BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

526 related articles for article (PubMed ID: 12584582)

  • 1. The most frequent APC mutations among Slovak familial adenomatous polyposis patients. Adenomatous polyposis coli.
    Zajac V; Kovác M; Kirchhoff T; Stevurková V; Tomka M
    Neoplasma; 2002; 49(6):356-61. PubMed ID: 12584582
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of APC exon 15 mutations in families suspected of familial adenomatous polyposis (FAP).
    Kirchhoff T; Zajac V; Krizan P; Repiská V; Stevurková V; Friedl W
    Folia Biol (Praha); 1997; 43(5):203-9. PubMed ID: 9595262
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis. Novel criteria of assessment and correlations with constitutional adenomatous polyposis coli gene mutations.
    Valanzano R; Cama A; Volpe R; Curia MC; Mencucci R; Palmirotta R; Battista P; Ficari F; Mariani-Costantini R; Tonelli F
    Cancer; 1996 Dec; 78(11):2400-10. PubMed ID: 8941012
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characterization of APC exon 15 germ-line mutation in FAP family with severe phenotype showing extracolonic symptoms.
    Kirchhoff T; Kulcsár L; Tomka M; Stevurková V; Zajac V
    Neoplasma; 1999; 46(5):290-4. PubMed ID: 10665844
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel mutations in the APC gene and clinical features in Swedish patients with polyposis coli.
    Nordling M; Engwall Y; Wahlström J; Wiklund L; Eriksson MA; Gustavsson B; Fasth S; Larsson PA; Martinsson T
    Anticancer Res; 1997; 17(6D):4275-80. PubMed ID: 9494520
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The combination of heteroduplex analysis and protein truncation test for exact detection of the APC gene mutations.
    Tomka M; Kirchhoff T; Kulcsár L; Stevurková V; Zajac V
    Neoplasma; 1998; 45(6):345-8. PubMed ID: 10210106
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutational screening of the APC gene in Chilean families with familial adenomatous polyposis: nine novel truncating mutations.
    De la Fuente MK; Alvarez KP; Letelier AJ; Bellolio F; Acuña ML; León FS; Pinto E; Carvallo P; López-Köstner F
    Dis Colon Rectum; 2007 Dec; 50(12):2142-8. PubMed ID: 17963004
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The spectrum of the APC pathogenic mutations in Slovak FAP patients.
    Matelova L; Stevurkova V; Zajac V
    Neuro Endocrinol Lett; 2008 Oct; 29(5):653-7. PubMed ID: 18987576
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Detection of APC gene deletion by double competitive polymerase chain reaction in patients with familial adenomatous polyposis.
    Takahashi M; Kikuchi M; Ohkura N; Yaguchi H; Nagamura Y; Ohnami S; Ushiama M; Yoshida T; Sugano K; Iwama T; Kosugi S; Tsukada T
    Int J Oncol; 2006 Aug; 29(2):413-21. PubMed ID: 16820884
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rapid RT-PCR-based protein truncation test in the screening for 5' located mutations of the APC gene.
    Kraus C; Günther K; Vogler A; Hohenberger W; Pfeiffer RA; Ballhausen WG
    Mol Cell Probes; 1998 Jun; 12(3):143-7. PubMed ID: 9664575
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Detection of adenomatous polyposis coli gene mutations in 31 familial adenomatous polyposis families by using denaturing high performance liquid chromatography].
    Cai SR; Zhang SZ; Zheng S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Apr; 25(2):164-7. PubMed ID: 18393237
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Familial adenomatous polyposis coli in the Czech population. I. Detection of an additional 3 mutations out of a total of 7 in exon 15 of the APC gene].
    Jirásek V; Olschwang S; Boisson C; Janda J; Thomas G; Martásek P
    Cas Lek Cesk; 1997 Dec; 136(23):733-8. PubMed ID: 9476377
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Germline mutations of the APC gene in Korean familial adenomatous polyposis patients.
    Won YJ; Park KJ; Kwon HJ; Lee JH; Kim JH; Kim YJ; Chun SH; Han HJ; Park JG
    J Hum Genet; 1999; 44(2):103-8. PubMed ID: 10083733
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital hypertrophy of the retinal pigment epithelium and APC mutations in two Chinese families with familial adenomatous polyposis.
    Pang CP; Keung JW; Tang NL; Fan DS; Lau JW; Lam DS
    Eye (Lond); 2000 Feb; 14 ( Pt 1)():18-22. PubMed ID: 10755094
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation analysis of the adenomatous polyposis coli (APC) gene in northwest Spanish patients with familial adenomatous polyposis (FAP) and sporadic colorectal cancer.
    Ruiz-Ponte C; Vega A; Carracedo A; Barros F
    Hum Mutat; 2001 Oct; 18(4):355. PubMed ID: 11668620
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial adenomatous polyposis coli: five novel mutations in exon 15 of the adenomatous polyposis coli (APC) gene in Italian patients. Mutations in brief no. 225. Online.
    Scarano MI; De Rosa M; Panariello L; Carlomagno N; Riegler G; Rossi GB; Bucci L; Pesce G; Toni F; Renda A; Izzo P
    Hum Mutat; 1999; 13(3):256-7. PubMed ID: 10090483
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Somatic mutations of the adenomatous polyposis coli gene in gastroduodenal tumors from patients with familial adenomatous polyposis.
    Toyooka M; Konishi M; Kikuchi-Yanoshita R; Iwama T; Miyaki M
    Cancer Res; 1995 Jul; 55(14):3165-70. PubMed ID: 7606737
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical features and genotype-phenotype correlations in 41 Italian families with adenomatosis coli.
    Ponz de Leon M; Benatti P; Percesepe A; Cacciatore A; Sassatelli R; Bertoni G; Sabadini G; Varesco L; Gismondi V; Mareni C; Montera M; Di Gregorio C; Landi P; Roncucci L
    Ital J Gastroenterol Hepatol; 1999 Dec; 31(9):850-60. PubMed ID: 10669993
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular analysis of the APC gene in 105 Dutch kindreds with familial adenomatous polyposis: 67 germline mutations identified by DGGE, PTT, and southern analysis.
    van der Luijt RB; Khan PM; Vasen HF; Tops CM; van Leeuwen-Cornelisse IS; Wijnen JT; van der Klift HM; Plug RJ; Griffioen G; Fodde R
    Hum Mutat; 1997; 9(1):7-16. PubMed ID: 8990002
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients.
    Mihalatos M; Apessos A; Dauwerse H; Velissariou V; Psychias A; Koliopanos A; Petropoulos K; Triantafillidis JK; Danielidis I; Fountzilas G; Agnantis NJ; Nasioulas G
    BMC Cancer; 2005 Apr; 5():40. PubMed ID: 15833136
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 27.