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Items: 1 to 20 of 167

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 15;57(22):5017-21.

2.

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.

PMID:
9811934
3.

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.

PMID:
9491322
4.

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.

PMID:
11174374
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, et al.

Hum Mol Genet. 1998 Mar;7(3):507-15.

PMID:
9467011
6.

A juvenile polyposis tumor suppressor locus at 10q22 is deleted from nonepithelial cells in the lamina propria.

Jacoby RF, Schlack S, Cole CE, Skarbek M, Harris C, Meisner LF.

Gastroenterology. 1997 Apr;112(4):1398-403.

PMID:
9098028
7.

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.

PMID:
9709978
8.

Allele loss in colorectal cancer at the Cowden disease/juvenile polyposis locus on 10q.

Frayling IM, Bodmer WF, Tomlinson IP.

Cancer Genet Cytogenet. 1997 Aug;97(1):64-9.

PMID:
9242220
9.

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.

PMID:
9443042
10.

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. Review.

PMID:
11352305
11.

Constipation, polyps, or cancer? Let PTEN predict your future.

Eng C.

Am J Med Genet A. 2003 Nov 1;122A(4):315-22. Review.

PMID:
14518069
12.

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 1;57(21):4710-3.

13.

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 1;58(23):5267-70.

14.

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 Mar-Apr;46(26):661-6. Review.

PMID:
10370593
15.

[Hamartomatous polyposis syndromes].

Bossone G, Salesi N, Alghisi F, Di Cocco B.

Recenti Prog Med. 2004 Feb;95(2):101-3. Review. Italian.

PMID:
15072395
16.

A gene for familial juvenile polyposis maps to chromosome 18q21.1.

Howe JR, Ringold JC, Summers RW, Mitros FA, Nishimura DY, Stone EM.

Am J Hum Genet. 1998 May;62(5):1129-36.

17.

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 15;60(22):6311-3.

18.

Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes.

Zhou XP, Woodford-Richens K, Lehtonen R, Kurose K, Aldred M, Hampel H, Launonen V, Virta S, Pilarski R, Salovaara R, Bodmer WF, Conrad BA, Dunlop M, Hodgson SV, Iwama T, Järvinen H, Kellokumpu I, Kim JC, Leggett B, Markie D, Mecklin JP, Neale K, Phillips R, Piris J, Rozen P, Houlston RS, Aaltonen LA, Tomlinson IP, Eng C.

Am J Hum Genet. 2001 Oct;69(4):704-11. Epub 2001 Aug 30.

19.

Analysis of the PTEN gene mutation in polyposis syndromes and sporadic gastrointestinal tumors in Japanese patients.

Negoro K, Takahashi S, Kinouchi Y, Takagi S, Hiwatashi N, Ichinohasama R, Shimosegawa T, Toyota T.

Dis Colon Rectum. 2000 Oct;43(10 Suppl):S29-33.

PMID:
11052475
20.

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. Review.

PMID:
15667510

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