrophils initially phagocytose the yeast and subsequently release neutrophi
284 n recipient splenic CD11c(+) dendritic cells phagocytosing the injected ECDI-SPs.
285 ons degenerated and radial glia responded by phagocytosing the resulting debris.
286 ; Dictyostelium chemotax toward bacteria and phagocytose them as food sources.
287 f red blood cells in the spleen, but fail to phagocytose these red blood cells efficiently, and devel
288 hanisms whereby uterine decidual macrophages phagocytose this bacterium and tested the hypothesis tha
289                         Macrophages can also phagocytose tissue debris and produce pro-healing cytoki
290 ages TLRs on a murine macrophage while it is phagocytosed triggers the autophagosome marker LC3 to be
291                The ability of macrophages to phagocytose tumor cells might be exploited therapeutical
292 ditioned macrophages expressed FcgammaRs and phagocytosed tumor cells in the presence of a tumor Ag-t
293 lose proximity to dead cells and efficiently phagocytose tumour cells.
294 teracting with intact donor ECDI-SPs not yet phagocytosed undergo limited proliferation and are subse
295  defects, Arpc2(-/-) macrophages competently phagocytose via FcR and chemotax toward CSF and CX3CL1.
296 t in whole blood was shown to bind and to be phagocytosed via CD47-SIRPalpha interactions.
297      For bacterial replication to occur, the phagocytosed viable cells must be grown to a low cell de
298  showed that peritoneal B cells were able to phagocytose virulent C. burnetii bacteria and form Coxie
299 s of the E: a fraction (</=15%) of the E was phagocytosed, while the remaining E were stripped of IC.
300   They almost completely lost the ability to phagocytose zymosan beads.

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