BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Endocrine gland cancer AND RARA, RAR, 5914, ENSG00000131759, NR1B1 AND Diagnosis
7 results:

  • 1. Analysis of BRAF(V600E) mutation and DNA methylation improves the diagnostics of thyroid fine needle aspiration biopsies.
    Zhang B; Liu S; Zhang Z; Wei J; Qu Y; Wu K; Yang Q; Hou P; Shi B
    Diagn Pathol; 2014 Mar; 9():45. PubMed ID: 24588959
    [TBL] [Abstract] [Full Text] [Related]  

  • 2. mRNA expression pattern of retinoic acid and retinoid X nuclear receptor subtypes in human thyroid papillary carcinoma.
    Macejová D; Galbavý S; Podoba J; Bialešová L; Brtko J
    Oncol Rep; 2013 Nov; 30(5):2371-8. PubMed ID: 23969901
    [TBL] [Abstract] [Full Text] [Related]  

  • 3. Retinoid acid receptor expression is helpful to distinguish between adenoma and well-differentiated carcinoma in the thyroid.
    Gauchotte G; Lacomme S; Brochin L; Tournier B; Cahn V; Monhoven N; Piard F; Klein M; Martinet N; Rochette-Egly C; Vignaud JM
    Virchows Arch; 2013 Jun; 462(6):619-32. PubMed ID: 23639973
    [TBL] [Abstract] [Full Text] [Related]  

  • 4. Retinoic acid receptor and retinoid X receptor subtype expression for the differential diagnosis of thyroid neoplasms.
    Hoftijzer HC; Liu YY; Morreau H; van Wezel T; Pereira AM; Corssmit EP; Romijn JA; Smit JW
    Eur J Endocrinol; 2009 Apr; 160(4):631-8. PubMed ID: 19155317
    [TBL] [Abstract] [Full Text] [Related]  

  • 5. Quantitative assessment of promoter methylation profiles in thyroid neoplasms.
    Hoque MO; Rosenbaum E; Westra WH; Xing M; Ladenson P; Zeiger MA; Sidransky D; Umbricht CB
    J Clin Endocrinol Metab; 2005 Jul; 90(7):4011-8. PubMed ID: 15840741
    [TBL] [Abstract] [Full Text] [Related]  

  • 6. Promoter hypermethylation of MGMT, CDH1, rar-beta and SYK tumour suppressor genes in granulosa cell tumours (GCTs) of ovarian origin.
    Dhillon VS; Young AR; Husain SA; Aslam M
    Br J Cancer; 2004 Feb; 90(4):874-81. PubMed ID: 14970867
    [TBL] [Abstract] [Full Text] [Related]  

  • 7. Translocation (15;17)(q22;q21) as a secondary chromosomal abnormality in a case of acute monoblastic leukemia with tetrasomy 8.
    Zhang XX; Robinson LJ; Stenzel TT; Qumsiyeh MB
    Cancer Genet Cytogenet; 1999 Aug; 113(1):9-13. PubMed ID: 10459339
    [TBL] [Abstract] [Full Text] [Related]  


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