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1 cluding effector CD8+ T cells from the tumor microenvironment.
2 al centre B cells and ASCs within the tumour microenvironment.
3 the same way by the local pressurized CO(2) microenvironment.
4 WAF1/CIP1) overexpression and protumorigenic microenvironment.
5 MCTs), supporting the formation of an acidic microenvironment.
6 as the specific source of FGF1 in the tumor microenvironment.
7 critical regulator of immunity in the tumour microenvironment.
8 and increased stromal cells within the tumor microenvironment.
9 sidered to be important players in the tumor microenvironment.
10 nformation on spatial position and the local microenvironment.
11 pecific proteases overexpressed in the tumor microenvironment.
12 or cell lineage in reprogramming the stromal microenvironment.
13 and regulatory pathways active in the aortic microenvironment.
14 lie the dual potential of TANs in the tumour microenvironment.
15 tial distributions and interactions with the microenvironment.
16 the ability of cells to interact with their microenvironment.
17 r heterogeneity, and complexity of the tumor microenvironment.
18 ch CXCR4 inhibition affects the tumor immune microenvironment.
19 hat host Wnt5a promotes an immunosuppressive microenvironment.
20 e to fluorescence quenching in the digestive microenvironment.
21 ithin the context of a disrupted bone marrow microenvironment.
22 stance and immunomodulation within the tumor microenvironment.
23 u) that leads to a highly vascularized tumor microenvironment.
24 -primed exhausted CD8 + T-cells in the tumor microenvironment.
25 well as the formation of a tumor-permissive microenvironment.
26 in diverse cell types that compose the tumor microenvironment.
27 ve despite nutrient limitations in the tumor microenvironment.
28 characterize the differences in their tumor microenvironment.
29 ct on angiogensis, a key factor in the tumor microenvironment.
30 populations reshape the immunological tumor microenvironment.
31 t hematopoietic cell type in the solid tumor microenvironment.
32 key characteristics and functions of in vivo microenvironment.
33 T regulatory cell distribution in the tumor microenvironment.
34 ing in small electrical changes in the tumor microenvironment.
35 neficial effects on the ovarian tumor immune microenvironment.
36 a proinflammatory and TGF-beta-low cytokine microenvironment.
37 of this critical cell type within the tumour microenvironment.
38 es with gene expression of LGP2 in the tumor microenvironment.
39 rveillance and sustain the suppressive tumor microenvironment.
40 osmotic pressures are altered in the tumour microenvironment.
41 which overcomes the immunosuppressive tumor microenvironment.
42 y regulation is complex and dependent on the microenvironment.
43 mmunosuppressive mechanisms within the tumor microenvironment.
44 erapy as a result of immunosuppressive tumor microenvironment.
45 ell cultures, thereby disrupting each cell's microenvironment.
46 ted with exclusion of T cells from the tumor microenvironment.
47 cell survival due to the harmful dystrophic microenvironment.
48 ncreased adenosine levels characterize tumor microenvironment.
49 ely create an inflammatory and profibrogenic microenvironment.
50 suggest the development of a malignant tumor microenvironment.
51 assessment of both tumor cells and the tumor microenvironment.
52 enotype of non-neoplastic cells in the tumor microenvironment.
53 te the development of a profibrotic cellular microenvironment.
54 onses in normal tissues as well as the tumor microenvironment.
55 lymphoma B-cells and other cells within the microenvironment.
56 d degree of immune infiltration in the tumor microenvironment.
57 immune suppression associated with the tumor microenvironment.
58 for effector T cell recruitment to the tumor microenvironment.
59 reveal how glioblastoma alters the neuronal microenvironment.
60 g, live lymph node sections and a live tumor microenvironment.
61 mitochondrial activity and the tumor immune microenvironment.
62 metastatic relapse by modulating the immune microenvironment.
63 epigenetic changes, and changes in the tumor microenvironment.
64 ven within a highly immune-suppressive tumor microenvironment.
65 different environments such as hypoxic tumor microenvironments.
66 for lung cancer pulmonary and the lung tumor microenvironments.
67 ation of localized biomolecular networks, or microenvironments.
68 the hemodynamic landscape within angiogenic microenvironments.
71 actors in the formation of the premetastatic microenvironment after resection of primary tumours.
72 ion, we show that increased stiffness of the microenvironment also induces phosphorylation of gammaH2
74 hibition of NAMPT modulates the tumor immune microenvironment and acts cooperatively with anti-PD-1 c
75 nd biophysical characteristics of the tumour microenvironment and aim to enable studies of cancer, an
76 link between lipid utilization in the tumor microenvironment and anti-tumor immunity in obese mice.
77 ator of global T-cell responses in the tumor microenvironment and as a negative regulator of T-cell t
78 her shown to induce a pro-inflammatory tumor microenvironment and boost anti-tumor T cell activity.
80 s in the accumulation of LMW-HA in the tumor microenvironment and cancer-related inflammation and ang
81 ying TGFbeta signalling in tumours and their microenvironment and discuss approaches to inhibit these
83 ypical normal host cell from the lung cancer microenvironment and found no effect of field exposure o
84 represent an abundant cell type in the tumor microenvironment and have been linked to poor outcomes a
85 of the physiological features of the tumour microenvironment and have been shown to be far superior
86 mmarizes current understandings of the tumor microenvironment and intercellular communications in CCA
87 s, and describe the composition of the tumor microenvironment and its putative role in tumorigenesis.
88 igated type 2 inflammation in the metastatic microenvironment and mediated recruitment of eosinophils
89 myeloid and fibroblastic cells in the tumour microenvironment and ongoing immune surveillance(4-6).
90 HCs evolve during healthy pregnancy and how microenvironment and ontogeny impact phenotype and funct
91 in beta-thalassemia induced by an altered BM microenvironment and provide novel and relevant insight
92 in the transcriptional control of the tumor microenvironment and suggests use of a synthetic LXR ago
93 ensive reprogramming of the pancreatic tumor microenvironment and that patients who progress on gemci
95 under the oxidizing conditions of the tumour microenvironment and the reducing intracellular conditio
96 f B cell progenitors in the bone marrow (BM) microenvironment and their progression through the pre-B
97 Here, we discuss the properties of the tumor microenvironment and transport considerations for intrat
98 hed light on interactions between the tumour microenvironment and tumour genotype are highlighted, pr
100 is characterized by an extensive and complex microenvironment, and is resistant to both chemotherapy
101 ve distinct gene expression profiles, immune microenvironments, and outcomes following immunochemothe
102 use with bystander neural cells in the tumor microenvironment; and cancer cell fusion is a direct rou
103 elopmental, metabolic, epigenomic) and tumor microenvironment (angiogenesis, checkpoint regulation).
104 ance, ability to provide a distinct internal microenvironment (apparent local pH, RNA partitioning),
106 transporters, or components of complex tumor microenvironment are under intense investigation as pote
107 r, and average dwell times in the respective microenvironments are determined from the cell trajector
108 ith increased immune activation in the tumor microenvironment as well as decreased adenovirus-reactiv
110 is due to the formation of a neuroinhibitory microenvironment at injury sites, which includes neuroin
111 ive inhalation exposure assessment of indoor microenvironments at six commercial printing centers in
112 T cells are susceptible to the low arginine microenvironment because of the low expression of the ar
113 e-assessment approach for studying the tumor microenvironment before or shortly after treatment initi
115 uppression and inflammation within the tumor microenvironment but is difficult to achieve due to the
116 PHOS function might also influence the tumor microenvironment by alleviating hypoxia and improving th
117 nd maintains vascular integrity in the tumor microenvironment by contributing to the recruitment of p
120 impaired immune system and inhibitory tumor microenvironment can further complicate the prospects fo
122 y behaviors of lymphocytes within the tissue microenvironment can provide valuable insight into their
124 ulation abundances were quantified using the microenvironment cell population-counter package and com
125 368 patients (DNA sequencing set) and tumour microenvironment characteristics were assessed in 507 pa
126 d extracellular acidity while they grow in a microenvironment characterized by increasing acidity and
127 d that immune-cell-excluded and inflammatory microenvironments coexist within the same individuals an
128 aits of cancer cells and of associated tumor microenvironment components have been shown to promote a
131 sis, partly because of the immunosuppressive microenvironment created by tumor-associated macrophages
132 obile hematopoietic cells within specialized microenvironments created by sessile stromal cells.
133 he engrafted HSPC population and bone marrow microenvironment degradation caused by pre-transplantati
134 Furthermore, deletion of Vegfc from the microenvironment delayed hematopoietic recovery after tr
137 The immunosuppressive state of the tumor microenvironment diminishes the efficacy of dendritic ce
138 fluoresce in the acidic extracellular tumor microenvironment due to the mechanism of nanoscale macro
140 ated in macrophages exposed to TB-associated microenvironments due to tunneling nanotube (TNT) format
141 ly characterized the whole bone marrow (WBM) microenvironment during premalignant, baseline, on treat
143 erestingly, MFP treatment reshaped the tumor microenvironment, enhancing the production of proinflamm
144 survival and migration and affect the immune microenvironment, especially macrophages in clearing dyi
149 loit the unique characteristics of the tumor microenvironment for precise targeting have been designe
150 ents with chronic hepatitis, which creates a microenvironment for the growth of hepatic progenitor ce
151 brane vesicles, which may provide a tailored microenvironment for viral RNA synthesis in the infected
152 e of treatment induces an immune stimulatory microenvironment harboring more tumor infiltrating lymph
154 ver and decreases heterogeneity of the tumor microenvironment, hence PI3Kbeta inhibition may be a use
155 ing tumour-specific antigens into the tumour microenvironment highlights the potential for mCD40L as
157 l metabolism in cells residing in low-oxygen microenvironments (hypoxia) such as in the liver, spleen
158 unknown heterogeneity within the bone marrow microenvironment, imposed by the stages of bone turnover
163 f novel approaches to re-engineer the tumour microenvironment in favour of effective anticancer respo
164 ins of the programmed-death ligand 1 (PD-L1) microenvironment in live lymphocytes and selectively lab
167 apy and shed light on the role of the immune microenvironment in response to HER2-targeted agents.
169 tudies show that the adventitia is a dynamic microenvironment in which adventitial and perivascular a
170 ration of antiviral resistance reflected the microenvironment in which the virus population replicate
172 has been designed where the stiffness of the microenvironment, in 3D culture, has been set at either
173 es profound changes in the pancreatic cancer microenvironment, including elevated TGFbeta signaling a
174 es profound changes in the pancreatic cancer microenvironment, including increased numbers of tumor-i
175 sential in the development of protumorigenic microenvironment induced by NCOA5 deficiency and metform
177 BC; (2) non-neural functions related to cell-microenvironment interactions and intracellular damage p
178 ication with important implications in tumor microenvironment interactions, tumor growth, and metasta
181 tate of the preexisting T cells in the tumor microenvironment is a key determinant for effective anti
183 ternal genetic programming, but the external microenvironment is increasingly recognized as a signifi
185 en pancreatic epithelium and the surrounding microenvironment is pivotal for pancreas formation and d
187 ar that disruption of the normal bone marrow microenvironment is sufficient to promote leukemic trans
188 creased hyaluronan and collagen in the tumor microenvironment, leading to an extensive remodeling of
192 g networks operating within the local tissue microenvironment may enhance malignant tumor progression
193 ruses and their ability to remodel the tumor microenvironment may help to recruit and potentiate the
196 chaperone that, translocated to the external microenvironment, mediates crucial host-parasite interac
197 nding of intratumor heterogeneity, the tumor microenvironment, metastasis, and therapeutic resistance
198 ll RCC tumour and peritumoral adipose tissue microenvironment might have clinical relevance and warra
199 physicochemical characteristics of the tumor microenvironment, namely, acidic pH, redox reactants, an
200 We observe that these self-induced hypoxic microenvironments not only contribute to filamentous fun
201 ular signaling system that uses the confined microenvironment of a giant vesicle, derived from a livi
202 lagen fibrils - potentially important in the microenvironment of actively dividing cells, such as can
206 spectra revealed that the tryptophan residue microenvironment of betaLG was affected by the vitamin B
207 n altered the systemic and peritoneal immune microenvironment of mice with endometriosis as demonstra
209 cancer-associated fibroblasts (CAFs) in the microenvironment of murine carcinomas, each endowed with
210 eloped a new method to capture the proteomic microenvironment of the neuronal endolysosomal network b
213 iposomes could remodel the immunosuppressive microenvironment of triple negative breast cancer and fa
214 Here we characterized the tumor and splenic microenvironment of two syngeneic subcutaneous (NXS2 and
216 tion of regular surface cavities with unique microenvironment on graphitic carbon nitride as "subnano
217 with driver mutations generating a conducive microenvironment on the epithelial boundary, which becom
218 activation state of neighboring cells in the microenvironment or within progression of a particular d
219 dely utilized, little is known about how the microenvironment, particularly confined aqueous environm
222 wever, recent studies suggest that the tumor microenvironment plays a key role in the progression and
223 ltrating lymphocytes (TILs) within the tumor microenvironment provides strong prognostic value, which
224 ility to adapt and colonize lipid-rich tumor microenvironments, providing an opportunity for specific
231 Currently, photosensitizers (PSs) that are microenvironment responsive and hypoxia active are scarc
232 ent growth and highlights how the metastatic microenvironment restores this malignant property of can
234 infers the emergent network biology of tumor microenvironment spatial domains revealing a spatially-m
235 sembly system that achieves lysosomal acidic microenvironment specifically inducing topological trans
239 oimmunity, and variable effects on the tumor microenvironment that can limit or worsen tumor progress
240 IL-33 as an orchestrator of the glioblastoma microenvironment that contributes to tumorigenesis.
241 highly stromal and weakly immunogenic tumor microenvironment that promotes tumor evolution and contr
242 Tumours leverage ECM remodelling to create a microenvironment that promotes tumourigenesis and metast
243 s induce dynamic changes in the tumor immune microenvironment that vary by subtype and pathologic res
244 meostasis and alters both systemic and local microenvironments that impact stem cell plasticity and i
245 cellular organisms relies on specific tissue microenvironments that nurture hematopoietic precursors
246 e areas include the immune system, the tumor microenvironment, the fibrotic response, and stem cell f
247 e interaction between cancer cells and brain microenvironment, thereby inducing brain metastatic comp
249 ears to establish an immunosuppressive tumor microenvironment through the activation of STAT3, and lo
250 ent cholangiocytes can modify the periductal microenvironment through their ability to secrete variou
251 in inducing immune suppression in the tumor microenvironment, through both targeted inhibition of RA
252 mune systems and regulating the inflammatory microenvironment, thus alleviating the inflammatory resp
253 ued after cell transplantation into a normal microenvironment, thus proving the active role of the BM
255 nces in systemic metabolism change the tumor microenvironment (TME) and impact anti-tumor immunity is
256 er, the degree of heterogeneity of the tumor microenvironment (TME) and its molecular underpinnings r
257 umor progression and remodeling of the tumor microenvironment (TME) by sustaining the calcium transie
258 , metabolic constraints imposed by the tumor microenvironment (TME) can dampen their ability to contr
259 cells are armed to combat tumors, the tumor microenvironment (TME) contains ROS, which suppress NK c
261 y in establishing an immunosuppressive tumor microenvironment (TME) for the support of tumor growth.
262 uelled ongoing efforts to exploit the tumour microenvironment (TME) for therapy, but strategies aimed
263 nature (GES) or high immunosuppressive tumor microenvironment (TME) GES levels at baseline; an immuno
265 naling within the breast tumor and its tumor microenvironment (TME) is linked to poor clinical outcom
270 tion, recruitment of NK cells into the tumor microenvironment (TME), blockade of inhibitory receptors
280 focusing on modulating the pancreatic tumour microenvironment to enhance the efficacy of the immunoth
282 term gemcitabine administration on the tumor microenvironment to identify potential therapeutic optio
283 e materials can form the basis of artificial microenvironments to promote cell infiltration and repro
285 tophagy can play opposing roles in the tumor microenvironment via non-cell-autonomous mechanisms.
286 ces a signal only in the protease-rich tumor microenvironment, was topically applied to 90 specimens
287 gions of tumor heterogeneity and the hypoxic microenvironment were observed based on the spatial dist
288 ed suppressor cells (MDSCs) within the tumor microenvironment, when compared with Lys-SNAs and simple
289 acteristics and key components of the aortic microenvironment, where the first hematopoietic stem cel
290 tion of circulating monocytes into the tumor microenvironment, where they mature into tumor-associate
291 ticularly hindering in geometrically complex microenvironments, where it leads to entanglement and ul
292 pression in multiple cell types of the tumor microenvironment, which could contribute to angiogenesis
294 Hypoxia is a common feature of the tumor microenvironment, which is characterized by tissue oxyge
295 enic and exceedingly immunosuppressive tumor microenvironment, which is enriched with dysfunctional a
296 , and lymphangiogenesis in the endometriotic microenvironment, which opens up new horizons in underst
297 s allows us to obtain snapshots of molecular microenvironments with nanometer resolution, facilitatin
298 retion may be intimately linked to a hypoxic microenvironment within keloid tumors and that HIF-1alph