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 progression of VHL-associated renal cysts to clear cell renal cell carcinoma.
2 r remains the optimal approach in metastatic clear cell renal cell carcinoma.
3 tor inhibitor sunitinib in patients with non-clear cell renal cell carcinoma.
4 L diseases, including sporadic and inherited clear cell renal cell carcinoma.
5 n an attempt to delay disease progression in clear cell renal cell carcinoma.
6 to improve prediction of recurrence risk in clear cell renal cell carcinoma.
7 eptor inhibitor, in patients with metastatic clear cell renal cell carcinoma.
8 ular network characteristic of conventional (clear) cell renal cell carcinoma.
9 rolled patients with advanced or metastatic, clear-cell, renal cell carcinoma.
10 4 was up-regulated within the vasculature of clear cell-renal cell carcinoma almost 9-fold more than
11 lysis, we assessed 145 patients with primary clear-cell renal-cell carcinoma and defined PBRM1 and BA
12 covered that BAP1 is mutated in about 15% of clear-cell renal-cell carcinoma, and that BAP1 and PBRM1
17 carcinomas and eight out of 44 (18%) primary clear cell renal cell carcinomas (CC-RCC) and in one out
18 u tumor suppressor protein are found in most clear cell renal cell carcinomas (CC-RCCs) but not other
19 he genetic hallmark of hemangioblastomas and clear cell-renal cell carcinomas (CC-RCCs) is loss-of-fu
20 ppressor protein pVHL is commonly mutated in clear cell renal cell carcinoma (ccRCC) and has been imp
21 f flux balance analysis in two cancer types, clear cell renal cell carcinoma (ccRCC) and prostate ade
22 tin 3 (TRPM3) channel promotes the growth of clear cell renal cell carcinoma (ccRCC) and stimulates M
23 inically, SCP1 and SCP3 are downregulated in clear cell renal cell carcinoma (ccRCC) and these events
24 scular area mask (VAM) in H&E micrographs of clear cell renal cell carcinoma (ccRCC) cases from The C
29 ysregulation of chromatin-modifying genes in clear cell renal cell carcinoma (ccRCC) has been uncover
33 nd a T cell infiltration score and find that clear cell renal cell carcinoma (ccRCC) is among the hig
48 in-depth immune profiling of samples from 73 clear cell renal cell carcinoma (ccRCC) patients and fiv
49 role for dysregulated TGF-beta signaling in clear cell renal cell carcinoma (ccRCC) progression and
50 tion factor (HIF) signaling pathway promotes clear cell renal cell carcinoma (ccRCC) progression and
51 ncer arising from the kidney in adults, with clear cell renal cell carcinoma (ccRCC) representing app
52 iptional profiling of a cohort of 50 primary clear cell renal cell carcinoma (ccRCC) samples from The
53 1) was revealed to be downregulated in human clear cell renal cell carcinoma (ccRCC) samples, which w
54 Recent studies have demonstrated that in clear cell renal cell carcinoma (ccRCC) several chromati
56 oit novel compounds with high selectivity to clear cell renal cell carcinoma (ccRCC) with common muta
57 nitinib is a first-line therapy for advanced clear cell renal cell carcinoma (ccRCC), a deadly form o
58 ly targeted therapies have been approved for clear cell renal cell carcinoma (ccRCC), a highly aggres
60 genesis is an important prognostic factor of clear cell renal cell carcinoma (ccRCC), as well as a fa
64 umor suppressor gene (VHL) are a hallmark of clear cell renal cell carcinoma (CCRCC), the most common
66 ted as an early event in almost all cases of clear cell renal cell carcinoma (ccRCC), the most freque
68 nderlie the tumorigenesis and progression of clear cell renal cell carcinoma (ccRCC), we studied the
69 ints-average sensitivity and specificity for clear cell renal cell carcinoma (ccRCC)-were compared be
86 rimethyltransferase, have been identified in clear cell renal cell carcinoma (ccRCC); however it is u
87 C is frequently inactivated in patients with clear cell renal cell carcinoma (ccRCC); however, it is
88 ancer subtypes from The Cancer Genome Atlas: clear cell renal cell carcinoma (ccRCC, also known as ki
90 essor gene is inactivated in the majority of clear cell renal cell carcinomas (ccRCC), but genetic ab
95 r suppressor gene in hereditary and sporadic clear-cell renal cell carcinoma (ccRCC) have led to new
100 von Hippel-Lindau (VHL) are major causes of clear-cell renal cell carcinoma (ccRCC) that may origina
107 suppressor is inactivated in the majority of clear cell renal cell carcinomas (ccRCCs), leading to in
110 ulation by the transcription factor HNF4A in clear cell renal cell carcinoma, despite no differential
112 Molecular characterization of the genome of clear cell renal cell carcinoma enabled identification o
113 rchival specimens of primary organ-confined, clear-cell, renal cell carcinoma from patients who had u
114 he other subtypes of kidney neoplasms (e.g., clear-cell renal cell carcinoma) harbored PIK3CA mutatio
115 iology of renal cell carcinoma, particularly clear cell renal cell carcinoma, have led to the develop
116 glioma multiforme, breast, colorectal, skin, clear cell renal cell carcinoma, hepatic and prostate ca
117 els of primary and metastatic pVHL-defective clear cell renal cell carcinoma in an on-target fashion.
118 ur recurrence after nephrectomy in localised clear cell renal cell carcinoma is well characterised by
121 years and older with advanced or metastatic clear-cell renal cell carcinoma, measurable disease, and
122 mors that included renal oncocytomas and non-clear cell renal cell carcinomas (nccRCCs), consisting o
123 gle-agent targeted therapies in advanced non-clear cell renal cell carcinoma (ncRCC) compared with cl
124 ll carcinoma and renal oncocytoma but not by clear cell renal cell carcinoma or by papillary renal ce
125 linical outcome in patients with stage I-III clear cell renal cell carcinoma, providing a more accura
126 in zebrafish and murine xenograft models of clear cell renal cell carcinoma (RCC) and pancreatic ade
127 iews the evolution of targeted therapies for clear cell renal cell carcinoma (RCC) and recent develop
130 l renal cell carcinoma (ncRCC) compared with clear cell renal cell carcinoma (RCC) supports the study
131 a pathway is well-known to be deregulated in clear cell renal cell carcinoma (RCC) whereas in papilla
132 e has a critical role in the pathogenesis of clear cell renal cell carcinoma (RCC), because VHL mutat
133 unction occurs in familial and most sporadic clear cell renal cell carcinoma (RCC), resulting in the
139 m patients before undergoing nephrectomy for clear cell renal cell carcinoma (RCC; n = 48), normal vo
143 75 genes were analyzed in four conventional (clear cell) renal cell carcinomas (RCC), one chromophobe
144 r endothelial growth factor in the growth of clear-cell renal cell carcinoma (RCC) has identified a p
145 ) has a critical role in the pathogenesis of clear-cell renal cell carcinoma (RCC), as VHL mutations
146 nactivation of the von Hippel-Lindau gene in clear-cell renal cell carcinomas (RCC) leads to overexpr
148 signaling and was highly expressed in 99% of clear cell renal cell carcinomas (RCCs), the most preval
149 0 cm) included in this study, 108 (55%) were clear cell renal cell carcinomas (RCCs); 30 (15%), papil
150 viously untreated metastatic or unresectable clear-cell renal-cell carcinoma received oral regorafeni
151 sphorylated STAT3 are remarkably elevated in clear-cell renal-cell carcinoma relative to adjacent nor
153 roarray samples from tumors of patients with clear cell renal cell carcinoma shows that increased CDC
155 tute a significant portion of aggressive non-clear cell renal cell carcinomas that have no standard t
156 is for a molecular genetic classification of clear-cell renal-cell carcinoma that could influence tre
158 ed 615 patients with locoregional, high-risk clear-cell renal-cell carcinoma to receive either suniti
159 with treatment-naive progressive metastatic clear cell renal cell carcinoma were enrolled between Se
160 A total of 361 patients with metastatic clear cell renal cell carcinoma were randomly assigned e
161 med metastatic or locally advanced (or both) clear-cell renal cell carcinoma were randomly assigned (
162 pression predisposes to hemangioblastoma and clear cell renal cell carcinoma, whereas specific point
163 pe of how cancer is treated, particularly in clear cell renal cell carcinoma, which is molecularly li
164 of 626 patients from France with stage I-III clear cell renal cell carcinoma who had also undergone n
165 cal outcome in 942 patients with stage I-III clear cell renal cell carcinoma who had undergone a neph
166 papillary, chromophobe, or unclassified non-clear cell renal cell carcinoma with no history of previ
167 ndings identify mutation-defined subtypes of clear-cell renal-cell carcinoma with distinct clinical o
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。