-
1
-
-
0035172596
-
Genomic imbalances in the progression of endocrine pancreatic tumors
-
J. Zhao, H. Moch, A.F. Scheidweiler, A. Baer, A.A. Schäffer, E.J.M. Speel, J. Roth, P.U. Heitz, and P. Komminoth Genomic imbalances in the progression of endocrine pancreatic tumors Genes Chromosomes Cancer 32 2001 364 372
-
(2001)
Genes Chromosomes Cancer
, vol.32
, pp. 364-372
-
-
Zhao, J.1
Moch, H.2
Scheidweiler, A.F.3
Baer, A.4
Schäffer, A.A.5
Speel, E.J.M.6
Roth, J.7
Heitz, P.U.8
Komminoth, P.9
-
2
-
-
0141724605
-
The genetics of pancreatic cancer
-
S.M. Cowgill, and P. Muscarella The genetics of pancreatic cancer Am J Surg 186 2003 279 286
-
(2003)
Am J Surg
, vol.186
, pp. 279-286
-
-
Cowgill, S.M.1
Muscarella, P.2
-
3
-
-
0036731786
-
Review of the clinical, histological, and molecular aspects of pancreatic endocrine neoplasms
-
A.A. Gumbs, P.S. Moore, M. Falconi, C. Bassi, S. Beghelli, I. Modlin, and A. Scarpa Review of the clinical, histological, and molecular aspects of pancreatic endocrine neoplasms J Surg Oncol 81 2002 45
-
(2002)
J Surg Oncol
, vol.81
, pp. 45
-
-
Gumbs, A.A.1
Moore, P.S.2
Falconi, M.3
Bassi, C.4
Beghelli, S.5
Modlin, I.6
Scarpa, A.7
-
4
-
-
0033853351
-
Chromosomal alterations in human pancreatic endocrine tumors
-
E. Stumpf, Y. Aalto, A. Hoog, M. Kjellman, T. Otonkoski, S. Knuutila, and C. Anderson Chromosomal alterations in human pancreatic endocrine tumors Genes Chromosomes Cancer 29 2000 83 87
-
(2000)
Genes Chromosomes Cancer
, vol.29
, pp. 83-87
-
-
Stumpf, E.1
Aalto, Y.2
Hoog, A.3
Kjellman, M.4
Otonkoski, T.5
Knuutila, S.6
Anderson, C.7
-
5
-
-
0035138085
-
High resolution allelotype of nonfunctional pancreatic endocrine tumors: Identification of two molecular subgroups with clinical implications
-
G. Rigaud, E. Missiaglia, P.S. Moore, G. Zamboni, M. Falconi, G. Talamini, A. Pesci, A. Baron, D. Lissandrini, G. Rindi, P. Grigolato, P. Pederzoli, and A. Scarpa High resolution allelotype of nonfunctional pancreatic endocrine tumors: identification of two molecular subgroups with clinical implications Cancer Res 61 2001 285 292
-
(2001)
Cancer Res
, vol.61
, pp. 285-292
-
-
Rigaud, G.1
Missiaglia, E.2
Moore, P.S.3
Zamboni, G.4
Falconi, M.5
Talamini, G.6
Pesci, A.7
Baron, A.8
Lissandrini, D.9
Rindi, G.10
Grigolato, P.11
Pederzoli, P.12
Scarpa, A.13
-
6
-
-
0036772376
-
Chromosome 22q in pancreatic endocrine tumors: Identification of a homozygous deletion and potential prognostic associations of allelic deletions
-
A. Wild, P. Langer, I. Celik, B. Chaloupka, and D.K. Bartsch Chromosome 22q in pancreatic endocrine tumors: identification of a homozygous deletion and potential prognostic associations of allelic deletions Eur J Endocrinol 147 2002 507 513
-
(2002)
Eur J Endocrinol
, vol.147
, pp. 507-513
-
-
Wild, A.1
Langer, P.2
Celik, I.3
Chaloupka, B.4
Bartsch, D.K.5
-
8
-
-
0027966172
-
Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors
-
O.P. Kallioniemi, A. Kallioniemi, J. Piper, J. Isola, F.M. Waldman, J.W. Gray, and D. Pinkel Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors Genes Chromosomes Cancer 10 1994 231 243
-
(1994)
Genes Chromosomes Cancer
, vol.10
, pp. 231-243
-
-
Kallioniemi, O.P.1
Kallioniemi, A.2
Piper, J.3
Isola, J.4
Waldman, F.M.5
Gray, J.W.6
Pinkel, D.7
-
9
-
-
0034131138
-
Pancreatic acinar carcinoma shows a distinct pattern of chromosomal imbalances by comparative genomic hybridization
-
D. Taruscio, S. Paradisi, G. Zamboni, G. Rigaud, M. Falconi, and A. Scarpa Pancreatic acinar carcinoma shows a distinct pattern of chromosomal imbalances by comparative genomic hybridization Genes Chromosomes Cancer 28 2000 294 299
-
(2000)
Genes Chromosomes Cancer
, vol.28
, pp. 294-299
-
-
Taruscio, D.1
Paradisi, S.2
Zamboni, G.3
Rigaud, G.4
Falconi, M.5
Scarpa, A.6
-
10
-
-
0035139644
-
Molecular characterization of pancreatic serous microcystic adenomas: Evidence for a tumor suppressor gene on chromosome 10q
-
P.S. Moore, G. Zamboni, A. Brighenti, D. Lissandrini, D. Antonello, P. Capelli, G. Rigaud, M. Falconi, and A. Scarpa Molecular characterization of pancreatic serous microcystic adenomas: evidence for a tumor suppressor gene on chromosome 10q Am J Pathol 158 2001 317 321
-
(2001)
Am J Pathol
, vol.158
, pp. 317-321
-
-
Moore, P.S.1
Zamboni, G.2
Brighenti, A.3
Lissandrini, D.4
Antonello, D.5
Capelli, P.6
Rigaud, G.7
Falconi, M.8
Scarpa, A.9
-
11
-
-
0035011834
-
Alteration of chromosome arm 6p is characteristic of primary mediastinal B-cell lymphoma, as identified by genome-wide allelotyping
-
G. Rigaud, P.S. Moore, D. Taruscio, M. Scardoni, M. Montresor, F. Menestrina, and A. Scarpa Alteration of chromosome arm 6p is characteristic of primary mediastinal B-cell lymphoma, as identified by genome-wide allelotyping Genes Chromosomes Cancer 31 2001 191 195
-
(2001)
Genes Chromosomes Cancer
, vol.31
, pp. 191-195
-
-
Rigaud, G.1
Moore, P.S.2
Taruscio, D.3
Scardoni, M.4
Montresor, M.5
Menestrina, F.6
Scarpa, A.7
-
12
-
-
2342504277
-
Genetic abnormalities in pancreatic cancer
-
P.S. Moore, S. Beghelli, G. Zamboni, and A. Scarpa Genetic abnormalities in pancreatic cancer Mol Cancer 2 2003 7 Available at: http://www.molecular- cancer.com/content/2/1/7. Accessed February 15, 2004
-
(2003)
Mol Cancer
, vol.2
, pp. 7
-
-
Moore, P.S.1
Beghelli, S.2
Zamboni, G.3
Scarpa, A.4
-
13
-
-
0032761852
-
Genetic differences in endocrine pancreatic tumor subtypes detected by comparative genomic hybridization
-
E.J. Speel, J. Richter, H. Moch, C. Egenter, P. Saremaslani, K. Rutimann, J. Zhao, A. Barghorn, J. Roth, P.U. Heitz, and P. Komminoth Genetic differences in endocrine pancreatic tumor subtypes detected by comparative genomic hybridization Am J Pathol 155 1999 1787 1794
-
(1999)
Am J Pathol
, vol.155
, pp. 1787-1794
-
-
Speel, E.J.1
Richter, J.2
Moch, H.3
Egenter, C.4
Saremaslani, P.5
Rutimann, K.6
Zhao, J.7
Barghorn, A.8
Roth, J.9
Heitz, P.U.10
Komminoth, P.11
-
14
-
-
0035394330
-
Genetic evidence for early divergence of small functioning and nonfunctioning endocrine pancreatic tumors: Gain of 9Q34 is an early event in insulinomas
-
E.J. Speel, A.F. Scheidweiler, J. Zhao, C. Matter, P. Saremaslani, J. Roth, P.U. Heitz, and P. Komminoth Genetic evidence for early divergence of small functioning and nonfunctioning endocrine pancreatic tumors: gain of 9Q34 is an early event in insulinomas Cancer Res 61 2001 5186 5192
-
(2001)
Cancer Res
, vol.61
, pp. 5186-5192
-
-
Speel, E.J.1
Scheidweiler, A.F.2
Zhao, J.3
Matter, C.4
Saremaslani, P.5
Roth, J.6
Heitz, P.U.7
Komminoth, P.8
-
15
-
-
0031957753
-
Comparative genomic hybridization analysis of sporadic neuroendocrine tumors of the digestive system
-
B. Terris, M. Meddeb, A. Marchio, G. Danglot, J. Flejou, J. Belghiti, P. Ruszniewski, and A. Bernheim Comparative genomic hybridization analysis of sporadic neuroendocrine tumors of the digestive system Genes Chromosomes Cancer 22 1998 50 56
-
(1998)
Genes Chromosomes Cancer
, vol.22
, pp. 50-56
-
-
Terris, B.1
Meddeb, M.2
Marchio, A.3
Danglot, G.4
Flejou, J.5
Belghiti, J.6
Ruszniewski, P.7
Bernheim, A.8
-
16
-
-
0033987633
-
A region of common deletion in 22q13.3 in human glioma associated with astrocytoma progression
-
N.T. Oskam, E.H. Bijleveld, and T.J. Hulsebos A region of common deletion in 22q13.3 in human glioma associated with astrocytoma progression Int J Cancer 85 2000 336 339
-
(2000)
Int J Cancer
, vol.85
, pp. 336-339
-
-
Oskam, N.T.1
Bijleveld, E.H.2
Hulsebos, T.J.3
-
17
-
-
0035872483
-
Whole genome amplification and high-throughput allelotyping identified five distinct deletion regions on chromosomes 5 and 6 in microdissected early-stage ovarian tumors
-
V.W. Wang, D.A. Bell, R.S. Berkowitz, and S.C. Mok Whole genome amplification and high-throughput allelotyping identified five distinct deletion regions on chromosomes 5 and 6 in microdissected early-stage ovarian tumors Cancer Res 61 2001 4169 4174
-
(2001)
Cancer Res
, vol.61
, pp. 4169-4174
-
-
Wang, V.W.1
Bell, D.A.2
Berkowitz, R.S.3
Mok, S.C.4
-
18
-
-
84862477347
-
-
Weizmann Institute of Science Gene Cards. Available at http://bioinfo.weizmann.ac.il/cards-bin/carddisp?ESR1&search=ESR. Accessed February 15, 2004.
-
Weizmann Institute of Science Gene Cards
-
-
-
19
-
-
0022653964
-
Human oestrogen receptor cDNA: Sequence, expression and homology to v-erb-A
-
S. Green, P. Walter, V. Kumar, A. Krust, J.M. Bornert, P. Argos, and P. Chambon Human oestrogen receptor cDNA: sequence, expression and homology to v-erb-A Nature 320 1986 134 139
-
(1986)
Nature
, vol.320
, pp. 134-139
-
-
Green, S.1
Walter, P.2
Kumar, V.3
Krust, A.4
Bornert, J.M.5
Argos, P.6
Chambon, P.7
-
20
-
-
19244368091
-
Isolation and chromosomal localization of GPR31, a human gene encoding a putative G protein-coupled receptor
-
A. Zingoni, M. Rocchi, C.T. Storlazzi, G. Bernardini, A. Santoni, and M. Napolitano Isolation and chromosomal localization of GPR31, a human gene encoding a putative G protein-coupled receptor Genomics 42 1997 519 523
-
(1997)
Genomics
, vol.42
, pp. 519-523
-
-
Zingoni, A.1
Rocchi, M.2
Storlazzi, C.T.3
Bernardini, G.4
Santoni, A.5
Napolitano, M.6
-
21
-
-
0022536710
-
Isolation and characterization of a new cellular oncogene encoding a protein with multiple transmembrane domains
-
D. Young, G. Waitches, C. Birchmeier, O. Fasano, and M. Wigler Isolation and characterization of a new cellular oncogene encoding a protein with multiple transmembrane domains Cell 45 1984 711 719
-
(1984)
Cell
, vol.45
, pp. 711-719
-
-
Young, D.1
Waitches, G.2
Birchmeier, C.3
Fasano, O.4
Wigler, M.5
-
22
-
-
0040920369
-
-
Online Mendelian Inheritance in Man. Available at http://www.ncbi.nlm. nih.gov:80/entrez/query.fcgi?CMD=search&DB=omim. Accessed February 15, 2004.
-
Online Mendelian Inheritance in Man
-
-
-
23
-
-
0030891372
-
A clinical overview of WT1 gene mutations
-
M. Little, and C. Wells A clinical overview of WT1 gene mutations Hum Mutat 9 1997 209 225
-
(1997)
Hum Mutat
, vol.9
, pp. 209-225
-
-
Little, M.1
Wells, C.2
-
24
-
-
0012645205
-
The role of WT1 in oncogenesis: Tumor suppressor or oncogene?
-
D.M. Loeb, and S. Sukumar The role of WT1 in oncogenesis: tumor suppressor or oncogene? Int J Hematol 76 2002 117 126
-
(2002)
Int J Hematol
, vol.76
, pp. 117-126
-
-
Loeb, D.M.1
Sukumar, S.2
-
25
-
-
0040061124
-
Cytogenetic and fluorescence in situ hybridization analyses of chromosome 19 aberrations in pancreatic carcinomas: Frequent loss of 19p13.3 and gain of 19q13.1-13.2
-
M. Hoglund, L. Gorunova, A. Andren-Sandberg, S. Dawiskiba, F. Mitelman, and B. Johansson Cytogenetic and fluorescence in situ hybridization analyses of chromosome 19 aberrations in pancreatic carcinomas: frequent loss of 19p13.3 and gain of 19q13.1-13.2 Genes Chromosomes Cancer 21 1998 8 16
-
(1998)
Genes Chromosomes Cancer
, vol.21
, pp. 8-16
-
-
Hoglund, M.1
Gorunova, L.2
Andren-Sandberg, A.3
Dawiskiba, S.4
Mitelman, F.5
Johansson, B.6
-
26
-
-
0035834386
-
A phosphatase associated with metastasis of colorectal cancer
-
S. Saha, A. Bardelli, P. Buckhaults, V.E. Velculescu, C. Rago, B. St Croix, K.E. Romans, M.A. Choti, C. Lengauer, K.W. Kinzler, and B. Vogelstein A phosphatase associated with metastasis of colorectal cancer Science 294 2001 1343 1346
-
(2001)
Science
, vol.294
, pp. 1343-1346
-
-
Saha, S.1
Bardelli, A.2
Buckhaults, P.3
Velculescu, V.E.4
Rago, C.5
St Croix, B.6
Romans, K.E.7
Choti, M.A.8
Lengauer, C.9
Kinzler, K.W.10
Vogelstein, B.11
-
27
-
-
0038587789
-
Genomic amplification and oncogenic properties of the KCNK9 potassium channel gene
-
D. Mu, L. Chen, X. Zhang, L.H. See, C.M. Koch, C. Yen, J.J. Tong, L. Spiegel, K.C. Nguyen, A. Servoss, Y. Peng, L. Pei, J.R. Marks, S. Lowe, T. Hoey, L.Y. Jan, W.R. McCombie, M.H. Wigler, and S. Powers Genomic amplification and oncogenic properties of the KCNK9 potassium channel gene Cancer Cell 3 2003 297 302
-
(2003)
Cancer Cell
, vol.3
, pp. 297-302
-
-
Mu, D.1
Chen, L.2
Zhang, X.3
See, L.H.4
Koch, C.M.5
Yen, C.6
Tong, J.J.7
Spiegel, L.8
Nguyen, K.C.9
Servoss, A.10
Peng, Y.11
Pei, L.12
Marks, J.R.13
Lowe, S.14
Hoey, T.15
Jan, L.Y.16
McCombie, W.R.17
Wigler, M.H.18
Powers, S.19
|