346 related articles for article (PubMed ID: 29446530)
21. Beta-catenin accumulation and mutation of the CTNNB1 gene in hepatoblastoma.
Bläker H; Hofmann WJ; Rieker RJ; Penzel R; Graf M; Otto HF
Genes Chromosomes Cancer; 1999 Aug; 25(4):399-402. PubMed ID: 10398436
[TBL] [Abstract][Full Text] [Related]
22. Germline APC mutations in hepatoblastoma.
Yang A; Sisson R; Gupta A; Tiao G; Geller JI
Pediatr Blood Cancer; 2018 Apr; 65(4):. PubMed ID: 29251405
[TBL] [Abstract][Full Text] [Related]
23. A novel pathogenic large germline deletion in adenomatous polyposis coli gene in a Chinese family with familial adenomatous polyposis.
Zhang Z; Liang S; Huang H; Wang D; Zhang X; Wu J; Chen H; Wang Y; Rong T; Zhou Y; Banerjee S
Oncotarget; 2016 Aug; 7(31):50392-50400. PubMed ID: 27391059
[TBL] [Abstract][Full Text] [Related]
24. A subset of cranial fasciitis is associated with dysregulation of the Wnt/beta-catenin pathway.
Rakheja D; Cunningham JC; Mitui M; Patel AS; Tomlinson GE; Weinberg AG
Mod Pathol; 2008 Nov; 21(11):1330-6. PubMed ID: 18587328
[TBL] [Abstract][Full Text] [Related]
25. Two subtypes of colorectal tumor with distinct molecular features in familial adenomatous polyposis.
Takane K; Matsusaka K; Ota S; Fukuyo M; Yue Y; Nishimura M; Sakai E; Matsushita K; Miyauchi H; Aburatani H; Nakatani Y; Takayama T; Matsubara H; Akagi K; Kaneda A
Oncotarget; 2016 Dec; 7(51):84003-84016. PubMed ID: 27563825
[TBL] [Abstract][Full Text] [Related]
26. Childhood hepatoblastomas frequently carry a mutated degradation targeting box of the beta-catenin gene.
Koch A; Denkhaus D; Albrecht S; Leuschner I; von Schweinitz D; Pietsch T
Cancer Res; 1999 Jan; 59(2):269-73. PubMed ID: 9927029
[TBL] [Abstract][Full Text] [Related]
27. Sporadic childhood hepatoblastomas show activation of beta-catenin, mismatch repair defects and p53 mutations.
Curia MC; Zuckermann M; De Lellis L; Catalano T; Lattanzio R; Aceto G; Veschi S; Cama A; Otte JB; Piantelli M; Mariani-Costantini R; Cetta F; Battista P
Mod Pathol; 2008 Jan; 21(1):7-14. PubMed ID: 17962810
[TBL] [Abstract][Full Text] [Related]
28. Multifocality in a Patient with Cribriform-Morular Variant of Papillary Thyroid Carcinoma Is an Important Clue for the Diagnosis of Familial Adenomatous Polyposis.
Park J; Kim JW; Park H; Park SY; Kim TH; Kim SW; Oh YL; Chung JH
Thyroid; 2019 Nov; 29(11):1606-1614. PubMed ID: 31469036
[No Abstract] [Full Text] [Related]
29. Gardner fibroma: a clinicopathologic and immunohistochemical analysis of 45 patients with 57 fibromas.
Coffin CM; Hornick JL; Zhou H; Fletcher CD
Am J Surg Pathol; 2007 Mar; 31(3):410-6. PubMed ID: 17325483
[TBL] [Abstract][Full Text] [Related]
30. Multifocal hepatic neoplasia in 3 children with APC gene mutation.
Gupta A; Sheridan RM; Towbin A; Geller JI; Tiao G; Bove KE
Am J Surg Pathol; 2013 Jul; 37(7):1058-66. PubMed ID: 23715166
[TBL] [Abstract][Full Text] [Related]
31. Human microRNA expression in sporadic and FAP-associated desmoid tumors and correlation with beta-catenin mutations.
Cavallini A; Rotelli MT; Lippolis C; Piscitelli D; Digennaro R; Covelli C; Carella N; Accetturo M; Altomare DF
Oncotarget; 2017 Jun; 8(26):41866-41875. PubMed ID: 28418912
[TBL] [Abstract][Full Text] [Related]
32. Germline APC mutations are not commonly seen in children with sporadic hepatoblastoma.
Harvey J; Clark S; Hyer W; Hadzic N; Tomlinson I; Hinds R
J Pediatr Gastroenterol Nutr; 2008 Nov; 47(5):675-7. PubMed ID: 18955873
[TBL] [Abstract][Full Text] [Related]
33. Identification of previously unrecognized FAP in children with Gardner fibroma.
Vieira J; Pinto C; Afonso M; do Bom Sucesso M; Lopes P; Pinheiro M; Veiga I; Henrique R; Teixeira MR
Eur J Hum Genet; 2015 May; 23(5):715-8. PubMed ID: 25074465
[TBL] [Abstract][Full Text] [Related]
34. Genetic Counselor Practices Involving Pediatric Patients with FAP: an Investigation of their Self-Reported Strategies for Genetic Testing and Hepatoblastoma Screening.
Lawson CE; Attard TM; Dai H; Septer S
J Genet Couns; 2017 Jun; 26(3):586-593. PubMed ID: 27913912
[TBL] [Abstract][Full Text] [Related]
35. Pediatric craniopharyngioma in association with familial adenomatous polyposis.
Dahl NA; Pratt D; Camelo-Piragua S; Kumar-Sinha C; Mody RJ; Septer S; Hankinson TC; Chinnaiyan AM; Koschmann C; Hoffman L
Fam Cancer; 2019 Jul; 18(3):327-330. PubMed ID: 30919136
[TBL] [Abstract][Full Text] [Related]
36. The spectrum of APC mutations in children with hepatoblastoma from familial adenomatous polyposis kindreds.
Hirschman BA; Pollock BH; Tomlinson GE
J Pediatr; 2005 Aug; 147(2):263-6. PubMed ID: 16126064
[TBL] [Abstract][Full Text] [Related]
37. Oncogenic KRAS is not necessary for Wnt signalling activation in APC-associated FAP adenomas.
Obrador-Hevia A; Chin SF; González S; Rees J; Vilardell F; Greenson JK; Cordero D; Moreno V; Caldas C; Capellá G
J Pathol; 2010 May; 221(1):57-67. PubMed ID: 20196079
[TBL] [Abstract][Full Text] [Related]
38. Activation of beta-catenin in epithelial and mesenchymal hepatoblastomas.
Wei Y; Fabre M; Branchereau S; Gauthier F; Perilongo G; Buendia MA
Oncogene; 2000 Jan; 19(4):498-504. PubMed ID: 10698519
[TBL] [Abstract][Full Text] [Related]
39. Barrett's esophagus in the patients with familial adenomatous polyposis.
Gatalica Z; Chen M; Snyder C; Mittal S; Lynch HT
Fam Cancer; 2014 Jun; 13(2):213-7. PubMed ID: 23771323
[TBL] [Abstract][Full Text] [Related]
40. A novel AXIN2 germline variant associated with attenuated FAP without signs of oligondontia or ectodermal dysplasia.
Rivera B; Perea J; Sánchez E; Villapún M; Sánchez-Tomé E; Mercadillo F; Robledo M; Benítez J; Urioste M
Eur J Hum Genet; 2014 Mar; 22(3):423-6. PubMed ID: 23838596
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
