Imprinting Mutation in the Beckwith-Wiedemann Syndrome Leads to Biallelic IGF2 expression through an H19 -Independent Pathway

By Brown Keith W.   Villar Angela J.   Bickmore Wendy   Clayton-Smith Jill   Catchpoole Daniel   Maher Eamonn R.   Reik Wolf  

Human Molecular Genetics, Vol. 5, Iss. 12, 1996-12 ,pp. : 2027-2032

Oxford University Press

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

By Sandovici I.  

Human Molecular Genetics, Vol. 12, Iss. 13, 2003-07 ,pp. : 1569-1578

Oxford University Press

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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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The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites

By Beygo Jasmin   Citro Valentina   Sparago Angela   De Crescenzo Agostina   Cerrato Flavia   Heitmann Melanie   Rademacher Katrin   Guala Andrea   Enklaar Thorsten   Anichini Cecilia   Cirillo Silengo Margherita   Graf Notker   Prawitt Dirk   Cubellis Maria Vittoria   Horsthemke Bernhard   Buiting Karin   Riccio Andrea  

Human Molecular Genetics, Vol. 22, Iss. 3, 2013-02 ,pp. : 544-557

Oxford University Press

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Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms’ tumorigenesis and methylation hyper-dependence of H19 imprinting

By Dao Diem   Walsh Colum P.   Yuan Luwa   Gorelov Dmitri   Feng Lin   Hensle Terrence   Nisen Perry   Yamashiro Darrell J.   Bestor Timothy H.   Tycko Benjamin   Moulton T.   Steenman M.J.   Taniguchi T.   Moulton T.   Leighton P.A.   Nicholls R.D.   Lee M.H.   Matsuoka S.   Qian N.   Dao D.   Oren R.   Hussey D.J.   Reeve A.E.   Wadey R.B.   Mannens M.   Coppes M.J.   Besnard-Guerin C.   Grundy P.   Karnik P.   Betts D.R.   Chung W.Y.   Zhang Y.   Okamoto K.   Hu R.J.   Gabriel J.M.   Smilinich N.J.   Guillemot F.   Lee M.P.   Maecker H.T.   Miyazaki T.   Caspary T.   O’Keefe D.   Tycko B.   Barletta J.M.   Li E.   Li E.   Walsh C.P.   Weksberg R.   Hatada I.   Lee M.P.   Reik W.   Catchpoole D.   Joyce J.A.   Soejima H.   Tsang P.   Moore T.   Jones B.K.   Christofori G.   Hao Y.   Isfort R.J.   Chao L.Y.   Bestor T.H.   Colot V.   Berger C.   Cairney A.E.   Baylin S.B.   Bender C.M.   Belinsky S.A.   Orita M.   Hu R.J.   Yuan L.   Cooper P.R.   Lee M.P.   Schwienbacher C.   Lee M.P.   Gould T.D.  

Human Molecular Genetics, Vol. 8, Iss. 7, 1999-07 ,pp. : 1337-1352

Oxford University Press

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