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 *

168 related articles for article (PubMed ID: 16451126)

  • 1. Altered gene silencing and human diseases.
    Perini G; Tupler R
    Clin Genet; 2006 Jan; 69(1):1-7. PubMed ID: 16451126
    [TBL] [Abstract][Full Text] [Related]  

  • 2. When enough is enough: genetic diseases associated with transcriptional derepression.
    Gabellini D; Green MR; Tupler R
    Curr Opin Genet Dev; 2004 Jun; 14(3):301-7. PubMed ID: 15172674
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The role of genetics in the establishment and maintenance of the epigenome.
    Huidobro C; Fernandez AF; Fraga MF
    Cell Mol Life Sci; 2013 May; 70(9):1543-73. PubMed ID: 23474979
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Lessons from two human chromatin diseases, ICF syndrome and Rett syndrome.
    Matarazzo MR; De Bonis ML; Vacca M; Della Ragione F; D'Esposito M
    Int J Biochem Cell Biol; 2009 Jan; 41(1):117-26. PubMed ID: 18786650
    [TBL] [Abstract][Full Text] [Related]  

  • 5. DNA methylation and human diseases.
    El-Maarri O
    Adv Exp Med Biol; 2003; 544():135-44. PubMed ID: 14713224
    [No Abstract]   [Full Text] [Related]  

  • 6. Epigenetic and chromatin modifiers as targeted therapy of hematologic malignancies.
    Bhalla KN
    J Clin Oncol; 2005 Jun; 23(17):3971-93. PubMed ID: 15897549
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Digenic inheritance and Mendelian disease.
    Lupski JR
    Nat Genet; 2012 Dec; 44(12):1291-2. PubMed ID: 23192179
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Epigenetic mechanisms of facioscapulohumeral muscular dystrophy.
    de Greef JC; Frants RR; van der Maarel SM
    Mutat Res; 2008 Dec; 647(1-2):94-102. PubMed ID: 18723032
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic syndromes caused by mutations in epigenetic genes.
    Berdasco M; Esteller M
    Hum Genet; 2013 Apr; 132(4):359-83. PubMed ID: 23370504
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Perturbations of chromatin structure in human genetic disease: recent advances.
    Bickmore WA; van der Maarel SM
    Hum Mol Genet; 2003 Oct; 12 Spec No 2():R207-13. PubMed ID: 12915455
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Epigenetic Deregulation in Human Primary Immunodeficiencies.
    Campos-Sanchez E; Martínez-Cano J; Del Pino Molina L; López-Granados E; Cobaleda C
    Trends Immunol; 2019 Jan; 40(1):49-65. PubMed ID: 30509895
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Genetics and Epigenetics of Facioscapulohumeral Muscular Dystrophy.
    Himeda CL; Jones PL
    Annu Rev Genomics Hum Genet; 2019 Aug; 20():265-291. PubMed ID: 31018108
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dynamic and reversibility of heterochromatic gene silencing in human disease.
    Zardo G; Fazi F; Travaglini L; Nervi C
    Cell Res; 2005 Sep; 15(9):679-90. PubMed ID: 16212874
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Normal histone modifications on the inactive X chromosome in ICF and Rett syndrome cells: implications for methyl-CpG binding proteins.
    Gartler SM; Varadarajan KR; Luo P; Canfield TK; Traynor J; Francke U; Hansen RS
    BMC Biol; 2004 Sep; 2():21. PubMed ID: 15377381
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Syndromes of disordered chromatin remodeling.
    Ausió J; Levin DB; De Amorim GV; Bakker S; Macleod PM
    Clin Genet; 2003 Aug; 64(2):83-95. PubMed ID: 12859401
    [TBL] [Abstract][Full Text] [Related]  

  • 16. DNA methyltransferase 3B (DNMT3B) mutations in ICF syndrome lead to altered epigenetic modifications and aberrant expression of genes regulating development, neurogenesis and immune function.
    Jin B; Tao Q; Peng J; Soo HM; Wu W; Ying J; Fields CR; Delmas AL; Liu X; Qiu J; Robertson KD
    Hum Mol Genet; 2008 Mar; 17(5):690-709. PubMed ID: 18029387
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Facioscapulohumeral muscular dystrophy as a model for epigenetic regulation and disease.
    Himeda CL; Jones TI; Jones PL
    Antioxid Redox Signal; 2015 Jun; 22(16):1463-82. PubMed ID: 25336259
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Epigenetic deregulation of genomic imprinting in human disorders and following assisted reproduction.
    Arnaud P; Feil R
    Birth Defects Res C Embryo Today; 2005 Jun; 75(2):81-97. PubMed ID: 16035043
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The epigenetics of nuclear envelope organization and disease.
    Schirmer EC
    Mutat Res; 2008 Dec; 647(1-2):112-21. PubMed ID: 18722388
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Heterochromatin dysregulation in human diseases.
    Hahn M; Dambacher S; Schotta G
    J Appl Physiol (1985); 2010 Jul; 109(1):232-42. PubMed ID: 20360431
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.