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4. 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]
5. 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]
6. 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]
7. Germline mutations of the PTEN/MMAC1 gene in Japanese patients with Cowden disease. Kohno T; Takahashi M; Fukutomi T; Ushio K; Yokota J Jpn J Cancer Res; 1998 May; 89(5):471-4. PubMed ID: 9685848 [TBL] [Abstract][Full Text] [Related]
8. The genetic basis of Cowden's syndrome: three novel mutations in PTEN/MMAC1/TEP1. Tsou HC; Ping XL; Xie XX; Gruener AC; Zhang H; Nini R; Swisshelm K; Sybert V; Diamond TM; Sutphen R; Peacocke M Hum Genet; 1998 Apr; 102(4):467-73. PubMed ID: 9600246 [TBL] [Abstract][Full Text] [Related]
9. The role of MMAC1 mutations in early-onset breast cancer: causative in association with Cowden syndrome and excluded in BRCA1-negative cases. Tsou HC; Teng DH; Ping XL; Brancolini V; Davis T; Hu R; Xie XX; Gruener AC; Schrager CA; Christiano AM; Eng C; Steck P; Ott J; Tavtigian SV; Peacocke M Am J Hum Genet; 1997 Nov; 61(5):1036-43. PubMed ID: 9345101 [TBL] [Abstract][Full Text] [Related]
10. 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]
12. 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]
13. Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis. Lynch ED; Ostermeyer EA; Lee MK; Arena JF; Ji H; Dann J; Swisshelm K; Suchard D; MacLeod PM; Kvinnsland S; Gjertsen BT; Heimdal K; Lubs H; Møller P; King MC Am J Hum Genet; 1997 Dec; 61(6):1254-60. PubMed ID: 9399897 [TBL] [Abstract][Full Text] [Related]
14. Mutational abrogation of the PTEN/MMAC1 gene in gastrointestinal polyps in patients with Cowden disease. Chi SG; Kim HJ; Park BJ; Min HJ; Park JH; Kim YW; Dong SH; Kim BH; Lee JI; Chang YW; Chang R; Kim WK; Yang MH Gastroenterology; 1998 Nov; 115(5):1084-9. PubMed ID: 9797362 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Mutation analysis of the PTEN / MMAC1 gene in Japanese patients with Cowden disease. Sawada T; Hamano N; Satoh H; Okada T; Takeda Y; Mabuchi H Jpn J Cancer Res; 2000 Jul; 91(7):700-5. PubMed ID: 10920277 [TBL] [Abstract][Full Text] [Related]
17. Mutation analysis of PTEN/MMAC 1 in sporadic thyroid tumors. Hsieh MC; Lin SF; Shin SJ; Liu TC; Chang JG; Lee JP Kaohsiung J Med Sci; 2000 Jan; 16(1):9-12. PubMed ID: 10741010 [TBL] [Abstract][Full Text] [Related]
18. 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]