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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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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Epigenetic analysis of the Dlk1–Gtl2 imprinted domain on mouse chromosome 12: implications for imprinting control from comparison with Igf2–H19

By Kelsey G.  

Human Molecular Genetics, Vol. 11, Iss. 1, 2002-01 ,pp. : 77-86

Oxford University Press

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Chromosome 11p15.5 Regional Imprinting: Comparative Analysis of KIP2 and H19 in Human Tissues and Wilms' Tumors

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Human Molecular Genetics, Vol. 5, Iss. 8, 1996-01 ,pp. : 1101-1108

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Different mechanisms cause imprinting defects at the IGF2 / H19 locus in BeckwithWiedemann syndrome and Wilms' tumour

By Cerrato Flavia   Sparago Angela   Verde Gaetano   De Crescenzo Agostina   Citro Valentina   Cubellis Maria Vittoria   Rinaldi Maria Michela   Boccuto Luigi   Neri Giovanni   Magnani Cinzia   D'Angelo Paolo   Collini Paola   Perotti Daniela   Sebastio Gianfranco   Maher Eamonn R.   Riccio Andrea  

Human Molecular Genetics, Vol. 17, Iss. 10, 2008-05 ,pp. : 1427-1435

Oxford University Press

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