153 related articles for article (PubMed ID: 11295050)
1. Germline mutation of the PTEN gene in a Japanese patient with Cowden's disease.
Kato N; Kimura K; Sugawara H; Aoyagi S; Ikeda T; Horii A
Int J Oncol; 2001 May; 18(5):1017-22. PubMed ID: 11295050
[TBL] [Abstract][Full Text] [Related]
2. Cowden's disease: clinical and molecular genetic findings in a patient with a novel PTEN germline mutation.
Reifenberger J; Rauch L; Beckmann MW; Megahed M; Ruzicka T; Reifenberger G
Br J Dermatol; 2003 May; 148(5):1040-6. PubMed ID: 12786840
[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. 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]
5. 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]
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. 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]
8. 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]
9. 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]
10. A novel PTEN mutation in a Japanese patient with Cowden disease.
Kubo Y; Urano Y; Hida Y; Ikeuchi T; Nomoto M; Kunitomo K; Arase S
Br J Dermatol; 2000 Jun; 142(6):1100-5. PubMed ID: 10848731
[TBL] [Abstract][Full Text] [Related]
11. Gastrointestinal polyposis with esophageal polyposis is useful for early diagnosis of Cowden's disease.
Umemura K; Takagi S; Ishigaki Y; Iwabuchi M; Kuroki S; Kinouchi Y; Shimosegawa T
World J Gastroenterol; 2008 Oct; 14(37):5755-9. PubMed ID: 18837096
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Novel mutation of the PTEN gene in an Italian Cowden's disease kindred.
Scala S; Bruni P; Lo Muzio L; Mignogna M; Viglietto G; Fusco A
Int J Oncol; 1998 Oct; 13(4):665-8. PubMed ID: 9735393
[TBL] [Abstract][Full Text] [Related]
15. Lhermitte-Duclos disease as a component of Cowden's syndrome. Case report and review of the literature.
Koch R; Scholz M; Nelen MR; Schwechheimer K; Epplen JT; Harders AG
J Neurosurg; 1999 Apr; 90(4):776-9. PubMed ID: 10193626
[TBL] [Abstract][Full Text] [Related]
16. Genital lentigines in a 6-year-old boy with a family history of Cowden's disease: clinical and genetic evidence of the linkage between Bannayan-Riley-Ruvacalba syndrome and Cowden's disease.
Blum RR; Rahimizadeh A; Kardon N; Lebwohl M; Wei H
J Cutan Med Surg; 2001; 5(3):228-30. PubMed ID: 11685670
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. Severe Lhermitte-Duclos disease with unique germline mutation of PTEN.
Sutphen R; Diamond TM; Minton SE; Peacocke M; Tsou HC; Root AW
Am J Med Genet; 1999 Feb; 82(4):290-3. PubMed ID: 10051160
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]