249 related articles for article (PubMed ID: 9616081)
1. Landscaping the cancer terrain.
Kinzler KW; Vogelstein B
Science; 1998 May; 280(5366):1036-7. PubMed ID: 9616081
[No Abstract] [Full Text] [Related]
2. Genetic conditions associated with intestinal juvenile polyps.
Merg A; Howe JR
Am J Med Genet C Semin Med Genet; 2004 Aug; 129C(1):44-55. PubMed ID: 15264272
[TBL] [Abstract][Full Text] [Related]
3. Mutations in the SMAD4/DPC4 gene in juvenile polyposis.
Howe JR; Roth S; Ringold JC; Summers RW; Järvinen HJ; Sistonen P; Tomlinson IP; Houlston RS; Bevan S; Mitros FA; Stone EM; Aaltonen LA
Science; 1998 May; 280(5366):1086-8. PubMed ID: 9582123
[TBL] [Abstract][Full Text] [Related]
4. Germline mutations in PTEN are present in Bannayan-Zonana syndrome.
Marsh DJ; Dahia PL; Zheng Z; Liaw D; Parsons R; Gorlin RJ; Eng C
Nat Genet; 1997 Aug; 16(4):333-4. PubMed ID: 9241266
[No Abstract] [Full Text] [Related]
5. PTEN and inherited hamartoma-cancer syndromes.
Eng C; Peacocke M
Nat Genet; 1998 Jul; 19(3):223. PubMed ID: 9662392
[No Abstract] [Full Text] [Related]
6. Cancer predisposition: where's the phosphate?
Smith A; Ashworth A
Curr Biol; 1998 Mar; 8(7):R241-3. PubMed ID: 9545192
[TBL] [Abstract][Full Text] [Related]
7. Epithelial-specific loss of PTEN results in colorectal juvenile polyp formation and invasive cancer.
Marsh Durban V; Jansen M; Davies EJ; Morsink FH; Offerhaus GJ; Clarke AR
Am J Pathol; 2014 Jan; 184(1):86-91. PubMed ID: 24200851
[TBL] [Abstract][Full Text] [Related]
8. Genetics of Cowden syndrome: through the looking glass of oncology.
Eng C
Int J Oncol; 1998 Mar; 12(3):701-10. PubMed ID: 9472113
[TBL] [Abstract][Full Text] [Related]
9. [Involvement of protein tyrosine phosphatases in cancer development].
Hinoda Y; Idogawa M; Imai K
Tanpakushitsu Kakusan Koso; 1998 Jun; 43(8 Suppl):1186-92. PubMed ID: 9655978
[No Abstract] [Full Text] [Related]
10. Absence of PTEN/MMAC1 germ-line mutations in sporadic Bannayan-Riley-Ruvalcaba syndrome.
Carethers JM; Furnari FB; Zigman AF; Lavine JE; Jones MC; Graham GE; Teebi AS; Huang HJ; Ha HT; Chauhan DP; Chang CL; Cavenee WK; Boland CR
Cancer Res; 1998 Jul; 58(13):2724-6. PubMed ID: 9661881
[TBL] [Abstract][Full Text] [Related]
11. Cowden syndrome: a rare, but recognisable cancer predisposition disorder.
Adlard JW
Clin Oncol (R Coll Radiol); 2005 Aug; 17(5):393. PubMed ID: 16097574
[No Abstract] [Full Text] [Related]
12. Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis.
Sweet K; Willis J; Zhou XP; Gallione C; Sawada T; Alhopuro P; Khoo SK; Patocs A; Martin C; Bridgeman S; Heinz J; Pilarski R; Lehtonen R; Prior TW; Frebourg T; Teh BT; Marchuk DA; Aaltonen LA; Eng C
JAMA; 2005 Nov; 294(19):2465-73. PubMed ID: 16287957
[TBL] [Abstract][Full Text] [Related]
13. PTEN: life as a tumor suppressor.
Simpson L; Parsons R
Exp Cell Res; 2001 Mar; 264(1):29-41. PubMed ID: 11237521
[TBL] [Abstract][Full Text] [Related]
14. Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation.
Marsh DJ; Coulon V; Lunetta KL; Rocca-Serra P; Dahia PL; Zheng Z; Liaw D; Caron S; Duboué B; Lin AY; Richardson AL; Bonnetblanc JM; Bressieux JM; Cabarrot-Moreau A; Chompret A; Demange L; Eeles RA; Yahanda AM; Fearon ER; Fricker JP; Gorlin RJ; Hodgson SV; Huson S; Lacombe D; Eng C
Hum Mol Genet; 1998 Mar; 7(3):507-15. PubMed ID: 9467011
[TBL] [Abstract][Full Text] [Related]
15. Frequent gastrointestinal polyps and colorectal adenocarcinomas in a prospective series of PTEN mutation carriers.
Heald B; Mester J; Rybicki L; Orloff MS; Burke CA; Eng C
Gastroenterology; 2010 Dec; 139(6):1927-33. PubMed ID: 20600018
[TBL] [Abstract][Full Text] [Related]
16. Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome.
Liaw D; Marsh DJ; Li J; Dahia PL; Wang SI; Zheng Z; Bose S; Call KM; Tsou HC; Peacocke M; Eng C; Parsons R
Nat Genet; 1997 May; 16(1):64-7. PubMed ID: 9140396
[TBL] [Abstract][Full Text] [Related]
17. Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease.
Nelen MR; van Staveren WC; Peeters EA; Hassel MB; Gorlin RJ; Hamm H; Lindboe CF; Fryns JP; Sijmons RH; Woods DG; Mariman EC; Padberg GW; Kremer H
Hum Mol Genet; 1997 Aug; 6(8):1383-7. PubMed ID: 9259288
[TBL] [Abstract][Full Text] [Related]
18. Hereditary breast cancer.
Ellisen LW; Haber DA
Annu Rev Med; 1998; 49():425-36. PubMed ID: 9509273
[TBL] [Abstract][Full Text] [Related]
19. Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease.
Arch EM; Goodman BK; Van Wesep RA; Liaw D; Clarke K; Parsons R; McKusick VA; Geraghty MT
Am J Med Genet; 1997 Sep; 71(4):489-93. PubMed ID: 9286463
[TBL] [Abstract][Full Text] [Related]
20. Absence of germline mutations in MINPP1, a phosphatase encoding gene centromeric of PTEN, in patients with Cowden and Bannayan-Riley-Ruvalcaba syndrome without germline PTEN mutations.
Dahia PM; Gimm O; Chi H; Marsh DJ; Reynolds PR; Eng C
J Med Genet; 2000 Sep; 37(9):715-7. PubMed ID: 11182934
[No Abstract] [Full Text] [Related]
[Next] [New Search]