Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci

By Azzi Salah   Rossignol Sylvie   Steunou Virginie   Sas Theo   Thibaud Nathalie   Danton Fabienne   Le Jule Maryline   Heinrichs Claudine   Cabrol Sylvie   Gicquel Christine   Le Bouc Yves   Netchine Irene  

Human Molecular Genetics, Vol. 18, Iss. 24, 2009-12 ,pp. : 4724-4733

Oxford University Press

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Maternal alleles acquiring paternal methylation patterns in biparental complete hydatidiform moles

By El-Maarri O.  

Human Molecular Genetics, Vol. 12, Iss. 12, 2003-06 ,pp. : 1405-1413

Oxford University Press

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Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion

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Human Molecular Genetics, Vol. 9, Iss. 11, 2000-07 ,pp. : 1587-1595

Oxford University Press

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CTCF binding sites promote transcription initiation and prevent DNA methylation on the maternal allele at the imprinted H19/Igf2 locus

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Human Molecular Genetics, Vol. 15, Iss. 19, 2006-10 ,pp. : 2945-2954

Oxford University Press

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Correlation of expression and methylation of imprinted genes with pluripotency of parthenogenetic embryonic stem cells

By Li Chao   Chen Zhisheng   Liu Zhong   Huang Junjiu   Zhang Wei   Zhou Lingjun   Keefe David L.   Liu Lin  

Human Molecular Genetics, Vol. 18, Iss. 12, 2009-06 ,pp. : 2177-2187

Oxford University Press

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