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 *

693 related articles for article (PubMed ID: 9467011)

  • 21. Pten is essential for embryonic development and tumour suppression.
    Di Cristofano A; Pesce B; Cordon-Cardo C; Pandolfi PP
    Nat Genet; 1998 Aug; 19(4):348-55. PubMed ID: 9697695
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Biallelic inactivating mutations and an occult germline mutation of PTEN in primary cervical carcinomas.
    Kurose K; Zhou XP; Araki T; Eng C
    Genes Chromosomes Cancer; 2000 Oct; 29(2):166-72. PubMed ID: 10959096
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome.
    Marsh DJ; Roth S; Lunetta KL; Hemminki A; Dahia PL; Sistonen P; Zheng Z; Caron S; van Orsouw NJ; Bodmer WF; Cottrell SE; Dunlop MG; Eccles D; Hodgson SV; Järvinen H; Kellokumpu I; Markie D; Neale K; Phillips R; Rozen P; Syngal S; Vijg J; Tomlinson IP; Aaltonen LA; Eng C
    Cancer Res; 1997 Nov; 57(22):5017-21. PubMed ID: 9371495
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. 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]  

  • 29. PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocol.
    Piccione M; Fragapane T; Antona V; Giachino D; Cupido F; Corsello G
    Am J Med Genet A; 2013 Nov; 161A(11):2902-8. PubMed ID: 24123798
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations.
    Nelen MR; Kremer H; Konings IB; Schoute F; van Essen AJ; Koch R; Woods CG; Fryns JP; Hamel B; Hoefsloot LH; Peeters EA; Padberg GW
    Eur J Hum Genet; 1999 Apr; 7(3):267-73. PubMed ID: 10234502
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype.
    Longy M; Coulon V; Duboué B; David A; Larrègue M; Eng C; Amati P; Kraimps JL; Bottani A; Lacombe D; Bonneau D
    J Med Genet; 1998 Nov; 35(11):886-9. PubMed ID: 9832032
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [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]  

  • 34. 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]  

  • 35. Severe Lhermitte-Duclos disease with unique germline mutation of PTEN.
    Sutphen R; Diamond TM; Minton SE; Peacocke M; Tsou HC; Root AW
    Am J Med Genet; 1999 Feb; 82(4):290-3. PubMed ID: 10051160
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes.
    Pezzolesi MG; Li Y; Zhou XP; Pilarski R; Shen L; Eng C
    Am J Hum Genet; 2006 Nov; 79(5):923-34. PubMed ID: 17033968
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Role of PTEN, a lipid phosphatase upstream effector of protein kinase B, in epithelial thyroid carcinogenesis.
    Eng C
    Ann N Y Acad Sci; 2002 Jun; 968():213-21. PubMed ID: 12119278
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A highly conserved processed PTEN pseudogene is located on chromosome band 9p21.
    Dahia PL; FitzGerald MG; Zhang X; Marsh DJ; Zheng Z; Pietsch T; von Deimling A; Haluska FG; Haber DA; Eng C
    Oncogene; 1998 May; 16(18):2403-6. PubMed ID: 9620558
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of a PTEN mutation in a family with Cowden syndrome and Bannayan-Zonana syndrome.
    Wanner M; Celebi JT; Peacocke M
    J Am Acad Dermatol; 2001 Feb; 44(2):183-7. PubMed ID: 11174374
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 35.