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

Author： 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.  

Publisher： Oxford University Press

ISSN： 1460-2083

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

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

Missense mutations in β-1,3- N -acetylglucosaminyltransferase 1 ( B3GNT1 ) cause Walker-Warburg syndrome

By Buysse Karen   Riemersma Moniek   Powell Gareth   van Reeuwijk Jeroen   Chitayat David   Roscioli Tony   Kamsteeg Erik-Jan   van den Elzen Christa   van Beusekom Ellen   Blaser Susan   Babul-Hirji Riyana   Halliday William   Wright Gavin J.   Stemple Derek L.   Lin Yung-Yao   Lefeber Dirk J.   van Bokhoven Hans  

Human Molecular Genetics, Vol. 22, Iss. 9, 2013-05 ,pp. : 1746-1754

Oxford University Press

Access to resources Recommend Favorite