-
1
-
-
34250715384
-
Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer)
-
DOI 10.1136/jmg.2007.048991
-
Vasen HFA, Möslein G, Alonso A et al (2007) Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer). J Med Genet 44:353-362 (Pubitemid 46953715)
-
(2007)
Journal of Medical Genetics
, vol.44
, Issue.6
, pp. 353-362
-
-
Vasen, H.F.A.1
Moslein, G.2
Alonso, A.3
Bernstein, I.4
Bertario, L.5
Blanco, I.6
Burn, J.7
Capella, G.8
Engel, C.9
Frayling, I.10
Friedl, W.11
Hes, F.J.12
Hodgson, S.13
Mecklin, J.-P.14
Moller, P.15
Nagengast, F.16
Parc, Y.17
Renkonen-Sinisalo, L.18
Sampson, J.R.19
Stormorken, A.20
Wijnen, J.21
more..
-
2
-
-
0034011564
-
Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer
-
Jarvinen HJ, Aarnio M, Mustonen H et al (2000) Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer. Gastroenterology 118:829-834 (Pubitemid 30243745)
-
(2000)
Gastroenterology
, vol.118
, Issue.5
, pp. 829-834
-
-
Jarvinen, H.J.1
Aarnio, M.2
Mustonen, H.3
AktanCollan, K.4
Aaltonen, L.A.5
Peltomaki, P.6
Chapelle, A.D.L.7
Mecklin, J.8
-
3
-
-
30944457531
-
Prophylactic surgery to reduce the risk of gynecologic cancers in the lynch syndrome
-
DOI 10.1056/NEJMoa052627
-
Schmeler KM, Lynch HT, Chen LM et al (2006) Prophylactic surgery to reduce the risk of gynecologic cancers in the Lynch syndrome. N Engl J Med 354:261-269 (Pubitemid 43113031)
-
(2006)
New England Journal of Medicine
, vol.354
, Issue.3
, pp. 261-269
-
-
Schmeler, K.M.1
Lynch, H.T.2
Chen, L.-M.3
Munsell, M.F.4
Soliman, P.T.5
Clark, M.B.6
Daniels, M.S.7
White, K.G.8
Boyd-Rogers, S.G.9
Conrad, P.G.10
Yang, K.Y.11
Rubin, M.M.12
Sun, C.C.13
Slomovitz, B.M.14
Gershenson, D.M.15
Lu, K.H.16
-
4
-
-
20244386256
-
Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: Familial colorectal cancer type X
-
DOI 10.1001/jama.293.16.1979
-
Lindor NM, Rabe K, Petersen GM et al (2005) Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X. JAMA 293:1979-1985 (Pubitemid 40570891)
-
(2005)
Journal of the American Medical Association
, vol.293
, Issue.16
, pp. 1979-1985
-
-
Lindor, N.M.1
Rabe, K.2
Petersen, G.M.3
Haile, R.4
Casey, G.5
Baron, J.6
Gallinger, S.7
Bapat, B.8
Aronson, M.9
Hopper, J.10
Jass, J.11
LeMarchand, L.12
Grove, J.13
Potter, J.14
Newcomb, P.15
Terdiman, J.P.16
Conrad, P.17
Moslein, G.18
Goldberg, R.19
Ziogas, A.20
Anton-Culver, H.21
De Andrade, M.22
Siegmund, K.23
Thibodeau, S.N.24
Boardman, L.A.25
Seminara, D.26
more..
-
5
-
-
34548191532
-
Who should be sent for genetic testing in hereditary colorectal cancer syndromes?
-
DOI 10.1200/JCO.2006.10.3119
-
Lynch HT, Boland CR, Rodriguez-Bigas MA et al (2007) Who should be sent for genetic testing in hereditary colorectal cancer syndromes? J Clin Oncol 25:3534-3542 (Pubitemid 47310892)
-
(2007)
Journal of Clinical Oncology
, vol.25
, Issue.23
, pp. 3534-3542
-
-
Lynch, H.T.1
Boland, C.R.2
Rodriguez-Bigas, M.A.3
Amos, C.4
Lynch, J.P.5
Lynch, P.M.6
-
6
-
-
57449097359
-
Feasibility of screening for Lynch syndrome among patients with colorectal cancer
-
Hampel H, Frankel WL, Martin E et al (2008) Feasibility of screening for Lynch syndrome among patients with colorectal cancer. J Clin Oncol 26:5783-5788
-
(2008)
J Clin Oncol
, vol.26
, pp. 5783-5788
-
-
Hampel, H.1
Frankel, W.L.2
Martin, E.3
-
7
-
-
20244386395
-
Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer
-
DOI 10.1001/jama.293.16.1986
-
Piñol V, Castells A, Andreu M et al (2005) Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer. JAMA 293:1986-1994 (Pubitemid 40570892)
-
(2005)
Journal of the American Medical Association
, vol.293
, Issue.16
, pp. 1986-1994
-
-
Pinol, V.1
Castells, A.2
Andreu, M.3
Castellvi-Bel, S.4
Alenda, C.5
Llor, X.6
Xicola, R.M.7
Rodriguez-Moranta, F.8
Paya, A.9
Jover, R.10
Bessa, X.11
-
8
-
-
36549086274
-
Prospective determination of prevalence of Lynch syndrome in young women with endometrial cancer
-
DOI 10.1200/JCO.2007.10.8597
-
Lu KH, Schorge JO, Rodabaugh KJ et al (2007) Prospective determination of prevalence of Lynch Syndrome in young women with endometrial cancer. J Clin Oncol 25:5158-5164 (Pubitemid 350232246)
-
(2007)
Journal of Clinical Oncology
, vol.25
, Issue.33
, pp. 5158-5164
-
-
Lu, K.H.1
Schorge, J.O.2
Rodabaugh, K.J.3
Daniels, M.S.4
Sun, C.C.5
Soliman, P.T.6
White, K.G.7
Luthra, R.8
Gershenson, D.M.9
Broaddus, R.R.10
-
9
-
-
37449019456
-
Validation and extension of the PREMM 1,2 model in a population-based cohort of colorectal cancer patients
-
Balaguer F, Balmaña J, Castellví-Bel S et al (2008) Validation and extension of the PREMM 1,2 model in a population-based cohort of colorectal cancer patients. Gastroenterology 134:39-46
-
(2008)
Gastroenterology
, vol.134
, pp. 39-46
-
-
Balaguer, F.1
Balmaña, J.2
Castellví-Bel, S.3
-
10
-
-
33745658837
-
Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer
-
DOI 10.1056/NEJMoa053493
-
Barnetson RA, Tenesa A, Farrington SM et al (2006) Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer. N Engl J Med 354:2751-2763 (Pubitemid 43974193)
-
(2006)
New England Journal of Medicine
, vol.354
, Issue.26
, pp. 2751-2763
-
-
Barnetson, R.A.1
Tenesa, A.2
Farrington, S.M.3
Nicholl, I.D.4
Cetnarskyj, R.5
Porteous, M.E.6
Campbell, H.7
Dunlop, M.G.8
-
11
-
-
10744233937
-
Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
-
Umar A, Boland CR, Terdiman JP et al (2004) Revised Bethesda guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst 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..
-
12
-
-
33749040947
-
Prediction of MLH1 and MSH2 mutations in lynch syndrome
-
DOI 10.1001/jama.296.12.1469
-
Balmaña J, Stockwell DH, Steyerberg EW et al (2006) Prediction of MLH1 and MSH2 mutations in Lynch syndrome. JAMA 296:1469-1478 (Pubitemid 44465511)
-
(2006)
Journal of the American Medical Association
, vol.296
, Issue.12
, pp. 1469-1478
-
-
Balmana, J.1
Stockwell, D.H.2
Steyerberg, E.W.3
Stoffel, E.M.4
Deffenbaugh, A.M.5
Reid, J.E.6
Ward, B.7
Scholl, T.8
Hendrickson, B.9
Tazelaar, J.10
Burbidge, L.A.11
Syngal, S.12
-
13
-
-
33749066191
-
Prediction of germline mutations and cancer risk in the lynch syndrome
-
DOI 10.1001/jama.296.12.1479
-
Chen S, Wang W, Lee S et al (2006) Prediction of germline mutations and cancer risk in the Lynch syndrome. JAMA 296:1479-1487 (Pubitemid 44465512)
-
(2006)
Journal of the American Medical Association
, vol.296
, Issue.12
, pp. 1479-1487
-
-
Chen, S.1
Wang, W.2
Lee, S.3
Nafa, K.4
Lee, J.5
Romans, K.6
Watson, P.7
Gruber, S.B.8
Euhus, D.9
Kinzler, K.W.10
Jass, J.11
Gallinger, S.12
Lindor, N.M.13
Casey, G.14
Ellis, N.15
Giardiello, F.M.16
Offit, K.17
Parmigiani, G.18
-
14
-
-
84860762191
-
Comparación de los modelos predictivos para identificación de portadores de mutación en MLH1/MSH2/ MSH6 (síndrome de Lynch) en una cohorte española
-
DOI:10.3252/pso.es.12seom.2009
-
Balmaña J, Valenzuela I, Rué M et al (2009) Comparación de los modelos predictivos para identificación de portadores de mutación en MLH1/MSH2/ MSH6 (síndrome de Lynch) en una cohorte española. XII Congreso Sociedad Española de Oncología Médica (SEOM). DOI:10.3252/pso.es.12seom.2009
-
(2009)
XII Congreso Sociedad Española de Oncología Médica (SEOM).
-
-
Balmaña, J.1
Valenzuela, I.2
Rué, M.3
-
15
-
-
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 (2008) 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 10:293-300 (Pubitemid 352019113)
-
(2008)
Journal of Molecular Diagnostics
, vol.10
, Issue.4
, pp. 293-300
-
-
Shia, J.1
-
16
-
-
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 (2004) Microsatellite instability, immunohistochemistry, and additional PMS2 staining in suspected hereditary nonpolyposis colorectal cancer. Clin Cancer Res 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
-
17
-
-
47649096866
-
Immunohistochemistry (IHC) as first-line screening tool for detecting colorectal cancer (CRC) patients at risk for Lynch syndrome: A 2-antibody panel is as predictive as a 4-antibody panel (Abstr)
-
Shia J, Vakiani E, Guillem J et al (2008) Immunohistochemistry (IHC) as first-line screening tool for detecting colorectal cancer (CRC) patients at risk for Lynch syndrome: a 2-antibody panel is as predictive as a 4-antibody panel (Abstr). Mod Pathol 21[Suppl 1]:138A
-
(2008)
Mod Pathol
, vol.21
, Issue.SUPPL. 1
-
-
Shia, J.1
Vakiani, E.2
Guillem, J.3
-
18
-
-
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 (2010) Immunohistochemistry for PMS2 and MSH6 alone can replace a four antibody panel for mismatch repair deficiency screening in colorectal adenocarcinoma. Pathology 42:209-213
-
(2010)
Pathology
, vol.42
, pp. 209-213
-
-
Hall, G.1
Clarkson, A.2
Shi, A.3
-
19
-
-
84860762636
-
-
Ley 14/2007, 3 de Julio, de Investigación Biomédica
-
Ley 14/2007, 3 de Julio, de Investigación Biomédica
-
-
-
-
20
-
-
34548141754
-
Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC
-
DOI 10.1111/j.1399-0004.2007.00856.x
-
Roncari B, Pedroni M, Maffei S et al (2007) Frequency of constitutional MSH6 mutations in a consecutive series of families with clinical suspicion of HNPCC. Clin Genet 72:230-237 (Pubitemid 47300026)
-
(2007)
Clinical Genetics
, vol.72
, Issue.3
, pp. 230-237
-
-
Roncari, B.1
Pedroni, M.2
Maffei, S.3
Di Gregorio, V.4
Ponti, G.5
Scarselli, A.6
Losi, L.7
Benatti, P.8
Roncucci, L.9
De Gaetani, E.10
Camellini, L.11
Lucci-Cordisco, E.12
Tricarico, R.13
Genuardi, M.14
De Leon, M.P.15
-
21
-
-
0035044718
-
Microsatellite instability and hMLH1 and hMSH2 expression analysis in familial and sporadic colorectal cancer
-
Salashor S, Koelble K, Rubio C et al (2001) Microsatellite instability and hMLH1 and hMSH2 expression analysis in familial and sporadic colorectal cancer. Lab Invest 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
-
22
-
-
4544310802
-
Mutations associated with HNPCC predisposition - Update of ICG-HNPCC/INSiGHT mutation database
-
Lynch Syndrome (HNPCC) and Microsatellite Instability
-
Peltomaki P, Vasen H (2004) Mutations associated with HNPCC predisposition-update of ICGHNPCC/INSiGHT mutation database. Dis Markers 20:269-276 (Pubitemid 40164099)
-
(2004)
Disease Markers
, vol.20
, Issue.4-5
, pp. 269-276
-
-
Peltomaki, P.1
Vasen, H.2
-
23
-
-
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 (2002) Evaluation of microsatellite instability and immunohistochemistry for the prediction of germline MSH2 and MLH1 mutations in hereditary nonpolyposis colon cancer families. Cancer Res 62:3485-3492 (Pubitemid 34651396)
-
(2002)
Cancer Research
, vol.62
, Issue.12
, pp. 3485-3492
-
-
Wahlberg, S.S.1
Schmeits, J.2
Thomas, G.3
Loda, M.4
Garber, J.5
Syngal, S.6
Kolodner, R.D.7
Fox, E.8
-
24
-
-
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 (2005) Tumors from MSH2 mutation carriers show loss of MSH2 expression but many tumors from MLH1 mutation carriers exhibit weak positive MLH1 staining. J Pathol 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
-
25
-
-
0036082617
-
Oxidative stress inactivates the human DNA mismatch repair system
-
Chang CL, Marra G, Chauhan DP et al (2002) Oxidative stress inactivates the human DNA mismatch repair system. Am J Physiol Cell Physiol 283:C148-C154 (Pubitemid 34670558)
-
(2002)
American Journal of Physiology - Cell Physiology
, vol.283
, Issue.1
-
-
Chang, C.L.1
Marra, G.2
Chauhan, D.P.3
Ha, H.T.4
Chang, D.K.5
Ricciardiello, L.6
Randolph, A.7
Carethers, J.M.8
Richard Boland, C.9
-
26
-
-
34547114718
-
Regulation of DNA repair in hypoxic cancer cells
-
DOI 10.1007/s10555-007-9061-3, Special issue on Hypoxia and Cancer, Guest Editor: Gregg L. Semenza
-
Bindra RS, Crosby ME, Glazer PM et al (2007) Regulation of DNA repair in hypoxic cancer cells. Cancer Metastasis Rev 26:249-260 (Pubitemid 47101664)
-
(2007)
Cancer and Metastasis Reviews
, vol.26
, Issue.2
, pp. 249-260
-
-
Bindra, R.S.1
Crosby, M.E.2
Glazer, P.M.3
-
27
-
-
9944243710
-
The utility of immunohistochemical detection of DNA mismatch repair gene proteins
-
DOI 10.1007/s00428-004-1090-5
-
Shia J, Ellis NA, Klimstra DS (2004) The utility of immunohistochemical detection of DNA mismatch repair gene proteins. Virchows Arch 445:431-441 (Pubitemid 39592745)
-
(2004)
Virchows Archiv
, vol.445
, Issue.5
, pp. 431-441
-
-
Shia, J.1
Ellis, N.A.2
Klimstra, D.S.3
-
28
-
-
47649101956
-
Immunohistochemistry versus microsatellite instability testing for screening colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome: Part II. The utility of microsatellite instability testing
-
DOI 10.2353/jmoldx.2008.080062
-
Zhang L (2008) Immunohistochemistry versus microsatellite instability testing for screening colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome. Part II. The utility of microsatellite instability testing. J Mol Diagn 10:301-307 (Pubitemid 352019114)
-
(2008)
Journal of Molecular Diagnostics
, vol.10
, Issue.4
, pp. 301-307
-
-
Zhang, L.1
-
29
-
-
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 (2002) Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant. Am J Hum Genet 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
-
30
-
-
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 (2004) Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history. Am J Hum Genet 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
-
31
-
-
3242670404
-
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: Impact on counseling and surveillance
-
DOI 10.1053/j.gastro.2004.03.068, PII S0016508504005785
-
Hendriks YM, Wagner A, Morreau H et al (2004) Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance. Gastroenterology 127:17-25 (Pubitemid 38962270)
-
(2004)
Gastroenterology
, vol.127
, Issue.1
, pp. 17-25
-
-
Hendriks, Y.M.C.1
Wagner, A.2
Morreau, H.3
Menko, F.4
Stormorken, A.5
Quehenberger, F.6
Sandkuijl, L.7
Moller, P.8
Genuardi, M.9
Van Houwelingen, H.10
Tops, C.11
Van Puijenbroek, M.12
Verkuijlen, P.13
Kenter, G.14
Van Mil, A.15
Meijers-Heijboer, H.16
Tan, G.B.17
Breuning, M.H.18
Fodde, R.19
Wijnen, J.T.H.20
Brocker-Vriends, A.H.J.T.21
Vasen, H.22
more..
-
32
-
-
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 (1996) hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6. Proc Natl Acad Sci U S A 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
-
33
-
-
0029868110
-
Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair
-
Marsischky GT, Filosi N, Kane MF et al (1996) Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair. Genes Dev 10:407-420 (Pubitemid 26085996)
-
(1996)
Genes and Development
, vol.10
, Issue.4
, pp. 407-420
-
-
Marsischky, G.T.1
Filosi, N.2
Kane, M.F.3
Kolodner, R.4
-
34
-
-
12844262940
-
Development of a fluorescent multiplex assay for detection of MSI-high tumors
-
Lynch Syndrome (HNPCC) and Microsatellite Instability
-
Bacher JW, Flanagan LA, Smalley RL et al (2004) Development of a ? uorescent multiplex assay for detection of MSI-high tumors. Dis Markers 20:237-250 (Pubitemid 40164096)
-
(2004)
Disease Markers
, vol.20
, Issue.4-5
, pp. 237-250
-
-
Bacher, J.W.1
Flanagan, L.A.2
Smalley, R.L.3
Nassif, N.A.4
Burgart, L.J.5
Halberg, R.B.6
Megid, W.M.A.7
Thibodeau, S.N.8
-
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 (2002) Evaluation of tumor microsatellite instability using five quasimonomorphic mononucleotide repeats and pentaplex PCR. Gastroenterology 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
-
-
74249097210
-
Recent insights into the pathogenesis of colorectal cancer
-
Goel A, Boland CR (2010) Recent insights into the pathogenesis of colorectal cancer. Curr Opin Gastroenterol 26:47-52
-
(2010)
Curr Opin Gastroenterol
, vol.26
, pp. 47-52
-
-
Goel, A.1
Boland, C.R.2
-
37
-
-
18444374405
-
Mutations of the BRAF gene in human cancer
-
DOI 10.1038/nature00766
-
Davies H, Bignell CR, Cox C et al (2002) Mutations of the BRAF gene in human cancer. Nature 417:949-954 (Pubitemid 34716871)
-
(2002)
Nature
, vol.417
, Issue.6892
, 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
Palmleri, 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..
-
38
-
-
0346057796
-
BRAF mutations characterize colon but not gastric cancer with mismatch repair deficiency
-
DOI 10.1038/sj.onc.1207061
-
Oliveira C, Pinto M, Duval A et al (2003) BRAF mutations characterize colon but not gastric cancer with mismatch repair deficiency. Oncogene 22:9192-9196 (Pubitemid 38067995)
-
(2003)
Oncogene
, vol.22
, Issue.57
, pp. 9192-9196
-
-
Oliveira, C.1
Pinto, M.2
Duval, A.3
Brennetot, C.4
Domingo, E.5
Espin, E.6
Armengol, M.7
Yamamoto, H.8
Hamelin, R.9
Seruca, R.10
Schwartz Jr., S.11
-
39
-
-
0037194728
-
RAF/RAS oncogenes and mismatch-repair status
-
DOI 10.1038/418934a
-
Rajagopalan H, Bardelli A, Lengauer C et al (2002) Tumorigenesis: RAF/RAS oncogenes and mismatch-repair status. Nature 418:934 (Pubitemid 34976022)
-
(2002)
Nature
, vol.418
, Issue.6901
, pp. 934
-
-
Rajagopalan, H.1
Bardelli, A.2
Lengauer, C.3
Kinzler, K.W.4
Vogelstein, B.5
Velculescu, V.E.6
-
40
-
-
1642535480
-
BRAF Mutation Is Frequently Present in Sporadic Colorectal Cancer with Methylated hMLH1, but Not in Hereditary Nonpolyposis Colorectal Cancer
-
DOI 10.1158/1078-0432.CCR-1118-3
-
Deng G, Bell I, Crawley S et al (2004) BRAF mutation is frequently present in sporadic colorectal cancer with methylated hMLH1, but not in hereditary nonpolyposis colorectal cancer. Clin Cancer Res 10:191-195 (Pubitemid 38114179)
-
(2004)
Clinical Cancer Research
, vol.10
, Issue.1
, 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
-
41
-
-
3242686837
-
BRAF mutation is associated with DNA methylation in serrated polyps and cancers of the colorectum
-
DOI 10.1136/gut.2003.037671
-
Kambara T, Simms LA, Whitehall VL et al (2004) BRAF mutation is associated with DNA methylation in serrated polyps and cancers of the colorectum. Gut 53:1137-1144 (Pubitemid 38961968)
-
(2004)
Gut
, vol.53
, Issue.8
, pp. 1137-1144
-
-
Kambara, T.1
Simms, L.A.2
Whitehall, V.L.J.3
Spring, K.J.4
Wynter, C.V.A.5
Walsh, M.D.6
Barker, M.A.7
Arnold, S.8
McGivern, A.9
Matsubara, N.10
Tanaka, N.11
Higuchi, T.12
Young, J.13
Jass, J.R.14
Leggett, B.A.15
-
42
-
-
20544437157
-
BRAF-V600E is not involved in the colorectal tumorigenesis of HNPCC in patients with functional MLH1 and MSH2 genes
-
DOI 10.1038/sj.onc.1208569
-
Domingo E, Niessen RC, Oliveira C et al (2005) BRAF-V600E is not involved in the colorectal tumorigenesis of HNPCC in patients with functional MLH1 and MSH2 genes. Oncogene 24:3995-3998 (Pubitemid 40896411)
-
(2005)
Oncogene
, vol.24
, Issue.24
, pp. 3995-3998
-
-
Domingo, E.1
Niessen, R.C.2
Oliveira, C.3
Alhopuro, P.4
Moutinho, C.5
Espin, E.6
Armengol, M.7
Sijmons, R.H.8
Kleibeuker, J.H.9
Seruca, R.10
Aaltonen, L.A.11
Imai, K.12
Yamamoto, H.13
Schwartz Jr., S.14
Hofstra, R.M.W.15
-
43
-
-
4444311092
-
BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing
-
DOI 10.1136/jmg.2004.020651
-
Domingo E, Laiho P, Ollikainen M et al (2004) BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing. J Med Genet 41:664-668 (Pubitemid 39208606)
-
(2004)
Journal of Medical Genetics
, vol.41
, Issue.9
, pp. 664-668
-
-
Domingo, E.1
Laiho, P.2
Ollikainen, M.3
Pinto, M.4
Wang, L.5
French, A.J.6
Westra, J.7
Frebourg, T.8
Espin, E.9
Armengol, M.10
Hamelin, R.11
Yamamoto, H.12
Hofstra, R.M.W.13
Seruca, R.14
Lindblom, A.15
Peltomaki, P.16
Thibodeau, S.N.17
Aaltonen, L.A.18
Schwartz Jr., S.19
-
44
-
-
36049029745
-
Relación de la alteración del gen BRAF y la metilación del gen reparador HMLH1 en tumores colorrectales
-
Veganzones S, Maestro ML, Vidaurreta M et al (2007) Relación de la alteración dl gen BRAF y la metilación del gen reparador HMLH1en tumores colorrectales. Química Clínica 26:207-212 (Pubitemid 350084010)
-
(2007)
Quimica Clinica
, vol.26
, Issue.4
, pp. 207-212
-
-
Veganzones, S.1
Maestro De Las Casas, M.L.2
Vidaurreta, M.3
Sanz-Casla, M.T.4
Rafael, S.5
Martinez, A.6
Herranz, M.D.7
Aguilera, C.8
Cerdan, J.9
Arroyo, M.10
-
45
-
-
13144266670
-
Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma
-
DOI 10.1073/pnas.95.12.6870
-
Herman JG, Umar A, Polyak K et al (1998) Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma. Proc Natl Acad Sci U S A 95:6870-6875 (Pubitemid 28278073)
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, Issue.12
, pp. 6870-6875
-
-
Herman, J.G.1
Umar, A.2
Polyak, K.3
Graff, J.R.4
Ahuja, N.5
Issa, J.-P.J.6
Markowitz, S.7
Willson, J.K.V.8
Hamilton, S.R.9
Kinzler, K.W.10
Kane, M.F.11
Kolodner, R.D.12
Vogelstein, B.13
Kunkel, T.A.14
Baylin, S.B.15
-
46
-
-
0842278570
-
Epigenetic changes in colorectal cancer
-
DOI 10.1023/A:1025806911782
-
Kondo Y, Issa JP (2004) Epigenetic changes in colorectal cancer. Cancer Metastasis Rev 23:29-39 (Pubitemid 38221595)
-
(2004)
Cancer and Metastasis Reviews
, vol.23
, Issue.1-2
, pp. 29-39
-
-
Kondo, Y.1
Issa, J.-P.J.2
-
47
-
-
0035185894
-
Features of colorectal cancers with high-level microsatellite instability occurring in familial and sporadic settings: Parallel pathways of tumorigenesis
-
Young J, Simms LA, Biden KG et al (2001) Features of colorectal cancers with high-level microsatellite instability occurring in familial and sporadic settings: parallel pathways of tumorigenesis. Am J Pathol 159:2107-2116 (Pubitemid 33104265)
-
(2001)
American Journal of Pathology
, vol.159
, Issue.6
, pp. 2107-2116
-
-
Young, J.1
Simms, L.A.2
Biden, K.G.3
Wynter, C.4
Whitehall, V.5
Karamatic, R.6
George, J.7
Goldblatt, J.8
Walpole, I.9
Robin, S.-A.10
Borten, M.M.11
Stitz, R.12
Searle, J.13
McKeone, D.14
Fraser, L.15
Purdie, D.R.16
Podger, K.17
Price, R.18
Buttenshaw, R.19
Walsh, M.D.20
Barker, M.21
Leggett, B.A.22
Jass, J.R.23
more..
-
48
-
-
34247619416
-
Heritable germline epimutation is not the same as transgenerational epigenetic inheritance [5]
-
DOI 10.1038/ng0507-574, PII NG0507574
-
Chong S, Youngson NA, Whitelaw E et al (2007) Heritable germline epimutation is not the same as transgenerational epigenetic inheritance. Nat Genet 39:574-575 (Pubitemid 46676092)
-
(2007)
Nature Genetics
, vol.39
, Issue.5
, pp. 574-575
-
-
Chong, S.1
Youngson, N.A.2
Whitelaw, E.3
-
50
-
-
55949124994
-
DNA methylation, epimutations and cancer predisposition
-
Dobrovic A, Kristensen LS (2009) DNA methylation, epimutations and cancer predisposition. Int J Biochem Cell Biol 41:34-39
-
(2009)
Int J Biochem Cell Biol
, vol.41
, pp. 34-39
-
-
Dobrovic, A.1
Kristensen, L.S.2
-
51
-
-
67650383819
-
Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome
-
Niessen RC, Hofstra RM, Westers H et al (2009) Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome. Genes Chromosomes Cancer 48:737-744
-
(2009)
Genes Chromosomes Cancer
, vol.48
, pp. 737-744
-
-
Niessen, R.C.1
Hofstra, R.M.2
Westers, H.3
-
52
-
-
33846973361
-
Inheritance of a cancer-associated MLH1 germ-line epimutation
-
Hitchins MP, Wong JJ, Suthers G et al (2007) Inheritance of a cancer-associated MLH1 germ-line epimutation. N Engl J Med 356:697-705
-
(2007)
N Engl J Med
, vol.356
, pp. 697-705
-
-
Hitchins, M.P.1
Wong, J.J.2
Suthers, G.3
-
53
-
-
35649021295
-
Erasure of MLH1 methylation in spermatozoa - Implications for epigenetic inheritance
-
DOI 10.1038/ng1107-1289, PII NG11071289
-
Hitchins MP, Ward RL (2007) Erasure of MLH1 methylation in spermatozoa-implications for epigenetic inheritance. Nat Genet 39:1289 (Pubitemid 350035008)
-
(2007)
Nature Genetics
, vol.39
, Issue.11
, pp. 1289
-
-
Hitchins, M.P.1
Ward, R.L.2
-
54
-
-
72749085056
-
Constitutional (germline) MLH1 epimutation as an aetiological mechanism for hereditary non-polyposis colorectal cancer
-
Hitchins MP, Ward RL (2009) Constitutional (germline) MLH1 epimutation as an aetiological mechanism for hereditary non-polyposis colorectal cancer. J Med Genet 46:793-802
-
(2009)
J Med Genet
, vol.46
, pp. 793-802
-
-
Hitchins, M.P.1
Ward, R.L.2
-
55
-
-
45749135888
-
Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC
-
DOI 10.1038/ejhg.2008.25, PII EJHG200825
-
Morak M, Schackert HK, Rahner N et al (2008) Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC. Eur J Hum Genet 16:804-811 (Pubitemid 351865678)
-
(2008)
European Journal of Human Genetics
, vol.16
, Issue.7
, pp. 804-811
-
-
Morak, M.1
Schackert, H.K.2
Rahner, N.3
Betz, B.4
Ebert, M.5
Walldorf, C.6
Royer-Pokora, B.7
Schulmann, K.8
Von Knebel-Doeberitz, M.9
Dietmaier, W.10
Keller, G.11
Kerker, B.12
Leitner, G.13
Holinski-Feder, E.14
-
56
-
-
59749085710
-
Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome
-
Kovacs ME, Papp J, Szentirmay Z et al (2009) Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome. Hum Mutat 30:197-203
-
(2009)
Hum Mutat
, vol.30
, pp. 197-203
-
-
Kovacs, M.E.1
Papp, J.2
Szentirmay, Z.3
-
57
-
-
58149144567
-
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1
-
Ligtenberg MJ, Kuiper RP, Chan TL et al (2009) Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1. Nat Genet 41:112-117
-
(2009)
Nat Genet
, vol.41
, pp. 112-117
-
-
Ligtenberg, M.J.1
Kuiper, R.P.2
Chan, T.L.3
-
58
-
-
77951049336
-
Somatic hypermethylation of MSH2 is a frequent event in Lynch syndrome colorectal cancers
-
Nagasaka T, Rhees J, Kloor M et al (2010) Somatic hypermethylation of MSH2 is a frequent event in Lynch syndrome colorectal cancers. Cancer Res 70:3098-3108
-
(2010)
Cancer Res
, vol.70
, pp. 3098-3108
-
-
Nagasaka, T.1
Rhees, J.2
Kloor, M.3
-
59
-
-
78449264515
-
Lynch syndrome TACSTD1 family with predominant colorectal cancer
-
abstr 1500
-
Lynch HT, Thibodeau SN, Snyder C et al (2010) Lynch syndrome TACSTD1 family with predominant colorectal cancer. J Clin Oncol 28[15s]:abstr 1500
-
(2010)
J Clin Oncol
, vol.28
-
-
Lynch, H.T.1
Thibodeau, S.N.2
Snyder, C.3
-
60
-
-
79952754996
-
Recurrence and variability of germline EPCAM deletions in Lynch syndrome
-
Kuiper RP, Vissers LE, Venkatachalam R et al (2011) Recurrence and variability of germline EPCAM deletions in Lynch syndrome. Hum Mutat 32:407-414
-
(2011)
Hum Mutat
, vol.32
, pp. 407-414
-
-
Kuiper, R.P.1
Vissers, L.E.2
Venkatachalam, R.3
-
61
-
-
78650692633
-
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: A cohort study
-
Kempers MJ, Kuiper RP, Ockeloen CW et al (2011) Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study. Lancet Oncol 12:49-55
-
(2011)
Lancet Oncol
, vol.12
, pp. 49-55
-
-
Kempers, M.J.1
Kuiper, R.P.2
Ockeloen, C.W.3
-
62
-
-
79951997249
-
Analysis of EPCAM protein expression in diagnostics of Lynch syndrome
-
Kloor M, Voigt AY, Schackert HK et al (2010) Analysis of EPCAM protein expression in diagnostics of Lynch syndrome. J Clin Oncol 29:223-227
-
(2010)
J Clin Oncol
, vol.29
, pp. 223-227
-
-
Kloor, M.1
Voigt, A.Y.2
Schackert, H.K.3
-
63
-
-
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 (2008) The biochemical basis of microsatellite instability and abnormal immunohistochemistry and clinical behavior in Lynch Syndrome: from bench to bedside. Fam Cancer 7:41-52
-
(2008)
Fam Cancer
, vol.7
, pp. 41-52
-
-
Boland, C.R.1
Koi, M.2
Chang, D.K.3
-
64
-
-
0034912314
-
Microsatellites in the eukaryotic DNA mismatch repair genes as modulators of evolutionary mutation rate
-
DOI 10.1101/gr.186301
-
Chang DK, Metzgar D, Wills C et al (2001) Microsatellites in the eukaryotic DNA mismatch repair genes as modulators of evolutionary mutation rate. Genome Res 11:1145-1146 (Pubitemid 32677287)
-
(2001)
Genome Research
, vol.11
, Issue.7
, pp. 1145-1146
-
-
Chang, D.K.1
Metzgar, D.2
Wills, C.3
Boland, C.R.4
|