-
1
-
-
12844275378
-
Lynch syndrome: History and current status
-
Lynch Syndrome (HNPCC) and Microsatellite Instability
-
Lynch HT, Lynch JF. Lynch syndrome: history and current status. Dis Markers 2004;20:181-198. (Pubitemid 40164092)
-
(2004)
Disease Markers
, vol.20
, Issue.4-5
, pp. 181-198
-
-
Lynch, H.T.1
Lynch, J.F.2
-
2
-
-
0027742295
-
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
-
DOI 10.1016/0092-8674(93)90546-3
-
Fishel R, Lescoe MK, Rao MR, et al. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer. Cell 1993;75:1027-1038. (Pubitemid 24014559)
-
(1993)
Cell
, vol.75
, Issue.5
, pp. 1027-1038
-
-
Fishel, R.1
Lescoe, M.K.2
Rao, M.R.S.3
Copeland, N.G.4
Jenkins, N.A.5
Garber, J.6
Kane, M.7
Kolodner, R.8
-
3
-
-
0028350601
-
Mutation of a mutL homolog in hereditary colon cancer
-
Papadopoulos N, Nicolaides NC, Wei YF, et al. Mutation of a mutL homolog in hereditary colon cancer. Science 1994;263:1625-1629. (Pubitemid 24128369)
-
(1994)
Science
, vol.263
, Issue.5153
, pp. 1625-1629
-
-
Papadopoulos, N.1
Nicolaides, N.C.2
Wei, Y.-F.3
Ruben, S.M.4
Carter, K.C.5
Rosen, C.A.6
Haseltine, W.A.7
Fleischmann, R.D.8
Fraser, C.M.9
Adams, M.D.10
Venter, J.C.11
Hamilton, S.R.12
Petersen, G.M.13
Watson, P.14
Lynch, H.T.15
Peltomaki, P.16
Mecklin, J.-P.17
De La Chapelle, A.18
Kinzler, K.W.19
Vogelstein, B.20
more..
-
4
-
-
0027145633
-
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
-
DOI 10.1016/0092-8674(93)90330-S
-
Leach FS, Nicolaides NC, Papadopoulos N, et al. Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. Cell 1993;75:1215-1225. (Pubitemid 24006117)
-
(1993)
Cell
, vol.75
, Issue.6
, pp. 1215-1225
-
-
Leach, F.S.1
Nicolaides, N.C.2
Papadopoulos, N.3
Liu, B.4
Jen, J.5
Parsons, R.6
Peltomaki, P.7
Sistonen, P.8
Aaltonen, L.A.9
Nystrom-Lahti, M.10
Guan, X.-Y.11
Zhang, J.12
Meltzer, P.S.13
Yu, J.-W.14
Kao, F.-T.15
Chen, D.J.16
Cerosaletti, K.M.17
Fournier, R.E.K.18
Todd, S.19
-
5
-
-
0028221943
-
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer
-
Bronner CE, Baker SM, Morrison PT, et al. Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer. Nature 1994;368:258-261.
-
(1994)
Nature
, vol.368
, pp. 258-261
-
-
Bronner, C.E.1
Baker, S.M.2
Morrison, P.T.3
-
6
-
-
27744512989
-
Testing for defective DNA mismatch repair in colorectal carcinoma: A practical guide
-
Burgart LJ. Testing for defective DNA mismatch repair in colorectal carcinoma: a practical guide. Arch Pathol Lab Med 2005;129:1385-1389. (Pubitemid 41587010)
-
(2005)
Archives of Pathology and Laboratory Medicine
, vol.129
, Issue.11
, pp. 1385-1389
-
-
Burgart, L.J.1
-
7
-
-
47649123223
-
Immunohistochemistry versus microsatellite instability testing for screening colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome: Part I. The utility of immunohistochemistry
-
DOI 10.2353/jmoldx.2008.080031
-
Shia J. Immunohistochemistry versus microsatellite instability testing for screening colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome. Part I. The utility of immunohistochemistry. J Mol Diagn 2008;10:293-300. (Pubitemid 352019113)
-
(2008)
Journal of Molecular Diagnostics
, vol.10
, Issue.4
, pp. 293-300
-
-
Shia, J.1
-
8
-
-
4544310802
-
Mutations associated with HNPCC predisposition - Update of ICG-HNPCC/INSiGHT mutation database
-
Lynch Syndrome (HNPCC) and Microsatellite Instability
-
Peltomaki P, Vasen H. Mutations associated with HNPCC predisposition-update of ICG-HNPCC/INSiGHT mutation database. Dis Markers 2004;20: 269-276. (Pubitemid 40164099)
-
(2004)
Disease Markers
, vol.20
, Issue.4-5
, pp. 269-276
-
-
Peltomaki, P.1
Vasen, H.2
-
9
-
-
32044450030
-
Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)
-
DOI 10.1053/j.gastro.2005.10.052, PII S0016508505022328
-
Hendriks YM, Jagmohan-Changur S, van der Klift HM, et al. Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome). Gastroenterology 2006;130:312-322. (Pubitemid 43202031)
-
(2006)
Gastroenterology
, vol.130
, Issue.2
, pp. 312-322
-
-
Hendriks, Y.M.C.1
Jagmohan-Changur, S.2
Van Der Klift, H.M.3
Morreau, H.4
Van Puijenbroek, M.5
Tops, C.6
Van Os, T.7
Wagner, A.8
Ausems, M.G.F.M.9
Gomez, E.10
Breuning, M.H.11
Brocker-Vriends, A.H.J.T.12
Vasen, H.F.A.13
Wijnen, J.Th.14
-
10
-
-
0032941343
-
Cancer risk in mutation carriers of DNA-mismatch-repair genes
-
Aarnio M, Sankila R, Pukkala E, et al. Cancer risk in mutation carriers of DNA-mismatch-repair genes. Int J Cancer 1999;81:214-218. (Pubitemid 29144749)
-
(1999)
International Journal of Cancer
, vol.81
, Issue.2
, pp. 214-218
-
-
Aarnio, M.1
Sankila, R.2
Pukkala, E.3
Salovaara, R.4
Aaltonen, L.A.5
De La Chapelle, A.6
Peltomaki, P.7
Mecklin, J.-P.8
Jarvinen, H.J.9
-
11
-
-
13944260884
-
Gynecologic cancer as a "sentinel cancer" for women with hereditary nonpolyposis colorectal cancer syndrome
-
DOI 10.1097/01.AOG.0000154885.44002.ae
-
Lu KH, Dinh M, Kohlmann W, et al. Gynecologic cancer as a "sentinel cancer" for women with hereditary nonpolyposis colorectal cancer syndrome. Obstet Gynecol 2005;105:569-574. (Pubitemid 40271224)
-
(2005)
Obstetrics and Gynecology
, vol.105
, Issue.3
, pp. 569-574
-
-
Lu, K.H.1
Dinh, M.2
Kohlmann, W.3
Watson, P.4
Green, J.5
Syngal, S.6
Bandipalliam, P.7
Chen, L.-M.8
Alien, B.9
Conrad, P.10
Terdiman, J.11
Sun, C.12
Daniels, M.13
Burke, T.14
Gershenson, D.M.15
Lynch, H.16
Lynch, P.17
Broaddus, R.R.18
-
12
-
-
33644864321
-
Decrease in mortality in Lynch syndrome families because of surveillance
-
DOI 10.1053/j.gastro.2005.11.032, PII S0016508505023930
-
de Jong AE, Hendriks YM, Kleibeuker JH, et al. Decrease in mortality in Lynch syndrome families because of surveillance. Gastroenterology 2006;130: 665-671. (Pubitemid 43374516)
-
(2006)
Gastroenterology
, vol.130
, Issue.3
, pp. 665-671
-
-
De Jong, A.E.1
Hendriks, Y.M.C.2
Kleibeuker, J.H.3
De Boer, S.Y.4
Cats, A.5
Griffioen, G.6
Nagengast, F.M.7
Nelis, F.G.8
Rookus, M.A.9
Vasen, H.F.A.10
-
13
-
-
39649093644
-
The frequency of Muir-Torre syndrome among Lynch syndrome families
-
DOI 10.1093/jnci/djm291
-
South CD, Hampel H, Comeras I, et al. The frequency of Muir-Torre syndrome among Lynch syndrome families. J Natl Cancer Inst 2008;100:277-281. (Pubitemid 351480531)
-
(2008)
Journal of the National Cancer Institute
, vol.100
, Issue.4
, pp. 277-281
-
-
South, C.D.1
Hampel, H.2
Comeras, I.3
Westman, J.A.4
Frankel, W.L.5
De La Chapelle, A.6
-
14
-
-
34547702208
-
Mismatch repair proteins expression and microsatellite instability in skin lesions with sebaceous differentiation: A study in different clinical subgroups with and without extracutaneous cancer
-
DOI 10.1097/DAD.0b013e318057713c, PII 0000037220070800000004
-
Cesinaro AM, Ubiali A, Sighinolfi P, et al. Mismatch repair proteins expression and microsatellite instability in skin lesions with sebaceous differentiation: a study in different clinical subgroups with and without extracutaneous cancer. Am J Dermatopathol 2007; 29:351-358. (Pubitemid 47220485)
-
(2007)
American Journal of Dermatopathology
, vol.29
, Issue.4
, pp. 351-358
-
-
Cesinaro, A.M.1
Ubiali, A.2
Sighinolfi, P.3
Trentini, G.P.4
Gentili, F.5
Facchetti, F.6
-
15
-
-
0034031078
-
Microsatellite instability and expression of hMLH-1 and hMSH-2 in sebaceous gland carcinomas as markers for Muir-Torre syndrome
-
Entius MM, Keller JJ, Drillenburg P, et al. Microsatellite instability and expression of hMLH-1 and hMSH-2 in sebaceous gland carcinomas as markers for Muir-Torre syndrome. Clin Cancer Res 2000;6: 1784-1789. (Pubitemid 30305072)
-
(2000)
Clinical Cancer Research
, vol.6
, Issue.5
, pp. 1784-1789
-
-
Entius, M.M.1
Keller, J.J.2
Drillenburg, P.3
Kuypers, K.C.4
Giardiello, F.M.5
Offerhaus, G.J.A.6
-
16
-
-
3142682207
-
A genotype-phenotype correlation in HNPCC: Strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome
-
Mangold E, Pagenstecher C, Leister M, et al. A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome. J Med Genet 2004;41:567-572. (Pubitemid 38932119)
-
(2004)
Journal of Medical Genetics
, vol.41
, Issue.7
, pp. 567-572
-
-
Mangold, E.1
Pagenstecher, C.2
Leister, M.3
Mathiak, M.4
Rutten, A.5
Friedl, W.6
Propping, P.7
Ruzicka, T.8
Kruse, R.9
-
17
-
-
0038636399
-
Frequency of microsatellite instability in unselected sebaceous gland neoplasias and hyperplasias
-
DOI 10.1046/j.1523-1747.2003.12125.x
-
Kruse R, Rutten A, Schweiger N, et al. Frequency of microsatellite instability in unselected sebaceous gland neoplasias and hyperplasias. J Invest Dermatol 2003;120:858-864. (Pubitemid 36529090)
-
(2003)
Journal of Investigative Dermatology
, vol.120
, Issue.5
, pp. 858-864
-
-
Kruse, R.1
Rutten, A.2
Schweiger, N.3
Jakob, E.4
Mathiak, M.5
Propping, P.6
Mangold, E.7
Bisceglia, M.8
Ruzicka, T.9
-
18
-
-
0036187460
-
Loss of DNA mismatch repair proteins in skin tumors from patients with Muir-Torre syndrome and MSH2 or MLH1 germline mutations: Establishment of immunohistochemical analysis as a screening test
-
DOI 10.1097/00000478-200203000-00007
-
Mathiak M, Rutten A, Mangold E, et al. Loss of DNA mismatch repair proteins in skin tumors from patients with Muir-Torre syndrome and MSH2 or MLH1 germline mutations: establishment of immunohistochemical analysis as a screening test. Am J Surg Pathol 2002;26:338-343. (Pubitemid 34184457)
-
(2002)
American Journal of Surgical Pathology
, vol.26
, Issue.3
, pp. 338-343
-
-
Mathiak, M.1
Rutten, A.2
Mangold, E.3
Fischer, H.-P.4
Ruzicka, T.5
Friedl, W.6
Propping, P.7
Kruse, R.8
-
19
-
-
67549086705
-
Towards identification of hereditary DNA mismatch repair deficiency: Sebaceous neoplasm warrants routine immunohistochemical screening regardless of patient's age or other clinical characteristics
-
Orta L, Klimstra DS, Qin J, et al. Towards identification of hereditary DNA mismatch repair deficiency: sebaceous neoplasm warrants routine immunohistochemical screening regardless of patient's age or other clinical characteristics. Am J Surg Pathol 2009;33: 934-944.
-
(2009)
Am J Surg Pathol
, vol.33
, pp. 934-944
-
-
Orta, L.1
Klimstra, D.S.2
Qin, J.3
-
20
-
-
0035044718
-
Microsatellite instability and hMLH1 and hMSH2 expression analysis in familial and sporadic colorectal cancer
-
Salahshor S, Koelble K, Rubio C, et al. Microsatellite instability and hMLH1 and hMSH2 expression analysis in familial and sporadic colorectal cancer. Lab Invest 2001;81:535-541. (Pubitemid 32298799)
-
(2001)
Laboratory Investigation
, vol.81
, Issue.4
, pp. 535-541
-
-
Salahshor, S.1
Koelble, K.2
Rubio, C.3
Lindblom, A.4
-
21
-
-
29744435357
-
Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining
-
DOI 10.1002/path.1858
-
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;207:385-395. (Pubitemid 43025686)
-
(2005)
Journal of Pathology
, vol.207
, Issue.4
, pp. 385-395
-
-
Mangold, E.1
Pagenstecher, C.2
Friedl, W.3
Fischer, H.-P.4
Merkelbach-Bruse, S.5
Ohlendorf, M.6
Friedrichs, N.7
Aretz, S.8
Buettner, R.9
Propping, P.10
Mathiak, M.11
-
22
-
-
10744232899
-
Microsatellite Instability, Immunohistochemistry, and Additional PMS2 Staining in Suspected Hereditary Nonpolyposis Colorectal Cancer
-
DOI 10.1158/1078-0432.CCR-0956-3
-
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; 10:972-980. (Pubitemid 38198898)
-
(2004)
Clinical Cancer Research
, vol.10
, Issue.3
, pp. 972-980
-
-
De Jong, A.E.1
Van Puijenbroek, M.2
Hendriks, Y.3
Tops, C.4
Wijnen, J.5
Ausems, M.G.E.M.6
Meijers-Heijboer, H.7
Wagner, A.8
Van Os, T.A.M.9
Brocker-Vriends, A.H.J.T.10
Vasen, H.F.A.11
Morreau, H.12
-
23
-
-
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;352:1851-1860.
-
(2005)
N Engl J Med
, vol.352
, pp. 1851-1860
-
-
Hampel, H.1
Frankel, W.L.2
Martin, E.3
-
24
-
-
26644441586
-
Use of molecular tumor characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer
-
DOI 10.1200/JCO.2005.04.671
-
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;23:6524-6532. (Pubitemid 46190244)
-
(2005)
Journal of Clinical Oncology
, vol.23
, Issue.27
, pp. 6524-6532
-
-
Southey, M.C.1
Jenkins, M.A.2
Mead, L.3
Whitty, J.4
Trivett, M.5
Tesoriero, A.A.6
Smith, L.D.7
Jennings, K.8
Grubb, G.9
Royce, S.G.10
Walsh, M.D.11
Barker, M.A.12
Young, J.P.13
Jass, J.R.14
St. John, D.J.B.15
Macrae, F.A.16
Giles, G.G.17
Hopper, J.L.18
-
25
-
-
33847794097
-
Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics
-
DOI 10.1093/jnci/djk051
-
Lagerstedt Robinson K, Liu T, Vandrovcova J, et al. Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics. J Natl Cancer Inst 2007;99: 291-299. (Pubitemid 47073492)
-
(2007)
Journal of the National Cancer Institute
, vol.99
, Issue.4
, pp. 291-299
-
-
Lagerstedt Robinson, K.1
Liu, T.2
Vandrovcova, J.3
Halvarsson, B.4
Clendenning, M.5
Frebourg, T.6
Papadopoulos, N.7
Kinzler, K.W.8
Vogelstein, B.9
Peltomaki, P.10
Kolodner, R.D.11
Nilbert, M.12
Lindblom, A.13
-
26
-
-
18244380349
-
Molecular and clinical characteristics of MSH6 variants: An analysis of 25 index carriers of a germline variant
-
DOI 10.1086/337944
-
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. (Pubitemid 34031695)
-
(2002)
American Journal of Human Genetics
, vol.70
, Issue.1
, pp. 26-37
-
-
Berends, M.J.W.1
Wu, Y.2
Sijmons, R.H.3
Mensink, R.G.J.4
Van Der Sluis, T.5
Hordijk-Hos, J.M.6
De Vries, E.G.E.7
Hollema, H.8
Karrenbeld, A.9
Buys, C.H.C.M.10
Van Der Zee, A.G.J.11
Hofstra, R.M.W.12
Kleibeuker, J.H.13
-
27
-
-
2442708840
-
Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history
-
DOI 10.1086/421332
-
Buttin BM, Powell MA, Mutch DG, et al. Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history. Am J Hum Genet 2004;74:1262-1269. (Pubitemid 38669325)
-
(2004)
American Journal of Human Genetics
, vol.74
, Issue.6
, pp. 1262-1269
-
-
Buttin, B.M.1
Powell, M.A.2
Mutch, D.G.3
Babb, S.A.4
Huettner, P.C.5
Edmonston, T.B.6
Herzog, T.J.7
Rader, J.S.8
Gibb, R.K.9
Whelan, A.J.10
Goodfellow, P.J.11
-
28
-
-
0030776227
-
Correction of hypermutability, N-Methyl-N'-nitro-N-nitrosoguanidine resistance, and defective dna mismatch repair by introducing chromosome 2 into human tumor cells with mutations in MSH2 and MSH6
-
Umar A, Koi M, Risinger JI, et al. Correction of hypermutability, N-methyl-N'-nitro-N-nitrosoguanidine resistance, and defective DNA mismatch repair by introducing chromosome 2 into human tumor cells with mutations in MSH2 and MSH6. Cancer Res 1997;57:3949-3955. (Pubitemid 27427682)
-
(1997)
Cancer Research
, vol.57
, Issue.18
, pp. 3949-3955
-
-
Umar, A.1
Koi, M.2
Risinger, J.I.3
Glaab, W.E.4
Tindall, K.R.5
Kolodner, R.D.6
Boland, C.R.7
Barrett, J.C.8
Kunkel, T.A.9
-
29
-
-
46449117172
-
The biochemical basis of microsatellite instability and abnormal immunohistochemistry and clinical behavior in Lynch syndrome: From bench to bedside
-
Boland CR, Koi M, Chang DK, et al. The biochemical basis of microsatellite instability and abnormal immunohistochemistry and clinical behavior in Lynch syndrome: from bench to bedside. Fam Cancer 2008;7:41-52.
-
(2008)
Fam Cancer
, vol.7
, pp. 41-52
-
-
Boland, C.R.1
Koi, M.2
Chang, D.K.3
-
30
-
-
0030465237
-
HMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6
-
DOI 10.1073/pnas.93.24.13629
-
Acharya S, Wilson T, Gradia S, et al. hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6. Proc Natl Acad Sci USA 1996;93:13629-13634. (Pubitemid 26424170)
-
(1996)
Proceedings of the National Academy of Sciences of the United States of America
, vol.93
, Issue.24
, pp. 13629-13634
-
-
Acharya, S.1
Wilson, T.2
Gradia, S.3
Kane, M.F.4
Guerrette, S.5
Marsischky, G.T.6
Kolodner, R.7
Fishel, R.8
-
31
-
-
70350437372
-
Immunohistochemistry as first-line screening for detecting colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome: A 2-antibody panel may be as predictive as a 4-antibody panel
-
Shia J, Tang LH, Vakiani E, et al. Immunohistochemistry as first-line screening for detecting colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome: a 2-antibody panel may be as predictive as a 4-antibody panel. Am J Surg Pathol 2009;33:1639-1645.
-
(2009)
Am J Surg Pathol
, vol.33
, pp. 1639-1645
-
-
Shia, J.1
Tang, L.H.2
Vakiani, E.3
-
32
-
-
77954784170
-
Immunohistochemistry for PMS2 and MSH6 alone can replace a four antibody panel for mismatch repair deficiency screening in colorectal adenocarcinoma
-
Hall G, Clarkson A, Shi A, et al. Immunohistochemistry for PMS2 and MSH6 alone can replace a four antibody panel for mismatch repair deficiency screening in colorectal adenocarcinoma. Pathology 2010; 42:409-413.
-
(2010)
Pathology
, vol.42
, pp. 409-413
-
-
Hall, G.1
Clarkson, A.2
Shi, A.3
-
33
-
-
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;96:261-268. (Pubitemid 38256271)
-
(2004)
Journal of the National Cancer Institute
, vol.96
, Issue.4
, pp. 261-268
-
-
Umar, A.1
Boland, C.R.2
Terdiman, J.P.3
Syngal, S.4
De La Chapelle, A.5
Ruschoff, J.6
Fishel, R.7
Lindor, N.M.8
Burgart, L.J.9
Hamelin, R.10
Hamilton, S.R.11
Hiatt, R.A.12
Jass, J.13
Lindblom, A.14
Lynch, H.T.15
Peltomaki, P.16
Ramsey, S.D.17
Rodriguez-Bigas, M.A.18
Vasen, H.F.A.19
Hawk, E.T.20
Barrett, J.C.21
Freedman, A.N.22
Srivastava, S.23
more..
-
34
-
-
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 in 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 in colorectal cancer. Cancer Res 1998;58:5248-5257. (Pubitemid 28521189)
-
(1998)
Cancer Research
, vol.58
, Issue.22
, 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.11
-
35
-
-
0036893598
-
Evaluation of tumor microsatellite instability using five quasimonomorphic mononucleotide repeats and pentaplex PCR
-
DOI 10.1053/gast.2002.37070
-
Suraweera N, Duval A, Reperant M, et al. Evaluation of tumor microsatellite instability using five quasimonomorphic mononucleotide repeats and pentaplex PCR. Gastroenterology 2002;123:1804-1811. (Pubitemid 35408304)
-
(2002)
Gastroenterology
, vol.123
, Issue.6
, pp. 1804-1811
-
-
Suraweera, N.1
Duval, A.2
Reperant, M.3
Vaury, C.4
Furlan, D.5
Leroy, K.6
Seruca, R.7
Iacopetta, B.8
Hamelin, R.9
-
36
-
-
13944279163
-
Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomas: Role of clinical features, microsatellite instability, and immunohistochemistry
-
DOI 10.1002/cncr.20873
-
Ponti G, Losi L, Di Gregorio C, et al. Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomas: role of clinical features, microsatellite instability, and immunohistochemistry. Cancer 2005;103:1018-1025. (Pubitemid 40270079)
-
(2005)
Cancer
, vol.103
, Issue.5
, pp. 1018-1025
-
-
Ponti, G.1
Losi, L.2
Di Gregorio, C.3
Roncucci, L.4
Pedroni, M.5
Scarselli, A.6
Benatti, P.7
Seidenari, S.8
Pellacani, G.9
Lembo, L.10
Rossi, G.11
Marino, M.12
Lucci-Cordisco, E.13
De Leon, M.P.14
-
37
-
-
33748796884
-
Value of MLH1 and MSH2 mutations in the appearance of Muir-Torre syndrome phenotype in HNPCC patients presenting sebaceous gland tumors or keratoacanthomas
-
DOI 10.1038/sj.jid.5700475, PII 5700475
-
Ponti G, Losi L, Pedroni M, et al. Value of MLH1 and MSH2 mutations in the appearance of Muir-Torre syndrome phenotype in HNPCC patients presenting sebaceous gland tumors or keratoacanthomas. J Invest Dermatol 2006;126:2302-2307. (Pubitemid 44413178)
-
(2006)
Journal of Investigative Dermatology
, vol.126
, Issue.10
, pp. 2302-2307
-
-
Ponti, G.1
Losi, L.2
Pedroni, M.3
Lucci-Cordisco, E.4
Di Gregorio, C.5
Pellacani, G.6
Seidenari, S.7
-
38
-
-
46249091417
-
Site and tumor type predicts DNA mismatch repair status in cutaneous sebaceous neoplasia
-
Singh RS, Grayson W, Redston M, et al. Site and tumor type predicts DNA mismatch repair status in cutaneous sebaceous neoplasia. Am J Surg Pathol 2008;32:936-942.
-
(2008)
Am J Surg Pathol
, vol.32
, pp. 936-942
-
-
Singh, R.S.1
Grayson, W.2
Redston, M.3
-
39
-
-
34247630047
-
Utility of immunohistochemistry in predicting microsatellite instability in endometrial carcinoma
-
DOI 10.1097/01.pas.0000213428.61374.06, PII 0000047820070500000013
-
Modica I, Soslow RA, Black D, et al. Utility of immunohistochemistry in predicting microsatellite instability in endometrial carcinoma. Am J Surg Pathol 2007;31:744-751. (Pubitemid 46684215)
-
(2007)
American Journal of Surgical Pathology
, vol.31
, Issue.5
, pp. 744-751
-
-
Modica, I.1
Soslow, R.A.2
Black, D.3
Tornos, C.4
Kauff, N.5
Shia, J.6
-
40
-
-
67549138793
-
Selection of endometrial carcinomas for DNA mismatch repair protein immunohistochemistry using patient age and tumor morphology enhances detection of mismatch repair abnormalities
-
Garg K, Leitao Jr MM, Kauff ND, et al. Selection of endometrial carcinomas for DNA mismatch repair protein immunohistochemistry using patient age and tumor morphology enhances detection of mismatch repair abnormalities. Am J Surg Pathol 2009;33:925-933.
-
(2009)
Am J Surg Pathol
, vol.33
, pp. 925-933
-
-
Garg, K.1
Leitao Jr., M.M.2
Kauff, N.D.3
-
41
-
-
67651160324
-
Prospective evaluation of DNA mismatch repair protein expression in primary endometrial cancer
-
Backes FJ, Leon ME, Ivanov I, et al. Prospective evaluation of DNA mismatch repair protein expression in primary endometrial cancer. Gynecol Oncol 2009;114:486-490.
-
(2009)
Gynecol Oncol
, vol.114
, pp. 486-490
-
-
Backes, F.J.1
Leon, M.E.2
Ivanov, I.3
-
42
-
-
77951917844
-
DNA mismatch repair deficiency in ampullary carcinoma: A morphologic and immunohistochemical study of 54 cases
-
Agaram NP, Shia J, Tang LH, et al. DNA mismatch repair deficiency in ampullary carcinoma: a morphologic and immunohistochemical study of 54 cases. Am J Clin Pathol 2010;133:772-780.
-
(2010)
Am J Clin Pathol
, vol.133
, pp. 772-780
-
-
Agaram, N.P.1
Shia, J.2
Tang, L.H.3
-
43
-
-
11144279281
-
Value of immunohistochemical detection of DNA mismatch repair proteins in predicting germline mutation in hereditary colorectal neoplasms
-
DOI 10.1097/01.pas.0000146009.85309.3b
-
Shia J, Klimstra DS, Nafa K, et al. Value of immunohistochemical detection of DNA mismatch repair proteins in predicting germline mutation in hereditary colorectal neoplasms. Am J Surg Pathol 2005;29: 96-104. (Pubitemid 40023956)
-
(2005)
American Journal of Surgical Pathology
, vol.29
, Issue.1
, pp. 96-104
-
-
Shia, J.1
Klimstra, D.S.2
Nafa, K.3
Offit, K.4
Guillem, J.G.5
Markowitz, A.J.6
Gerald, W.L.7
Ellis, N.A.8
-
44
-
-
79953198017
-
Immunohistochemistry for DNA mismatch repair proteins in colorectal carcinoma: What does scanty staining for MSH6 mean?
-
Guo M, Klimstra DS, Tang LH, et al. Immunohistochemistry for DNA mismatch repair proteins in colorectal carcinoma: what does scanty staining for MSH6 mean? Mod Pathol 2010;23(Suppl 1):433A.
-
(2010)
Mod Pathol
, vol.23
, Issue.SUPPL. 1
-
-
Guo, M.1
Klimstra, D.S.2
Tang, L.H.3
-
45
-
-
79960009495
-
Neoadjuvant therapy induces loss of MSH6 expression in colorectal carcinoma
-
Bao F, Rennert H, Yantiss RK. Neoadjuvant therapy induces loss of MSH6 expression in colorectal carcinoma. Mod Pathol 2010;23(Suppl 1):136A.
-
(2010)
Mod Pathol
, vol.23
, Issue.SUPPL. 1
-
-
Bao, F.1
Rennert, H.2
Yantiss, R.K.3
-
46
-
-
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
-
PII S0959804999002087
-
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. (Pubitemid 30035343)
-
(2000)
European Journal of Cancer
, vol.36
, Issue.1
, pp. 49-54
-
-
Debniak, T.1
Kurzawski, G.2
Gorski, B.3
Kladny, J.4
Domagala, W.5
Lubinski, J.6
|