These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
444 related articles for article (PubMed ID: 11238682)
1. Male breast cancer in Cowden syndrome patients with germline PTEN mutations. Fackenthal JD; Marsh DJ; Richardson AL; Cummings SA; Eng C; Robinson BG; Olopade OI J Med Genet; 2001 Mar; 38(3):159-64. PubMed ID: 11238682 [TBL] [Abstract][Full Text] [Related]
2. PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome. Marsh DJ; Kum JB; Lunetta KL; Bennett MJ; Gorlin RJ; Ahmed SF; Bodurtha J; Crowe C; Curtis MA; Dasouki M; Dunn T; Feit H; Geraghty MT; Graham JM; Hodgson SV; Hunter A; Korf BR; Manchester D; Miesfeldt S; Murday VA; Nathanson KL; Parisi M; Pober B; Romano C; Eng C Hum Mol Genet; 1999 Aug; 8(8):1461-72. PubMed ID: 10400993 [TBL] [Abstract][Full Text] [Related]
4. Germline PTEN mutations in three families with Cowden syndrome. Celebi JT; Ping XL; Zhang H; Remington T; Sulica VI; Tsou HC; Peacocke M Exp Dermatol; 2000 Apr; 9(2):152-6. PubMed ID: 10772390 [TBL] [Abstract][Full Text] [Related]
5. Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway. Zhou XP; Waite KA; Pilarski R; Hampel H; Fernandez MJ; Bos C; Dasouki M; Feldman GL; Greenberg LA; Ivanovich J; Matloff E; Patterson A; Pierpont ME; Russo D; Nassif NT; Eng C Am J Hum Genet; 2003 Aug; 73(2):404-11. PubMed ID: 12844284 [TBL] [Abstract][Full Text] [Related]
6. Two novel mutations of PTEN gene in Japanese patients with Cowden syndrome. Sawada T; Okada T; Miwa K; Satoh H; Asano A; Mabuchi H Am J Med Genet A; 2004 Jul; 128A(1):12-4. PubMed ID: 15211648 [TBL] [Abstract][Full Text] [Related]
7. Germline mutations in the PTEN gene in Israeli patients with Bannayan-Riley-Ruvalcaba syndrome and women with familial breast cancer. Figer A; Kaplan A; Frydman M; Lev D; Paswell J; Papa MZ; Goldman B; Friedman E Clin Genet; 2002 Oct; 62(4):298-302. PubMed ID: 12372056 [TBL] [Abstract][Full Text] [Related]
8. Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTEN. Celebi JT; Tsou HC; Chen FF; Zhang H; Ping XL; Lebwohl MG; Kezis J; Peacocke M J Med Genet; 1999 May; 36(5):360-4. PubMed ID: 10353779 [TBL] [Abstract][Full Text] [Related]
10. Breast cancer risk and clinical implications for germline PTEN mutation carriers. Ngeow J; Sesock K; Eng C Breast Cancer Res Treat; 2017 Aug; 165(1):1-8. PubMed ID: 26700035 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Activation of a cryptic splice site of PTEN and loss of heterozygosity in benign skin lesions in Cowden disease. Trojan J; Plotz G; Brieger A; Raedle J; Meltzer SJ; Wolter M; Zeuzem S J Invest Dermatol; 2001 Dec; 117(6):1650-3. PubMed ID: 11886535 [TBL] [Abstract][Full Text] [Related]
13. Identification of a novel PTEN mutation (L139X) in a patient with Cowden disease and Sjögren's syndrome. Raizis AM; Ferguson MM; Robinson BA; Atkinson CH; George PM Mol Pathol; 1998 Dec; 51(6):339-41. PubMed ID: 10193515 [TBL] [Abstract][Full Text] [Related]
14. Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases. Hendriks YM; Verhallen JT; van der Smagt JJ; Kant SG; Hilhorst Y; Hoefsloot L; Hansson KB; van der Straaten PJ; Boutkan H; Breuning MH; Vasen HF; Bröcker-Vriends AH Fam Cancer; 2003; 2(2):79-85. PubMed ID: 14574156 [TBL] [Abstract][Full Text] [Related]
15. A heterozygous germline mutation of the PTEN/MMAC1 gene in a patient with Cowden disease. Iida S; Nakamura Y; Fujii H; Kimura M; Moriwaki K Int J Mol Med; 1998 Mar; 1(3):565-8. PubMed ID: 9852263 [TBL] [Abstract][Full Text] [Related]
16. Germline PTEN mutation in a family with Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome. Zori RT; Marsh DJ; Graham GE; Marliss EB; Eng C Am J Med Genet; 1998 Dec; 80(4):399-402. PubMed ID: 9856571 [TBL] [Abstract][Full Text] [Related]
17. PTEN mutations in eight Spanish families and one Brazilian family with Cowden syndrome. Bussaglia E; Pujol RM; Gil MJ; Martí RM; Tuneu A; Febrer MI; Garcia-Patos V; Ruiz EM; Barnadas M; Alegre M; Serrano S; Matias-Guiu X J Invest Dermatol; 2002 Apr; 118(4):639-44. PubMed ID: 11918710 [TBL] [Abstract][Full Text] [Related]
18. Novel germline mutation of the PTEN gene in a Japanese family with Cowden disease. Harada N; Sugimura T; Yoshimura R; Motomura S; Shirahama S; Naramoto J; Chijiiwa Y; Nakamura K; Ito K; Nawata H J Gastroenterol; 2003; 38(1):87-91. PubMed ID: 12560928 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]