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Melanie Ehrlich et al.
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Roles for Dnmt3b in mammalian development: a mouse model for the ICF syndrome
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Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF)
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Interphase chromosomal abnormalities and mitotic missegregation of hypomethylated sequences in ICF syndrome cells
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CHROMOSOMA (2005)
Inactivation of Dnmt3b in mouse embryonic fibroblasts results in DNA hypomethylation, chromosomal instability, and spontaneous immortalization
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Normal histone modifications on the inactive X chromosome in ICF and Rett syndrome cells: implications for methyl-CpG binding proteins
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Molecular enzymology of the catalytic domains of the Dnmt3a and Dnmt3b DNA methyltransferases
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JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
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Prolonged culture of normal chorionic villus cells yields ICF syndrome-like chromatin decondensation and rearrangements
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Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2
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DNA methylation and chromosome instability in lymphoblastoid cell lines
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DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients
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