189 related articles for article (PubMed ID: 12173026)
1. Pathogenic mutations and rare variants of the APC gene identified in 75 Belgian patients with familial adenomatous polyposis by fluorescent enzymatic mutation detection (EMD).
Michils G; Tejpar S; Fryns JP; Legius E; Van Cutsem E; Cassiman JJ; Matthijs G
Eur J Hum Genet; 2002 Sep; 10(9):505-10. PubMed ID: 12173026
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Analysis of germline mutations in the APC gene in familial adenomatous polyposis patients.
Liu XR; Shan XN; Friedl W; Uhlhaas S; Propping P; Wang YP
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):261-4. PubMed ID: 15952110
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Characterization of two novel adenomatous polyposis coli (APC) gene mutations in patients with familial adenomatous polyposis (FAP).
Bapat B; Berk T; Mitri A; Cohen Z; Gallinger S; Stern H
Hum Mutat; 1994; 4(4):253-6. PubMed ID: 7866403
[TBL] [Abstract][Full Text] [Related]
7. Implication of adenomatous polyposis coli and MUTYH mutations in familial colorectal polyposis.
De Rosa M; Galatola M; Borriello S; Duraturo F; Masone S; Izzo P
Dis Colon Rectum; 2009 Feb; 52(2):268-74. PubMed ID: 19279422
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. APC germline mutations identified in Czech patients with familial adenomatous polyposis.
Kohoutová M; Stekrová J; Jirásek V; Kapras J
Hum Mutat; 2002 Apr; 19(4):460-1. PubMed ID: 11933206
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. First genotype characterization of Argentinean FAP patients: identification of 14 novel APC mutations.
De Rosa M; Dourisboure RJ; Morelli G; Graziano A; Gutiérrez A; Thibodeau S; Halling K; Avila KC; Duraturo F; Podesta EJ; Izzo P; Solano AR
Hum Mutat; 2004 May; 23(5):523-4. PubMed ID: 15108288
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Nontruncating APC germ-line mutations and mismatch repair deficiency play a minor role in APC mutation-negative polyposis.
Heinimann K; Thompson A; Locher A; Furlanetto T; Bader E; Wolf A; Meier R; Walter K; Bauerfeind P; Marra G; Müller H; Foernzler D; Dobbie Z
Cancer Res; 2001 Oct; 61(20):7616-22. PubMed ID: 11606402
[TBL] [Abstract][Full Text] [Related]
15. [Genetic diagnosis of familial adenomatous polyposis: detection of APC gene mutations based on an in vitro synthetized protein].
Albuquerque C; Fidalgo P; Chagas C; Suspiro A; Cravo M; Ramalho E; Leitão CN; Mira FC
Acta Med Port; 1998 Jan; 11(1):25-32. PubMed ID: 9580364
[TBL] [Abstract][Full Text] [Related]
16. Familial adenomatous polyposis: aberrant splicing due to missense or silent mutations in the APC gene.
Aretz S; Uhlhaas S; Sun Y; Pagenstecher C; Mangold E; Caspari R; Möslein G; Schulmann K; Propping P; Friedl W
Hum Mutat; 2004 Nov; 24(5):370-80. PubMed ID: 15459959
[TBL] [Abstract][Full Text] [Related]
17. Screening for mutations of the APC gene in 66 Italian familial adenomatous polyposis patients: evidence for phenotypic differences in cases with and without identified mutation.
Giarola M; Stagi L; Presciuttini S; Mondini P; Radice MT; Sala P; Pierotti MA; Bertario L; Radice P
Hum Mutat; 1999; 13(2):116-23. PubMed ID: 10094547
[TBL] [Abstract][Full Text] [Related]
18. Large deletions of the APC gene in 15% of mutation-negative patients with classical polyposis (FAP): a Belgian study.
Michils G; Tejpar S; Thoelen R; van Cutsem E; Vermeesch JR; Fryns JP; Legius E; Matthijs G
Hum Mutat; 2005 Feb; 25(2):125-34. PubMed ID: 15643602
[TBL] [Abstract][Full Text] [Related]
19. Somatic APC mosaicism: a frequent cause of familial adenomatous polyposis (FAP).
Aretz S; Stienen D; Friedrichs N; Stemmler S; Uhlhaas S; Rahner N; Propping P; Friedl W
Hum Mutat; 2007 Oct; 28(10):985-92. PubMed ID: 17486639
[TBL] [Abstract][Full Text] [Related]
20. Mutation spectrum of the APC gene in 83 Korean FAP families.
Kim DW; Kim IJ; Kang HC; Park HW; Shin Y; Park JH; Jang SG; Yoo BC; Lee MR; Hong CW; Park KJ; Oh NG; Kim NK; Sung MK; Lee BW; Kim YJ; Lee H; Park JG
Hum Mutat; 2005 Sep; 26(3):281. PubMed ID: 16088911
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
