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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
13                                          Non-clear cell renal cell carcinomas are histologically and
14             Among patients with locoregional clear-cell renal-cell carcinoma at high risk for tumor r
15           A common genetic mutation found in clear cell renal cell carcinoma (CC-RCC) is the loss of
16                                              Clear cell renal cell carcinoma (CC-RCC) is the most let
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
25                   In agreement, SETD2-mutant clear cell renal cell carcinoma (ccRCC) cells displayed
26      The presence of sarcomatoid features in clear cell renal cell carcinoma (ccRCC) confers a poor p
27                                              Clear cell renal cell carcinoma (CCRCC) evolves due to m
28                                              Clear cell renal cell carcinoma (ccRCC) has been previou
29 ysregulation of chromatin-modifying genes in clear cell renal cell carcinoma (ccRCC) has been uncover
30                         However, its role in clear cell renal cell carcinoma (ccRCC) has not been des
31           Recent genomic studies of sporadic clear cell renal cell carcinoma (ccRCC) have uncovered n
32                                              Clear cell renal cell carcinoma (ccRCC) is a gender-bias
33 nd a T cell infiltration score and find that clear cell renal cell carcinoma (ccRCC) is among the hig
34                                              Clear cell renal cell carcinoma (ccRCC) is an aggressive
35                                              Clear cell renal cell carcinoma (CCRCC) is an incurable
36                                              Clear cell renal cell carcinoma (ccRCC) is characterized
37                                              Clear cell renal cell carcinoma (ccRCC) is characterized
38                                              Clear cell renal cell carcinoma (CCRCC) is characterized
39                                              Clear cell renal cell carcinoma (ccRCC) is cytogenetical
40                  The long-term prognosis for clear cell renal cell carcinoma (ccRCC) is dramatically
41                                              Clear cell renal cell carcinoma (ccRCC) is histologicall
42                                              Clear cell renal cell carcinoma (ccRCC) is the most comm
43                                              Clear cell renal cell carcinoma (ccRCC) is the most comm
44                                              Clear cell renal cell carcinoma (ccRCC) is the most comm
45                                              Clear cell renal cell carcinoma (ccRCC) is the most comm
46                                              Clear cell renal cell carcinoma (ccRCC) is the most comm
47                                        Human clear cell renal cell carcinoma (ccRCC) is therapy resis
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
55                           On the other hand, clear cell renal cell carcinoma (ccRCC) strongly deviate
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
59                                              Clear cell renal cell carcinoma (ccRCC), a tubular epith
60 genesis is an important prognostic factor of clear cell renal cell carcinoma (ccRCC), as well as a fa
61              In the most common form of RCC, clear cell renal cell carcinoma (ccRCC), inactivation of
62                        Some cancers, such as clear cell renal cell carcinoma (ccRCC), require exogeno
63                                     Sporadic clear cell renal cell carcinoma (ccRCC), the most common
64 umor suppressor gene (VHL) are a hallmark of clear cell renal cell carcinoma (CCRCC), the most common
65                                              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
67                                          For clear cell renal cell carcinoma (ccRCC), three of the fi
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
70  six tandem BDs and is frequently mutated in clear cell renal cell carcinoma (ccRCC).
71 rface glycoprotein ubiquitously expressed in clear cell renal cell carcinoma (ccRCC).
72 otein expression, and methylation changes in clear cell renal cell carcinoma (ccRCC).
73 on, multiple renal cysts, and early onset of clear cell renal cell carcinoma (ccRCC).
74  central nervous system hemangioblastoma and clear cell renal cell carcinoma (CCRCC).
75 d of care for first-line therapy of advanced clear cell renal cell carcinoma (ccRCC).
76 ed as a therapeutic target for patients with clear cell renal cell carcinoma (ccRCC).
77  major hurdle in improving the management of clear cell renal cell carcinoma (ccRCC).
78 odeler, is implicated in the pathogenesis of clear cell renal cell carcinoma (ccRCC).
79  genomic ITH has previously been reported in clear cell renal cell carcinoma (ccRCC).
80  outcomes for African American patients with clear cell renal cell carcinoma (ccRCC).
81 dau (VHL) gene mutations are associated with clear cell renal cell carcinoma (ccRCC).
82 ection of miR-204 and miR-210 related to the clear cell Renal Cell Carcinoma (ccRCC).
83 s a direct transcriptional target of HIFs in clear cell renal cell carcinoma (ccRCC).
84 eases, including both sporadic and inherited clear cell renal cell carcinoma (ccRCC).
85 mor suppressor VHL, the most common event in clear cell renal cell carcinoma (ccRCC).
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
89                             More than 90% of clear cell renal cell carcinomas (ccRCC) exhibit inactiv
90 essor gene is inactivated in the majority of clear cell renal cell carcinomas (ccRCC), but genetic ab
91                                VHL-deficient clear cell renal cell carcinomas (ccRCC), the most commo
92  tumor-suppressor gene (VHL) is lost in most clear cell renal cell carcinomas (ccRCC).
93 d to the hereditary VHL disease and sporadic clear cell renal cell carcinomas (CCRCC).
94  VEGF, which drives abnormal angiogenesis in clear cell renal cell carcinomas (ccRCC).
95 r suppressor gene in hereditary and sporadic clear-cell renal cell carcinoma (ccRCC) have led to new
96                                              Clear-cell renal cell carcinoma (ccRCC) is a common aggr
97                                 Importantly, clear-cell renal cell carcinoma (ccRCC) is frequently as
98                                  Surgery for clear-cell renal cell carcinoma (ccRCC) might benefit fr
99 n and tumor growth in selected VHL-deficient clear-cell renal cell carcinoma (ccRCC) models.
100  von Hippel-Lindau (VHL) are major causes of clear-cell renal cell carcinoma (ccRCC) that may origina
101                                           In clear-cell renal cell carcinoma (ccRCC), inactivation of
102 or the development of adjuvant treatments in clear-cell renal cell carcinoma (ccRCC).
103 ad to benign and malignant tumors, including clear-cell renal cell carcinoma (ccRCC).
104                                              Clear cell renal cell carcinomas (ccRCCs) are characteri
105                                              Clear cell renal cell carcinomas (ccRCCs) display diverg
106            A subset of familial and sporadic clear cell renal cell carcinomas (ccRCCs) is believed to
107 suppressor is inactivated in the majority of clear cell renal cell carcinomas (ccRCCs), leading to in
108                               pVHL-defective clear cell renal cell carcinoma cell lines display unexp
109                                Intriguingly, clear cell renal cell carcinoma cells (ccRCC) have a dys
110 ulation by the transcription factor HNF4A in clear cell renal cell carcinoma, despite no differential
111                                              Clear-cell renal-cell carcinomas display divergent clini
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
119                                              Clear-cell renal cell carcinoma is a frequent cause of d
120                                              Clear cell renal cell carcinoma masses are more likely t
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
128                                              Clear cell renal cell carcinoma (RCC) is considered an i
129                                              Clear cell renal cell carcinoma (RCC) is the most common
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
134 tionship between tumor size and perfusion in clear cell renal cell carcinoma (RCC).
135 ll as the majority of patients with sporadic clear cell renal cell carcinoma (RCC).
136  significant clinical activity in metastatic clear cell renal cell carcinoma (RCC).
137  (VHL) is an early event in >60% of sporadic clear cell renal cell carcinoma (RCC).
138 e revolutionized the treatment of metastatic clear cell renal cell carcinoma (RCC).
139 m patients before undergoing nephrectomy for clear cell renal cell carcinoma (RCC; n = 48), normal vo
140                                              Clear cell renal cell carcinomas (RCC) frequently displa
141                                   In all, 39 clear cell renal cell carcinomas (RCC), seven primary an
142                                              Clear cell renal cell carcinomas (RCC), the major histol
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
147 r suppressor pVHL is lost in the majority of clear-cell renal cell carcinomas (RCC).
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
152 mmune infiltrates in lung adenocarcinoma and clear cell renal cell carcinoma, respectively.
153 roarray samples from tumors of patients with clear cell renal cell carcinoma shows that increased CDC
154              In patients with metastatic non-clear cell renal cell carcinoma, sunitinib improved prog
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
157                                              Clear cell renal cell carcinoma, the most common form of
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

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