-
1
-
-
0032555020
-
Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease
-
Aaltonen LA, Salovaara R, Kristo P, Canzian F, Hemminki A, Peltomaki P, Chadwick RB, Kaariainen H, Eskelinen M, Jarvinen H, Mecklin JP, de la Chapelle A. Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. N Engl J Med 1998;338:1481-7.
-
(1998)
N Engl J Med
, vol.338
, pp. 1481-1487
-
-
Aaltonen, L.A.1
Salovaara, R.2
Kristo, P.3
Canzian, F.4
Hemminki, A.5
Peltomaki, P.6
Chadwick, R.B.7
Kaariainen, H.8
Eskelinen, M.9
Jarvinen, H.10
Mecklin, J.P.11
De La Chapelle, A.12
-
2
-
-
0027285475
-
Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis
-
Ionov Y, Peinado MA, Malkhosyan S, Shibata D, Perucho M. Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis. Nature 1993;363:558-61.
-
(1993)
Nature
, vol.363
, pp. 558-561
-
-
Ionov, Y.1
Peinado, M.A.2
Malkhosyan, S.3
Shibata, D.4
Perucho, M.5
-
3
-
-
0027158031
-
Clues to the pathogenesis of familial colorectal cancer
-
Aaltonen LA, Peltomaki P, Leach FS, Sistonen P, Pylkkanen L, Mecklin JP, Jarvinen H, Powell SM, Jen J, Hamilton SR. Clues to the pathogenesis of familial colorectal cancer. Science 1993;260:812-6.
-
(1993)
Science
, vol.260
, pp. 812-816
-
-
Aaltonen, L.A.1
Peltomaki, P.2
Leach, F.S.3
Sistonen, P.4
Pylkkanen, L.5
Mecklin, J.P.6
Jarvinen, H.7
Powell, S.M.8
Jen, J.9
Hamilton, S.R.10
-
4
-
-
0027140481
-
Microsatellite instability is associated with tumours that characterise the hereditary non-polyposis colorectal carcinoma syndrome
-
Peltomaki P, Lothe RA, Aaltonen LA, Pylkkanen L, Nystrom-Lahti M, Seruca R, David L, Holm R, Ryberg D, Haugen A. Microsatellite instability is associated with tumours that characterise the hereditary non-polyposis colorectal carcinoma syndrome. Cancer Res 1993;53:5853-5.
-
(1993)
Cancer Res
, vol.53
, pp. 5853-5855
-
-
Peltomaki, P.1
Lothe, R.A.2
Aaltonen, L.A.3
Pylkkanen, L.4
Nystrom-Lahti, M.5
Seruca, R.6
David, L.7
Holm, R.8
Ryberg, D.9
Haugen, A.10
-
5
-
-
0027314411
-
Microsatellite instability in cancer of the proximal colon
-
Thibodeau SN, Bren G, Schaid D. Microsatellite instability in cancer of the proximal colon. Science 1993;260:816-9.
-
(1993)
Science
, vol.260
, pp. 816-819
-
-
Thibodeau, S.N.1
Bren, G.2
Schaid, D.3
-
6
-
-
0032730774
-
Genetic susceptibility to nonpolyposis colorectal cancer
-
Lynch HT, de la Chapelle A. Genetic susceptibility to nonpolyposis colorectal cancer. J Med Genet 1999;36:801-18.
-
(1999)
J Med Genet
, vol.36
, pp. 801-818
-
-
Lynch, H.T.1
De La Chapelle, A.2
-
7
-
-
0029089259
-
Hereditary nonpolyposis colorectal cancer: The syndrome, the genes, and historical perspectives
-
Marra G, Boland CR. Hereditary nonpolyposis colorectal cancer: the syndrome, the genes, and historical perspectives. J Natl Cancer Inst 1995;87:1114-25.
-
(1995)
J Natl Cancer Inst
, vol.87
, pp. 1114-1125
-
-
Marra, G.1
Boland, C.R.2
-
8
-
-
0031278322
-
Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer
-
Miyaki M, Konishi M, Tanaka K, Kikuchi-Yanoshita R, Muraoka M, Yasuno M, Igari T, Koike M, Chiba M, Mori T. Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer. Nat Genet 1997;17:271-2.
-
(1997)
Nat Genet
, vol.17
, pp. 271-272
-
-
Miyaki, M.1
Konishi, M.2
Tanaka, K.3
Kikuchi-Yanoshita, R.4
Muraoka, M.5
Yasuno, M.6
Igari, T.7
Koike, M.8
Chiba, M.9
Mori, T.10
-
9
-
-
0025848680
-
The international collaborative group on hereditary nonpolyposis colorectal cancer (ICG-HNPCC)
-
Vasen HFA, Mecklin J-P, Khan PM, Lynch HT. The international collaborative group on hereditary nonpolyposis colorectal cancer (ICG-HNPCC). Dis Colon Rectum 1991;34:424-5.
-
(1991)
Dis Colon Rectum
, vol.34
, pp. 424-425
-
-
Vasen, H.F.A.1
Mecklin, J.-P.2
Khan, P.M.3
Lynch, H.T.4
-
10
-
-
0033063711
-
New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the international collaborative group on HNPCC
-
Vasen HFA, Watson P, Mecklin J-P, Lynch HT. New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the international collaborative group on HNPCC. Gastroenterology 1999;116:1453-6.
-
(1999)
Gastroenterology
, vol.116
, pp. 1453-1456
-
-
Vasen, H.F.A.1
Watson, P.2
Mecklin, J.-P.3
Lynch, H.T.4
-
11
-
-
0031551963
-
A National Cancer Institute workshop on hereditary colorectal cancer syndrome: Meeting highlights and Bethesda Guidelines
-
Rodriguez-Bigas MA, Boland CR, Hamilton SR, Henson DE, Jass JR, Khan PM, Lynch H, Perucho M, Smyrk T, Sobin L, Srivastava S. A National Cancer Institute workshop on hereditary colorectal cancer syndrome: meeting highlights and Bethesda Guidelines. J Natl Cancer Inst 1997;89:1758-62.
-
(1997)
J Natl Cancer Inst
, vol.89
, pp. 1758-1762
-
-
Rodriguez-Bigas, M.A.1
Boland, C.R.2
Hamilton, S.R.3
Henson, D.E.4
Jass, J.R.5
Khan, P.M.6
Lynch, H.7
Perucho, M.8
Smyrk, T.9
Sobin, L.10
Srivastava, S.11
-
12
-
-
0028845693
-
Founding mutations and Alu-mediated recombination in hereditary colon cancer
-
Nyström-Lahti M, Kristo P, Nicolaides NC, Chang SY, Aaltonen LA, Moisio AL, Jarvinen HJ, Mecklin JP, Kinzler KW, Vogelstein B. Founding mutations and Alu-mediated recombination in hereditary colon cancer. Nat Med 1995;1:1203-6.
-
(1995)
Nat Med
, vol.1
, pp. 1203-1206
-
-
Nyström-Lahti, M.1
Kristo, P.2
Nicolaides, N.C.3
Chang, S.Y.4
Aaltonen, L.A.5
Moisio, A.L.6
Jarvinen, H.J.7
Mecklin, J.P.8
Kinzler, K.W.9
Vogelstein, B.10
-
13
-
-
0035899935
-
Cost-effectiveness of microsatellite screening as a method for detecting hereditary nonpolyposis colorectal cancer
-
Ramsey SD, Clarke L, Tzioni R, Higashi M, Berry K, Urban N. Cost-effectiveness of microsatellite screening as a method for detecting hereditary nonpolyposis colorectal cancer. Ann Intern Med 2001;135:577-88.
-
(2001)
Ann Intern Med
, vol.135
, pp. 577-588
-
-
Ramsey, S.D.1
Clarke, L.2
Tzioni, R.3
Higashi, M.4
Berry, K.5
Urban, N.6
-
14
-
-
0036840371
-
Comparison of selection strategies for genetic testing of patients with hereditary nonpolyposis colorectal carcinoma: Effectiveness and cost-effectiveness
-
Reyes CM, Allen BA, Terdiman JP, Wilson LS. Comparison of selection strategies for genetic testing of patients with hereditary nonpolyposis colorectal carcinoma: effectiveness and cost-effectiveness. Cancer 2002;95:1848-50.
-
(2002)
Cancer
, vol.95
, pp. 1848-1850
-
-
Reyes, C.M.1
Allen, B.A.2
Terdiman, J.P.3
Wilson, L.S.4
-
15
-
-
0031017268
-
Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumours and mismatch repair defective human tumor cell lines
-
Kane MF, Loda M, Gaida GM, Lipman J, Mishra R, Goldman H, Jessup JM, Kolodner R. Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumours and mismatch repair defective human tumor cell lines. Cancer Res 1997;57:808-11.
-
(1997)
Cancer Res
, vol.57
, pp. 808-811
-
-
Kane, M.F.1
Loda, M.2
Gaida, G.M.3
Lipman, J.4
Mishra, R.5
Goldman, H.6
Jessup, J.M.7
Kolodner, R.8
-
16
-
-
13144307115
-
Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers
-
Veigl ML, Kasturi L, Olechnowicz J, Ma AH, Lutterbaugh JD, Periyasamy S, Li GM, Drummond J, Modrich PL, Sedwick WD, Morkowitz SD. Biallelic inactivation of hMLH1 by epigenetic gene silencing, a novel mechanism causing human MSI cancers. Proc Natl Acad Sci U S A 1998;95:8698-702.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 8698-8702
-
-
Veigl, M.L.1
Kasturi, L.2
Olechnowicz, J.3
Ma, A.H.4
Lutterbaugh, J.D.5
Periyasamy, S.6
Li, G.M.7
Drummond, J.8
Modrich, P.L.9
Sedwick, W.D.10
Morkowitz, S.D.11
-
17
-
-
0034129240
-
Population-based molecular detection of hereditary nonpolyposis colorectal cancer [correction appeared in J Clin Oncol 2000;18:3456]
-
Salovaara R, Loukola A, Kristo P, Kaariainen H, Ahtola H, Eskelinen M, Horkonen N, Julkunen R, Kangas E, Ojala S, Tulikoura J, Valkamo E, Jarvinen H, Mecklin JP, Aaltonen LA, de la Chapelle A. Population-based molecular detection of hereditary nonpolyposis colorectal cancer [correction appeared in J Clin Oncol 2000;18:3456]. J Clin Oncol 2000;18:2193-200.
-
(2000)
J Clin Oncol
, vol.18
, pp. 2193-2200
-
-
Salovaara, R.1
Loukola, A.2
Kristo, P.3
Kaariainen, H.4
Ahtola, H.5
Eskelinen, M.6
Horkonen, N.7
Julkunen, R.8
Kangas, E.9
Ojala, S.10
Tulikoura, J.11
Valkamo, E.12
Jarvinen, H.13
Mecklin, J.P.14
Aaltonen, L.A.15
De La Chapelle, A.16
-
18
-
-
1442269853
-
Activating BRAF and N-Ras mutations in sporadic primary melanomas: An inverse association with allelic loss on chromosome 9
-
Kumar R, Angelini S, Hemminki K. Activating BRAF and N-Ras mutations in sporadic primary melanomas: an inverse association with allelic loss on chromosome 9. Oncogene 2003;22:9217-24.
-
(2003)
Oncogene
, vol.22
, pp. 9217-9224
-
-
Kumar, R.1
Angelini, S.2
Hemminki, K.3
-
19
-
-
18444374405
-
Mutations of the BRAF gene in human cancer
-
Davies H, Bignell GR, Cox C, Stephens P, Edkins S, Clegg S, Teague J, Woffendin H, Garnett MJ, Bottomley W, Davis N, Dicks E, Ewing R, Floyd Y, Gray K, Hall S, Hawes R, Hughes J, Kosmidou V, Menzies A, Mould C, Parker A, Stevens C, Watt S, Hooper S, Wilson R, Jayatilake H, Gusterson BA, Cooper C, Shipley J, Hargrave D, Pritchard-Jones K, Maitland N, Chenevix-Trench G, Riggins GJ, Bigner DD, Palmieri G, Cossu A, Flanagan A, Nicholson A, Ho JWC, Leung SY, Yuen ST, Weber BL, Seigler HF, Darrow TL, Paterson H, Marais R, Marshall CJ, Wooster R, Stratton MR, Futreal PA. Mutations of the BRAF gene in human cancer. Nature 2002;417:949-54.
-
(2002)
Nature
, vol.417
, pp. 949-954
-
-
Davies, H.1
Bignell, G.R.2
Cox, C.3
Stephens, P.4
Edkins, S.5
Clegg, S.6
Teague, J.7
Woffendin, H.8
Garnett, M.J.9
Bottomley, W.10
Davis, N.11
Dicks, E.12
Ewing, R.13
Floyd, Y.14
Gray, K.15
Hall, S.16
Hawes, R.17
Hughes, J.18
Kosmidou, V.19
Menzies, A.20
Mould, C.21
Parker, A.22
Stevens, C.23
Watt, S.24
Hooper, S.25
Wilson, R.26
Jayatilake, H.27
Gusterson, B.A.28
Cooper, C.29
Shipley, J.30
Hargrave, D.31
Pritchard-Jones, K.32
Maitland, N.33
Chenevix-Trench, G.34
Riggins, G.J.35
Bigner, D.D.36
Palmieri, G.37
Cossu, A.38
Flanagan, A.39
Nicholson, A.40
Ho, J.W.C.41
Leung, S.Y.42
Yuen, S.T.43
Weber, B.L.44
Seigler, H.F.45
Darrow, T.L.46
Paterson, H.47
Marais, R.48
Marshall, C.J.49
Wooster, R.50
Stratton, M.R.51
Futreal, P.A.52
more..
-
20
-
-
0037194728
-
RAF/RAS oncogenes and mismatch-repair status
-
Rajagopalan H, Bardelli A, Lengauer C, Kinzler KW, Vogelstein B, Velculescu VE. RAF/RAS oncogenes and mismatch-repair status. Nature 2002;418:934.
-
(2002)
Nature
, vol.418
, pp. 934
-
-
Rajagopalan, H.1
Bardelli, A.2
Lengauer, C.3
Kinzler, K.W.4
Vogelstein, B.5
Velculescu, V.E.6
-
21
-
-
0141593677
-
BRAF mutations in colon cancer are not likely attributable to defective DNA mismatch repair
-
Wang L, Cunningham JM, Winters JL, Guenther JC, French AJ, Boardman LA, Burgart LJ, McDonnell SK, Schaid DJ, Thibodeau SN. BRAF mutations in colon cancer are not likely attributable to defective DNA mismatch repair. Cancer Res 2003;63:5209-12.
-
(2003)
Cancer Res
, vol.63
, pp. 5209-5212
-
-
Wang, L.1
Cunningham, J.M.2
Winters, J.L.3
Guenther, J.C.4
French, A.J.5
Boardman, L.A.6
Burgart, L.J.7
McDonnell, S.K.8
Schaid, D.J.9
Thibodeau, S.N.10
-
22
-
-
9144271690
-
Activated BRAF targets proximal colon tumours with mismatch repair deficiency and hMLH1 inactivation
-
Domingo E, Espin E, Armengol M, Oliveira C, Pinto M, Duval A, Brennetot C, Seruca R, Hamelin R, Yamamoto H, Schwartz S Jr. Activated BRAF targets proximal colon tumours with mismatch repair deficiency and hMLH1 inactivation. Genes Chromosomes Cancer 2004;39:138-42.
-
(2004)
Genes Chromosomes Cancer
, vol.39
, pp. 138-142
-
-
Domingo, E.1
Espin, E.2
Armengol, M.3
Oliveira, C.4
Pinto, M.5
Duval, A.6
Brennetot, C.7
Seruca, R.8
Hamelin, R.9
Yamamoto, H.10
Schwartz Jr., S.11
-
23
-
-
1642535480
-
BRAF mutation is frequently present in sporadic colorectal cancer with methylated hMLH1, but not in hereditary nonpolyposis colorectal cancer
-
Deng G, Bell I, Crawley S, Gum J, Terdiman JP, Allen BA, Truta B, Sleisenger MH, Kim YS. BRAF mutation is frequently present in sporadic colorectal cancer with methylated hMLH1, but not in hereditary nonpolyposis colorectal cancer. Clin Cancer Res 2004;10:191-5.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 191-195
-
-
Deng, G.1
Bell, I.2
Crawley, S.3
Gum, J.4
Terdiman, J.P.5
Allen, B.A.6
Truta, B.7
Sleisenger, M.H.8
Kim, Y.S.9
-
24
-
-
0032534069
-
A National Cancer Institute workshop on microsatellite instability for cancer detection and familial predisposition: Development of international criteria for the determination of microsotellite instability in colorectal cancer
-
Boland CR, Thibodeau SN, Hamilton SR, Sidransky D, Eshleman JR, Burt RW, Meltzer SJ, Rodriguez-Bigas MA, Fodde R, Ranzani GN, Srivastava SA. A National Cancer Institute workshop on microsatellite instability for cancer detection and familial predisposition: development of international criteria for the determination of microsotellite instability in colorectal cancer. Cancer Res 1998;58:5248-57.
-
(1998)
Cancer Res
, vol.58
, pp. 5248-5257
-
-
Boland, C.R.1
Thibodeau, S.N.2
Hamilton, S.R.3
Sidransky, D.4
Eshleman, J.R.5
Burt, R.W.6
Meltzer, S.J.7
Rodriguez-Bigas, M.A.8
Fodde, R.9
Ranzani, G.N.10
Srivastava, S.A.11
-
25
-
-
0031015728
-
BAT-26, an indicator of the replication error phenotype in colorectal cancers and cell lines
-
Hoang JM, Cottu PH, Thuille B, Salmon RJ, Thomas G, Hamelin R. BAT-26, an indicator of the replication error phenotype in colorectal cancers and cell lines. Cancer Res 1997;57:300-3.
-
(1997)
Cancer Res
, vol.57
, pp. 300-303
-
-
Hoang, J.M.1
Cottu, P.H.2
Thuille, B.3
Salmon, R.J.4
Thomas, G.5
Hamelin, R.6
-
26
-
-
9144273165
-
Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC
-
Di Fiore F, Charbonnier F, Martin C, Frerat S, Olschwang S, Wang Q, Boisson C, Buisine MP, Nilbert M, Lindblom A, Frebourg T. Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC. J Med Genet 2004;41:18-20.
-
(2004)
J Med Genet
, vol.41
, pp. 18-20
-
-
Di Fiore, F.1
Charbonnier, F.2
Martin, C.3
Frerat, S.4
Olschwang, S.5
Wang, Q.6
Boisson, C.7
Buisine, M.P.8
Nilbert, M.9
Lindblom, A.10
Frebourg, T.11
-
27
-
-
18644386133
-
Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach
-
Gille JJ, Hogervorst FB, Pals G, Wijnen JT, van Schooten RJ, Dommering CJ, Meijer GA, Craanen ME, Nederlof PM, de Jong D, McElgunn CJ, Schouten JP, Menko FH. Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach. Br J Cancer 2002;87:892-7.
-
(2002)
Br J Cancer
, vol.87
, pp. 892-897
-
-
Gille, J.J.1
Hogervorst, F.B.2
Pals, G.3
Wijnen, J.T.4
Van Schooten, R.J.5
Dommering, C.J.6
Meijer, G.A.7
Craanen, M.E.8
Nederlof, P.M.9
De Jong, D.10
McElgunn, C.J.11
Schouten, J.P.12
Menko, F.H.13
-
28
-
-
0032820317
-
Various mutation screening techniques in the DNA mismatch repair genes hMSH2 and hMLH1
-
Wahlberg S, Liu T, Lindblom P, Lindblom A. Various mutation screening techniques in the DNA mismatch repair genes hMSH2 and hMLH1. Genet Test 1999;3:259-64.
-
(1999)
Genet Test
, vol.3
, pp. 259-264
-
-
Wahlberg, S.1
Liu, T.2
Lindblom, P.3
Lindblom, A.4
-
29
-
-
0034827025
-
The frequency of hereditary defective mismatch repair in a prospective series of unselectea colorectal carcinomas
-
Cunningham JM, Kim C-Y, Christensen ER, Tester DJ, Parc Y, Burgart LJ, Hailing KC, McDonnell SK, Schaid DJ, Walsh Vockley C, Kubly V, Nelson H, Michels VV, Thibodeau SN. The frequency of hereditary defective mismatch repair in a prospective series of unselectea colorectal carcinomas. Am J Hum Genet 2001;69:780-90.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 780-790
-
-
Cunningham, J.M.1
Kim, C.-Y.2
Christensen, E.R.3
Tester, D.J.4
Parc, Y.5
Burgart, L.J.6
Hailing, K.C.7
McDonnell, S.K.8
Schaid, D.J.9
Walsh Vockley, C.10
Kubly, V.11
Nelson, H.12
Michels, V.V.13
Thibodeau, S.N.14
-
30
-
-
0003964361
-
-
Atlanta: American Cancer Society
-
American Cancer Society. Cancer facts and figures 1999. Atlanta: American Cancer Society, 1999.
-
(1999)
Cancer Facts and Figures 1999
-
-
-
31
-
-
0027518250
-
Surveillance in hereditary nonpolyposis colorectal cancer: An international cooperative study on 165 families
-
Vasen HF, Mecklin J-P, Watson P, Utsunomiya J, Bertario L, Lynch P, Svendsen LB, Cristofaro G, Muller H, Meera Khan P, Lynch HT (The International Collaborative Group on HNPCC). Surveillance in hereditary nonpolyposis colorectal cancer: an international cooperative study on 165 families. Dis Colon Rectum 1993;36:1-4.
-
(1993)
Dis Colon Rectum
, vol.36
, pp. 1-4
-
-
Vasen, H.F.1
Mecklin, J.-P.2
Watson, P.3
Utsunomiya, J.4
Bertario, L.5
Lynch, P.6
Svendsen, L.B.7
Cristofaro, G.8
Muller, H.9
Meera Khan, P.10
Lynch, H.T.11
-
32
-
-
0038002279
-
Tumor microsatellite-instability status as a predictor of benefit from fluorouracil-based adjuvant chemotherapy for colon cancer
-
Ribic CM, Sargent DJ, Moore MJ, Thibodeau SN, French AJ, Goldberg RM, Hamilton SR, Laurent-Puig P, Gryfe R, Shepherd LE, Tu D, Redston M, Gallinger S. Tumor microsatellite-instability status as a predictor of benefit from fluorouracil-based adjuvant chemotherapy for colon cancer. N Engl J Med 2003;349:247-57.
-
(2003)
N Engl J Med
, vol.349
, pp. 247-257
-
-
Ribic, C.M.1
Sargent, D.J.2
Moore, M.J.3
Thibodeau, S.N.4
French, A.J.5
Goldberg, R.M.6
Hamilton, S.R.7
Laurent-Puig, P.8
Gryfe, R.9
Shepherd, L.E.10
Tu, D.11
Redston, M.12
Gallinger, S.13
-
33
-
-
0141731323
-
Microsatellite instability is a predictive factor of the tumor response to irinotecan in patients with advanced colorectal cancer
-
Fallik D, Borrini F, Boige V, Viguier J, Jacob S, Miquel C, Sabourin JC, Ducreux M, Praz F. Microsatellite instability is a predictive factor of the tumor response to irinotecan in patients with advanced colorectal cancer. Cancer Res 2003;63:5738-44.
-
(2003)
Cancer Res
, vol.63
, pp. 5738-5744
-
-
Fallik, D.1
Borrini, F.2
Boige, V.3
Viguier, J.4
Jacob, S.5
Miquel, C.6
Sabourin, J.C.7
Ducreux, M.8
Praz, F.9
|