BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

256 related articles for article (PubMed ID: 11918710)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 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. 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]  

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

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 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. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases.
    Hendriks YM; Verhallen JT; van der Smagt JJ; Kant SG; Hilhorst Y; Hoefsloot L; Hansson KB; van der Straaten PJ; Boutkan H; Breuning MH; Vasen HF; Bröcker-Vriends AH
    Fam Cancer; 2003; 2(2):79-85. PubMed ID: 14574156
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.