These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

223 related articles for article (PubMed ID: 11792608)

  • 1. [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]  

  • 2. 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]  

  • 3. [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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Evaluation of germline PTEN mutations in endometrial cancer patients.
    Black D; Bogomolniy F; Robson ME; Offit K; Barakat RR; Boyd J
    Gynecol Oncol; 2005 Jan; 96(1):21-4. PubMed ID: 15589575
    [TBL] [Abstract][Full Text] [Related]  

  • 7. PTEN: one gene, many syndromes.
    Eng C
    Hum Mutat; 2003 Sep; 22(3):183-98. PubMed ID: 12938083
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Silencing of the PTEN tumor-suppressor gene in anaplastic thyroid cancer.
    Frisk T; Foukakis T; Dwight T; Lundberg J; Höög A; Wallin G; Eng C; Zedenius J; Larsson C
    Genes Chromosomes Cancer; 2002 Sep; 35(1):74-80. PubMed ID: 12203792
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. High incidence of breast and endometrial neoplasia resembling human Cowden syndrome in pten+/- mice.
    Stambolic V; Tsao MS; Macpherson D; Suzuki A; Chapman WB; Mak TW
    Cancer Res; 2000 Jul; 60(13):3605-11. PubMed ID: 10910075
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. PTEN mutations in eight Spanish families and one Brazilian family with Cowden syndrome.
    Bussaglia E; Pujol RM; Gil MJ; Martí RM; Tuneu A; Febrer MI; Garcia-Patos V; Ruiz EM; Barnadas M; Alegre M; Serrano S; Matias-Guiu X
    J Invest Dermatol; 2002 Apr; 118(4):639-44. PubMed ID: 11918710
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.