238 related articles for article (PubMed ID: 24801760)
21. Clinical characterization and mutation spectrum in patients with familial adenomatous polyposis in China.
Li N; Kang Q; Yang L; Zhao XJ; Xue LJ; Wang X; Li AQ; Li CG; Sheng JQ
J Gastroenterol Hepatol; 2019 Sep; 34(9):1497-1503. PubMed ID: 31062380
[TBL] [Abstract][Full Text] [Related]
22. Exome sequencing of familial adenomatous polyposis-like individuals identifies both known and novel causative genes.
Xavier A; Scott RJ; Talseth-Palmer B
Clin Genet; 2021 Oct; 100(4):478-483. PubMed ID: 34259353
[TBL] [Abstract][Full Text] [Related]
23. The genetics of familial adenomatous polyposis (FAP) and MutYH-associated polyposis (MAP).
Claes K; Dahan K; Tejpar S; De Paepe A; Bonduelle M; Abramowicz M; Verellen C; Franchimont D; Van Cutsem E; Kartheuser A
Acta Gastroenterol Belg; 2011 Sep; 74(3):421-6. PubMed ID: 22103048
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Colorectal Adenomatous Polyposis: Heterogeneity of Susceptibility Gene Mutations and Phenotypes in a Cohort of Italian Patients.
Marabelli M; Molinaro V; Abou Khouzam R; Berrino E; Panero M; Balsamo A; Venesio T; Ranzani GN
Genet Test Mol Biomarkers; 2016 Dec; 20(12):777-785. PubMed ID: 27705013
[TBL] [Abstract][Full Text] [Related]
26. The first mutations in the MYH gene reported in Moroccan colon cancer patients.
Laarabi FZ; Cherkaoui Jaouad I; Baert-Desurmont S; Ouldim K; Ibrahimi A; Kanouni N; Frebourg T; Sefiani A
Gene; 2012 Mar; 496(1):55-8. PubMed ID: 22266422
[TBL] [Abstract][Full Text] [Related]
27. Burden and Profile of Somatic Mutation in Duodenal Adenomas from Patients with Familial Adenomatous- and
Thomas LE; Hurley JJ; Meuser E; Jose S; Ashelford KE; Mort M; Idziaszczyk S; Maynard J; Brito HL; Harry M; Walters A; Raja M; Walton SJ; Dolwani S; Williams GT; Morgan M; Moorghen M; Clark SK; Sampson JR
Clin Cancer Res; 2017 Nov; 23(21):6721-6732. PubMed ID: 28790112
[No Abstract] [Full Text] [Related]
28. Novel mutations and phenotypic associations identified through APC, MUTYH, NTHL1, POLD1, POLE gene analysis in Indian Familial Adenomatous Polyposis cohort.
Khan N; Lipsa A; Arunachal G; Ramadwar M; Sarin R
Sci Rep; 2017 May; 7(1):2214. PubMed ID: 28533537
[TBL] [Abstract][Full Text] [Related]
29. NTHL1 biallelic mutations seldom cause colorectal cancer, serrated polyposis or a multi-tumor phenotype, in absence of colorectal adenomas.
Belhadj S; Quintana I; Mur P; Munoz-Torres PM; Alonso MH; Navarro M; Terradas M; Piñol V; Brunet J; Moreno V; Lázaro C; Capellá G; Valle L
Sci Rep; 2019 Jun; 9(1):9020. PubMed ID: 31227763
[TBL] [Abstract][Full Text] [Related]
30. The Diagnostic Yield of Genetic Testing in Patients With Multiple Colorectal Adenomas: A Specialist Center Cohort Study.
Mak S; Alexander JL; Clark SK; Hawkins M; Cuthill V; Latchford A; Monahan KJ
Clin Transl Gastroenterol; 2024 Jan; 15(1):e00645. PubMed ID: 37856205
[TBL] [Abstract][Full Text] [Related]
31. Adenoma development in familial adenomatous polyposis and MUTYH-associated polyposis: somatic landscape and driver genes.
Rashid M; Fischer A; Wilson CH; Tiffen J; Rust AG; Stevens P; Idziaszczyk S; Maynard J; Williams GT; Mustonen V; Sampson JR; Adams DJ
J Pathol; 2016 Jan; 238(1):98-108. PubMed ID: 26414517
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Increased risk for colorectal adenomas and cancer in mono-allelic MUTYH mutation carriers: results from a cohort of North-African Jews.
Rosner G; Bercovich D; Daniel YE; Strul H; Fliss-Isakov N; Ben-Yehoiada M; Santo E; Halpern Z; Kariv R
Fam Cancer; 2015 Sep; 14(3):427-36. PubMed ID: 25822476
[TBL] [Abstract][Full Text] [Related]
34. Multiple rare nonsynonymous variants in the adenomatous polyposis coli gene predispose to colorectal adenomas.
Azzopardi D; Dallosso AR; Eliason K; Hendrickson BC; Jones N; Rawstorne E; Colley J; Moskvina V; Frye C; Sampson JR; Wenstrup R; Scholl T; Cheadle JP
Cancer Res; 2008 Jan; 68(2):358-63. PubMed ID: 18199528
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3.
Dallosso AR; Dolwani S; Jones N; Jones S; Colley J; Maynard J; Idziaszczyk S; Humphreys V; Arnold J; Donaldson A; Eccles D; Ellis A; Evans DG; Frayling IM; Hes FJ; Houlston RS; Maher ER; Nielsen M; Parry S; Tyler E; Moskvina V; Cheadle JP; Sampson JR
Gut; 2008 Sep; 57(9):1252-5. PubMed ID: 18515411
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Similar colorectal cancer risk in patients with monoallelic and biallelic mutations in the MYH gene identified in a population with adenomatous polyposis.
Olschwang S; Blanché H; de Moncuit C; Thomas G
Genet Test; 2007; 11(3):315-20. PubMed ID: 17949294
[TBL] [Abstract][Full Text] [Related]
39. Integrated genotype-phenotype analysis of familial adenomatous polyposis-associated hepatocellular adenomas.
Tóth M; Kirchner M; Longerich T; Stenzinger A; Schirmacher P
Virchows Arch; 2024 Apr; 484(4):587-595. PubMed ID: 37872280
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
