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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

Paternal imprints can be established on the maternal Igf2-H19 locus without altering replication timing of DNA

By Cerrato Flavia  

Human Molecular Genetics, Vol. 12, Iss. 23, 2003-12 ,pp. : 3123-3132

Oxford University Press

Access to resources Recommend Favorite

Heritable rather than age-related environmental and stochastic factors dominate variation in DNA methylation of the human IGF2/H19 locus

By Heijmans Bastiaan T.   Kremer Dennis   Tobi Elmar W.   Boomsma Dorret I.   Slagboom P. Eline  

Human Molecular Genetics, Vol. 16, Iss. 5, 2007-03 ,pp. : 547-554

Oxford University Press

Access to resources Recommend Favorite

Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith–Wiedemann syndrome and Silver–Russell syndrome

By Nativio Raffaella   Sparago Angela   Ito Yoko   Weksberg Rosanna   Riccio Andrea   Murrell Adele  

Human Molecular Genetics, Vol. 20, Iss. 7, 2011-04 ,pp. : 1363-1374

Oxford University Press

Access to resources Recommend Favorite