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1 y genes and a predominant M1-like macrophage infiltrate.
2 cantly negatively associated with the immune infiltrate.
3  the intratumoral localization of the immune infiltrate.
4 elial cells within a dense inflammatory cell infiltrate.
5 sociated with the tumour spheroids that they infiltrate.
6 ature and intensity of the inflammatory skin infiltrate.
7 tch1 mutant tumours have an increased immune infiltrate.
8 ose chest X-rays were obtained had bilateral infiltrates.
9 ial origin of fibroblasts within fibro-fatty infiltrates.
10 me did not require the presence of bilateral infiltrates.
11 y (CAV) is associated with intragraft B cell infiltrates.
12  clinical outcomes than those with bilateral infiltrates.
13 demonstrate an increase in neuroinflammatory infiltrates.
14 -IAB22M2C again was able to detect CD8 tumor infiltrates.
15 ortant to determine the significance of such infiltrates.
16 and fibroblasts were detected in fibro-fatty infiltrates.
17 nown as Quilty effect or nodular endocardial infiltrates.
18 dle-shaped cells with prominent neutrophilic infiltrates.
19 tality was higher in those without bilateral infiltrates (14% vs 8%; p = 0.04).
20  that vacant lands citywide may cumulatively infiltrate 51-54% additional annual rainfall volume as c
21                                              Infiltrating adipose tissue (inFAT) is a newly recognize
22 nance of polymorphonuclear cell inflammatory infiltrate and a reduced extent of fibrosis were observe
23 and MMPs, together with apparent mononuclear infiltrate and increased collagenolysis confirm that hyp
24 -RWE, as indicated by lung inflammatory cell infiltrate and mediators, mucus hypersecretion, and seru
25 n vivo to an improved ability for T cells to infiltrate and repress tumors.
26 ' was defined to quantify the in situ T cell infiltrate and was demonstrated to be superior to the AJ
27 Delta3A-infected tumors have elevated T cell infiltrates and decreased expression of the CLEC2D recep
28 atic steatosis, portal fibrosis, lymphocytic infiltrates and ductular proliferation, lobular cholesta
29 erns and spatial distribution of lymphocytic infiltrates and facilitate improved quantification of TI
30 ciated with favorable changes in immune cell infiltrates and gene expression profiles in both the gut
31 nvestigating the associations between immune infiltrates and genetic or clinical features, and four m
32 f eosinophils also exhibit robust CD8 T cell infiltrates and have a better prognosis than patients wi
33 e was similar to controls but chronic immune infiltrates and pro-inflammatory gene activation, includ
34 nflammatory cytokines, alveolar inflammatory infiltrates and vascular microthrombi.
35 ory in the patient presenting with pulmonary infiltrates and/or fibrosis.
36 ained with this interface were examined with infiltrating and noninfiltrating tumors, and were compar
37 text of acute inflammation and discover both infiltrating and tissue-resident immune cells to be visi
38      We analyzed lung inflammation, cellular infiltrate, and airway hyperresponsiveness.
39 lls promote a neutrophilic inflammatory cell infiltrate, and persistent arthritis, via GM-CSF product
40  were performed to test 1) whether bilateral infiltrates are associated with elevated interleukin-1 r
41 st or interleukin-8 and 2) whether bilateral infiltrates are associated with worse clinical outcomes.
42               Glioblastoma-associated immune infiltrates are dominated by tumor-associated macrophage
43 LC) patients, and identify subtypes of tumor-infiltrated B cells and their diverse functions in the p
44 ciated with the intratumoral accumulation of infiltrated B cells.
45                                        Tumor-infiltrating B cells are heterogeneous, and their roles
46         In fact, a large proportion of islet-infiltrating B lymphocytes in the NOD mouse model of T1D
47 ed tumor cell areas, tumor stroma, and tumor-infiltrating blood vessels.
48  of the placenta revealed a dense macrophage infiltrate, but no evidence for the vasculopathy typical
49  caused them to form smaller tumors in mice, infiltrated by higher numbers of CD8(+) T cells that exp
50                CRC patients whose tumors are infiltrated by large numbers of eosinophils also exhibit
51                      Allografts were rapidly infiltrated by recipient leukocytes, which recapitulated
52 -Df-IAB22M2C) to monitor CD8(+) T-cell tumor infiltrates by PET.
53 ociated increase of both activated STAT3 and infiltrated CD11b+ cells in 4T1 model.
54 sident CD11b/CD45(int)Ly6C(-) microglia, and infiltrating CD11b(+)/CD45(high) monocytes/macrophages c
55 r rejection, associated with increased tumor-infiltrating CD4 and CD8 T cells.
56                  Surprisingly, sciatic nerve-infiltrating CD4(+) cells had an expansion of IFN-gamma(
57                              Nerve and islet-infiltrating CD4(+) T cells also differed by expression
58  depletion promoted GzmB expression by tumor-infiltrating CD4(+), and this was prevented by interleuk
59 ze was negatively associated with numbers of infiltrating CD4+ T cells, CD4+CD127+ T cells, and CD8+C
60 Carbon monoxide did not affect the number of infiltrating CD45(+) cells in the prostates of E. coli-
61 is often correlates with the number of tumor-infiltrating CD8 T cells, but many of these cells recogn
62  significantly increased the number of tumor-infiltrating CD8(+) T and natural killer cells, slowed t
63  increase fat uptake with HFD, whereas tumor-infiltrating CD8(+) T cells do not.
64 s, a comparison of these cells with melanoma-infiltrating CD8(+) T cells revealed upregulated cytokin
65 expression concomitant with higher number of infiltrating CD8(+) T cells.
66               There was no increase in tumor infiltrating CD8+ T cells expressing "exhaustion" marker
67                                        Tumor-infiltrating CD8+ T cells mediate antitumor immune respo
68 roposed to explain how these multiple tumour-infiltrating cell types block the development of an effe
69 med an unbiased examination of diverse islet-infiltrating cells during autoimmune diabetes in the non
70 e-cell analysis of intrinsic renal cells and infiltrating cells from patients with LN is a new approa
71                            Analysis of tumor-infiltrating cells in dual PARP-1/PARP-2-deficiency host
72 mitigation of the inflammatory status of the infiltrating cells, improved electrophysiologic visual f
73 myeloid, mesenchymal) and abundance of tumor-infiltrating cells.
74 ation, where inflammation was defined as >14 infiltrating cells/mm(2).
75  the first time complete regression of a non-infiltrating ciliary body medulloepithelioma with seedin
76 yzed by immunohistochemistry for immune cell infiltrate composition, by in situ RT-PCR and quantitati
77  pancreas and lung cancer are differences in infiltrating conventional dendritic cells (cDCs).
78 the extent of connective tissue inflammatory infiltrate (CTII) using the following markers (CD4, CD5,
79 ape, the data shows that spherical particles infiltrate deeper than fragments and fibers.
80 mantic segmentation method to identify tumor-infiltrated diagnostic regions within SRH images.
81 3), the most common histologic subtypes were infiltrating ductal carcinoma (IDC, 84.9%) and luminal A
82 er analyzed ex vivo the glomerular leukocyte infiltrate during NTN.
83            We also find that peritoneal LPMs infiltrate early ovarian tumours and that RXR deletion d
84          ALK5(DeltaCD8) mice have more tumor-infiltrating effector CD8(+) T cells, with more cytotoxi
85 lammatory cytokines (e.g., IL1B) from immune infiltrates, ELF3 in tumor cells was upregulated to trig
86                                 Knowledge of infiltrating endometriosis and its ultrasonographic feat
87      This paper illustrates the findings for infiltrating endometriosis involving the bowel and urina
88 culating human memory T cells preferentially infiltrated ES and showed diverse functional profiles of
89 stric biopsies showed a small-sized lymphoid infiltrate, expanding the lamina propria, with a non-des
90 f deleted genes while those with high immune infiltrate expressed higher levels of adaptive resistanc
91  characterized by a lack of prominent T cell infiltrates, extensive intratumoral heterogeneity, poor
92 essed in TMEs and induces apoptosis in tumor-infiltrating, Fas receptor-positive lymphocytes.
93 of graft failure increases with the level of infiltrated fat.
94 cell subsets were also characterized in lung infiltrates from critical COVID-19 patients.
95 containing protein 3 (TIM-3) expressed by TG infiltrating gB-specific CD8(+) T cells from the HSV-1 0
96 sy-proven patient data identified as diffuse infiltrating glioma patients whose disease progressed/re
97 ignificant challenge in follow-up of diffuse infiltrating gliomas, particularly high grade, which lea
98 by phagocytic resident liver macrophages and infiltrating Gr-1(+) myeloid cells.
99  cell infiltration and the migratory path of infiltrating H3K27M DMG cells into other midline structu
100                      Samples with low immune infiltrate had higher number of deleted genes while thos
101                                       B cell infiltrates have been associated with steroid resistance
102                                              Infiltrating host mononuclear cells are a likely source
103                         Patients with immune-infiltrated "hot" tumors demonstrate higher treatment re
104 umber of comorbidities (HR 5.41, P = 0.004), infiltrates (HR 3.08, P = 0.032), and neutropenia (HR 1.
105  Axl+Siglec-6+ DCs (ASDC), was also found to infiltrate human skin during wounding.
106 aring BDCA-2+CD123int DC subset that rapidly infiltrates human skin wounds and comprises a major DC p
107  Finally, a higher proportion of bone marrow-infiltrating ICOShigh/PD-1- Treg cells is a highly signi
108                             The inflammatory infiltrates identified were of chronic inflammatory cell
109 romoting the expansion of peripheral and CNS-infiltrating IL-10(+) T cells.
110 nd late DUX4 target genes, therefore, muscle-infiltrated immune cells may contribute the molecular la
111 nalysis of genomic, transcriptomic and tumor-infiltrating immune cell profiles demonstrated alignment
112                                        Tumor-infiltrating immune cells comprise a previously unrecogn
113 e tumor microenvironment (TME) that prevents infiltrating immune cells from performing their anticanc
114                        We characterize tumor-infiltrating immune cells from transplant and primary tu
115 examined steroid hormone receptors and tumor-infiltrating immune cells in metastatic lesions with or
116 bution of Notch3 expression in tissue versus infiltrating immune cells is unknown.
117                         The ability of tumor-infiltrating immune cells to promote tumor growth via th
118                                              Infiltrating immune cells were predominately neutrophils
119  an interferon signature in the skin without infiltrating immune cells, but with interferon-kappa pro
120 onally, by modulating the reuptake of tissue-infiltrating immune cells, lymphatics regulate immune re
121 s evaluated by immunohistochemistry in tumor infiltrating immune cells, while PD-L1 expression in the
122 rosstalk between stressed resident cells and infiltrating immune cells.
123 ers in a scRNAseq experiment involving tumor-infiltrating immune cells.
124                        The diverse leukocyte infiltrate in atherosclerotic mouse aortas was recently
125                                 The cellular infiltrate in protocol liver biopsies (PB) following ped
126 ty, increased perfusion and reduced cellular infiltrate in the allograft, when compared with conventi
127  stricturing by day 16, with an inflammatory infiltrate in the neuromuscular layers including eosinop
128  epicardial thickening and dense fibro-fatty infiltrates in atrial tissue sections from patients aged
129 ajority of cells comprising the inflammatory infiltrates in kidney allografts undergoing acute and/or
130  among tumor cells, stromal cells and immune infiltrates in the TME.
131 erum proinflammatory cytokines, inflammatory infiltrates in various organs, and amyloid deposits in t
132  juvenile mice displayed a sustained myeloid infiltrate (including monocytes and neutrophils) with in
133 t the quality of the tumor-associated T-cell infiltrate informs patient prognosis in primary Merkel c
134 ss (by 10% to 25%) and increased mononuclear infiltrate inside the membrane.
135                     However, how these cells infiltrate into the kidney are not fully elucidated.
136  that this flow causes inert microspheres to infiltrate into tumour spheroids via advection from the
137       Both infected and uninfected microglia infiltrated into hBORGs resulting in a triculture system
138                            However, bacteria infiltrated into the plant tissue are as virulent as the
139 as a reduction in the number of immune cells infiltrating into the brain, mitigation of the inflammat
140 ver, 0.4% and 2.0% ripasudil reduced CD45(+)-infiltrated leukocyte frequency, Cd11b and Cd11c mRNA le
141 3 d after CMH started), apoptotic removal of infiltrated leukocytes during the remission phase was ma
142 e antigen-4 (CTLA-4), respectively, on tumor-infiltrating leukocytes eliciting immunosuppression.
143 onclusion: (18)F-FAC PET can visualize brain-infiltrating leukocytes in a mouse MS model and can moni
144  suggest that (18)F-FAC accumulates in brain-infiltrating leukocytes in this model.
145 itated the targeted gene expression in tumor-infiltrating leukocytes, including antigen-presenting de
146 is (EAE) is a mouse disease model with brain-infiltrating leukocytes.
147 s in malignant and stromal cells, as well as infiltrating leukocytes.
148 tumor cells showed >80% GFP marking in tumor-infiltrating leukocytes.
149 18)F-FAC PET could noninvasively image brain-infiltrating leukocytes.
150 actions with cancer cells and crosstalk with infiltrating leukocytes.
151  effect of an immunomodulatory drug on brain-infiltrating leukocytes.
152 odel, the frequency of PD-1-expressing tumor-infiltrating LSD1-deficient CD8 T cells was greater than
153 oint blockade and adoptive transfer of tumor-infiltrating lymphocyte (TIL)-based therapies.
154 hocytes in a subset of TNBCs with high tumor-infiltrating lymphocyte content.
155 esolution subgroup significantly depended on infiltrating lymphocyte counts, with patients who showed
156 tions between functional hypoxia imaging and infiltrating lymphocyte levels as a potential predictor
157                        We also mined a tumor-infiltrating lymphocyte sample from a patient with melan
158 vestigation, we explored the effect of tumor-infiltrating lymphocyte subpopulations on lung cancer bi
159  nodal status (N0 vs rest), number of tumour-infiltrating lymphocytes (continuous variable), subtype
160             Direct competition between tumor-infiltrating lymphocytes (TIL) and cancer cells for meta
161    Here, we show that P2X7 activity in tumor-infiltrating lymphocytes (TIL) induces cellular senescen
162 DAC led to increased CD4(+) and CD8(+) tumor-infiltrating lymphocytes (TIL), PD1 expression, and tumo
163 en-specific, activated effector CD8(+) tumor-infiltrating lymphocytes (TILs) after interaction with t
164 d the role of CD226 in the function of tumor-infiltrating lymphocytes (TILs) and resistance to immuno
165 latory microenvironment harboring more tumor infiltrating lymphocytes (TILs) and up-regulation of inf
166                                        Tumor-infiltrating lymphocytes (TILs) are an important histopa
167 ACT) using ex vivo-expanded autologous tumor-infiltrating lymphocytes (TILs) can mediate complete reg
168 enhances the expansion and function of tumor-infiltrating lymphocytes (TILs) for treating cancer pati
169 ultifunctionality of CD8 + splenic and tumor-infiltrating lymphocytes (TILs) was impaired and associa
170                    The distribution of tumor-infiltrating lymphocytes (TILs) within the tumor microen
171 cell therapy (ACT) of ex vivo expanded tumor-infiltrating lymphocytes (TILs).
172 d a higher response of patient-matched tumor infiltrating lymphocytes against antigens diferentially
173 d, inhibits RANK pathway and increases tumor infiltrating lymphocytes and CD8(+) T cells.
174 at MHC class II (MHCII) expression and tumor infiltrating lymphocytes are important prognostic factor
175                          Generation of tumor-infiltrating lymphocytes begins when tumor antigens reac
176                                 CD8(+) tumor-infiltrating lymphocytes displayed low expression of CD2
177 n the presence of Wnt5A-depleted MDSC, tumor-infiltrating lymphocytes expressed decreased PD-1 and LA
178 FK_pY416 staining was also observed in tumor-infiltrating lymphocytes in a subset of TNBCs with high
179 y of this tool by using it to classify tumor-infiltrating lymphocytes in breast carcinoma and cutaneo
180 ssion is increased in keratinocytes and skin-infiltrating lymphocytes of psoriatic lesions in human s
181 omeostatic myeloid cells were outnumbered by infiltrating lymphocytes which modulated the local cell-
182 clinical-pathological data on stromal tumour-infiltrating lymphocytes, PAM50 subtypes, and expression
183 18 (IL-18) pathway are upregulated on tumour-infiltrating lymphocytes, suggesting that IL-18 therapy
184 -L1 expression in both tumor cells and tumor-infiltrating lymphocytes, suggesting that immune checkpo
185  and immunohistochemical stainings for tumor-infiltrating lymphocytes, tissue-based hypoxia, and micr
186 iers to the metabolism and activity of tumor infiltrating lymphocytes.
187  reflecting an increase in a subset of tumor-infiltrating M2-polarized macrophages.
188   Conditional knockout of TAK1 in microglial/infiltrated macrophages and neuronal lineages sensitizes
189 persistent DNA damage accumulation in tissue-infiltrating macrophages carrying an ERCC1-XPF DNA repai
190 signature and CD274 gene expression in tumor-infiltrating macrophages in humans.
191                                              Infiltrating macrophages promote inflammation and simult
192             TREM2 is also expressed by tumor-infiltrating macrophages.
193 genes shared between a microglia cluster and infiltrating macrophages.
194  innate immune response and increasing tumor infiltrating macrophages.
195 cular analysis are not performed, the subtle infiltrate may be easily overlooked.
196                                        Tumor-infiltrating MDSC from control animals showed a strong p
197 ddition, our investigation showed that tumor-infiltrating MDSCs from 6 GAC patients consisted of >35%
198 f activity is attributed to their ability to infiltrate microbial membranes.
199 mals occurred primarily in microglia and not infiltrated monocyte-derived macrophages.
200 onal abundance of tissue-resident microglia, infiltrating monocyte-derived macrophages, neutrophils,
201 cular integrity and accelerated apoptosis of infiltrated monocytes.
202 s, including neurons, astrocytes, microglia, infiltrating monocytes/macrophages, lymphocytes, and oth
203   Here, we report that STAT3 is activated in infiltrating monocytic cells near active MS lesions and
204                      Patients with bilateral infiltrates more often had a primary diagnosis of pneumo
205             Gamma delta (gammadelta) T cells infiltrate most human tumors, but current immunotherapie
206                     Nonetheless, eosinophils infiltrate multiple tumours and are equipped to regulate
207  phenotypic profile resembling that of tumor infiltrating myeloid and lymphoid populations, but with
208 th resulted in significantly decreased brain-infiltrating myeloid cells as well as attenuated cachexi
209 s cytometry revealed a wide heterogeneity of infiltrating myeloid cells with increased infiltration o
210   Understanding the migratory patterns of CP-infiltrating myeloid cells with intact and disrupted CX3
211 re splaying of muscle fibers by inflammatory infiltrates (n = 9) and mild fibrosis (n = 8) in the end
212 s well as the number and functions of tumour-infiltrating natural-killer and CD8(+) T lymphocytes.
213                                 Importantly, infiltrating nerves not only influence the tumor cells t
214 is currently known about the origin of tumor-infiltrating nerves, how they may be recruited to tumors
215 We demonstrated in a recent study that tumor-infiltrating neutrophil density correlated with TC size.
216 rface CD62L and upregulation of Cxcr4, heart infiltrating neutrophils acquired a unique SiglecF(hi) s
217 targeting versus CD56 for detection of tumor infiltrating NK cells.
218 , and NKp46 to determine expression on tumor-infiltrating NK cells.
219                  Finally, we find that tumor infiltrating NKT cells are highly enriched for the YY1(l
220         T cells isolated from the pancreatic infiltrates of nonobese diabetic mice have been shown to
221 syndrome oxygenation criteria with bilateral infiltrates on chest radiograph experience a more intens
222  days before symptom onset and had pulmonary infiltrates on imaging and whose illnesses were not attr
223                       Moreover, CD8-MP cells infiltrate oncogene-driven prostate tumors and express h
224 al healing at 3 days, 3 weeks, and 3 months, infiltrate or scar size at 3 weeks and 3 months, 3-day s
225                   There was no difference in infiltrate or scar size, percentage of epithelialized or
226 ging specific characteristics of immune cell infiltrates or aspects of the tumor microenvironment tha
227 , 95% confidence interval 1.09-2.52); >=2 mm infiltrate (OR 4.74, 2.68-8.40); and <=3 mm from corneal
228  (body temperature >38 degrees C), pulmonary infiltrates, or the need for supplemental oxygen in orde
229 mmation (glomerulitis, peritubular capillary infiltrates; p-values <=0.001) and segmental glomerulosc
230                      Here we show that ILC2s infiltrate pancreatic ductal adenocarcinomas (PDACs) to
231 (+) and CX(3)CR1(+) macrophages in the tumor infiltrate, paralleled by expansion of myeloid subsets e
232 ttractant pathway markedly reduced monocytic infiltrates, perineuronal nets, and autistic-like behavi
233                 These estimated tumor immune infiltrate populations have been associated with genomic
234 , including their interaction with allograft-infiltrating recipient immune cells and potential therap
235 nfiltration coincide with G1 arrest in tumor infiltrated Siah2(-/-) Tregs in vivo or following T cell
236 ronment, inhibition of SHP2 modulated T-cell infiltrates similar to checkpoint blockade.
237 covered a significant heterogeneity of tumor-infiltrating slan(+) -cells, including a macrophage-like
238 d features to explain the robust lymphocytic infiltrate, such as loss of mismatch repair protein expr
239 ression correlated with varying tumor immune infiltrates suggesting that the interaction between tumo
240 mation, which is reflected by high levels of infiltrating T cells and interferon-gamma (IFNgamma) sig
241                        There were more tumor-infiltrating T cells and MHCII(hi)-immune cells in tumor
242 omise in a variety of cancers, but how tumor-infiltrating T cells are activated remains unclear.
243 s the expression of CTLA-4 molecule on tumor-infiltrating T cells by siRNA-loaded chitosan-lactate (C
244                        The majority of tumor-infiltrating T cells exhibit a terminally exhausted phen
245            Gene expression analyses of tumor-infiltrating T cells following Yap deletion implicates Y
246 ished tumors promotes re-activation of tumor-infiltrating T cells for tumor control.
247                                        Tumor-infiltrating T cells mainly displayed exhausted and regu
248                            Presence of tumor-infiltrating T cells, but not programmed death-ligand 1
249 onment, including increased numbers of tumor-infiltrating T cells, elevated IFN signaling, and immune
250 ed to the downregulation of CTLA-4 on tumor -infiltrating T cells, which was associated with tumor re
251 eases MLK3 and Ppia gene expression in tumor-infiltrating T cells.
252  growth by suppressing the activity of tumor-infiltrating T cells.
253 sms of resistance of liver tumors in mice to infiltrating T cells.
254 hared antigenic epitopes recognized by tumor-infiltrating T lymphocytes (TILs) from eight melanoma pa
255 olic fitness and antitumor activity of tumor-infiltrating T lymphocytes (TILs).
256 h NGAL-deficient neutrophils with more renal infiltrating T(H)17 cells.
257                         Although plasma cell infiltrates tend to be more diffuse, B cells tend to agg
258                             Plasma cell-rich infiltrates tend to occur later, may be associated with
259 ted the involvement of virus-specific, joint-infiltrating Th1 cells as one of the main pathogenic med
260  oxygen species generation, and neutrophilic infiltrate that characterize the severe asthmatic phenot
261               We show here that glioma cells infiltrate the brain collectively as multicellular netwo
262  In this context, the B cell phenotypes that infiltrate the central nervous system during human immun
263 el10 homozygotes, neural crest cells fail to infiltrate the developing SV intermediate layer.
264 uenced by virus-specific CD8(+) T cells that infiltrate the ganglia at the onset of latency and contr
265 In type1 diabetes (T1D) autoreactive T-cells infiltrate the islets of Langerhans, depleting insulin-s
266                  During obesity, macrophages infiltrate the visceral adipose tissue and promote infla
267  pDCs, macrophages, neutrophils, and B cells infiltrated the CNS.
268 monstrated that in steady state, neutrophils infiltrated the mouse liver following a circadian patter
269 ed by a concurrent wild-type flank infection infiltrated the TG and were retained long term, suggesti
270 e cells appear to respond to noise damage by infiltrating the organ of Corti.
271  subset bias was observed among GC Tfh cells infiltrating the pancreas of NOD mice, which was enhance
272  main trajectory of human slan(+) -monocytes infiltrating the tonsil tissue is toward a macrophage-li
273 nal form of EB have significantly more cells infiltrating their wounds compared with patients with re
274 ttle is known as to how comparably large NCs infiltrate this vital intracellular barrier to enter the
275 argeted elimination of ALT cancer cells that infiltrate tissues and organs to become devastating tumo
276 erculosis (ATB), and IL-35-producing B cells infiltrated to tuberculous granuloma of patients with AT
277 , comparing histological features and immune infiltrates to previously published data on human neurob
278 decreased mucus production, reduced cellular infiltrates to the lung (especially ILC2s), and decrease
279  molecules preferentially expressed on tumor-infiltrating Tregs.
280 yrosine kinase-like orphan receptor 1 (ROR1) infiltrate tumors poorly and become dysfunctional.
281 de (Cy) transiently control tumor growth but infiltrate tumors poorly and lose function, similar to w
282  cells respond rapidly during infection, and infiltrate tumors, where they express high amounts of PD
283                   Our analysis revealed that infiltrated tumors are depleted of favorable PBRM1 mutat
284 somal losses of 9p21.3, as compared with non-infiltrated tumors, demonstrating how the potential inte
285  The pathology revealed diffusely and deeply infiltrating tumour cells extending through the dermis,
286 ilt and fine sand, while the particles might infiltrate up to 13 cm into sediment consisting of coars
287  the detection of intratumoral CD8(+) T-cell infiltrates upon either single or combination treatment
288  we studied the clonal composition of B cell infiltrates using 4 graft specimens with CAV.
289                            Deep stromal/ring infiltrate was associated with single-file round/ovoid o
290 of oxygenation defect, presence of bilateral infiltrates was associated with longer duration of mecha
291 eration, necrosis, and mononuclear leukocyte infiltrates, was observed in the dorsal root, autonomic,
292 -induced lung inflammation, focal neutrophil infiltrates were increased in CGD compared with WT mice
293                                       Tumors infiltrated with CD8(+) T cells (immune-active tumors) a
294 olent liver metastasis from a class 1B UM is infiltrated with clonally expanded plasma cells, indicat
295                                Tumors become infiltrated with diverse adaptive and innate immune cell
296 's syndrome (pSS) the exocrine glands become infiltrated with lymphocytes instigating severe damage t
297 ase symptoms was observed in silenced plants infiltrated with Pseudomonas syringae pv. tabaci express
298 tory distress syndrome but without bilateral infiltrates would have different inflammatory biomarker
299 n excess of 100 million per day, continually infiltrate wound dressings.
300 ls are major inflammatory cells that rapidly infiltrate wounds to provide antimicrobial functions.

 
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