257 related articles for article (PubMed ID: 11918710)
21. 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]
22. Identification of PTEN mutations in five families with Bannayan-Zonana syndrome.
Tok Celebi J; Chen FF; Zhang H; Ping XL; Tsou HC; Peacocke M
Exp Dermatol; 1999 Apr; 8(2):134-9. PubMed ID: 10232405
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. Association of splicing defects in PTEN leading to exon skipping or partial intron retention in Cowden syndrome.
Celebi JT; Wanner M; Ping XL; Zhang H; Peacocke M
Hum Genet; 2000 Sep; 107(3):234-8. PubMed ID: 11071384
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. [Cowden disease].
Sawada T; Hamano N; Suzuki A; Okada T; Mabuchi H
Nihon Rinsho; 2000 Jul; 58(7):1479-83. PubMed ID: 10921327
[TBL] [Abstract][Full Text] [Related]
27. GI polyposis and glycogenic acanthosis of the esophagus associated with PTEN mutation positive Cowden syndrome in the absence of cutaneous manifestations.
McGarrity TJ; Wagner Baker MJ; Ruggiero FM; Thiboutot DM; Hampel H; Zhou XP; Eng C
Am J Gastroenterol; 2003 Jun; 98(6):1429-34. PubMed ID: 12818292
[TBL] [Abstract][Full Text] [Related]
28. Absence of PTEN germ-line mutations in men with a potential inherited predisposition to prostate cancer.
Cooney KA; Tsou HC; Petty EM; Miesfeldt S; Ping XL; Gruener AC; Peacocke M
Clin Cancer Res; 1999 Jun; 5(6):1387-91. PubMed ID: 10389923
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. 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]
31. Identification of germline mutation of PTEN gene and analysis of apoptosis resistance of the lymphocytes in a patient with Cowden disease.
Kanaseki T; Torigoe T; Hirohashi Y; Hirai I; Himi T; Sato N
Pathobiology; 2002; 70(1):34-9. PubMed ID: 12415190
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Mutations of the human PTEN gene.
Bonneau D; Longy M
Hum Mutat; 2000; 16(2):109-22. PubMed ID: 10923032
[TBL] [Abstract][Full Text] [Related]
34. The role of PTEN, a phosphatase gene, in inherited and sporadic nonmedullary thyroid tumors.
Eng C
Recent Prog Horm Res; 1999; 54():441-52; discussion 453. PubMed ID: 10548886
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype.
Longy M; Coulon V; Duboué B; David A; Larrègue M; Eng C; Amati P; Kraimps JL; Bottani A; Lacombe D; Bonneau D
J Med Genet; 1998 Nov; 35(11):886-9. PubMed ID: 9832032
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations.
Nelen MR; Kremer H; Konings IB; Schoute F; van Essen AJ; Koch R; Woods CG; Fryns JP; Hamel B; Hoefsloot LH; Peeters EA; Padberg GW
Eur J Hum Genet; 1999 Apr; 7(3):267-73. PubMed ID: 10234502
[TBL] [Abstract][Full Text] [Related]
39. Biallelic inactivating mutations and an occult germline mutation of PTEN in primary cervical carcinomas.
Kurose K; Zhou XP; Araki T; Eng C
Genes Chromosomes Cancer; 2000 Oct; 29(2):166-72. PubMed ID: 10959096
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
