216 related articles for article (PubMed ID: 14691304)
1. APC haploinsufficiency, but not CTNNB1 or CDH1 gene mutations, accounts for a fraction of familial adenomatous polyposis patients without APC truncating mutations.
Venesio T; Balsamo A; Rondo-Spaudo M; Varesco L; Risio M; Ranzani GN
Lab Invest; 2003 Dec; 83(12):1859-66. PubMed ID: 14691304
[TBL] [Abstract][Full Text] [Related]
2. Germline APC mutation on the beta-catenin binding site is associated with a decreased apoptotic level in colorectal adenomas.
Venesio T; Balsamo A; Scordamaglia A; Bertolaso M; Arrigoni A; Sprujevnik T; Rossini FP; Risio M
Mod Pathol; 2003 Jan; 16(1):57-65. PubMed ID: 12527714
[TBL] [Abstract][Full Text] [Related]
3. Analysis of somatic APC mutations in rare extracolonic tumors of patients with familial adenomatous polyposis coli.
Bläker H; Sutter C; Kadmon M; Otto HF; Von Knebel-Doeberitz M; Gebert J; Helmke BM
Genes Chromosomes Cancer; 2004 Oct; 41(2):93-8. PubMed ID: 15287021
[TBL] [Abstract][Full Text] [Related]
4. Germline mutations are frequent in the APC gene but absent in the beta-catenin gene in familial adenomatous polyposis patients.
Cao X; Eu KW; Seow-Choen F; Cheah PY
Genes Chromosomes Cancer; 1999 Aug; 25(4):396-8. PubMed ID: 10398435
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. High frequency of MYH gene mutations in a subset of patients with familial adenomatous polyposis.
Venesio T; Molatore S; Cattaneo F; Arrigoni A; Risio M; Ranzani GN
Gastroenterology; 2004 Jun; 126(7):1681-5. PubMed ID: 15188161
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Whole-gene APC deletions cause classical familial adenomatous polyposis, but not attenuated polyposis or "multiple" colorectal adenomas.
Sieber OM; Lamlum H; Crabtree MD; Rowan AJ; Barclay E; Lipton L; Hodgson S; Thomas HJ; Neale K; Phillips RK; Farrington SM; Dunlop MG; Mueller HJ; Bisgaard ML; Bulow S; Fidalgo P; Albuquerque C; Scarano MI; Bodmer W; Tomlinson IP; Heinimann K
Proc Natl Acad Sci U S A; 2002 Mar; 99(5):2954-8. PubMed ID: 11867715
[TBL] [Abstract][Full Text] [Related]
11. The type of somatic mutation at APC in familial adenomatous polyposis is determined by the site of the germline mutation: a new facet to Knudson's 'two-hit' hypothesis.
Lamlum H; Ilyas M; Rowan A; Clark S; Johnson V; Bell J; Frayling I; Efstathiou J; Pack K; Payne S; Roylance R; Gorman P; Sheer D; Neale K; Phillips R; Talbot I; Bodmer W; Tomlinson I
Nat Med; 1999 Sep; 5(9):1071-5. PubMed ID: 10470088
[TBL] [Abstract][Full Text] [Related]
12. Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP).
Ghadamyari F; Heidari MM; Zeinali S; Khatami M; Merat S; Bagherian H; Rejali L; Ghasemi F
J Clin Lab Anal; 2021 May; 35(5):e23768. PubMed ID: 33769591
[TBL] [Abstract][Full Text] [Related]
13. Inactivation of germline mutant APC alleles by attenuated somatic mutations: a molecular genetic mechanism for attenuated familial adenomatous polyposis.
Su LK; Barnes CJ; Yao W; Qi Y; Lynch PM; Steinbach G
Am J Hum Genet; 2000 Sep; 67(3):582-90. PubMed ID: 10924409
[TBL] [Abstract][Full Text] [Related]
14. Beta-catenin and adenomatous polyposis coli (APC) mutations in adenomas from hereditary non-polyposis colorectal cancer patients.
Akiyama Y; Nagasaki H; Yagi KO; Nomizu T; Yuasa Y
Cancer Lett; 2000 Sep; 157(2):185-91. PubMed ID: 10936679
[TBL] [Abstract][Full Text] [Related]
15. Adenomatous Polyposis Coli Gene Mutations in 22 Chinese Pedigrees with Familial Adenomatous Polyposis.
Wang D; Zhang Z; Li Y; Xu C; Yu Y; Li M; Chen C; Zhang X
Med Sci Monit; 2019 May; 25():3796-3803. PubMed ID: 31113927
[TBL] [Abstract][Full Text] [Related]
16. A novel pathogenic splice acceptor site germline mutation in intron 14 of the APC gene in a Chinese family with familial adenomatous polyposis.
Wang D; Liang S; Zhang Z; Zhao G; Hu Y; Liang S; Zhang X; Banerjee S
Oncotarget; 2017 Mar; 8(13):21327-21335. PubMed ID: 28423518
[TBL] [Abstract][Full Text] [Related]
17. APC mutation in the alternatively spliced region of exon 9 associated with late onset familial adenomatous polyposis.
van der Luijt RB; Vasen HF; Tops CM; Breukel C; Fodde R; Meera Khan P
Hum Genet; 1995 Dec; 96(6):705-10. PubMed ID: 8522331
[TBL] [Abstract][Full Text] [Related]
18. Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary.
Papp J; Kovacs ME; Matrai Z; Orosz E; Kásler M; Børresen-Dale AL; Olah E
Fam Cancer; 2016 Jan; 15(1):85-97. PubMed ID: 26446593
[TBL] [Abstract][Full Text] [Related]
19. Familial adenomatous polyposis: from bedside to benchside.
O'Sullivan MJ; McCarthy TV; Doyle CT
Am J Clin Pathol; 1998 May; 109(5):521-6. PubMed ID: 9576568
[TBL] [Abstract][Full Text] [Related]
20. Low frequency of AXIN2 mutations and high frequency of MUTYH mutations in patients with multiple polyposis.
Lejeune S; Guillemot F; Triboulet JP; Cattan S; Mouton C; ; Porchet N; Manouvrier S; Buisine MP
Hum Mutat; 2006 Oct; 27(10):1064. PubMed ID: 16941501
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]