-
1
-
-
0032975473
-
Microsatellile instability in multiple colorectal tumors
-
Pedroni M, Tamassia MG, Percesepe A, et al. Microsatellile instability in multiple colorectal tumors. Int J Cancer 1999;81:1-5.
-
(1999)
Int J Cancer
, vol.81
, pp. 1-5
-
-
Pedroni, M.1
Tamassia, M.G.2
Percesepe, A.3
-
4
-
-
0025848680
-
The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)
-
Vasen HF, Mecklin JP, Khan PM, et al. The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC). Dis Colon Rectum 1991;34:424-5.
-
(1991)
Dis Colon Rectum
, vol.34
, pp. 424-425
-
-
Vasen, H.F.1
Mecklin, J.P.2
Khan, P.M.3
-
5
-
-
0033063711
-
New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC
-
Vasen HF, Watson P, Mecklin JP, et al. 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.1
Watson, P.2
Mecklin, J.P.3
-
6
-
-
0033971331
-
Value of pedigree/clinical data, immunohistochemistry and microsatellite instability analyses in reducing the cost of determining hMLH1 and hMSH2 gene mutations in patients with colorectal cancer
-
Debniak T, Kurzawski G, Gorski B, et al. Value of pedigree/clinical data, immunohistochemistry and microsatellite instability analyses in reducing the cost of determining hMLH1 and hMSH2 gene mutations in patients with colorectal cancer. Eur J Cancer 2000;36:49-54.
-
(2000)
Eur J Cancer
, vol.36
, pp. 49-54
-
-
Debniak, T.1
Kurzawski, G.2
Gorski, B.3
-
7
-
-
26644441586
-
Use of molecular tumor characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer
-
Southey MC, Jenkins MA, Mead L, et al. Use of molecular tumor characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer. J Clin Oncol 2005;23:6524-32.
-
(2005)
J Clin Oncol
, vol.23
, pp. 6524-6532
-
-
Southey, M.C.1
Jenkins, M.A.2
Mead, L.3
-
8
-
-
17944362664
-
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer)
-
Hampel H, Frankel WL, Martin E, et al. Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer). N Engl J Med 2005;352:1851-60.
-
(2005)
N Engl J Med
, vol.352
, pp. 1851-1860
-
-
Hampel, H.1
Frankel, W.L.2
Martin, E.3
-
9
-
-
27944464473
-
Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer
-
Engel C, Forberg J, Holinski-Feder E, et al. Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer. Int J Cancer 2006; 118:115-22.
-
(2006)
Int J Cancer
, vol.118
, pp. 115-122
-
-
Engel, C.1
Forberg, J.2
Holinski-Feder, E.3
-
10
-
-
0037083484
-
Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors
-
Lindor NM, Burgart LJ, Leontovich O, et al. Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors. J Clin Oncol 2002;20:1043-8.
-
(2002)
J Clin Oncol
, vol.20
, pp. 1043-1048
-
-
Lindor, N.M.1
Burgart, L.J.2
Leontovich, O.3
-
11
-
-
20244386395
-
Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer
-
Pinol V, Castells A, Andreu M, et al. Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer. JAMA 2005;293:1986-94.
-
(2005)
JAMA
, vol.293
, pp. 1986-1994
-
-
Pinol, V.1
Castells, A.2
Andreu, M.3
-
12
-
-
6444245757
-
The reliability of immunohistochemistry as a prescreening method for the diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC)-results of an international collaborative study
-
Müller W, Burgart U, Krause-Paulus R, et al. The reliability of immunohistochemistry as a prescreening method for the diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC)-results of an international collaborative study. Familial Cancer 2001;1:87-92.
-
(2001)
Familial Cancer
, vol.1
, pp. 87-92
-
-
Müller, W.1
Burgart, U.2
Krause-Paulus, R.3
-
13
-
-
0033825587
-
Sensitivity and specificity of clinical criteria for hereditary non-polyposis colorectal cancer associated mutations in MSH2 and MLH1
-
Syngal S, Fox EA, Eng C, et al. Sensitivity and specificity of clinical criteria for hereditary non-polyposis colorectal cancer associated mutations in MSH2 and MLH1. J Med Genet 2000;37:641-5.
-
(2000)
J Med Genet
, vol.37
, pp. 641-645
-
-
Syngal, S.1
Fox, E.A.2
Eng, C.3
-
14
-
-
0037096801
-
Evaluation of microsatellite instability and immunohistochemistry for the prediction of germ-line MSH2 and MLH1 mutations in hereditary nonpolyposis colon cancer families
-
Wahlberg SS, Schmeits J, Thomas G, et al. Evaluation of microsatellite instability and immunohistochemistry for the prediction of germ-line MSH2 and MLH1 mutations in hereditary nonpolyposis colon cancer families. Cancer Res 2002;62:3485-92.
-
(2002)
Cancer Res
, vol.62
, pp. 3485-3492
-
-
Wahlberg, S.S.1
Schmeits, J.2
Thomas, G.3
-
15
-
-
0036890171
-
Antibody-based screening for hereditary nonpolyposis colorectal carcinoma compared with microsatellite analysis and sequencing
-
Christensen M, Katballe N, Wikman F, et al. Antibody-based screening for hereditary nonpolyposis colorectal carcinoma compared with microsatellite analysis and sequencing. Cancer 2002;95:2422-30.
-
(2002)
Cancer
, vol.95
, pp. 2422-2430
-
-
Christensen, M.1
Katballe, N.2
Wikman, F.3
-
16
-
-
6444245421
-
Prediction of the outcome of genetic testing in HNPCC kindreds using the revised Amsterdam criteria and immunohistochemistry
-
Stormorken AT, Müller W, Lemkemeyer B, et al. Prediction of the outcome of genetic testing in HNPCC kindreds using the revised Amsterdam criteria and immunohistochemistry. Fam Cancer 2001;1:169-73.
-
(2001)
Fam Cancer
, vol.1
, pp. 169-173
-
-
Stormorken, A.T.1
Müller, W.2
Lemkemeyer, B.3
-
17
-
-
0031551963
-
A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting highlights and Bethesda guidelines
-
Rodriguez-Bigas MA, Boland CR, Hamilton SR, et al. A National Cancer Institute Workshop on Hereditary Nonpolyposis 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
-
18
-
-
10744233937
-
Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
-
Umar A, Boland CR, Terdiman JP, et al. Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst 2004;96:261-8.
-
(2004)
J Natl Cancer Inst
, vol.96
, pp. 261-268
-
-
Umar, A.1
Boland, C.R.2
Terdiman, J.P.3
-
19
-
-
0035672948
-
Patient accuracy of reporting on hereditary non-polyposis colorectal cancer-related malignancy in family members
-
Katballe N, Juul S, Christensen M, et al. Patient accuracy of reporting on hereditary non-polyposis colorectal cancer-related malignancy in family members. Br J Surg 2001;88:1228-33.
-
(2001)
Br J Surg
, vol.88
, pp. 1228-1233
-
-
Katballe, N.1
Juul, S.2
Christensen, M.3
-
20
-
-
0034077306
-
Accuracy of family history of cancer: Clinical genetic implications
-
Sijmons RH, Boonstra AE, Reefhuis J, et al. Accuracy of family history of cancer: clinical genetic implications. Eur J Hum Genet 2000;8:181-6.
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 181-186
-
-
Sijmons, R.H.1
Boonstra, A.E.2
Reefhuis, J.3
-
21
-
-
18244380349
-
Molecular and clinical characteristics of MSH6 variants: An analysis of 25 index carriers of a germline variant
-
Berends MJ, Wu Y, Sijmons RH, et al. Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant. Am J Hum Genet 2002;70:26-37.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 26-37
-
-
Berends, M.J.1
Wu, Y.2
Sijmons, R.H.3
-
22
-
-
0032749569
-
Germ-line msh6 mutations in colorectal cancer families
-
Kolodner RD, Tytell JD, Schmeits JL, et al. Germ-line msh6 mutations in colorectal cancer families. Cancer Res 1999;59:5068-74.
-
(1999)
Cancer Res
, vol.59
, pp. 5068-5074
-
-
Kolodner, R.D.1
Tytell, J.D.2
Schmeits, J.L.3
-
24
-
-
33745728357
-
A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2. Application in a Dutch cancer clinic setting
-
Van der Hout AH, Van den Ouweland AM, Van der Luijt RB, et al. A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2. Application in a Dutch cancer clinic setting. Hum Mutat 2006;27:654-66.
-
(2006)
Hum Mutat
, vol.27
, pp. 654-666
-
-
Van Der Hout, A.H.1
Van Den Ouweland, A.M.2
Van Der Luijt, R.B.3
-
25
-
-
18644386133
-
Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach
-
Gille JJ, Hogervorst FB, Pals G, et al. 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
-
26
-
-
0031795020
-
MSH2 genomic deletions are a frequent cause of HNPCC
-
Wijnen J, Van der Klift H, Vasen H, et al. MSH2 genomic deletions are a frequent cause of HNPCC. Nat Genet 1998;20:326-8.
-
(1998)
Nat Genet
, vol.20
, pp. 326-328
-
-
Wijnen, J.1
Van Der Klift, H.2
Vasen, H.3
-
27
-
-
0032534069
-
A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: Development of international criteria for the determination of microsatellite instability to colorectal cancer
-
Boland CR, Thibodeau SN, Hamilton SR, et al. A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability to 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
-
28
-
-
23044453645
-
Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancer
-
Stormorken AT, Bowitz-Lothe IM, Noren T, et al. Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancer. J Clin Oncol 2005;23:4705-12.
-
(2005)
J Clin Oncol
, vol.23
, pp. 4705-4712
-
-
Stormorken, A.T.1
Bowitz-Lothe, I.M.2
Noren, T.3
-
29
-
-
9444227024
-
What is the best way to assess microsatellite instability status in colorectal cancer? Study on a population base of 462 colorectal cancers
-
Chapusot C, Martin L, Puig PL, et al. What is the best way to assess microsatellite instability status in colorectal cancer? Study on a population base of 462 colorectal cancers. Am J Surg Pathol 2004;28:1553-9.
-
(2004)
Am J Surg Pathol
, vol.28
, pp. 1553-1559
-
-
Chapusot, C.1
Martin, L.2
Puig, P.L.3
-
30
-
-
29744435357
-
Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining
-
Mangold E, Pagenstecher C, Friedl W, et al. Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining. J Pathol 2005;207:385-95.
-
(2005)
J Pathol
, vol.207
, pp. 385-395
-
-
Mangold, E.1
Pagenstecher, C.2
Friedl, W.3
-
31
-
-
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;260:816-19.
-
(1993)
Science
, vol.260
, pp. 816-819
-
-
Thibodeau, S.N.1
Bren, G.2
Schaid, D.3
-
32
-
-
0036206948
-
Hereditary nonpolyposis colorectal cancer in young colorectal cancer patients: High-risk clinic versus population-based registry
-
Terdiman JP, Levin TR, Allen BA, et al. Hereditary nonpolyposis colorectal cancer in young colorectal cancer patients: high-risk clinic versus population-based registry. Gastroenterology 2002;122:940-7.
-
(2002)
Gastroenterology
, vol.122
, pp. 940-947
-
-
Terdiman, J.P.1
Levin, T.R.2
Allen, B.A.3
-
33
-
-
0032555020
-
Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease
-
Aaltonen LA, Salovaara R, Kristo P, et al. 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
-
34
-
-
0032796919
-
Prevalence of germline mutations of hMLH1, hMSH2, hPMS1, hPMS2, and hMSH6 genes in 75 French kindreds with nonpolyposis colorectal cancer
-
Wang Q, Lasset C, Desseigne F, et al. Prevalence of germline mutations of hMLH1, hMSH2, hPMS1, hPMS2, and hMSH6 genes in 75 French kindreds with nonpolyposis colorectal cancer. Hum Genet 1999;105:79-85.
-
(1999)
Hum Genet
, vol.105
, pp. 79-85
-
-
Wang, Q.1
Lasset, C.2
Desseigne, F.3
-
35
-
-
0033962257
-
Extensive molecular screening for hereditary non-polyposis colorectal cancer
-
Dieumegard B, Grandjouan S, Sabourin JC, et al. Extensive molecular screening for hereditary non-polyposis colorectal cancer. Br J Cancer 2000;82:871-80.
-
(2000)
Br J Cancer
, vol.82
, pp. 871-880
-
-
Dieumegard, B.1
Grandjouan, S.2
Sabourin, J.C.3
-
36
-
-
0034222153
-
Mutational germline analysis of hMSH2 and hMLH1 genes in early onset colorectal cancer patients
-
Montera M, Resta N, Simone C, et al. Mutational germline analysis of hMSH2 and hMLH1 genes in early onset colorectal cancer patients. J Med Genet 2000;37:E7.
-
(2000)
J Med Genet
, vol.37
-
-
Montera, M.1
Resta, N.2
Simone, C.3
-
37
-
-
0037341912
-
Early-age-at-onset colorectal cancer and microsatellite instability as markers of hereditary nonpolyposis colorectal cancer
-
Pucciarelli S, Agostini M, Viel A, et al. Early-age-at-onset colorectal cancer and microsatellite instability as markers of hereditary nonpolyposis colorectal cancer. Dis Colon Rectum 2003;46:305-12.
-
(2003)
Dis Colon Rectum
, vol.46
, pp. 305-312
-
-
Pucciarelli, S.1
Agostini, M.2
Viel, A.3
-
38
-
-
0034129240
-
Population-based molecular detection of hereditary nonpolyposis colorectal cancer
-
Salovaara R, Loukola A, Kristo P, et al. Population-based molecular detection of hereditary nonpolyposis colorectal cancer. 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
-
39
-
-
23244443650
-
Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: Later age of onset
-
Hampel H, Stephens JA, Pukkala E, et al. Cancer risk in hereditary nonpolyposis colorectal cancer syndrome: later age of onset. Gastroenterology 2005;129:415-21.
-
(2005)
Gastroenterology
, vol.129
, pp. 415-421
-
-
Hampel, H.1
Stephens, J.A.2
Pukkala, E.3
-
40
-
-
20544467125
-
Risk of colorectal and endometrial cancer for carriers of mutations of the hMLH1 and HMSH2 gene: Correction for ascertainment
-
Quehenberger F, Vasen HF, van Houwelingen HC. Risk of colorectal and endometrial cancer for carriers of mutations of the hMLH1 and HMSH2 gene: correction for ascertainment. J Med Genet 2005;42:491-6.
-
(2005)
J Med Genet
, vol.42
, pp. 491-496
-
-
Quehenberger, F.1
Vasen, H.F.2
Van Houwelingen, H.C.3
-
41
-
-
3142748325
-
Mismatch repair gene PMS2: Disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation
-
Nakagawa H, Lockman JC, Frankel WL, et al. Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation. Cancer Res 2004;64:4721-7.
-
(2004)
Cancer Res
, vol.64
, pp. 4721-4727
-
-
Nakagawa, H.1
Lockman, J.C.2
Frankel, W.L.3
-
42
-
-
21044440847
-
Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer
-
Truninger K, Menigatti M, Luz J, et al. Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer. Gastroenterology 2005;128:1160-71.
-
(2005)
Gastroenterology
, vol.128
, pp. 1160-1171
-
-
Truninger, K.1
Menigatti, M.2
Luz, J.3
-
43
-
-
19044363122
-
Familial mutations in PMS2 can cause autosomal dominant hereditary nonpolyposis colorectal cancer
-
Worthley DL, Walsh MD, Barker M, et al. Familial mutations in PMS2 can cause autosomal dominant hereditary nonpolyposis colorectal cancer. Gastroenterology 2005;128:1431-6.
-
(2005)
Gastroenterology
, vol.128
, pp. 1431-1436
-
-
Worthley, D.L.1
Walsh, M.D.2
Barker, M.3
-
44
-
-
1242263318
-
Hereditary non-polyposis colorectal cancer and the role of hPMS2 and hEXO1 mutations
-
Thompson E, Meldrum CJ, Crooks R, et al. Hereditary non-polyposis colorectal cancer and the role of hPMS2 and hEXO1 mutations. Clin Genet 2004;65:215-25.
-
(2004)
Clin Genet
, vol.65
, pp. 215-225
-
-
Thompson, E.1
Meldrum, C.J.2
Crooks, R.3
-
45
-
-
10744232899
-
Microsatellite instability, immunohistochemistry, and additional PMS2 staining in suspected hereditary nonpolyposis colorectal cancer
-
De Jong AE, van Puijenbroek M, Hendriks Y, et al. Microsatellite instability, immunohistochemistry, and additional PMS2 staining in suspected hereditary nonpolyposis colorectal cancer. Clin Cancer Res 2004;10:972-80.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 972-980
-
-
De Jong, A.E.1
Van Puijenbroek, M.2
Hendriks, Y.3
-
46
-
-
0042828931
-
Genomic rearrangements of hMSH6 contribute to the genetic predisposition in suspected hereditary non-polyposis colorectal cancer syndrome
-
Plaschke J, Ruschoff J, Schackert HK. Genomic rearrangements of hMSH6 contribute to the genetic predisposition in suspected hereditary non-polyposis colorectal cancer syndrome. J Med Genet 2003;40:597-600.
-
(2003)
J Med Genet
, vol.40
, pp. 597-600
-
-
Plaschke, J.1
Ruschoff, J.2
Schackert, H.K.3
-
47
-
-
0036144263
-
Mutational analysis of promoters of mismatch repair genes hMSH2 and hMLH1 in hereditary nonpolyposis colorectal cancer and early onset colorectal cancer patients: Identification of three novel germ-line mutations in promoter of the hMSH2 gene
-
Shin KH, Shin JH, Kim JH, et al. Mutational analysis of promoters of mismatch repair genes hMSH2 and hMLH1 in hereditary nonpolyposis colorectal cancer and early onset colorectal cancer patients: identification of three novel germ-line mutations in promoter of the hMSH2 gene. Cancer Res 2002;62:38-42.
-
(2002)
Cancer Res
, vol.62
, pp. 38-42
-
-
Shin, K.H.1
Shin, J.H.2
Kim, J.H.3
|