352 related articles for article (PubMed ID: 9399897)
1. 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]
2. Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in primary breast carcinomas.
Rhei E; Kang L; Bogomolniy F; Federici MG; Borgen PI; Boyd J
Cancer Res; 1997 Sep; 57(17):3657-9. PubMed ID: 9288766
[TBL] [Abstract][Full Text] [Related]
3. 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]
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. 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]
7. 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]
8. 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. PubMed ID: 11052475
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. A novel loss-of-function mutation (N48K) in the PTEN gene in a Spanish patient with Cowden disease.
Vega A; Torres J; Torres M; Cameselle-Teijeiro J; Macia M; Carracedo A; Pulido R
J Invest Dermatol; 2003 Dec; 121(6):1356-9. PubMed ID: 14675182
[TBL] [Abstract][Full Text] [Related]
13. Germline PTEN mutations in Cowden syndrome-like families.
Marsh DJ; Dahia PL; Caron S; Kum JB; Frayling IM; Tomlinson IP; Hughes KS; Eeles RA; Hodgson SV; Murday VA; Houlston R; Eng C
J Med Genet; 1998 Nov; 35(11):881-5. PubMed ID: 9832031
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Genetic heterogeneity in familial juvenile polyposis.
Huang SC; Chen CR; Lavine JE; Taylor SF; Newbury RO; Pham TT; Ricciardiello L; Carethers JM
Cancer Res; 2000 Dec; 60(24):6882-5. PubMed ID: 11156385
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Somatic mutations of the PTEN tumor suppressor gene in sporadic follicular thyroid tumors.
Halachmi N; Halachmi S; Evron E; Cairns P; Okami K; Saji M; Westra WH; Zeiger MA; Jen J; Sidransky D
Genes Chromosomes Cancer; 1998 Nov; 23(3):239-43. PubMed ID: 9790504
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Germline mutations in PTEN are an infrequent cause of genetic predisposition to breast cancer.
FitzGerald MG; Marsh DJ; Wahrer D; Bell D; Caron S; Shannon KE; Ishioka C; Isselbacher KJ; Garber JE; Eng C; Haber DA
Oncogene; 1998 Aug; 17(6):727-31. PubMed ID: 9715274
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]