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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]