The long non-coding RNA Meg3 mediates imprinted gene expression during stem cell differentiation von Farhadova, Sabina, Ghousein, Amani, Charon, François, Surcis, Caroline, Gomez-Velazques, Melisa, Roidor, Clara, Di Michele, Flavio, Borensztein, Maud, De Sario, Albertina, Esnault, Cyril, Noordermeer, Daan, Moindrot, Benoit, Feil, Robert

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Blood co-expression modules identify potential modifier genes of diabetes and lung function in cystic fibrosis von Pineau, Fanny, Caimmi, Davide, Magalhães, Milena, Fremy, Enora, Mohamed, Abdillah, Mely, Laurent, Leroy, Sylvie, Murris, Marlène, Claustres, Mireille, Chiron, Raphael, De Sario, Albertina

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Nasal epithelial cells: a tool to study DNA methylation in airway diseases von Bergougnoux, Anne, Claustres, Mireille, De Sario, Albertina

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Dynamic changes of DNA methylation and lung disease in cystic fibrosis: lessons from a monogenic disease von Magalhães, Milena, Tost, Jörg, Pineau, Fanny, Rivals, Isabelle, Busato, Florence, Alary, Nathan, Mely, Laurent, Leroy, Sylvie, Murris, Marlène, Caimmi, Davide, Claustres, Mireille, Chiron, Raphaël, Sario, Albertina De

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Clinical and molecular overview of inherited disorders resulting from epigenomic dysregulation von De Sario, Albertina

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Heterochromatic genes undergo epigenetic changes and escape silencing in immunodeficiency, centromeric instability, facial anomalies (ICF) syndrome von Brun, Marie-Elisabeth, Lana, Erica, Rivals, Isabelle, Lefranc, Gérard, Sarda, Pierre, Claustres, Mireille, Mégarbané, André, De Sario, Albertina

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DNA methylation changes in cystic fibrosis: Cause or consequence? von Scott, Madeleine, De Sario, Albertina

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DNA replication is altered in Immunodeficiency Centromeric instability Facial anomalies (ICF) cells carrying DNMT3B mutations von LANA, Erica, MEGARBANE, Andre, TOURRIERE, Helene, SARDA, Pierre, LEFRANC, Gerard, CLAUSTRES, Mireille, DE SARIO, Albertina

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BAGE Hypomethylation, A New Epigenetic Biomarker for Colon Cancer Detection von Grunau, Christoph, Brun, Me, Rivals, I., Selves, Janick, Hindermann, W., Favre-Mercuret, M., Granier, G., de Sario, Albertina

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The long non-coding RNA Meg3 mediates imprinted gene expression during stem cell differentiation von Farhadova, Sabina, Ghousein, Amani, Charon, François, Surcis, Caroline, Gomez-Velazques, Melisa, Roidor, Clara, Di Michele, Flavio, Borensztein, Maud, de Sario, Albertina, Esnault, Cyril, Noordermeer, Daan, Moindrot, Benoit, Feil, Robert

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New BAGE (B melanoma antigen) genes mapping to the juxtacentromeric regions of human chromosomes 13 and 21 have a cancer/testis expression profile von Ruault, Myriam, van der Bruggen, Pierre, Brun, Marie-Elisabeth, Boyle, Shelagh, Roizès, Gérard, De Sario, Albertina

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BAGE Hypomethylation Is an Early Event in Colon Transformation and Is Frequent in Histologically Advanced Adenomas von Lana, Erica, Brun, Marie-Elisabeth, Rivals, Isabelle, Selves, Janick, Kirzin, Sylvain, Lutsyk, Andriy P, Gordiyuk, Vasily V, Bibeau, Frédéric, Rynditch, Alla, De Sario, Albertina

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The HDAC inhibitor SAHA does not rescue CFTR membrane expression in Cystic Fibrosis von Bergougnoux, Anne, Petit, Aurélie, Knabe, Lucie, Bribes, Estelle, Chiron, Raphaël, De Sario, Albertina, Claustres, Mireille, Molinari, Nicolas, Vachier, Isabelle, Taulan-Cadars, Magali, Bourdin, Arnaud

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DNA Methylation at ATP11A cg11702988 Is a Biomarker of Lung Disease Severity in Cystic Fibrosis: A Longitudinal Study von Pineau, Fanny, Caimmi, Davide, Taviaux, Sylvie, Reveil, Maurane, Brosseau, Laura, Rivals, Isabelle, Drevait, Margot, Vachier, Isabelle, Claustres, Mireille, Chiron, Raphaël, De Sario, Albertina

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DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosis von Magalhães, Milena, Rivals, Isabelle, Claustres, Mireille, Varilh, Jessica, Thomasset, Mélodie, Bergougnoux, Anne, Mely, Laurent, Leroy, Sylvie, Corvol, Harriet, Guillot, Loïc, Murris, Marlène, Beyne, Emmanuelle, Caimmi, Davide, Vachier, Isabelle, Chiron, Raphaël, De Sario, Albertina

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Frequent DNA hypomethylation of human juxtacentromericBAGE loci in cancer von Grunau, Christoph, Sanchez, Cecilia, Ehrlich, Melanie, van der Bruggen, Pierre, Hindermann, Winfried, Rodriguez, Carmen, Krieger, Sophie, Dubeau, Louis, Fiala, Emerich, De Sario, Albertina

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MLL3, a new human member of the TRX/MLL gene family, maps to 7q36, a chromosome region frequently deleted in myeloid leukaemia von Ruault, Myriam, Brun, Marie Elisabeth, Ventura, Mario, Roizès, Gérard, De Sario, Albertina

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A balance between activating and repressive histone modifications regulates cystic fibrosis transmembrane conductance regulator (CFTR) expression in vivo von Bergougnoux, Anne, Rivals, Isabelle, Liquori, Alessandro, Raynal, Caroline, Varilh, Jessica, Magalhães, Milena, Perez, Marie-José, Bigi, Nicole, Des Georges, Marie, Chiron, Raphaël, Squalli-Houssaini, Ahmed Saad, Claustres, Mireille, De Sario, Albertina

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Heterochromatic Genes Undergo Epigenetic Changes and Escape Silencing in Immunodeficiency, Centromeric Instability, Facial Anomalies von Brun, Marie-Elisabeth, Lana, Erica, Rivals, Isabelle, Lefranc, Gérard, Sarda, Pierre, Claustres, Mireille, Mégarbané, André, De Sario, Albertina

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Mapping of the juxtacentromeric heterochromatin-euchromatin frontier of human chromosome 21 von Grunau, Christoph, Buard, Jérome, Brun, Marie-Elisabeth, De Sario, Albertina

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