コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 op an aggressive malignancy resembling human diffuse large B cell lymphoma.
2 opathy, Waldenstrom's macroglobulinemia, and diffuse large B cell lymphoma.
3 ecially for those with aggressive forms like diffuse large B-cell lymphoma.
4 able to transform into germinal center-type diffuse large B-cell lymphoma.
5 efiting patients with follicular lymphoma or diffuse large B-cell lymphoma.
6 tality for anal cancer, Hodgkin lymphoma, or diffuse large B-cell lymphoma.
7 development of FL and its transformation to diffuse large B-cell lymphoma.
8 Genetic markers have helped to prognosticate diffuse large B-cell lymphoma.
9 oblastic leukemia, plasma cell neoplasms, or diffuse large B-cell lymphoma.
10 (EFS24) is a clinically useful end point in diffuse large B-cell lymphoma.
11 notherapy in untreated elderly patients with diffuse large B-cell lymphoma.
12 issues when treating patients with high-risk diffuse large B-cell lymphoma.
13 a quarter of Burkitt lymphoma and GC-derived diffuse large B-cell lymphoma.
14 prove the outcome of high-risk patients with diffuse large B-cell lymphomas.
15 cated for the routine staging of HL and most diffuse large B-cell lymphomas.
16 st common mature noncutaneous lymphomas were diffuse large B-cell lymphomas (32.4%), follicular lymph
17 remission occurred in 6 of 14 patients with diffuse large B-cell lymphoma (43%; 95% CI, 18 to 71) an
18 ese, 12 (21%) had Hodgkin lymphoma, 22 (39%) diffuse large B-cell lymphoma, 5 (9%) Burkitt lymphoma,
21 ctory cancers, such as activated B cell-like diffuse large B cell lymphoma (ABC DLBCL), are likely re
22 ted in the activated B-cell-like subgroup of diffuse large B-cell lymphoma (ABC DLBCL) to drive aberr
23 scriptional network of activated B-cell-like diffuse large B-cell lymphoma (ABC-DLBCL), an aggressive
25 Additionally, BCL-W was overexpressed in diffuse large B cell lymphoma and correlated with decrea
26 rmed B cells in vitro; however, EBV-positive diffuse large B cell lymphomas and Burkitt lymphomas oft
27 iling in 177 cancer cell lines revealed that diffuse large B cell lymphomas and renal cell carcinomas
28 cytic leukemia, 29% of activated B-cell type diffuse large B-cell lymphoma and 90% of Waldenstrom mac
29 uently in follicular lymphoma and aggressive diffuse large B-cell lymphoma and are associated with H3
30 e in the treatment of relapsed or refractory diffuse large B-cell lymphoma and follicular lymphoma.
31 requently mutated in germinal center-derived diffuse large B-cell lymphoma and follicular lymphoma.
32 perior to the 5-point scale in patients with diffuse large B-cell lymphoma and may also improve the a
34 h FOXP1 expression is frequently observed in diffuse large B-cell lymphoma and mucosa-associated lymp
35 consolidation radiotherapy in patients with diffuse large B-cell lymphoma and primary mediastinal B-
36 nrolled patients with relapsed or refractory diffuse large B-cell lymphoma and relapsed or refractory
38 lymphomas had some of the characteristics of diffuse large B-cell lymphomas and contained monoclonal,
39 ld be detected in the serum of patients with diffuse large-B-cell lymphoma and used to predict clinic
40 , an enhanced expression was observed in HL, diffuse large B-cell lymphoma, and lymphoblastoid cell l
41 acetylation signature in the ABC subgroup of diffuse large B-cell lymphoma, and one of the most frequ
42 ent, and viral components in 41 AIDS-related diffuse large B-cell lymphomas (AR-DLBCLs) in the pre- a
43 nversely, the D2HGDH mutants that we find in diffuse large B-cell lymphoma are enzymatically inert.
45 ic active B-cell receptor (BCR) signaling in diffuse large B-cell lymphoma as a model system to estab
48 chemotherapy in older patients with advanced diffuse large B-cell lymphoma, but further comparative s
49 chemotherapy in older patients with advanced diffuse large B-cell lymphoma, but further comparative s
50 he vast majority of cases are histologically diffuse large B-cell lymphoma, but rarer subtypes are cl
54 re, RNF181 limits the proliferation of human diffuse large B cell lymphoma cells that depend upon abe
56 utcomes in patients older than 60 years with diffuse large B-cell lymphoma compared with CHOP every 3
58 nts represent promising treatment targets in diffuse large B cell lymphoma (DLBCL) and additional B c
59 rent and occur early during tumorigenesis in diffuse large B cell lymphoma (DLBCL) and follicular lym
60 tutively activate CARMA1 occur frequently in diffuse large B cell lymphoma (DLBCL) and mediate essent
61 on mutations that are frequently observed in diffuse large B cell lymphoma (DLBCL) and that disrupt I
62 ogenic BCL6 and EZH2 cooperate to accelerate diffuse large B cell lymphoma (DLBCL) development and co
63 of CD37 on neoplastic cells in patients with diffuse large B cell lymphoma (DLBCL) directly correlate
67 oyment of rationally developed therapies for diffuse large B cell lymphoma (DLBCL) requires rapid ass
68 f the activated B cell-like (ABC) subtype of diffuse large B cell lymphoma (DLBCL), engages the CARD1
69 n the activated B cell-like (ABC) subtype of diffuse large B cell lymphoma (DLBCL), the oncogenic MYD
75 port integrative genetic characterization of diffuse large B cell lymphomas (DLBCL), including large-
76 expression of these miRNAs also occurred in diffuse large B cell lymphomas (DLBCL), which are strong
77 ]), follicular lymphoma (FL) (23% [n = 20]), diffuse large B-cell lymphoma (DLBCL) (10% [n = 9]), man
78 cell lymphoma (MCL) (6.8% [18 of 263]), and diffuse large B-cell lymphoma (DLBCL) (4.6% [12 of 263).
79 arge B-cell lymphoma (PMBCL) is a subtype of diffuse large B-cell lymphoma (DLBCL) accounting for 2%
82 The PI3K-mTORC pathway is upregulated in diffuse large B-cell lymphoma (DLBCL) and can be targete
83 ing of the pathogenesis and heterogeneity of diffuse large B-cell lymphoma (DLBCL) and follicular lym
84 The standardized incidence ratios (SIRs) of diffuse large B-cell lymphoma (DLBCL) and follicular lym
85 antibody, was superior to rituximab in human diffuse large B-cell lymphoma (DLBCL) and mantle-cell ly
86 oncogene in activated B-cell-like subtype of diffuse large B-cell lymphoma (DLBCL) and mucosa-associa
87 Here, we interrogate the MNK-eIF4E axis in diffuse large B-cell lymphoma (DLBCL) and show a distinc
88 promotes degradation of Aiolos and Ikaros in diffuse large B-cell lymphoma (DLBCL) and T cells in vit
90 e-expressor lymphomas (DELs) are subtypes of diffuse large B-cell lymphoma (DLBCL) associated with po
93 ably, inhibition of the miR-17~92 cluster in diffuse large B-cell lymphoma (DLBCL) cell lines diminis
94 we used the miR-155 knockout (KO) mouse and diffuse large B-cell lymphoma (DLBCL) cell lines ectopic
95 e Lymph2Cx digital gene expression assay for diffuse large B-cell lymphoma (DLBCL) cell-of-origin det
96 nce that GLI1 contributes to the survival of diffuse large B-cell lymphoma (DLBCL) cells and that thi
98 me data from a large cohort of patients with diffuse large B-cell lymphoma (DLBCL) compared with norm
99 f transplant-eligible patients with relapsed diffuse large B-cell lymphoma (DLBCL) consists of rituxi
100 nical features from 1650 adults with de novo diffuse large B-cell lymphoma (DLBCL) diagnosed from 200
101 ospectively enrolled cohort of patients with diffuse large B-cell lymphoma (DLBCL) from the United St
103 Up to 40% of elderly patients with untreated diffuse large B-cell lymphoma (DLBCL) given a regimen of
105 ostic significance of MDM2 overexpression in diffuse large B-cell lymphoma (DLBCL) has not been defin
106 er latency to the development of BCL6-driven diffuse large B-cell lymphoma (DLBCL) in a murine model.
108 llance imaging of asymptomatic patients with diffuse large B-cell lymphoma (DLBCL) in first remission
109 urpose The general outlook for patients with diffuse large B-cell lymphoma (DLBCL) in first remission
117 pose The standard treatment of patients with diffuse large B-cell lymphoma (DLBCL) is rituximab in co
132 utility of routine surveillance imaging for diffuse large B-cell lymphoma (DLBCL) patients achieving
134 complete genome sequence analysis of primary diffuse large B-cell lymphoma (DLBCL) primary tumors and
135 phoma patients, transformation to aggressive diffuse large B-cell lymphoma (DLBCL) reduces median sur
136 The activated B-cell-like (ABC) subtype of diffuse large B-cell lymphoma (DLBCL) relies on chronic
137 apy plus consolidative radiotherapy (RT) for diffuse large B-cell lymphoma (DLBCL) remains controvers
138 apy (RT) after chemotherapy in limited-stage diffuse large B-cell lymphoma (DLBCL) remains controvers
139 he introduction of rituximab, survival after diffuse large B-cell lymphoma (DLBCL) remains heterogene
140 l-like (ABC) and germinal center B-cell-like diffuse large B-cell lymphoma (DLBCL) represent the 2 ma
143 uishes the aggressive activated B cell (ABC) diffuse large B-cell lymphoma (DLBCL) subtype from the b
145 tinal B-cell lymphoma (PMBL) is a subtype of diffuse large B-cell lymphoma (DLBCL) that is putatively
146 ant to human NHL, we also analyzed 148 human diffuse large B-cell lymphoma (DLBCL) tumors and identif
149 PET) biopsies from 344 patients with de novo diffuse large B-cell lymphoma (DLBCL) uniformly treated
150 lity therapy for patients with limited-stage diffuse large B-cell lymphoma (DLBCL) was shown in the S
153 iR-28 reexpression in human Burkitt (BL) and diffuse large B-cell lymphoma (DLBCL) xenografts blocked
154 evaluated in neuroblastoma, medulloblastoma, diffuse large B-cell lymphoma (DLBCL), and EOC microarra
155 including Burkitt lymphoma, Hodgkin disease, diffuse large B-cell lymphoma (DLBCL), and posttransplan
156 cance of MYC and BCL2 genetic alterations in diffuse large B-cell lymphoma (DLBCL), apart from transl
157 e to improving the survival of patients with diffuse large B-cell lymphoma (DLBCL), especially those
158 sented by the histologic transformation to a diffuse large B-cell lymphoma (DLBCL), is associated wit
159 eligible if they had relapsed or refractory diffuse large B-cell lymphoma (DLBCL), mantle-cell lymph
160 n the activated B-cell-like (ABC) subtype of diffuse large B-cell lymphoma (DLBCL), NF-kappaB activit
161 relapsed follicular lymphoma (FL), relapsed diffuse large B-cell lymphoma (DLBCL), or refractory agg
163 pathway may be usurped by tumors, including diffuse large B-cell lymphoma (DLBCL), to evade immune s
165 n-Hodgkin lymphoma (NHL) subtypes, including diffuse large B-cell lymphoma (DLBCL), variably express
202 viduals did not receive cancer treatment for diffuse large B-cell lymphoma (DLBCL; adjusted odds rati
203 ; n = 28), follicular lymphoma (FL; n = 29), diffuse large B-cell lymphoma (DLBCL; n = 34), DLBCL ari
204 ed the global microRNA (miRNA) expression in diffuse large B-cell lymphoma (DLBCL; n = 79), Burkitt l
205 es occurred in the subgroup of patients with diffuse large B-cell lymphoma (DLBCL; n=9), and three oc
206 ution to the diagnosis of CNS lymphoma in 91 diffuse large B-cell lymphomas (DLBCL) and 22 Burkitt ly
207 MYC rearrangements occur in 5% to 10% of diffuse large B-cell lymphomas (DLBCL) and confer an inc
212 tify HGBL-DH and will reclassify a subset of diffuse large B-cell lymphomas (DLBCLs) and HGBLs with f
214 Aggressive double- and triple-hit (DH/TH) diffuse large B-cell lymphomas (DLBCLs) feature activati
215 we show that patients with PRDM11-deficient diffuse large B-cell lymphomas (DLBCLs) have poorer over
216 series of Epstein-Barr virus-positive (EBV+) diffuse large B-cell lymphomas (DLBCLs) in young patient
217 tonic B-cell receptor (BCR) signal-dependent diffuse large B-cell lymphomas (DLBCLs) inhibits cellula
219 negative prognostic impact in patients with diffuse large B-cell lymphomas (DLBCLs) treated with imm
220 terminal hydrolase L1 (UCH-L1) is induced in diffuse large B-cell lymphomas (DLBCLs), and that levels
221 previously reported that early-stage gastric diffuse large B-cell lymphomas (DLBCLs), including DLBCL
225 ients with follicular lymphoma (FL), 16 with diffuse large B-cell lymphoma (DLCL), and 17 with mantle
226 the study: eight with relapsed or refractory diffuse large B-cell lymphoma (due to progressive diseas
227 y rearranged in PMBCL (20%) as compared with diffuse large B-cell lymphoma, follicular lymphoma, and
228 day), and six additional patients (two with diffuse large B-cell lymphoma, four with indolent lympho
232 place of JAK2 inhibitors in the treatment of diffuse large B-cell lymphoma has not been defined; we s
234 e lymphomas, which occur in <10% of cases of diffuse large B-cell lymphoma, have been referred to as
235 -cell lymphomas, including Burkitt lymphoma, diffuse large B-cell lymphoma, Hodgkin lymphoma, and pri
236 as limited prognostic value in patients with diffuse large B-cell lymphoma homogeneously treated with
237 tly mutated genes in follicular lymphoma and diffuse large B cell lymphoma; however, the biological c
238 s to predict survival time for patients with diffuse large B-cell lymphoma, illustrate the behavior o
241 lity in patients with follicular lymphoma or diffuse large B-cell lymphoma in five large European are
244 aggressive activated B cell-like subtype of diffuse large B-cell lymphoma is characterized by aberra
246 lthough survival for follicular lymphoma and diffuse large B-cell lymphoma is improving, the results
247 CT) as first-line treatment in patients with diffuse large B-cell lymphomas is still a matter of deba
250 P is a frequent feature of primary cutaneous diffuse large B-cell lymphoma, leg-type (PCLBCL-LT), rep
251 ose-escalation phase (part 1), patients with diffuse large B-cell lymphoma, mantle-cell lymphoma, or
252 40% among patients with follicular lymphoma, diffuse large B-cell lymphoma, mycosis fungoides, and pe
253 node biopsy samples, including FL (n = 20), diffuse large B-cell lymphoma (n = 10), classical Hodgki
254 rate was 69% across NHL subtypes and 55% for diffuse large B-cell lymphoma (n = 11); median response
255 s were treated (follicular lymphoma, n = 10; diffuse large B-cell lymphoma, n = 11; other B-cell lymp
256 with Hodgkin's lymphoma, Burkitt's lymphoma, diffuse large B-cell lymphomas, nasopharyngeal carcinoma
258 patients with nongerminal center B-cell-like diffuse large B-cell lymphoma (non-GCB DLBCL) were rando
259 ciated with increased NHL risk, specifically diffuse large B-cell lymphoma (odds ratio (OR) = 3.11, 9
260 directed CAR (CTL019) to treat patients with diffuse large B-cell lymphoma or follicular lymphoma tha
262 CI), 1.35-8.71] and, based on small numbers, diffuse large B-cell lymphoma (OR, 5.31; 95% CI, 1.54-18
266 ted genetic variants that predict outcome in diffuse large B-cell lymphoma patients treated with immu
268 1.29) and was significantly associated with diffuse large B cell lymphoma (pooled HR per SD: 1.47; 9
270 h bulky stage 2-3 or stage 3-4 CD20-positive diffuse large B-cell lymphoma, previously untreated, and
271 phase 2 trial, we enrolled 111 patients with diffuse large B-cell lymphoma, primary mediastinal B-cel
273 exposure was associated with a lower risk of diffuse large B-cell lymphoma (relative risk = 0.68, 95%
274 me for elderly patients with newly diagnosed diffuse large B-cell lymphoma remains suboptimal in the
275 ents with various NHL histologies, including diffuse large B-cell lymphoma, Richter's transformation,
276 ggressive lymphomas, the association between diffuse large B-cell lymphoma risk and slope was restric
277 gle-agent polatuzumab vedotin (14 of 25 with diffuse large B-cell lymphoma, seven of 15 with indolent
278 ed with the activated B cell-like subtype of diffuse large B cell lymphoma somehow perturb ID-mediate
279 y, oncogenic CARD11 variants associated with diffuse large B cell lymphoma spontaneously induce Lin(U
280 sisted of follicular lymphoma misgrading and diffuse large B-cell lymphoma subtype misclassification.
281 ed a new category of lymphoma, separate from diffuse large B-cell lymphoma, termed high-grade B-cell
282 ion-based signatures have been identified in diffuse large B-cell lymphoma that are predictive for su
283 on, which is impaired in approximately 6% of diffuse large B-cell lymphomas that carry inactivating g
284 nal B-cell lymphoma is a distinct subtype of diffuse large-B-cell lymphoma that is closely related to
285 HOP-21 chemotherapy for previously untreated diffuse large B-cell lymphoma; therefore, R-CHOP-21 rema
286 -based signatures on 2 sets of patients with diffuse large B-cell lymphoma treated with CHOP or R-CHO
287 .2 and 6q21 with EFS and OS in patients with diffuse large B-cell lymphoma treated with immunochemoth
290 dgkin lymphoma and eight of 20 patients with diffuse large B-cell lymphoma vs one of 15 patients with
291 alignancies, including mantle cell lymphoma, diffuse large B-cell lymphoma, Waldenstroms macroglobuli
295 elapsed/refractory NHL, who included 14 with diffuse large B-cell lymphoma, were enrolled; 42 receive
296 ion and STAT3 DNA binding in two subtypes of diffuse large B-cell Lymphoma, were used for benchmarkin
297 on after chemoimmunotherapy in patients with diffuse large B-cell lymphoma who are not candidates for
298 llow-up of 28.6 months, 86% of patients with diffuse large B-cell lymphoma who had a response (95% CI
300 to 50% of patients with Hodgkin lymphoma and diffuse large B-cell lymphoma will relapse, requiring ad
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。