Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regions

By Sandovici Ionel   Leppert Mark   Hawk Patricia Red   Suarez Alexander   Linares Yendi   Sapienza Carmen  

Human Molecular Genetics, Vol. 13, Iss. 7, 2004-04 ,pp. : 781-781

Oxford University Press

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Promoter-restricted histone code, not the differentially methylated DNA regions or antisense transcripts, marks the imprinting status of IGF2R in human and mouse

By Vu Thanh H.   Li Tao  

Human Molecular Genetics, Vol. 13, Iss. 19, 2004-10 ,pp. : 2233-2245

Oxford University Press

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Loss of imprinting of IGF2 and H19 in osteosarcoma is accompanied by reciprocal methylation changes of a CTCF-binding site

By Ladanyi M.  

Human Molecular Genetics, Vol. 12, Iss. 5, 2003-03 ,pp. : 535-549

Oxford University Press

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The H19 methylation imprint is erased and re‐established differentially on the parental alleles during male germ cell development

By Davis Tamara L.   Yang Grace J.   McCarrey JohnR.   Bartolomei MarisaS.  

Human Molecular Genetics, Vol. 9, Iss. 19, 2000-11 ,pp. : 2885-2894

Oxford University Press

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Deletion of a nuclease-sensitive region between the Igf2 and H19 genes leads to Igf2 misregulation and increased adiposity

By Jones B.K.   Levorse J.   Tilghman S.M.  

Human Molecular Genetics, Vol. 10, Iss. 8, 2001-04 ,pp. : 807-814

Oxford University Press

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