BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 15375702)

  • 1. Association of HNPCC and endometrial cancers.
    Banno K; Susumu N; Yanokura M; Hirao T; Iwata T; Hirasawa A; Aoki D; Sugano K; Nozawa S
    Int J Clin Oncol; 2004 Aug; 9(4):262-9. PubMed ID: 15375702
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Refining the Amsterdam Criteria and Bethesda Guidelines: testing algorithms for the prediction of mismatch repair mutation status in the familial cancer clinic.
    Lipton LR; Johnson V; Cummings C; Fisher S; Risby P; Eftekhar Sadat AT; Cranston T; Izatt L; Sasieni P; Hodgson SV; Thomas HJ; Tomlinson IP
    J Clin Oncol; 2004 Dec; 22(24):4934-43. PubMed ID: 15611508
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Women with synchronous primary cancers of the endometrium and ovary: do they have Lynch syndrome?
    Soliman PT; Broaddus RR; Schmeler KM; Daniels MS; Gonzalez D; Slomovitz BM; Gershenson DM; Lu KH
    J Clin Oncol; 2005 Dec; 23(36):9344-50. PubMed ID: 16361634
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients.
    de Leeuw WJ; Dierssen J; Vasen HF; Wijnen JT; Kenter GG; Meijers-Heijboer H; Brocker-Vriends A; Stormorken A; Moller P; Menko F; Cornelisse CJ; Morreau H
    J Pathol; 2000 Nov; 192(3):328-35. PubMed ID: 11054716
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular epidemiological and mutational analysis of DNA mismatch repair (MMR) genes in endometrial cancer patients with HNPCC-associated familial predisposition to cancer.
    Hirai Y; Banno K; Suzuki M; Ichikawa Y; Udagawa Y; Sugano K; Miki Y
    Cancer Sci; 2008 Sep; 99(9):1715-9. PubMed ID: 18624996
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular analysis of endometrial hyperplasia in HNPCC-suspicious patients may predict progression to endometrial carcinoma.
    Sutter C; Dallenbach-Hellweg G; Schmidt D; Baehring J; Bielau S; von Knebel Doeberitz M; Gebert J
    Int J Gynecol Pathol; 2004 Jan; 23(1):18-25. PubMed ID: 14668545
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Gynecologic manifestations of hereditary nonpolyposis colorectal cancer. From inherited to sporadic disease.
    Taylor N; Mutch DG
    Oncology (Williston Park); 2006 Jan; 20(1):85-94; discussion 94-6, 100. PubMed ID: 16572595
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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 MM; Kauff ND; Hansen J; Kosarin K; Shia J; Soslow RA
    Am J Surg Pathol; 2009 Jun; 33(6):925-33. PubMed ID: 19238076
    [TBL] [Abstract][Full Text] [Related]  

  • 9. High frequency of microsatellite instability and loss of mismatch-repair protein expression in patients with double primary tumors of the endometrium and colorectum.
    Planck M; Rambech E; Möslein G; Müller W; Olsson H; Nilbert M
    Cancer; 2002 May; 94(9):2502-10. PubMed ID: 12015776
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Essential to discover hereditary colorectal and endometrial cancer. Mutations in "HNPCC individuals" can cause several different tumors].
    Nilbert M; Grönberg H; Lindblom A
    Lakartidningen; 2002 Aug; 99(34):3296-300. PubMed ID: 12362848
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Two cases of endometrial cancer meeting new clinical criteria for hereditary nonpolyposis colorectal cancer.
    Sagawa T; Yamada H; Yamamoto R; Sakuragi N; Fujimoto S
    Gynecol Oncol; 2000 Nov; 79(2):327-31. PubMed ID: 11063667
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two mismatch repair gene mutations found in a colon cancer patient--which one is pathogenic?
    Kariola R; Otway R; Lönnqvist KE; Raevaara TE; Macrae F; Vos YJ; Kohonen-Corish M; Hofstra RM; Nyström-Lahti M
    Hum Genet; 2003 Feb; 112(2):105-9. PubMed ID: 12522549
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic alterations and MSI status in primary, synchronous, and metachronous tumors in a family with hereditary nonpolyposis colorectal cancer (HNPCC).
    González-Aguilera JJ; Nejda N; Fernández FJ; Medina V; González-Hermoso F; Barrios Y; Moreno Azcoita M; Fernández-Peralta AM
    Am J Clin Oncol; 2003 Aug; 26(4):386-91. PubMed ID: 12902892
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The genetics of HNPCC: application to diagnosis and screening.
    Abdel-Rahman WM; Mecklin JP; Peltomäki P
    Crit Rev Oncol Hematol; 2006 Jun; 58(3):208-20. PubMed ID: 16434208
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas].
    Olschwang S; Bonaïti C; Feingold J; Frébourg T; Grandjouan S; Lasset C; Laurent-Puig P; Lecuru F; Millat B; Sobol H; Thomas G; Eisinger F
    Bull Cancer; 2004 Apr; 91(4):303-15. PubMed ID: 15242312
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel missense germline mutation in exon 2 of the hMSH2 gene in a HNPCC family from Southern Italy.
    Baudi F; Fersini G; Lavecchia A; Terracciano R; Leone F; Quaresima B; Faniello MC; De Paola L; Doldo P; Cuda G; Costanzo F; Venuta S
    Cancer Lett; 2005 Jun; 223(2):285-91. PubMed ID: 15896463
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Microsatellite instability in early onset and familial colorectal cancer.
    Brassett C; Joyce JA; Froggatt NJ; Williams G; Furniss D; Walsh S; Miller R; Evans DG; Maher ER
    J Med Genet; 1996 Dec; 33(12):981-5. PubMed ID: 9004127
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [From gene to disease; from DNA 'mismatch' repair genes to hereditary non-polyposis colorectal carcinoma].
    Wijnen JT; Morreau H; Vasen HF
    Ned Tijdschr Geneeskd; 2001 Apr; 145(16):780-2. PubMed ID: 11346916
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Multiple epithelial and nonepithelial tumors in hereditary nonpolyposis colorectal cancer: characterization of germline and somatic mutations of the MSH2 gene and heterogeneity of replication error phenotypes.
    Huang RL; Chao CF; Ding DC; Yu CP; Chang CC; Lai HC; Yu MH; Liu HS; Chu TY
    Cancer Genet Cytogenet; 2004 Sep; 153(2):108-14. PubMed ID: 15350299
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genomic DNA-based hMSH2 and hMLH1 mutation screening in 32 Eastern United States hereditary nonpolyposis colorectal cancer pedigrees.
    Weber TK; Conlon W; Petrelli NJ; Rodriguez-Bigas M; Keitz B; Pazik J; Farrell C; O'Malley L; Oshalim M; Abdo M; Anderson G; Stoler D; Yandell D
    Cancer Res; 1997 Sep; 57(17):3798-803. PubMed ID: 9288790
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.