187 related articles for article (PubMed ID: 35978432)
21. Brain tumors in individuals with familial adenomatous polyposis: a cancer registry experience and pooled case report analysis.
Attard TM; Giglio P; Koppula S; Snyder C; Lynch HT
Cancer; 2007 Feb; 109(4):761-6. PubMed ID: 17238184
[TBL] [Abstract][Full Text] [Related]
22. Cribriform variant papillary thyroid cancer: a characteristic of familial adenomatous polyposis.
Fenton PA; Clarke SE; Owen W; Hibbert J; Hodgson SV
Thyroid; 2001 Feb; 11(2):193-7. PubMed ID: 11288991
[TBL] [Abstract][Full Text] [Related]
23. A Patient With Desmoid Tumors and Familial FAP Having Frame Shift Mutation of the APC Gene.
Sadighi S; Ghaffari-Moghaddam M; Saffari M; Mohagheghi MA; Shirkoohi R
Acta Med Iran; 2017 Feb; 55(2):134-138. PubMed ID: 28282712
[TBL] [Abstract][Full Text] [Related]
24. The role of pediatricians in families with a history of familial adenomatous polyposis.
Augustyn AM; Wallerstein R
Clin Pediatr (Phila); 2009 Jul; 48(6):623-6. PubMed ID: 19336753
[TBL] [Abstract][Full Text] [Related]
25. Cranial desmoid tumor associated with homozygous inactivation of the adenomatous polyposis coli gene in a 2-year-old girl with familial adenomatous polyposis.
de Silva DC; Wright MF; Stevenson DA; Clark C; Gray ES; Holmes JD; Dean JC; Haites NE; Dunlop MG
Cancer; 1996 Mar; 77(5):972-6. PubMed ID: 8608492
[TBL] [Abstract][Full Text] [Related]
26. Evidence for genetic predisposition to desmoid tumours in familial adenomatous polyposis independent of the germline APC mutation.
Sturt NJ; Gallagher MC; Bassett P; Philp CR; Neale KF; Tomlinson IP; Silver AR; Phillips RK
Gut; 2004 Dec; 53(12):1832-6. PubMed ID: 15542524
[TBL] [Abstract][Full Text] [Related]
27. Germ-line and somatic mutations of the APC gene in patients with Turcot syndrome and analysis of APC mutations in brain tumors.
Mori T; Nagase H; Horii A; Miyoshi Y; Shimano T; Nakatsuru S; Aoki T; Arakawa H; Yanagisawa A; Ushio Y
Genes Chromosomes Cancer; 1994 Mar; 9(3):168-72. PubMed ID: 7515658
[TBL] [Abstract][Full Text] [Related]
28. A novel APC gene mutation associated with a severe phenotype in a patient with Turcot syndrome.
Fritch Lilla SA; Yi JS; Hall BA; Moertel CL
J Pediatr Hematol Oncol; 2014 Apr; 36(3):e177-9. PubMed ID: 24309598
[TBL] [Abstract][Full Text] [Related]
29. The effect of a germline mutation in the APC gene on β-catenin in human embryonic stem cells.
Yedid N; Kalma Y; Malcov M; Amit A; Kariv R; Caspi M; Rosin-Arbesfeld R; Ben-Yosef D
BMC Cancer; 2016 Dec; 16(1):952. PubMed ID: 28010732
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Analysis of Wnt/Beta catenin signalling in desmoid tumors.
Tejpar S; Michils G; Denys H; Van Dam K; Nik SA; Jadidizadeh A; Cassiman JJ
Acta Gastroenterol Belg; 2005; 68(1):5-9. PubMed ID: 15832580
[TBL] [Abstract][Full Text] [Related]
32. Loss of p53 but not ARF accelerates medulloblastoma in mice heterozygous for patched.
Wetmore C; Eberhart DE; Curran T
Cancer Res; 2001 Jan; 61(2):513-6. PubMed ID: 11212243
[TBL] [Abstract][Full Text] [Related]
33. Family history, surgery, and APC mutation are risk factors for desmoid tumors in familial adenomatous polyposis: an international cohort study.
Nieuwenhuis MH; Lefevre JH; Bülow S; Järvinen H; Bertario L; Kernéis S; Parc Y; Vasen HF
Dis Colon Rectum; 2011 Oct; 54(10):1229-34. PubMed ID: 21904137
[TBL] [Abstract][Full Text] [Related]
34. Approach to screening for Familial Adenomatous Polyposis (FAP) in a cohort of 226 patients with Desmoid-type Fibromatosis (DF): experience of a specialist center in the UK.
Cojocaru E; Gennatas S; Thway K; Fisher C; Smrke A; Strauss D; Hayes A; Smith M; Jones RL; Benson C; McVeigh TP
Fam Cancer; 2022 Jan; 21(1):69-74. PubMed ID: 33547536
[TBL] [Abstract][Full Text] [Related]
35. Estrogen receptor α/prolactin receptor bilateral crosstalk promotes bromocriptine resistance in prolactinomas.
Xiao Z; Yang X; Zhang K; Liu Z; Shao Z; Song C; Wang X; Li Z
Int J Med Sci; 2020; 17(18):3174-3189. PubMed ID: 33173437
[TBL] [Abstract][Full Text] [Related]
36. Inactivation of the APC gene is constant in adrenocortical tumors from patients with familial adenomatous polyposis but not frequent in sporadic adrenocortical cancers.
Gaujoux S; Pinson S; Gimenez-Roqueplo AP; Amar L; Ragazzon B; Launay P; Meatchi T; Libé R; Bertagna X; Audebourg A; Zucman-Rossi J; Tissier F; Bertherat J
Clin Cancer Res; 2010 Nov; 16(21):5133-41. PubMed ID: 20978149
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Mutations of adenomatous polyposis coli (APC) gene are uncommon in sporadic desmoid tumours.
Giarola M; Wells D; Mondini P; Pilotti S; Sala P; Azzarelli A; Bertario L; Pierotti MA; Delhanty JD; Radice P
Br J Cancer; 1998 Sep; 78(5):582-7. PubMed ID: 9744495
[TBL] [Abstract][Full Text] [Related]
39. Recurrent giant cranial desmoid tumor in a 3-year-old boy with familial adenomatous polyposis requiring bifrontoparietal cranioplasty: case report.
Li L; Jensen JN; Szabo S; VanTuinen P; Lew SM
J Neurosurg Pediatr; 2016 Dec; 25(6):703-707. PubMed ID: 27635978
[TBL] [Abstract][Full Text] [Related]
40. Germline Prolactin Receptor Mutation Is Not a Major Cause of Sporadic Prolactinoma in Humans.
Bernard V; Bouilly J; Beau I; Broutin I; Chanson P; Young J; Binart N
Neuroendocrinology; 2016; 103(6):738-45. PubMed ID: 26641246
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]