Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome-Reference-Cited by-同舟云学术

Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome

Published:2014-06-10 Issue:21 Volume:23 Page:5763-5773
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Abi Habib Walid,Azzi Salah,Brioude Frédéric,Steunou Virginie,Thibaud Nathalie,Neves Cristina Das,Le Jule Marilyne,Chantot-Bastaraud Sandra,Keren Boris,Lyonnet Stanislas,Michot Caroline,Rossi Massimiliano,Pasquier Laurent,Gicquel Christine,Rossignol Sylvie,Le Bouc Yves,Netchine Irène

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

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3. 11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations;J. Clin. Endocrinol. Metab.,2007

4. An enhancer deletion affects both H19 and Igf2 expression;Genes Dev.,1995

5. Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor;J. Biol. Chem.,1999

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