These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
148 related articles for article (PubMed ID: 24498269)
21. Clinical characterization and mutation spectrum in Caribbean Hispanic families with Lynch syndrome. Cruz-Correa M; Diaz-Algorri Y; Pérez-Mayoral J; Suleiman-Suleiman W; Gonzalez-Pons Mdel M; Bertrán C; Casellas N; Rodríguez N; Pardo S; Rivera K; Mosquera R; Rodriguez-Quilichini S Fam Cancer; 2015 Sep; 14(3):415-25. PubMed ID: 25782445 [TBL] [Abstract][Full Text] [Related]
22. Genotype-phenotype correlation in MMR mutation-positive families with Lynch syndrome. Pérez-Cabornero L; Infante M; Velasco E; Lastra E; Miner C; Durán M Int J Colorectal Dis; 2013 Sep; 28(9):1195-201. PubMed ID: 23588873 [TBL] [Abstract][Full Text] [Related]
23. Familial colorectal cancer: eleven years of data from a registry program in Switzerland. Kovac M; Laczko E; Haider R; Jiricny J; Mueller H; Heinimann K; Marra G Fam Cancer; 2011 Sep; 10(3):605-16. PubMed ID: 21671081 [TBL] [Abstract][Full Text] [Related]
24. Detection of DNA mismatch repair proteins in fresh human blood lymphocytes--towards a novel method for hereditary non-polyposis colorectal cancer (Lynch syndrome) screening. Hassen S; Boman BM; Ali N; Parker M; Somerman C; Ali-Khan Catts ZJ; Ali AA; Fields JZ J Exp Clin Cancer Res; 2011 Oct; 30(1):100. PubMed ID: 22017758 [TBL] [Abstract][Full Text] [Related]
25. Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: a comprehensive analysis of 3,671 families. Steinke V; Holzapfel S; Loeffler M; Holinski-Feder E; Morak M; Schackert HK; Görgens H; Pox C; Royer-Pokora B; von Knebel-Doeberitz M; Büttner R; Propping P; Engel C; Int J Cancer; 2014 Jul; 135(1):69-77. PubMed ID: 24493211 [TBL] [Abstract][Full Text] [Related]
26. Smoking and colorectal cancer in Lynch syndrome: results from the Colon Cancer Family Registry and the University of Texas M.D. Anderson Cancer Center. Pande M; Lynch PM; Hopper JL; Jenkins MA; Gallinger S; Haile RW; LeMarchand L; Lindor NM; Campbell PT; Newcomb PA; Potter JD; Baron JA; Frazier ML; Amos CI Clin Cancer Res; 2010 Feb; 16(4):1331-9. PubMed ID: 20145170 [TBL] [Abstract][Full Text] [Related]
27. BRAF mutation analysis is a valid tool to implement in Lynch syndrome diagnosis in patients classified according to the Bethesda guidelines. Molinari F; Signoroni S; Lampis A; Bertan C; Perrone F; Sala P; Mondini P; Crippa S; Bertario L; Frattini M Tumori; 2014; 100(3):315-20. PubMed ID: 25076244 [TBL] [Abstract][Full Text] [Related]
28. Microsatellite instability and novel mismatch repair gene mutations in northern Chinese population with hereditary non-polyposis colorectal cancer. Sheng JQ; Chan TL; Chan YW; Huang JS; Chen JG; Zhang MZ; Guo XL; Mu H; Chan AS; Li SR; Yuen ST; Leung SY Chin J Dig Dis; 2006; 7(4):197-205. PubMed ID: 17054581 [TBL] [Abstract][Full Text] [Related]
29. Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome. Win AK; Lindor NM; Winship I; Tucker KM; Buchanan DD; Young JP; Rosty C; Leggett B; Giles GG; Goldblatt J; Macrae FA; Parry S; Kalady MF; Baron JA; Ahnen DJ; Marchand LL; Gallinger S; Haile RW; Newcomb PA; Hopper JL; Jenkins MA J Natl Cancer Inst; 2013 Feb; 105(4):274-9. PubMed ID: 23385444 [TBL] [Abstract][Full Text] [Related]
30. A new strategy to screen MMR genes in Lynch Syndrome: HA-CAE, MLPA and RT-PCR. Perez-Cabornero L; Velasco E; Infante M; Sanz D; Lastra E; Hernández L; Miner C; Duran M Eur J Cancer; 2009 May; 45(8):1485-93. PubMed ID: 19250818 [TBL] [Abstract][Full Text] [Related]
31. DNA mismatch repair deficiency and hereditary syndromes in Latino patients with colorectal cancer. Ricker CN; Hanna DL; Peng C; Nguyen NT; Stern MC; Schmit SL; Idos GE; Patel R; Tsai S; Ramirez V; Lin S; Shamasunadara V; Barzi A; Lenz HJ; Figueiredo JC Cancer; 2017 Oct; 123(19):3732-3743. PubMed ID: 28640387 [TBL] [Abstract][Full Text] [Related]
32. Lynch-like syndrome: characterization and comparison with EPCAM deletion carriers. Kang SY; Park CK; Chang DK; Kim JW; Son HJ; Cho YB; Yun SH; Kim HC; Kwon M; Kim KM Int J Cancer; 2015 Apr; 136(7):1568-78. PubMed ID: 25110875 [TBL] [Abstract][Full Text] [Related]
33. DNA methylation changes and somatic mutations as tumorigenic events in Lynch syndrome-associated adenomas retaining mismatch repair protein expression. Mäki-Nevala S; Valo S; Ristimäki A; Sarhadi V; Knuutila S; Nyström M; Renkonen-Sinisalo L; Lepistö A; Mecklin JP; Peltomäki P EBioMedicine; 2019 Jan; 39():280-291. PubMed ID: 30578081 [TBL] [Abstract][Full Text] [Related]
34. Breast carcinoma and Lynch syndrome: molecular analysis of tumors arising in mutation carriers, non-carriers, and sporadic cases. Lotsari JE; Gylling A; Abdel-Rahman WM; Nieminen TT; Aittomäki K; Friman M; Pitkänen R; Aarnio M; Järvinen HJ; Mecklin JP; Kuopio T; Peltomäki P Breast Cancer Res; 2012 Jun; 14(3):R90. PubMed ID: 22691310 [TBL] [Abstract][Full Text] [Related]
35. Hereditary non-polyposis colorectal cancer/Lynch syndrome in three dimensions. Kravochuck SE; Church JM ANZ J Surg; 2017 Dec; 87(12):1006-1010. PubMed ID: 26990828 [TBL] [Abstract][Full Text] [Related]
36. Validation of predictive models for germline mutations in DNA mismatch repair genes in colorectal cancer. Monzon JG; Cremin C; Armstrong L; Nuk J; Young S; Horsman DE; Garbutt K; Bajdik CD; Gill S Int J Cancer; 2010 Feb; 126(4):930-9. PubMed ID: 19653273 [TBL] [Abstract][Full Text] [Related]
37. Telomere Instability in Lynch Syndrome Families Leads to Some Shorter Telomeres in Garrido-Navas MC; Tippins F; Barwell J; Hoffman J; Codd V; Royle NJ Life (Basel); 2020 Oct; 10(11):. PubMed ID: 33142697 [TBL] [Abstract][Full Text] [Related]
38. Risk of pancreatic cancer in families with Lynch syndrome. Kastrinos F; Mukherjee B; Tayob N; Wang F; Sparr J; Raymond VM; Bandipalliam P; Stoffel EM; Gruber SB; Syngal S JAMA; 2009 Oct; 302(16):1790-5. PubMed ID: 19861671 [TBL] [Abstract][Full Text] [Related]
39. Current clinical criteria for Lynch syndrome are not sensitive enough to identify MSH6 mutation carriers. Sjursen W; Haukanes BI; Grindedal EM; Aarset H; Stormorken A; Engebretsen LF; Jonsrud C; Bjørnevoll I; Andresen PA; Ariansen S; Lavik LA; Gilde B; Bowitz-Lothe IM; Maehle L; Møller P J Med Genet; 2010 Sep; 47(9):579-85. PubMed ID: 20587412 [TBL] [Abstract][Full Text] [Related]
40. Prognostic impact of mismatch repair genes germline defects in colorectal cancer patients: are all mutations equal? Maccaroni E; Bracci R; Giampieri R; Bianchi F; Belvederesi L; Brugiati C; Pagliaretta S; Del Prete M; Scartozzi M; Cascinu S Oncotarget; 2015 Nov; 6(36):38737-48. PubMed ID: 26485756 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]