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 *

230 related articles for article (PubMed ID: 15580563)

  • 1. DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.
    Jiang YL; Rigolet M; Bourc'his D; Nigon F; Bokesoy I; Fryns JP; Hultén M; Jonveaux P; Maraschio P; Mégarbané A; Moncla A; Viegas-Péquignot E
    Hum Mutat; 2005 Jan; 25(1):56-63. PubMed ID: 15580563
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic variation in ICF syndrome: evidence for genetic heterogeneity.
    Wijmenga C; Hansen RS; Gimelli G; Björck EJ; Davies EG; Valentine D; Belohradsky BH; van Dongen JJ; Smeets DF; van den Heuvel LP; Luyten JA; Strengman E; Weemaes C; Pearson PL
    Hum Mutat; 2000 Dec; 16(6):509-17. PubMed ID: 11102980
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Satellite 2 methylation patterns in normal and ICF syndrome cells and association of hypomethylation with advanced replication.
    Hassan KM; Norwood T; Gimelli G; Gartler SM; Hansen RS
    Hum Genet; 2001 Oct; 109(4):452-62. PubMed ID: 11702227
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene.
    Xu GL; Bestor TH; Bourc'his D; Hsieh CL; Tommerup N; Bugge M; Hulten M; Qu X; Russo JJ; Viegas-Péquignot E
    Nature; 1999 Nov; 402(6758):187-91. PubMed ID: 10647011
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Three novel DNMT3B mutations in Japanese patients with ICF syndrome.
    Shirohzu H; Kubota T; Kumazawa A; Sado T; Chijiwa T; Inagaki K; Suetake I; Tajima S; Wakui K; Miki Y; Hayashi M; Fukushima Y; Sasaki H
    Am J Med Genet; 2002 Sep; 112(1):31-7. PubMed ID: 12239717
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Subcellular distribution of HP1 proteins is altered in ICF syndrome.
    Luciani JJ; Depetris D; Missirian C; Mignon-Ravix C; Metzler-Guillemain C; Megarbane A; Moncla A; Mattei MG
    Eur J Hum Genet; 2005 Jan; 13(1):41-51. PubMed ID: 15470359
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in DNA methyltransferase DNMT3B in ICF syndrome affect its regulation by DNMT3L.
    Xie ZH; Huang YN; Chen ZX; Riggs AD; Ding JP; Gowher H; Jeltsch A; Sasaki H; Hata K; Xu GL
    Hum Mol Genet; 2006 May; 15(9):1375-85. PubMed ID: 16543361
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hypomethylation of subtelomeric regions in ICF syndrome is associated with abnormally short telomeres and enhanced transcription from telomeric regions.
    Yehezkel S; Segev Y; Viegas-Péquignot E; Skorecki K; Selig S
    Hum Mol Genet; 2008 Sep; 17(18):2776-89. PubMed ID: 18558631
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome).
    Hagleitner MM; Lankester A; Maraschio P; Hultén M; Fryns JP; Schuetz C; Gimelli G; Davies EG; Gennery A; Belohradsky BH; de Groot R; Gerritsen EJ; Mattina T; Howard PJ; Fasth A; Reisli I; Furthner D; Slatter MA; Cant AJ; Cazzola G; van Dijken PJ; van Deuren M; de Greef JC; van der Maarel SM; Weemaes CM
    J Med Genet; 2008 Feb; 45(2):93-9. PubMed ID: 17893117
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel deletion in ZBTB24 in a Lebanese family with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2.
    Chouery E; Abou-Ghoch J; Corbani S; El Ali N; Korban R; Salem N; Castro C; Klayme S; Azoury-Abou Rjeily M; Khoury-Matar R; Debo G; Germanos-Haddad M; Delague V; Lefranc G; Mégarbané A
    Clin Genet; 2012 Nov; 82(5):489-93. PubMed ID: 21906047
    [TBL] [Abstract][Full Text] [Related]  

  • 12. ICF syndrome mutations cause a broad spectrum of biochemical defects in DNMT3B-mediated de novo DNA methylation.
    Moarefi AH; Chédin F
    J Mol Biol; 2011 Jun; 409(5):758-72. PubMed ID: 21549127
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome.
    Dupont C; Guimiot F; Perrin L; Marey I; Smiljkovski D; Le Tessier D; Lebugle C; Baumann C; Bourdoncle P; Tabet AC; Aboura A; Benzacken B; Dupont JM
    Clin Genet; 2012 Aug; 82(2):187-92. PubMed ID: 21554265
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dissecting de novo methylation.
    Reik W; Kelsey G; Walter J
    Nat Genet; 1999 Dec; 23(4):380-2. PubMed ID: 10581015
    [No Abstract]   [Full Text] [Related]  

  • 15. Genome-Wide DNA Methylation Analysis Identifies Novel Hypomethylated Non-Pericentromeric Genes with Potential Clinical Implications in ICF Syndrome.
    Simo-Riudalbas L; Diaz-Lagares A; Gatto S; Gagliardi M; Crujeiras AB; Matarazzo MR; Esteller M; Sandoval J
    PLoS One; 2015; 10(7):e0132517. PubMed ID: 26161907
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Regulation of DNA methylation activity through Dnmt3L promoter methylation by Dnmt3 enzymes in embryonic development.
    Hu YG; Hirasawa R; Hu JL; Hata K; Li CL; Jin Y; Chen T; Li E; Rigolet M; Viegas-Péquignot E; Sasaki H; Xu GL
    Hum Mol Genet; 2008 Sep; 17(17):2654-64. PubMed ID: 18544626
    [TBL] [Abstract][Full Text] [Related]  

  • 17. X inactivation-specific methylation of LINE-1 elements by DNMT3B: implications for the Lyon repeat hypothesis.
    Hansen RS
    Hum Mol Genet; 2003 Oct; 12(19):2559-67. PubMed ID: 12925568
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hematopoietic stem cell transplantation corrects the immunologic abnormalities associated with immunodeficiency-centromeric instability-facial dysmorphism syndrome.
    Gennery AR; Slatter MA; Bredius RG; Hagleitner MM; Weemaes C; Cant AJ; Lankester AC
    Pediatrics; 2007 Nov; 120(5):e1341-4. PubMed ID: 17908720
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Defective de novo methylation of viral and cellular DNA sequences in ICF syndrome cells.
    Tao Q; Huang H; Geiman TM; Lim CY; Fu L; Qiu GH; Robertson KD
    Hum Mol Genet; 2002 Sep; 11(18):2091-102. PubMed ID: 12189161
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome.
    Hansen RS; Wijmenga C; Luo P; Stanek AM; Canfield TK; Weemaes CM; Gartler SM
    Proc Natl Acad Sci U S A; 1999 Dec; 96(25):14412-7. PubMed ID: 10588719
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.