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1 rmal tumor, and one desmoplastic small round cell tumor).
2 inal stromal tumor, leiomyosarcoma, granular cell tumor).
3 ally named PEComas (perivascular epithelioid cell tumors).
4 pathological features of tenosynovial giant-cell tumor.
5 fication of the specific Ig genes from the B-cell tumor.
6 f skin surface and dermis is related to mast cell tumor.
7 al events in patients with a history of germ cell tumor.
8 d in the aggressive desmoplastic small round cell tumor.
9 oach from the Brazilian GCT-99 study on germ cell tumors.
10 ma skin cancer (NMSC), particularly squamous cell tumors.
11 a potential target for the therapy of Leydig cell tumors.
12 rs, lung and mammary carcinomas, and spindle cell tumors.
13 echanism that controls cell growth in Leydig cell tumors.
14 with newly diagnosed non-germinomatous germ cell tumors.
15 with newly diagnosed non-germinomatous germ cell tumors.
16 RAS/LKB1-mutant adenocarcinomas and squamous cell tumors.
17 gene is elevated in most tenosynovial giant-cell tumors.
18 e inactivated in a majority of lung squamous cell tumors.
19 y in flies, worms, zebrafish, and human germ cell tumors.
20 tral nervous system tumors, or renal or germ-cell tumors.
21 rge B cell lymphoma (DLBCL) and additional B cell tumors.
22 the development of adenocarinoma and spindle cell tumors.
23 either seminomas or nonseminomas/mixed germ cell tumors.
24 the survival of mice with implanted human B-cell tumors.
25 ightly stronger for B-cell tumors than for T-cell tumors.
26 are at increased risk of developing Sertoli cell tumors.
27 ovarian serous adenocarcinomas and granulosa cell tumors.
28 the poor outcome reported in all MHC II(-) B-cell tumors.
29 ficacy should be examined in patients with B-cell tumors.
30 PIK3CA were previously described in squamous cell tumors.
31 ent of certain categories of testicular germ cell tumors.
32 omatography to membrane preparations of beta-cell tumors.
33 29% of clear cell samples and 8% of nonclear cell tumors.
34 rtility and are associated with ovarian germ cell tumors.
35 a key determinant of oncogenic fate in germ-cell tumors.
36 or misexpression of Chinmo results in blood cell tumors.
37 nd immunophenotype, such as small round blue cell tumors.
38 into how cell identity is lost in some germ cell tumors.
39 rom 0.669 for signet cell to 0.75 for goblet cell tumors.
40 a, mesothelioma, melanoma, gastric, and germ cell tumors.
41 transcriptional regulator in prostatic basal cell tumors.
42 e most prevalent molecular features of clear cell tumors.
43 s, systemic mastocytosis, and localized mast cell tumors.
44 typical prolonged washout observed in Leydig cell tumors (12 of 21 patients, P < .001 when compared w
46 umors (29%), predominantly in Sertoli-Leydig cell tumors (26 of 43, or 60%), including 4 tumors with
47 primitive neuroectodermal tumors, 57.8; germ cell tumors, 63.5; ependymoma or high-grade glioma, 69.8
48 h hepatoblastoma or desmoplastic small round cell tumor achieved a partial response; eight patients h
49 cells (Tregs) and myeloid-derived suppressor cells, tumor Ag-specific Tregs interfere with the detect
50 or is pathognomonic for adult-type granulosa cell tumors (AGCT) and a diagnostic marker for this tumo
53 ductive system, including proliferative germ-cell tumors and uterine masses that express neuronal and
55 a target of chromosomal translocations in T-cell tumors and was activated by retroviral vector inser
56 ion can be abrogated by exposing susceptible cells (tumor and mycobacteria-infected cells, or aminobi
57 serve as binding sites on the breast cancer cells/tumor and the LHRH-conjugated drugs inhibited the
58 nd paraganglioma, pericardial cyst, Purkinje cell tumor, and papillary fibroelastoma (n = 1, each).
59 lution in relation to retinoblastoma or germ cell tumors, and both cancers are rare, these findings r
60 sion was validated in Ewing sarcoma cells, B-cell tumors, and human keratinocytes where NOTCH dysregu
61 expression is deregulated in testicular germ cell tumors, and loss of imprinting occurs frequently in
62 ype-specific variations, chromophobes, clear-cell tumors, and oncocytomas were composed exclusively o
64 vel marker for this lymphoma across mature B-cell tumors, and support the distinction of NMZL as an i
65 SCN-like epithelial cases, small-round-blue cell tumors, and unexpectedly in hematological malignanc
67 d-glucose (6-[(18)F]FDG) was studied in EMT6 cells, tumors, and muscle and correlated to GLUT1 and GL
68 ic antigen receptors (CAR) specific to the B cell tumor antigen CD19 can successfully eradicate syste
75 te Phf7 expression, is also observed in germ cell tumors arising from the loss of bag of marbles (bam
77 d-MyD88 infection of primary human dendritic cells, tumor-associated fibroblasts, and colorectal carc
79 ular immune modulators, such as regulatory T cells, tumor-associated macrophages, and myeloid-derived
81 ose proximity to colonies of prostate cancer cells, tumor-associated stromal cells and newly formed w
82 alterations, and gene expression and immune cell-tumor axis changes in a mouse model of oviductal se
84 therapeutics to manage various B cell and T cell tumors, because failure to open DNA hairpins and ac
85 the diagnosis of adrenomedullary chromaffin cell tumors can be jeopardized by physiologic uptake by
89 We analyzed three pairs of testicular germ cell tumor cell lines using Affymetrix expression microa
90 SPN knockout in AML cell lines facilitated T cell-tumor cell clustering and enhanced CD3 bsAb-mediate
95 be killed by CD8(+)alphabetaT or gammadeltaT cells; tumor cell killing was partially restored by trea
96 acteria in tumors and proliferation of tumor cells, tumor-cell DNA damage, and an inflammatory respon
97 of PD-L1 expression in both tumor and immune cells (tumor cells: 22c3, 2.96; 28-8, 3.26; SP142, 1.99;
98 their proximity to potential immune effector cells, tumor cells grow aggressively on these immune agg
101 eurofibromas are benign nerve sheath Schwann cell tumors characterized by biallelic mutations in the
102 g NKG2D ligands had increased incidence of B cell tumors, confirming that the inability to clear NKG2
105 nografted with human EGFRvIII-expressing GBM cells, tumor-derived suPAR was detected in the plasma, a
108 lar pathogenesis of desmoplastic small round cell tumor (DSRCT), a fatal malignancy occurring primari
110 al translocation in desmoplastic small round-cell tumors (DSRCT), a rare but aggressive soft tissue s
112 c niche consisting of transformed epithelial cells, tumor-educated fibroblasts, endothelial cells, an
114 endocrine tumors (pNET), also known as islet cell tumors, exhibit a wide range of biologic behaviors
116 veral human B cell cancer lines, and human B cell tumors expressing AID at high levels have genomic u
118 a critical role in the progression of Hut78 cell tumor formation in skin, thus providing a new thera
121 tivated by retroviral vector insertions in T-cell tumors from X-SCID patients in gene therapy trials.
122 rowth, were enriched in NMZL across mature B-cell tumors, functionally caused the loss of the phospha
123 rpose Patients with relapsed metastatic germ cell tumor (GCT) can be cured with second-line and even
124 in patients with metastatic testicular germ cell tumor (GCT) is of unknown prognostic significance.
126 re conducted on 488 North American male germ cell tumor (GCT) survivors in relation to cumulative cis
127 nicopathologic heterogeneity, malignant germ cell tumors (GCT) share molecular abnormalities that are
128 than the classic markers of testicular germ cell tumors (GCTs) and are applicable toward both semino
129 sitivity, most patients with metastatic germ cell tumors (GCTs) are cured with cisplatin-based chemot
134 granulosa cells causes metastatic granulosa cell tumors (GCTs) in female mice and phenocopies human
136 alignant lesions that develop into granulosa cell tumors (GCTs) spontaneously later in life or follow
137 in two thirds of patients with advanced germ cell tumors (GCTs) who relapsed after first-line chemoth
138 mainstay of treatment for disseminated germ cell tumors (GCTs), is associated with venous thromboemb
143 e-wide association study for testicular germ cell tumor, genotyping 298,782 SNPs in 979 affected indi
145 Inhibiting Sod2 expression reduces OCCC ES-2 cell tumor growth and metastasis in a chorioallantoic me
146 y, chronic MAF overexpression enhanced MPNST cell tumor growth in vivo, correlating with elevated pS6
149 t cells were injected along with WT parental cells, tumor growth was enhanced with mutant cells becom
150 inhibitor imatinib after injection of cancer cells; tumor growth was measured based on bioluminescenc
151 n study, 12 patients with tenosynovial giant-cell tumors had a partial response and 7 patients had st
152 spectrum of human neoplasms, including germ cell tumors, high-grade and low-grade carcinomas and ben
153 0.96), was lower after nonseminomatous germ cell tumor (HR, 0.58; 95% CI, 0.35 to 0.96) and decrease
154 cell clones were often observed in T- and NK-cell tumors in a percentage higher than observed in reac
161 d slows the growth of these "addicted" pre-B-cell tumors in vivo, suggesting a promising therapeutic
163 s in 1 of 14 nonseminomatous testicular germ-cell tumors, in 2 of 5 embryonal rhabdomyosarcomas, and
164 hydra analysis framework to small blue round cell tumors (including rhabdomyosarcoma, synovial sarcom
165 rated lymphocytes, low level of regulatory T-cell tumor-infiltrated lymphocytes, and low PD-L1 expres
167 ability of this tracer to quantify CD8(+) T-cell tumor infiltrates was evaluated in preclinical stud
169 recognized that rapidly proliferating cancer cells, tumor-infiltrating lymphocytes, and vascular endo
170 guish them from mature lymphatic endothelial cells, tumor-infiltrating lymphoid cells, and tissue-res
171 DQB2, HLA-DMA, and HLA-DOA), increased CD8 T-cell tumor infiltration (P=7.6x10(-5)), and trans-regula
172 okine receptor 4 (CXCR4) blockade promotes T cell tumor infiltration and is synergistic with anti-PD-
173 environment and as a negative regulator of T-cell tumor infiltration and patient survival in diverse
175 growth, increased antigen-specific CD8(+) T-cell tumor infiltration, and increased median survival,
177 enes, impaired IFN gene expression, anemic T cell tumor infiltration, poor tumor immunity, and shorte
179 zation of cancer in which only a fraction of cells, tumor-initiating cells (TICs), can sustain tumor
180 ith menin knockdown, in MEN1-associated beta cell tumors (insulinomas), and also in human sporadic in
183 idence interval (CI): 2.65, 3.50), with germ cell tumors (IRR = 5.19, 95% CI: 2.67, 9.41), retinoblas
184 etween chlordane isomers and testicular germ cell tumors, it is reasonable to assume that chlordanes
186 n treatment of TRAF3-deficient B cells and B cell tumor lines with c-Myc inhibitors enhanced their se
187 g peptide that specifically recognizes tumor cells, tumor lymphatics, and tumor-associated macrophage
188 tramer-positive CD8 T cells, increased CD8 T-cell tumor lytic activity, augmented antigen-specific IF
189 iota of 11 dogs affected by spontaneous mast cell tumor (MCT), using skin contralateral sites as intr
191 Effects against mitochondria and general cell tumor metabolism were noted at higher concentration
192 s with intermediate-risk (IR) malignant germ cell tumors (MGCT) if the administration of cisplatin, e
194 ting of a genetic disease, the B-cell/plasma cell tumor microenvironment (TME) contributes significan
195 spontaneous translocations in other mouse B-cell tumor models, CP B-cell tumor translocations were n
197 vival outcomes in metastatic testicular germ cell tumor (MT-GCT), but how the initial risk changes ov
198 own as HHV8) is the causative agent of two B cell tumors, multicentric Castleman disease (MCD) and pr
199 tivation of genes expressed in retinal glial cells, tumor necrosis factor-alpha, and transforming gro
200 kers to differentiate non-germinomatous germ cell tumors (NGGCTs) from germinomas are critical, as th
202 thologic stage (PS) IIA nonseminomatous germ cell tumors (NSGCTs) is 10%-20% but increases to >= 50%
207 -year-old man with a history of a mixed germ cell tumor of the testis presented with acute-onset, rig
208 ndings are mirrored in G34W-containing giant cell tumors of bone where patient-derived stromal cells
215 ciplinary approach to the management of germ cell tumors of the testis has resulted in survival rates
216 e the surgical management of metastatic germ cell tumors of the testis, highlighting the indications
217 ratio (OR) = 1.05; 95% CI: 1.01, 1.10]; germ cell tumors (OR = 1.16; 95% CI: 1.04, 1.29), particularl
219 riplatin in the National Cancer Institute 60-cell tumor panel screen revealed a spectrum of activity
224 f the resected tissue showed metastatic germ cell tumor predominantly consisting of a yolk sac elemen
230 induction promoted drug resistance in MCF-7 cells, tumor regeneration in Du145 cells and, most impor
233 ably, hydra analysis of all small blue round cell tumors revealed similar subtypes, characterized by
235 ve been reported with IFNgamma-producing Th1 cells, tumor-specific Th2 cells have been largely neglec
236 d antimetastasis activity in two-dimensional cells, tumor spheroids, subcutaneous transplantation mou
241 hepatoblastomas (HBs), 1 transitional liver cell tumor (TCLT), 1 hepatocellular carcinoma, and 2 mal
242 necrosis (20%), viable nonteratomatous germ cell tumor +/- teratoma (41%), and secondary somatic-typ
245 association (GWA) studies of testicular germ cell tumor (TGCT) have identified 18 susceptibility loci
247 aggressive fibromatosis, tenosynovial giant cell tumor (TGCT) or diffuse-type pigmented villonodular
248 molecular pathogenesis of tenosynovial giant cell tumor (TGCT) or pigmented villonodular synovitis (P
249 conventional inheritance for testicular germ cell tumor (TGCT) risk both in humans and mice implicate
250 yzed population-wide data on testicular germ-cell tumor (TGCT) status in 1,135,320 two-generational N
254 -wide association studies of testicular germ cell tumor (TGCT; 3,558 cases and 13,970 controls) to id
262 actor for the development of testicular germ cell tumors (TGCT), but the initiating event linking the
263 tworks in two major types of testicular germ cell tumors (TGCT): seminoma (SE) and non-seminoma (NSE)
266 e enhances susceptibility to testicular germ cell tumors (TGCTs) in mice, in part by interacting epig
270 tanding of susceptibility to testicular germ cell tumors (TGCTs), but much of the heritability remain
271 so are misregulated in human testicular germ cell tumors (TGCTs), suggesting similar etiology between
276 l zone lymphoma (NMZL) is a rare, indolent B-cell tumor that is distinguished from splenic marginal z
277 agnosis and therapy of malignant small round cell tumors that affect children, particularly in rhabdo
279 slowly proliferating, insulin-producing beta cell tumors that provide a molecular "recipe" or "roadma
280 is, leading to the accumulation of granulosa cell tumors that reactivates the epithelial program from
281 rtoli cells also caused testicular granulosa cell tumors that showed gene expression patterns that pa
282 preclinical canine study of spontaneous mast cell tumors, the treatment led to a 67% response rate (t
284 with the widespread expression in epithelial cells, tumor tissues, and macrophages detected using BTN
286 ons in other mouse B-cell tumor models, CP B-cell tumor translocations were not recurrent and did not
287 ere indeed found in 7% of 43 testicular germ cell tumor trios; this percentage exceeds background CNV
288 s expression levels in human testicular germ cell tumors using patient tissues, model cell lines, and
291 importance of versican in this smooth muscle cell tumor, we used versican-directed siRNA to knock dow
292 ociated with lymphomas and some ovarian germ cell tumors, we present a case of calcitriol overproduct
296 treatment of patients with nonseminoma germ cell tumor, whereas radiotherapy, as a standard treatmen
297 my, and pathology showed a 1.5-cm mixed germ cell tumor with 85% embryonal, 10% yolk sac tumor, and 5
298 skin developed significantly fewer squamous cell tumors with a delayed onset when compared with wild
300 529 was highly active against subcutaneous B-cell tumor xenografts in severe combined immunodeficient