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1 , increased cholangiocyte proliferation, and intrahepatic cholangiocarcinoma.
2 ed for radioembolization in locally advanced intrahepatic cholangiocarcinoma.
3 with the highest incidences among those with intrahepatic cholangiocarcinoma.
4 up to 25% of cholangiocarcinomas, especially intrahepatic cholangiocarcinoma.
5 % were hepatocellular carcinoma and 20% were intrahepatic cholangiocarcinoma.
6 llular carcinoma with stem cell features and intrahepatic cholangiocarcinoma.
7 a target of transformation and an origin of intrahepatic cholangiocarcinoma.
8 epatocytes in this model as well as in human intrahepatic cholangiocarcinoma.
9 itumor effects in an orthotopic rat model of intrahepatic cholangiocarcinoma.
10 ncreasing in frequency as is that of primary intrahepatic cholangiocarcinoma.
11 ors, several others could be associated with intrahepatic cholangiocarcinoma.
12 ce, mortality, and survival rates of primary intrahepatic cholangiocarcinoma.
13 served in hepatocellular carcinoma (HCC) and intrahepatic cholangiocarcinomas.
14 soforms 1 or 2 occur in approximately 15% of intrahepatic cholangiocarcinomas.
15 ehydrogenase (IDH) is recurrently mutated in intrahepatic cholangiocarcinomas.
16 tly expanded the genetic characterization of intrahepatic cholangiocarcinomas.
17 and IDH2 genes encoding metabolic enzymes in intrahepatic cholangiocarcinomas.
18 role of dysregulated chromatin remodeling in intrahepatic cholangiocarcinomas.
19 osis and most of the tumors that formed were intrahepatic cholangiocarcinomas.
21 occur in approximately 13% of patients with intrahepatic cholangiocarcinoma, a relatively uncommon c
23 broblast growth factor receptor-2 fusions in intrahepatic cholangiocarcinoma, among others) is changi
25 ate the prevalence of known risk factors for intrahepatic cholangiocarcinoma and explore other potent
26 f patients with hepatocellular carcinoma and intrahepatic cholangiocarcinoma and identify two subsets
27 contrast enhancement is a typical feature of intrahepatic cholangiocarcinoma and may aid in the detec
28 tic reviews of all series on TO indications (intrahepatic cholangiocarcinoma and perihilar cholangioc
29 103 patients obtained from meta-analyses on intrahepatic cholangiocarcinoma and phCC, and liver meta
30 ondary glioblastoma, acute myeloid leukemia, intrahepatic cholangiocarcinoma, and chondrosarcomas, le
31 s, acute-on-chronic liver failure, hilar and intrahepatic cholangiocarcinoma, and unresectable liver
32 hepatocellular carcinoma, hepatoblastoma and intrahepatic cholangiocarcinoma are analyzed, obtaining
33 cers, including hepatocellular carcinoma and intrahepatic cholangiocarcinoma, are leading causes of c
35 een increasingly used to treat patients with intrahepatic cholangiocarcinoma, as well as metastatic d
36 cancers including hepatocellular carcinomas, intrahepatic cholangiocarcinomas, basal cell carcinomas,
37 markers made progresses slowly compared with intrahepatic cholangiocarcinoma because of surgical comp
38 constitute a novel therapeutic approach for intrahepatic cholangiocarcinoma, because this protein al
42 e to enrich for cell surface proteins of the intrahepatic cholangiocarcinoma cell line CC-SW-1 was de
44 equencing of 133 combined hepatocellular and intrahepatic cholangiocarcinoma (cHCC-ICC) cases, includ
46 1 activity was high throughout the course of intrahepatic cholangiocarcinomas development and low dur
47 ve consortium of malignancies, consisting of intrahepatic cholangiocarcinoma, extrahepatic cholangioc
48 inactivation of Vgll4 dramatically enhanced intrahepatic cholangiocarcinoma formation in Nf2-deficie
49 t also produced a significant suppression of intrahepatic cholangiocarcinoma growth when administered
51 sociated fibroblastic cells in the stroma of intrahepatic cholangiocarcinoma has recently been demons
52 ly encompassing hepatocellular carcinoma and intrahepatic cholangiocarcinoma, has become the second l
55 ), bile ducts and liver (CD/UC), liver (CD), intrahepatic cholangiocarcinoma (IBDs), bile ducts (CD),
57 owth Factor Receptor 2 (FGFR2) are common in intrahepatic cholangiocarcinoma (ICC) and confer sensiti
58 ed unresectable or metastatic BTC, including intrahepatic cholangiocarcinoma (ICC) and extrahepatic c
61 s study aimed to estimate incidence rates of intrahepatic cholangiocarcinoma (ICC) and non-Hodgkin ly
63 at mediate the initiation and development of intrahepatic cholangiocarcinoma (ICC) associated with he
65 rom combined hepatocellular liver cancer and intrahepatic cholangiocarcinoma (ICC) has increased and
66 rates of hepatocellular carcinoma (HCC) and intrahepatic cholangiocarcinoma (ICC) have increased in
77 rgical tumor resection (R0) for treatment of intrahepatic cholangiocarcinoma (ICC) is potentially cur
81 st common liver cancer, can be classified as intrahepatic cholangiocarcinoma (ICC) or extrahepatic ch
83 ions between diabetes, smoking, obesity, and intrahepatic cholangiocarcinoma (ICC) risk remain inconc
84 on of overall survival (OS) in patients with Intrahepatic Cholangiocarcinoma (ICC) who underwent conv
86 232R) of PTPN3, a frequent mutation found in intrahepatic cholangiocarcinoma (ICC), disables its role
88 on and aggressive malignancy of mass-forming intrahepatic cholangiocarcinoma (ICC), we modeled ICC de
89 cells treated with wild-type or IDH1 mutant intrahepatic cholangiocarcinoma (ICC)-derived EVs uncove
94 Primary liver cancer (PLC), which includes intrahepatic cholangiocarcinoma (iCCA) and hepatocellula
98 he 3-year overall survival (OS) for advanced intrahepatic cholangiocarcinoma (iCCA) confined to the l
99 Limited treatment options in patients with intrahepatic cholangiocarcinoma (iCCA) demand the introd
109 performed proteogenomic characterization of intrahepatic cholangiocarcinoma (iCCA) using paired tumo
110 We report a case of a 55-year-old male with intrahepatic cholangiocarcinoma (iCCA) who underwent liv
112 activation of YAP/TAZ, rapid development of intrahepatic cholangiocarcinoma (iCCA), and early lethal
113 er comprises hepatocellular carcinoma (HCC), intrahepatic cholangiocarcinoma (iCCA), and other rare t
114 Biliary tract cancers (BTCs), including intrahepatic cholangiocarcinoma (iCCA), extrahepatic cho
116 inhibitors (FGFRi) are used for treatment of intrahepatic cholangiocarcinoma (iCCA), understanding po
122 102 hepatocellular carcinomas (HCCs), three intrahepatic cholangiocarcinomas (ICCs), one neuroendocr
124 ata suggesting a rising worldwide incidence, intrahepatic cholangiocarcinoma (IHC) remains an uncommo
125 Standard therapies for localized inoperable intrahepatic cholangiocarcinoma (IHCC) are ineffective.
127 among the most common genetic alterations in intrahepatic cholangiocarcinoma (IHCC), a deadly liver c
128 increase in the incidence and mortality from intrahepatic cholangiocarcinoma in the United States in
129 termine recent trends in the epidemiology of intrahepatic cholangiocarcinoma in the United States.
132 in endemic areas; moreover, the incidence of intrahepatic cholangiocarcinoma is rising globally.
133 1997, the incidence and mortality rates from intrahepatic cholangiocarcinoma markedly increased, with
134 ver tumors (hepatocellular carcinoma: n = 3, intrahepatic cholangiocarcinoma: n = 2, extrahepatic cho
135 ocellular carcinoma and 1.06 (1.01-1.11) for intrahepatic cholangiocarcinoma (p(heterogeneity)=0.82).
136 ngiocarcinoma cells in relation to promoting intrahepatic cholangiocarcinoma progression is only just
140 , despite significant genetic heterogeneity, intrahepatic cholangiocarcinoma relies on a limited numb
141 f cHCC-ICC with hepatocellular carcinoma and intrahepatic cholangiocarcinoma revealed that combined a
144 e vs recurrent) and primary tumour location (intrahepatic cholangiocarcinoma vs extrahepatic cholangi
146 could classify hepatocellular carcinoma and intrahepatic cholangiocarcinoma with an sensitivity and
147 BDEsp cells yielded only small nonmetastatic intrahepatic cholangiocarcinomas without bile duct obstr