A developmental window of opportunity for imprinted gene silencing mediated by DNA methylation and the Kcnq1ot1 noncoding RNA

By Green Kelly   Lewis Annabelle   Dawson Claire   Dean Wendy   Reinhart Bonnie   Chaillet J.   Reik Wolf  

Mammalian Genome, Vol. 18, Iss. 1, 2007-01 ,pp. : 32-42

Springer Publishing Company

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Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith–Wiedemann syndrome

By Olney A.  

Human Molecular Genetics, Vol. 11, Iss. 11, 2002-05 ,pp. : 1317-1325

Oxford University Press

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The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell syndrome cases

By Chiesa Nicoletta   De Crescenzo Agostina   Mishra Kankadeb   Perone Lucia   Carella Massimo   Palumbo Orazio   Mussa Alessandro   Sparago Angela   Cerrato Flavia   Russo Silvia   Lapi Elisabetta   Cubellis Maria Vittoria   Kanduri Chandrasekhar   Cirillo Silengo Margherita   Riccio Andrea   Ferrero Giovanni Battista  

Human Molecular Genetics, Vol. 21, Iss. 1, 2012-01 ,pp. : 10-25

Oxford University Press

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Tumor development in the Beckwith–Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1

By Weksberg Rosanna  

Human Molecular Genetics, Vol. 10, Iss. 26, 2001-12 ,pp. : 2989-3000

Oxford University Press

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Heightened susceptibility to chronic gastritis, hyperplasia and metaplasia in Kcnq1 mutant mice

By Elso Colleen M.  

Human Molecular Genetics, Vol. 13, Iss. 22, 2004-11 ,pp. : 2813-2821

Oxford University Press

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