Mutations in DNA methyltransferase DNMT3B in ICF syndrome affect its regulation by DNMT3L

By Xie Zheng-Hua   Huang Yan-Nv   Chen Zhao-Xia   Riggs Arthur D.   Ding Jian-Ping   Gowher Humaira   Jeltsch Albert   Sasaki Hiroyuki   Hata Kenichiro   Xu Guo-Liang  

Human Molecular Genetics, Vol. 15, Iss. 9, 2006-05 ,pp. : 1375-1385

Oxford University Press

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Hypomethylation of subtelomeric regions in ICF syndrome is associated with abnormally short telomeres and enhanced transcription from telomeric regions

By Yehezkel Shiran   Segev Yardena   Viegas-Pquignot Evani   Skorecki Karl   Selig Sara  

Human Molecular Genetics, Vol. 17, Iss. 18, 2008-09 ,pp. : 2776-2789

Oxford University Press

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DNA methyltransferase 3B (DNMT3B) mutations in ICF syndrome lead to altered epigenetic modifications and aberrant expression of genes regulating development, neurogenesis and immune function

By Jin Bilian   Tao Qian   Peng Jinrong   Soo Hui Meng   Wu Wei   Ying Jianming   Fields C. Robert   Delmas Amber L.   Liu Xuefeng   Qiu Jingxin   Robertson Keith D.  

Human Molecular Genetics, Vol. 17, Iss. 5, 2008-03 ,pp. : 690-709

Oxford University Press

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Stochastic imprinting in the progeny of Dnmt3L −/− females

By Arnaud Philippe   Hata Kenichiro   Kaneda Masahiro   Li En   Sasaki Hiroyuki   Feil Robert   Kelsey Gavin  

Human Molecular Genetics, Vol. 15, Iss. 4, 2006-02 ,pp. : 589-598

Oxford University Press

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DNMT3B interacts with constitutive centromere protein CENP-C to modulate DNA methylation and the histone code at centromeric regions

By Gopalakrishnan Suhasni   Sullivan Beth A.   Trazzi Stefania   Della Valle Giuliano   Robertson Keith D.  

Human Molecular Genetics, Vol. 18, Iss. 17, 2009-09 ,pp. : 3178-3193

Oxford University Press

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