141 related articles for article (PubMed ID: 38467732)
21. Molecular analysis of the APC gene in Sicilian patients with familial adenomatous polyposis (F.A.P.).
Russo A; Catania VE; Cavallaro A; Ficili B; Lanteri E; Tralongo P; Cappellani A; Randazzo C; Cammisuli F; Madeddu R; Trichilo V; Libra M; Travali S
Int J Surg; 2014; 12 Suppl 2():S125-S129. PubMed ID: 25183641
[TBL] [Abstract][Full Text] [Related]
22. A novel large germ line deletion in adenomatous polyposis coli (APC) gene associated with familial adenomatous polyposis.
Pouya F; Mojtabanezhad Shariatpanahi A; Ghaffarzadegan K; Tabatabaee Yazdi SA; Golmohammadzadeh H; Soltani G; Aminian Toosi K; Kerachian MA
Mol Genet Genomic Med; 2018 Nov; 6(6):1031-1040. PubMed ID: 30259713
[TBL] [Abstract][Full Text] [Related]
23. Gastric polyposis and desmoid tumours as a new familial adenomatous polyposis clinical variant associated with
Disciglio V; Fasano C; Cariola F; Forte G; Grossi V; Sanese P; Lepore Signorile M; Resta N; Lotesoriere C; Stella A; Lolli I; Simone C
J Med Genet; 2020 May; 57(5):356-360. PubMed ID: 31591141
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Use of sanger and next-generation sequencing to screen for mosaic and intronic APC variants in unexplained colorectal polyposis patients.
Elsayed FA; Tops CMJ; Nielsen M; Morreau H; Hes FJ; van Wezel T
Fam Cancer; 2022 Jan; 21(1):79-83. PubMed ID: 33683519
[TBL] [Abstract][Full Text] [Related]
26. A novel pathogenic germline mutation in the adenomatous polyposis coli gene in a Chinese family with familial adenomatous coli.
Jiang SS; Li JJ; Li Y; He LJ; Wang QJ; Weng DS; Pan K; Liu Q; Zhao JJ; Pan QZ; Zhang XF; Tang Y; Chen CL; Zhang HX; Xu GL; Zeng YX; Xia JC
Oncotarget; 2015 Sep; 6(29):27267-74. PubMed ID: 26311738
[TBL] [Abstract][Full Text] [Related]
27. Detection of a heterozygous germline APC mutation in a three-generation family with familial adenomatous polyposis using targeted massive parallel sequencing in Vietnam.
Giang H; Nguyen VT; Nguyen SD; Nguyen HP; Vo BT; Nguyen TM; Nguyen NH; Truong KD; Do TT; Phan MD; Nguyen HN
BMC Med Genet; 2018 Oct; 19(1):188. PubMed ID: 30340471
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Colon cancer prevention by detection of APC gene mutation in a family with attenuated familial adenomatous polyposis.
Poovorawan K; Suksawatamnuay S; Sahakitrungruang C; Treeprasertsuk S; Wisedopas N; Komolmit P; Poovorawan Y
Asian Pac J Cancer Prev; 2012; 13(10):5101-4. PubMed ID: 23244118
[TBL] [Abstract][Full Text] [Related]
30. Clinical characterization and mutation spectrum in Hispanic families with adenomatous polyposis syndromes.
Cruz-Correa M; Diaz-Algorri Y; Mendez V; Vazquez PJ; Lozada ME; Freyre K; Lathroum L; Gonzalez-Pons M; Hernandez-Marrero J; Giardiello F; Rodriguez-Quilichini S
Fam Cancer; 2013 Sep; 12(3):555-62. PubMed ID: 23460355
[TBL] [Abstract][Full Text] [Related]
31. APC transcription studies and molecular diagnosis of familial adenomatous polyposis.
Short E; Thomas LE; Davies A; Bolton A; Maynard J; Giles P; Mort M; Consoli C; Egner I; Jundi H; Sampson JR
Eur J Hum Genet; 2020 Jan; 28(1):118-121. PubMed ID: 31383941
[TBL] [Abstract][Full Text] [Related]
32. Thyroid Carcinomas That Occur in Familial Adenomatous Polyposis Patients Recurrently Harbor Somatic Variants in
Nieminen TT; Walker CJ; Olkinuora A; Genutis LK; O'Malley M; Wakely PE; LaGuardia L; Koskenvuo L; Arola J; Lepistö AH; Brock P; Yilmaz AS; Eisfeld AK; Church JM; Peltomäki P; de la Chapelle A
Thyroid; 2020 Mar; 30(3):380-388. PubMed ID: 32024448
[No Abstract] [Full Text] [Related]
33. Variant profiling of colorectal adenomas from three patients of two families with MSH3-related adenomatous polyposis.
Perne C; Peters S; Cartolano M; Horpaopan S; Grimm C; Altmüller J; Sommer AK; Hillmer AM; Thiele H; Odenthal M; Möslein G; Adam R; Sivalingam S; Kirfel J; Schweiger MR; Peifer M; Spier I; Aretz S
PLoS One; 2021; 16(11):e0259185. PubMed ID: 34843512
[TBL] [Abstract][Full Text] [Related]
34. Correlations between mutation site in APC and phenotype of familial adenomatous polyposis (FAP): a review of the literature.
Nieuwenhuis MH; Vasen HF
Crit Rev Oncol Hematol; 2007 Feb; 61(2):153-61. PubMed ID: 17064931
[TBL] [Abstract][Full Text] [Related]
35. APC or MUTYH mutations account for the majority of clinically well-characterized families with FAP and AFAP phenotype and patients with more than 30 adenomas.
Filipe B; Baltazar C; Albuquerque C; Fragoso S; Lage P; Vitoriano I; Mão de Ferro S; Claro I; Rodrigues P; Fidalgo P; Chaves P; Cravo M; Nobre Leitão C
Clin Genet; 2009 Sep; 76(3):242-55. PubMed ID: 19793053
[TBL] [Abstract][Full Text] [Related]
36. Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers.
Ghorbanoghli Z; Nieuwenhuis MH; Houwing-Duistermaat JJ; Jagmohan-Changur S; Hes FJ; Tops CM; Wagner A; Aalfs CM; Verhoef S; Gómez García EB; Sijmons RH; Menko FH; Letteboer TG; Hoogerbrugge N; van Wezel T; Vasen HF; Wijnen JT
Fam Cancer; 2016 Oct; 15(4):563-70. PubMed ID: 26880076
[TBL] [Abstract][Full Text] [Related]
37. Resorting the function of the colorectal cancer gatekeeper adenomatous polyposis coli.
Kariv R; Caspi M; Fliss-Isakov N; Shorer Y; Shor Y; Rosner G; Brazowski E; Beer G; Cohen S; Rosin-Arbesfeld R
Int J Cancer; 2020 Feb; 146(4):1064-1074. PubMed ID: 31283021
[TBL] [Abstract][Full Text] [Related]
38. Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.
Rohlin A; Rambech E; Kvist A; Törngren T; Eiengård F; Lundstam U; Zagoras T; Gebre-Medhin S; Borg Å; Björk J; Nilbert M; Nordling M
Fam Cancer; 2017 Apr; 16(2):195-203. PubMed ID: 27696107
[TBL] [Abstract][Full Text] [Related]
39. Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases.
Spier I; Drichel D; Kerick M; Kirfel J; Horpaopan S; Laner A; Holzapfel S; Peters S; Adam R; Zhao B; Becker T; Lifton RP; Perner S; Hoffmann P; Kristiansen G; Timmermann B; Nöthen MM; Holinski-Feder E; Schweiger MR; Aretz S
J Med Genet; 2016 Mar; 53(3):172-9. PubMed ID: 26613750
[TBL] [Abstract][Full Text] [Related]
40. Singapore familial adenomatous polyposis (FAP) patients with classical adenomatous polyposis but undetectable APC mutations have accelerated cancer progression.
Cao X; Hong Y; Eu KW; Loi C; Cheah PY
Am J Gastroenterol; 2006 Dec; 101(12):2810-7. PubMed ID: 17026565
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]