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 *

374 related articles for article (PubMed ID: 18432406)

  • 1. ICF, an immunodeficiency syndrome: DNA methyltransferase 3B involvement, chromosome anomalies, and gene dysregulation.
    Ehrlich M; Sanchez C; Shao C; Nishiyama R; Kehrl J; Kuick R; Kubota T; Hanash SM
    Autoimmunity; 2008 May; 41(4):253-71. PubMed ID: 18432406
    [TBL] [Abstract][Full Text] [Related]  

  • 2. DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes.
    Ehrlich M; Buchanan KL; Tsien F; Jiang G; Sun B; Uicker W; Weemaes CM; Smeets D; Sperling K; Belohradsky BH; Tommerup N; Misek DE; Rouillard JM; Kuick R; Hanash SM
    Hum Mol Genet; 2001 Dec; 10(25):2917-31. PubMed ID: 11741835
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF).
    Ehrlich M; Jackson K; Weemaes C
    Orphanet J Rare Dis; 2006 Mar; 1():2. PubMed ID: 16722602
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. DNA hypomethylation, cancer, the immunodeficiency, centromeric region instability, facial anomalies syndrome and chromosomal rearrangements.
    Ehrlich M
    J Nutr; 2002 Aug; 132(8 Suppl):2424S-2429S. PubMed ID: 12163705
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients.
    Tuck-Muller CM; Narayan A; Tsien F; Smeets DF; Sawyer J; Fiala ES; Sohn OS; Ehrlich M
    Cytogenet Cell Genet; 2000; 89(1-2):121-8. PubMed ID: 10894953
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The ICF syndrome, a DNA methyltransferase 3B deficiency and immunodeficiency disease.
    Ehrlich M
    Clin Immunol; 2003 Oct; 109(1):17-28. PubMed ID: 14585272
    [TBL] [Abstract][Full Text] [Related]  

  • 9. DNA replication is altered in Immunodeficiency Centromeric instability Facial anomalies (ICF) cells carrying DNMT3B mutations.
    Lana E; Mégarbané A; Tourrière H; Sarda P; Lefranc G; Claustres M; De Sario A
    Eur J Hum Genet; 2012 Oct; 20(10):1044-50. PubMed ID: 22378288
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Prolonged culture of normal chorionic villus cells yields ICF syndrome-like chromatin decondensation and rearrangements.
    Tsien F; Fiala ES; Youn B; Long TI; Laird PW; Weissbecker K; Ehrlich M
    Cytogenet Genome Res; 2002; 98(1):13-21. PubMed ID: 12584436
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Heterochromatic genes undergo epigenetic changes and escape silencing in immunodeficiency, centromeric instability, facial anomalies (ICF) syndrome.
    Brun ME; Lana E; Rivals I; Lefranc G; Sarda P; Claustres M; Mégarbané A; De Sario A
    PLoS One; 2011 Apr; 6(4):e19464. PubMed ID: 21559330
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells.
    Gisselsson D; Shao C; Tuck-Muller CM; Sogorovic S; Pålsson E; Smeets D; Ehrlich M
    Chromosoma; 2005 Jul; 114(2):118-26. PubMed ID: 15856360
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO-1 and UBC9.
    Kloeckener-Gruissem B; Betts DR; Zankl A; Berger W; Güngör T
    Am J Med Genet A; 2005 Jul; 136(1):31-7. PubMed ID: 15952214
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Epigenetic alteration of microRNAs in DNMT3B-mutated patients of ICF syndrome.
    Gatto S; Della Ragione F; Cimmino A; Strazzullo M; Fabbri M; Mutarelli M; Ferraro L; Weisz A; D'Esposito M; Matarazzo MR
    Epigenetics; 2010 Jul; 5(5):427-43. PubMed ID: 20448464
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Subtelomeric methylation distinguishes between subtypes of Immunodeficiency, Centromeric instability and Facial anomalies syndrome.
    Toubiana S; Velasco G; Chityat A; Kaindl AM; Hershtig N; Tzur-Gilat A; Francastel C; Selig S
    Hum Mol Genet; 2018 Oct; 27(20):3568-3581. PubMed ID: 30010917
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.