-
1
-
-
62949143802
-
Burden of digestive diseases in the United States Part III: Liver, biliary tract, and pancreas
-
Everhart, J. E. & Ruhl, C. E. Burden of digestive diseases in the United States Part III: Liver, biliary tract, and pancreas. Gastroenterology 136, 1134-1144 (2009).
-
(2009)
Gastroenterology
, vol.136
, pp. 1134-1144
-
-
Everhart, J.E.1
Ruhl, C.E.2
-
2
-
-
80052552459
-
Clinical diagnosis and staging of cholangiocarcinoma
-
Blechacz, B. et al. Clinical diagnosis and staging of cholangiocarcinoma. Nat. Rev. Gastroenterol. Hepatol. 8, 512-522 (2011).
-
(2011)
Nat. Rev. Gastroenterol. Hepatol.
, vol.8
, pp. 512-522
-
-
Blechacz, B.1
-
3
-
-
84856298658
-
Frequent mutation of isocitrate dehydrogenase IDH1 and IDH2 in cholangiocarcinoma identified through broad-based tumor genotyping
-
Borger, D. R. et al. Frequent mutation of isocitrate dehydrogenase IDH1 and IDH2 in cholangiocarcinoma identified through broad-based tumor genotyping. Oncologist 17, 72-79 (2012).
-
(2012)
Oncologist
, vol.17
, pp. 72-79
-
-
Borger, D.R.1
-
4
-
-
84879224082
-
Molecular profiling of cholangiocarcinoma shows potential for targeted therapy treatment decisions
-
Voss, J. S. et al. Molecular profiling of cholangiocarcinoma shows potential for targeted therapy treatment decisions. Hum. Pathol. 44, 1216-1222 (2013).
-
(2013)
Hum. Pathol.
, vol.44
, pp. 1216-1222
-
-
Voss, J.S.1
-
5
-
-
79951677877
-
KRAS and PIK3CA but not BRAF genes are frequently mutated in Chinese cholangiocarcinoma patients
-
Xu, R. F. et al. KRAS and PIK3CA but not BRAF genes are frequently mutated in Chinese cholangiocarcinoma patients. Biomed. Pharmacother. 65, 22-26 (2011).
-
(2011)
Biomed. Pharmacother.
, vol.65
, pp. 22-26
-
-
Xu, R.F.1
-
6
-
-
12144249804
-
Immunohistochemical study of DPC4 and p53 proteins in gallbladder and bile duct cancers
-
Chuang, S. C. et al. Immunohistochemical study of DPC4 and p53 proteins in gallbladder and bile duct cancers. World J. Surg. 28, 995-1000 (2004).
-
(2004)
World J. Surg.
, vol.28
, pp. 995-1000
-
-
Chuang, S.C.1
-
7
-
-
0036056617
-
Genetic and epigenetic alterations of the INK4a-ARF pathway in cholangiocarcinoma
-
Tannapfel, A. et al. Genetic and epigenetic alterations of the INK4a-ARF pathway in cholangiocarcinoma. J. Pathol. 197, 624-631 (2002).
-
(2002)
J. Pathol.
, vol.197
, pp. 624-631
-
-
Tannapfel, A.1
-
8
-
-
60849115270
-
IDH1 and IDH2 mutations in gliomas
-
Yan, H. et al. IDH1 and IDH2 mutations in gliomas. N. Engl. J. Med. 360, 765-773 (2009).
-
(2009)
N. Engl. J. Med.
, vol.360
, pp. 765-773
-
-
Yan, H.1
-
9
-
-
0345790165
-
Immunohistochemical and genetic analysis of non-small cell and small cell gallbladder carcinoma and their precursor lesions
-
DOI 10.1097/01.MP.0000062656.60581.AA
-
Parwani, A. V. et al. Immunohistochemical and genetic analysis of non-small cell and small cell gallbladder carcinoma and their precursor lesions. Mod. Pathol. 16, 299-308 (2003). (Pubitemid 36443978)
-
(2003)
Modern Pathology
, vol.16
, Issue.4
, pp. 299-308
-
-
Parwani, A.V.1
Geradts, J.2
Caspers, E.3
Offerhaus, G.J.4
Yeo, C.J.5
Cameron, J.L.6
Klimstra, D.S.7
Maitra, A.8
Hruban, R.H.9
Argani, P.10
-
10
-
-
0035134978
-
More frequent β-catenin exon 3 mutations in gallbladder adenomas than in carcinomas indicate different lineages
-
Yanagisawa, N. et al. More frequent ?-catenin exon 3 mutations in gallbladder adenomas than in carcinomas indicate different lineages. Cancer Res. 61, 19-22 (2001). (Pubitemid 32095691)
-
(2001)
Cancer Research
, vol.61
, Issue.1
, pp. 19-22
-
-
Yanagisawa, N.1
Mikami, T.2
Saegusa, M.3
Okayasu, I.4
-
11
-
-
84873827063
-
Tumours associated with BAP1 mutations
-
Murali, R. et al. Tumours associated with BAP1 mutations. Pathology 45, 116-126 (2013).
-
(2013)
Pathology
, vol.45
, pp. 116-126
-
-
Murali, R.1
-
12
-
-
84857467474
-
Somatic mutations in the chromatin remodeling gene ARID1A occur in several tumor types
-
Jones, S. et al. Somatic mutations in the chromatin remodeling gene ARID1A occur in several tumor types. Hum. Mutat. 33, 100-103 (2012).
-
(2012)
Hum. Mutat.
, vol.33
, pp. 100-103
-
-
Jones, S.1
-
13
-
-
79251635938
-
Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma
-
Varela, I. et al. Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma. Nature 469, 539-542 (2011).
-
(2011)
Nature
, vol.469
, pp. 539-542
-
-
Varela, I.1
-
14
-
-
70349100446
-
Histone deacetylase inhibitors: Current status and overview of recent clinical trials
-
Ma, X. et al. Histone deacetylase inhibitors: current status and overview of recent clinical trials. Drugs 69, 1911-1934 (2009).
-
(2009)
Drugs
, vol.69
, pp. 1911-1934
-
-
Ma, X.1
-
15
-
-
84861581233
-
Exome sequencing of liver fluke-associated cholangiocarcinoma
-
Ong, C. K. et al. Exome sequencing of liver fluke-associated cholangiocarcinoma. Nat. Genet. 44, 690-693 (2012).
-
(2012)
Nat. Genet.
, vol.44
, pp. 690-693
-
-
Ong, C.K.1
-
16
-
-
84879418850
-
Mutations in isocitrate dehydrogenase 1 and 2 occur frequently in intrahepatic cholangiocarcinomas and share hypermethylation targets with glioblastomas
-
Wang, P. et al. Mutations in isocitrate dehydrogenase 1 and 2 occur frequently in intrahepatic cholangiocarcinomas and share hypermethylation targets with glioblastomas. Oncogene 32, 3091-3100 (2013).
-
(2013)
Oncogene
, vol.32
, pp. 3091-3100
-
-
Wang, P.1
-
17
-
-
34250829395
-
Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes
-
DOI 10.1038/sj.onc.1210529, PII 1210529
-
Pollock, P. M. et al. Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes. Oncogene 26, 7158-7162 (2007). (Pubitemid 350059681)
-
(2007)
Oncogene
, vol.26
, Issue.50
, pp. 7158-7162
-
-
Pollock, P.M.1
Gartside, M.G.2
Dejeza, L.C.3
Powell, M.A.4
Mallon, M.A.5
Davies, H.6
Mohammadi, M.7
Futreal, P.A.8
Stratton, M.R.9
Trent, J.M.10
Goodfellow, P.J.11
-
18
-
-
84878781242
-
Identification of targetable FGFR gene fusions in diverse cancers
-
Wu, Y. M. et al. Identification of targetable FGFR gene fusions in diverse cancers. Cancer Discov. 3, 636-647 (2013).
-
(2013)
Cancer Discov.
, vol.3
, pp. 636-647
-
-
Wu, Y.M.1
-
19
-
-
33749993417
-
The consensus coding sequences of human breast and colorectal cancers
-
DOI 10.1126/science.1133427
-
Sjöblom, T. et al. The consensus coding sequences of human breast and colorectal cancers. Science 314, 268-274 (2006). (Pubitemid 44571966)
-
(2006)
Science
, vol.314
, Issue.5797
, pp. 268-274
-
-
Sjoblom, T.1
Jones, S.2
Wood, L.D.3
Parsons, D.W.4
Lin, J.5
Barber, T.D.6
Mandelker, D.7
Leary, R.J.8
Ptak, J.9
Silliman, N.10
Szabo, S.11
Buckhaults, P.12
Farrell, C.13
Meeh, P.14
Markowitz, S.D.15
Willis, J.16
Dawson, D.17
Willson, J.K.V.18
Gazdar, A.F.19
Hartigan, J.20
Wu, L.21
Liu, C.22
Parmigiani, G.23
Park, B.H.24
Bachman, K.E.25
Papadopoulos, N.26
Vogelstein, B.27
Kinzler, K.W.28
Velculescu, V.E.29
more..
-
20
-
-
77955660663
-
Diverse somatic mutation patterns and pathway alterations in human cancers
-
Kan, Z. et al. Diverse somatic mutation patterns and pathway alterations in human cancers. Nature 466, 869-873 (2010).
-
(2010)
Nature
, vol.466
, pp. 869-873
-
-
Kan, Z.1
-
21
-
-
10844247982
-
Combining probability values from independent permutation tests: A discrete analog of Fisher's classical method
-
Mielke, P. W. et al. Combining probability values from independent permutation tests: a discrete analog of Fisher's classical method. Psychol. Rep. 95, 449-458 (2004).
-
(2004)
Psychol. Rep.
, vol.95
, pp. 449-458
-
-
Mielke, P.W.1
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