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: 9915974)

  • 21. 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]  

  • 22. 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]  

  • 23. 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]  

  • 24. Absence of PTEN/MMAC1 germ-line mutations in sporadic Bannayan-Riley-Ruvalcaba syndrome.
    Carethers JM; Furnari FB; Zigman AF; Lavine JE; Jones MC; Graham GE; Teebi AS; Huang HJ; Ha HT; Chauhan DP; Chang CL; Cavenee WK; Boland CR
    Cancer Res; 1998 Jul; 58(13):2724-6. PubMed ID: 9661881
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in primary breast carcinomas.
    Rhei E; Kang L; Bogomolniy F; Federici MG; Borgen PI; Boyd J
    Cancer Res; 1997 Sep; 57(17):3657-9. PubMed ID: 9288766
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Genetics of Cowden syndrome: through the looking glass of oncology.
    Eng C
    Int J Oncol; 1998 Mar; 12(3):701-10. PubMed ID: 9472113
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease.
    Arch EM; Goodman BK; Van Wesep RA; Liaw D; Clarke K; Parsons R; McKusick VA; Geraghty MT
    Am J Med Genet; 1997 Sep; 71(4):489-93. PubMed ID: 9286463
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Mutational abrogation of the PTEN/MMAC1 gene in gastrointestinal polyps in patients with Cowden disease.
    Chi SG; Kim HJ; Park BJ; Min HJ; Park JH; Kim YW; Dong SH; Kim BH; Lee JI; Chang YW; Chang R; Kim WK; Yang MH
    Gastroenterology; 1998 Nov; 115(5):1084-9. PubMed ID: 9797362
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. 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]  

  • 35. 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]  

  • 36. 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]  

  • 37. Infrequent genetic alterations of the PTEN gene in Japanese patients with sporadic prostate cancer.
    Orikasa K; Fukushige S; Hoshi S; Orikasa S; Kondo K; Miyoshi Y; Kubota Y; Horii A
    J Hum Genet; 1998; 43(4):228-30. PubMed ID: 9852672
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 9.