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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DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes

By Belohradsky B.H.  

Human Molecular Genetics, Vol. 10, Iss. 25, 2001-12 ,pp. : 2917-2931

Oxford University Press

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A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylation

By El-Maarri Osman   Kareta Michael S.   Mikeska Thomas   Becker Tim   Diaz-Lacava Amalia   Junen Judith   Nsgen Nicole   Behne Frank   Wienker Thomas   Waha Andreas   Oldenburg Johannes   Chdin Frdric  

Human Molecular Genetics, Vol. 18, Iss. 10, 2009-05 ,pp. : 1755-1768

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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