263 related articles for article (PubMed ID: 9371495)
1. Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome.
Marsh DJ; Roth S; Lunetta KL; Hemminki A; Dahia PL; Sistonen P; Zheng Z; Caron S; van Orsouw NJ; Bodmer WF; Cottrell SE; Dunlop MG; Eccles D; Hodgson SV; Järvinen H; Kellokumpu I; Markie D; Neale K; Phillips R; Rozen P; Syngal S; Vijg J; Tomlinson IP; Aaltonen LA; Eng C
Cancer Res; 1997 Nov; 57(22):5017-21. PubMed ID: 9371495
[TBL] [Abstract][Full Text] [Related]
2. Identification of a PTEN mutation in a family with Cowden syndrome and Bannayan-Zonana syndrome.
Wanner M; Celebi JT; Peacocke M
J Am Acad Dermatol; 2001 Feb; 44(2):183-7. PubMed ID: 11174374
[TBL] [Abstract][Full Text] [Related]
3. Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic loci.
Stratakis CA; Kirschner LS; Taymans SE; Tomlinson IP; Marsh DJ; Torpy DJ; Giatzakis C; Eccles DM; Theaker J; Houlston RS; Blouin JL; Antonarakis SE; Basson CT; Eng C; Carney JA
J Clin Endocrinol Metab; 1998 Aug; 83(8):2972-6. PubMed ID: 9709978
[TBL] [Abstract][Full Text] [Related]
4. Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases.
Houlston R; Bevan S; Williams A; Young J; Dunlop M; Rozen P; Eng C; Markie D; Woodford-Richens K; Rodriguez-Bigas MA; Leggett B; Neale K; Phillips R; Sheridan E; Hodgson S; Iwama T; Eccles D; Bodmer W; Tomlinson I
Hum Mol Genet; 1998 Nov; 7(12):1907-12. PubMed ID: 9811934
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Somatic deletions and mutations in the Cowden disease gene, PTEN, in sporadic thyroid tumors.
Dahia PL; Marsh DJ; Zheng Z; Zedenius J; Komminoth P; Frisk T; Wallin G; Parsons R; Longy M; Larsson C; Eng C
Cancer Res; 1997 Nov; 57(21):4710-3. PubMed ID: 9354427
[TBL] [Abstract][Full Text] [Related]
7. Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome.
Gruber SB; Entius MM; Petersen GM; Laken SJ; Longo PA; Boyer R; Levin AM; Mujumdar UJ; Trent JM; Kinzler KW; Vogelstein B; Hamilton SR; Polymeropoulos MH; Offerhaus GJ; Giardiello FM
Cancer Res; 1998 Dec; 58(23):5267-70. PubMed ID: 9850045
[TBL] [Abstract][Full Text] [Related]
8. Allelic imbalance, including deletion of PTEN/MMACI, at the Cowden disease locus on 10q22-23, in hamartomas from patients with Cowden syndrome and germline PTEN mutation.
Marsh DJ; Dahia PL; Coulon V; Zheng Z; Dorion-Bonnet F; Call KM; Little R; Lin AY; Eeles RA; Goldstein AM; Hodgson SV; Richardson AL; Robinson BG; Weber HC; Longy M; Eng C
Genes Chromosomes Cancer; 1998 Jan; 21(1):61-9. PubMed ID: 9443042
[TBL] [Abstract][Full Text] [Related]
9. Molecular and phenotypic markers of hamartomatous polyposis syndromes in the gastrointestinal tract.
Entius MM; Westerman AM; van Velthuysen ML; Wilson JH; Hamilton SR; Giardiello FM; Offerhaus GJ
Hepatogastroenterology; 1999; 46(26):661-6. PubMed ID: 10370593
[TBL] [Abstract][Full Text] [Related]
10. [Hamartomatous polyposis syndromes].
Bossone G; Salesi N; Alghisi F; Di Cocco B
Recenti Prog Med; 2004 Feb; 95(2):101-3. PubMed ID: 15072395
[TBL] [Abstract][Full Text] [Related]
11. Constipation, polyps, or cancer? Let PTEN predict your future.
Eng C
Am J Med Genet A; 2003 Nov; 122A(4):315-22. PubMed ID: 14518069
[TBL] [Abstract][Full Text] [Related]
12. Somatic mutations of LKB1 and beta-catenin genes in gastrointestinal polyps from patients with Peutz-Jeghers syndrome.
Miyaki M; Iijima T; Hosono K; Ishii R; Yasuno M; Mori T; Toi M; Hishima T; Shitara N; Tamura K; Utsunomiya J; Kobayashi N; Kuroki T; Iwama T
Cancer Res; 2000 Nov; 60(22):6311-3. PubMed ID: 11103790
[TBL] [Abstract][Full Text] [Related]
13. The hamartomatous polyposis syndromes: a clinical and molecular review.
Schreibman IR; Baker M; Amos C; McGarrity TJ
Am J Gastroenterol; 2005 Feb; 100(2):476-90. PubMed ID: 15667510
[TBL] [Abstract][Full Text] [Related]
14. Analysis of PTEN gene mutations in Korean patients with Cowden syndrome and polyposis syndrome.
Kim DK; Myung SJ; Yang SK; Hong SS; Kim KJ; Byeon JS; Lee GH; Kim JH; Min YI; Lee SM; Jeong JY; Song K; Jung SA
Dis Colon Rectum; 2005 Sep; 48(9):1714-22. PubMed ID: 16007494
[TBL] [Abstract][Full Text] [Related]
15. Hamartomatous polyposis syndromes: molecular genetics, neoplastic risk, and surveillance recommendations.
Wirtzfeld DA; Petrelli NJ; Rodriguez-Bigas MA
Ann Surg Oncol; 2001 May; 8(4):319-27. PubMed ID: 11352305
[TBL] [Abstract][Full Text] [Related]
16. Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis.
Hemminki A; Tomlinson I; Markie D; Järvinen H; Sistonen P; Björkqvist AM; Knuutila S; Salovaara R; Bodmer W; Shibata D; de la Chapelle A; Aaltonen LA
Nat Genet; 1997 Jan; 15(1):87-90. PubMed ID: 8988175
[TBL] [Abstract][Full Text] [Related]
17. Mapping of a translocation breakpoint in a Peutz-Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11-negative PJS cases.
Hearle N; Lucassen A; Wang R; Lim W; Ross F; Wheeler R; Moore I; Shipley J; Houlston R
Genes Chromosomes Cancer; 2004 Oct; 41(2):163-9. PubMed ID: 15287029
[TBL] [Abstract][Full Text] [Related]
18. Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome.
Tsuchiya KD; Wiesner G; Cassidy SB; Limwongse C; Boyle JT; Schwartz S
Genes Chromosomes Cancer; 1998 Feb; 21(2):113-8. PubMed ID: 9491322
[TBL] [Abstract][Full Text] [Related]
19. Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinomas.
Marsh DJ; Zheng Z; Zedenius J; Kremer H; Padberg GW; Larsson C; Longy M; Eng C
Cancer Res; 1997 Feb; 57(3):500-3. PubMed ID: 9012481
[TBL] [Abstract][Full Text] [Related]
20. A family with juvenile polyposis linked to the BMPR1A locus: cryptic mutation or closely linked gene?
Chow E; Lipton L; Carvajal-Carmona LG; Arthur G; Bhathal P; Kaur G; Jaeger E; Woodford-Richens K; Howarth K; Tomlinson I; Macrae F
J Gastroenterol Hepatol; 2007 Dec; 22(12):2292-7. PubMed ID: 17573831
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
