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 *

161 related articles for article (PubMed ID: 15211648)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 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. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

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

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.