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.


Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

549 related articles for article (PubMed ID: 15449173)

  • 1. Mutational analysis of OGG1, MYH, MTH1 in FAP, HNPCC and sporadic colorectal cancer patients: R154H OGG1 polymorphism is associated with sporadic colorectal cancer patients.
    Kim IJ; Ku JL; Kang HC; Park JH; Yoon KA; Shin Y; Park HW; Jang SG; Lim SK; Han SY; Shin YK; Lee MR; Jeong SY; Shin HR; Lee JS; Kim WH; Park JG
    Hum Genet; 2004 Nov; 115(6):498-503. PubMed ID: 15449173
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH.
    Sieber OM; Lipton L; Crabtree M; Heinimann K; Fidalgo P; Phillips RK; Bisgaard ML; Orntoft TF; Aaltonen LA; Hodgson SV; Thomas HJ; Tomlinson IP
    N Engl J Med; 2003 Feb; 348(9):791-9. PubMed ID: 12606733
    [TBL] [Abstract][Full Text] [Related]  

  • 3. MYH, OGG1, MTH1, and APC alterations involved in the colorectal tumorigenesis of Korean patients with multiple adenomas.
    Kim JC; Ka IH; Lee YM; Koo KH; Kim HC; Yu CS; Jang SJ; Kim YS; Lee HI; Lee KH
    Virchows Arch; 2007 Mar; 450(3):311-9. PubMed ID: 17252231
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis.
    Mur P; Jemth AS; Bevc L; Amaral N; Navarro M; Valdés-Mas R; Pons T; Aiza G; Urioste M; Valencia A; Lázaro C; Moreno V; Puente XS; Stenmark P; Warpman-Berglund U; Capellá G; Helleday T; Valle L
    Hum Mutat; 2018 Sep; 39(9):1214-1225. PubMed ID: 29900613
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Germline mutations but not somatic changes at the MYH locus contribute to the pathogenesis of unselected colorectal cancers.
    Halford SE; Rowan AJ; Lipton L; Sieber OM; Pack K; Thomas HJ; Hodgson SV; Bodmer WF; Tomlinson IP
    Am J Pathol; 2003 May; 162(5):1545-8. PubMed ID: 12707038
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of the oxidative damage repair genes NUDT1, OGG1, and MUTYH in patients from mismatch repair proficient HNPCC families (MSS-HNPCC).
    Garre P; Briceño V; Xicola RM; Doyle BJ; de la Hoya M; Sanz J; Llovet P; Pescador P; Puente J; Díaz-Rubio E; Llor X; Caldés T
    Clin Cancer Res; 2011 Apr; 17(7):1701-12. PubMed ID: 21355073
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Analysis of somatic molecular changes, clinicopathological features, family history, and germline mutations in colorectal cancer families: evidence for efficient diagnosis of HNPCC and for the existence of distinct groups of non-HNPCC families.
    Johnson V; Lipton LR; Cummings C; Eftekhar Sadat AT; Izatt L; Hodgson SV; Talbot IC; Thomas HJ; Silver AJ; Tomlinson IP
    J Med Genet; 2005 Oct; 42(10):756-62. PubMed ID: 15788729
    [TBL] [Abstract][Full Text] [Related]  

  • 8. First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genes.
    Morak M; Massdorf T; Sykora H; Kerscher M; Holinski-Feder E
    Eur J Cancer; 2011 May; 47(7):1046-55. PubMed ID: 21195604
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exon 3 beta-catenin mutations are specifically associated with colorectal carcinomas in hereditary non-polyposis colorectal cancer syndrome.
    Johnson V; Volikos E; Halford SE; Eftekhar Sadat ET; Popat S; Talbot I; Truninger K; Martin J; Jass J; Houlston R; Atkin W; Tomlinson IP; Silver AR
    Gut; 2005 Feb; 54(2):264-7. PubMed ID: 15647192
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas.
    Gismondi V; Meta M; Bonelli L; Radice P; Sala P; Bertario L; Viel A; Fornasarig M; Arrigoni A; Gentile M; Ponz de Leon M; Anselmi L; Mareni C; Bruzzi P; Varesco L
    Int J Cancer; 2004 May; 109(5):680-4. PubMed ID: 14999774
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prevalence of MYH germline mutations in Swiss APC mutation-negative polyposis patients.
    Russell AM; Zhang J; Luz J; Hutter P; Chappuis PO; Berthod CR; Maillet P; Mueller H; Heinimann K
    Int J Cancer; 2006 Apr; 118(8):1937-40. PubMed ID: 16287072
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Role of inherited defects of MYH in the development of sporadic colorectal cancer.
    Kambara T; Whitehall VL; Spring KJ; Barker MA; Arnold S; Wynter CV; Matsubara N; Tanaka N; Young JP; Leggett BA; Jass JR
    Genes Chromosomes Cancer; 2004 May; 40(1):1-9. PubMed ID: 15034862
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk.
    Croitoru ME; Cleary SP; Di Nicola N; Manno M; Selander T; Aronson M; Redston M; Cotterchio M; Knight J; Gryfe R; Gallinger S
    J Natl Cancer Inst; 2004 Nov; 96(21):1631-4. PubMed ID: 15523092
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutational analysis of the transforming growth factor beta receptor type II gene in hereditary nonpolyposis colorectal cancer and early-onset colorectal cancer patients.
    Shin KH; Park YJ; Park JG
    Clin Cancer Res; 2000 Feb; 6(2):536-40. PubMed ID: 10690536
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Analysis of K-ras, APC, and beta-catenin in aberrant crypt foci in sporadic adenoma, cancer, and familial adenomatous polyposis.
    Takayama T; Ohi M; Hayashi T; Miyanishi K; Nobuoka A; Nakajima T; Satoh T; Takimoto R; Kato J; Sakamaki S; Niitsu Y
    Gastroenterology; 2001 Sep; 121(3):599-611. PubMed ID: 11522744
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic investigation of DNA-repair pathway genes PMS2, MLH1, MSH2, MSH6, MUTYH, OGG1 and MTH1 in sporadic colon cancer.
    Schafmayer C; Buch S; Egberts JH; Franke A; Brosch M; El Sharawy A; Conring M; Koschnick M; Schwiedernoch S; Katalinic A; Kremer B; Fölsch UR; Krawczak M; Fändrich F; Schreiber S; Tepel J; Hampe J
    Int J Cancer; 2007 Aug; 121(3):555-8. PubMed ID: 17417778
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Investigation of pathogenic mechanisms in multiple colorectal adenoma patients without germline APC or MYH/MUTYH mutations.
    Thirlwell C; Howarth KM; Segditsas S; Guerra G; Thomas HJ; Phillips RK; Talbot IC; Gorman M; Novelli MR; Sieber OM; Tomlinson IP
    Br J Cancer; 2007 Jun; 96(11):1729-34. PubMed ID: 17505512
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; Wynter C; Whitehall V; Karamatic R; George J; Goldblatt J; Walpole I; Robin SA; Borten MM; Stitz R; Searle J; McKeone D; Fraser L; Purdie DR; Podger K; Price R; Buttenshaw R; Walsh MD; Barker M; Leggett BA; Jass JR
    Am J Pathol; 2001 Dec; 159(6):2107-16. PubMed ID: 11733361
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Both BRAF and KRAS mutations are rare in colorectal carcinomas from patients with hereditary nonpolyposis colorectal cancer.
    Miyaki M; Iijima T; Yamaguchi T; Kadofuku T; Funata N; Mori T
    Cancer Lett; 2004 Jul; 211(1):105-9. PubMed ID: 15194222
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic predisposition to colorectal cancer: new pieces in the pediatric puzzle.
    Durno CA; Gallinger S
    J Pediatr Gastroenterol Nutr; 2006 Jul; 43(1):5-15. PubMed ID: 16819371
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 28.