BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 14569134)

  • 1. PTEN hamartoma tumour syndrome: variability of an entity.
    Merks JH; de Vries LS; Zhou XP; Nikkels P; Barth PG; Eng C; Hennekam RC
    J Med Genet; 2003 Oct; 40(10):e111. PubMed ID: 14569134
    [No Abstract]   [Full Text] [Related]  

  • 2. Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome.
    Pilarski R; Eng C
    J Med Genet; 2004 May; 41(5):323-6. PubMed ID: 15121767
    [No Abstract]   [Full Text] [Related]  

  • 3. Granular cell tumor in a PHTS patient with a novel germline PTEN mutation.
    Marchese C; Montera M; Torrini M; Goldoni F; Mareni C; Forni M; Locatelli L
    Am J Med Genet A; 2003 Jul; 120A(2):286-8. PubMed ID: 12833416
    [No Abstract]   [Full Text] [Related]  

  • 4. A novel germline mutation of the PTEN/MMAC1 gene in a patient with Cowden disease.
    Sanson M; Zhou XP; Brault JL; Hoang-Xuan K; Hamelin R
    Acta Oncol; 1999; 38(7):973-5. PubMed ID: 10606430
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. [Cowden disease and the PTEN gene: a successfully clinical and biological combined approach].
    Longy M
    Bull Cancer; 2001 Dec; 88(12):1153-8. PubMed ID: 11792608
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Will the real Cowden syndrome please stand up: revised diagnostic criteria.
    Eng C
    J Med Genet; 2000 Nov; 37(11):828-30. PubMed ID: 11073535
    [No Abstract]   [Full Text] [Related]  

  • 9. Variant manifestation of Cowden disease in Japan: hamartomatous polyposis of the digestive tract with mutation of the PTEN gene.
    Kurose K; Araki T; Matsunaka T; Takada Y; Emi M
    Am J Hum Genet; 1999 Jan; 64(1):308-10. PubMed ID: 9915974
    [No Abstract]   [Full Text] [Related]  

  • 10. PTEN and inherited hamartoma-cancer syndromes.
    Eng C; Peacocke M
    Nat Genet; 1998 Jul; 19(3):223. PubMed ID: 9662392
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Hamartoma and lentiginosis syndromes: clinical and molecular aspects.
    Marsh DJ; Stratakis CA
    Front Horm Res; 2001; 28():167-213. PubMed ID: 11443851
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromes.
    Zhou X; Hampel H; Thiele H; Gorlin RJ; Hennekam RC; Parisi M; Winter RM; Eng C
    Lancet; 2001 Jul; 358(9277):210-1. PubMed ID: 11476841
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndrome.
    Parisi MA; Dinulos MB; Leppig KA; Sybert VP; Eng C; Hudgins L
    J Med Genet; 2001 Jan; 38(1):52-8. PubMed ID: 11332402
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. Recognition of genetic syndromes in families with suspected hereditary colon cancer syndromes.
    Lindor NM
    Clin Gastroenterol Hepatol; 2004 May; 2(5):366-75. PubMed ID: 15118973
    [No Abstract]   [Full Text] [Related]  

  • 20. Cowden syndrome: a rare, but recognisable cancer predisposition disorder.
    Adlard JW
    Clin Oncol (R Coll Radiol); 2005 Aug; 17(5):393. PubMed ID: 16097574
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.