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.


Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 9012481)

  • 1. Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinomas.
    Marsh DJ; Zheng Z; Zedenius J; Kremer H; Padberg GW; Larsson C; Longy M; Eng C
    Cancer Res; 1997 Feb; 57(3):500-3. PubMed ID: 9012481
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Somatic deletions and mutations in the Cowden disease gene, PTEN, in sporadic thyroid tumors.
    Dahia PL; Marsh DJ; Zheng Z; Zedenius J; Komminoth P; Frisk T; Wallin G; Parsons R; Longy M; Larsson C; Eng C
    Cancer Res; 1997 Nov; 57(21):4710-3. PubMed ID: 9354427
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fine-structure deletion mapping of 10q22-24 identifies regions of loss of heterozygosity and suggests that sporadic follicular thyroid adenomas and follicular thyroid carcinomas develop along distinct neoplastic pathways.
    Yeh JJ; Marsh DJ; Zedenius J; Dwight T; Delbridge L; Robinson BG; Eng C
    Genes Chromosomes Cancer; 1999 Dec; 26(4):322-8. PubMed ID: 10534767
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Differential loss of heterozygosity at 7q31.2 in follicular and papillary thyroid tumors.
    Zhang JS; Nelson M; McIver B; Hay ID; Goellner JR; Grant CS; Eberhardt NL; Smith DI
    Oncogene; 1998 Aug; 17(6):789-93. PubMed ID: 9715281
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regions.
    Kerangueven F; Eisinger F; Noguchi T; Allione F; Wargniez V; Eng C; Padberg G; Theillet C; Jacquemier J; Longy M; Sobol H; Birnbaum D
    Oncogene; 1997 Jan; 14(3):339-47. PubMed ID: 9018120
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Sporadic breast cancers exhibit loss of heterozygosity on chromosome segment 10q23 close to the Cowden disease locus.
    Singh B; Ittmann MM; Krolewski JJ
    Genes Chromosomes Cancer; 1998 Feb; 21(2):166-71. PubMed ID: 9491329
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Frequent loss of heterozygosity on chromosome 14 occurs in advanced colorectal carcinomas.
    Young J; Leggett B; Ward M; Thomas L; Buttenshaw R; Searle J; Chenevix-Trench G
    Oncogene; 1993 Mar; 8(3):671-5. PubMed ID: 8437850
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Somatic mutation and germline variants of MINPP1, a phosphatase gene located in proximity to PTEN on 10q23.3, in follicular thyroid carcinomas.
    Gimm O; Chi H; Dahia PL; Perren A; Hinze R; Komminoth P; Dralle H; Reynolds PR; Eng C
    J Clin Endocrinol Metab; 2001 Apr; 86(4):1801-5. PubMed ID: 11297621
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Distinct target regions for chromosome 1p deletions in parathyroid adenomas and carcinomas.
    Välimäki S; Forsberg L; Farnebo LO; Larsson C
    Int J Oncol; 2002 Oct; 21(4):727-35. PubMed ID: 12239610
    [TBL] [Abstract][Full Text] [Related]  

  • 11. High frequency of loss of heterozygosity in imprinted, compared with nonimprinted, genomic regions in follicular thyroid carcinomas and atypical adenomas.
    Sarquis MS; Weber F; Shen L; Broelsch CE; Jhiang SM; Zedenius J; Frilling A; Eng C
    J Clin Endocrinol Metab; 2006 Jan; 91(1):262-9. PubMed ID: 16249278
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Genetic and epigenetic changes in the APC gene in sporadic colorectal carcinoma with synchronous adenoma.
    Kim JC; Koo KH; Roh SA; Cho YK; Kim HC; Yu CS; Kim HJ; Kim JS; Cho MK
    Int J Colorectal Dis; 2003 May; 18(3):203-9. PubMed ID: 12673484
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial D-Loop instability in thyroid tumours is not a marker of malignancy.
    Máximo V; Lima J; Soares P; Botelho T; Gomes L; Sobrinho-Simões M
    Mitochondrion; 2005 Oct; 5(5):333-40. PubMed ID: 16183030
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Somatic mutations of the PTEN tumor suppressor gene in sporadic follicular thyroid tumors.
    Halachmi N; Halachmi S; Evron E; Cairns P; Okami K; Saji M; Westra WH; Zeiger MA; Jen J; Sidransky D
    Genes Chromosomes Cancer; 1998 Nov; 23(3):239-43. PubMed ID: 9790504
    [TBL] [Abstract][Full Text] [Related]  

  • 16. High resolution loss of heterozygosity mapping of 17p13 in thyroid cancer: Hurthle cell carcinomas exhibit a small 411-kilobase common region of allelic imbalance, probably containing a novel tumor suppressor gene.
    Farrand K; Delahunt B; Wang XL; McIver B; Hay ID; Goellner JR; Eberhardt NL; Grebe SK
    J Clin Endocrinol Metab; 2002 Oct; 87(10):4715-21. PubMed ID: 12364463
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Low frequency of numerical chromosomal aberrations in follicular thyroid tumors detected by comparative genomic hybridization.
    Frisk T; Kytölä S; Wallin G; Zedenius J; Larsson C
    Genes Chromosomes Cancer; 1999 Aug; 25(4):349-53. PubMed ID: 10398428
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sporadic follicular thyroid tumors show loss of a 200-kb region in 11q13 without evidence for mutations in the MEN1 gene.
    Nord B; Larsson C; Wong FK; Wallin G; Teh BT; Zedenius J
    Genes Chromosomes Cancer; 1999 Sep; 26(1):35-9. PubMed ID: 10441003
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Studies of allelic loss in thyroid tumors reveal major differences in chromosomal instability between papillary and follicular carcinomas.
    Ward LS; Brenta G; Medvedovic M; Fagin JA
    J Clin Endocrinol Metab; 1998 Feb; 83(2):525-30. PubMed ID: 9467569
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Localization of the gene for Cowden disease to chromosome 10q22-23.
    Nelen MR; Padberg GW; Peeters EA; Lin AY; van den Helm B; Frants RR; Coulon V; Goldstein AM; van Reen MM; Easton DF; Eeles RA; Hodgsen S; Mulvihill JJ; Murday VA; Tucker MA; Mariman EC; Starink TM; Ponder BA; Ropers HH; Kremer H; Longy M; Eng C
    Nat Genet; 1996 May; 13(1):114-6. PubMed ID: 8673088
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.