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Blood co-expression modules identify potential modifier genes of diabetes and lung function in cystic fibrosis

PloS one, 2020-04, Vol.15 (4), p.e0231285-e0231285

2020

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Nasal epithelial cells: a tool to study DNA methylation in airway diseases

Epigenomics, 2015-02, Vol.7 (1), p.119-126

2015

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Dynamic changes of DNA methylation and lung disease in cystic fibrosis: lessons from a monogenic disease

Epigenomics, 2018-08, Vol.10 (8), p.1131-1145

2018

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DNA Methylation at ATP11A cg11702988 Is a Biomarker of Lung Disease Severity in Cystic Fibrosis: A Longitudinal Study

Genes, 2021-03, Vol.12 (3), p.441

2021

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Clinical and molecular overview of inherited disorders resulting from epigenomic dysregulation

European journal of medical genetics, 2009-11, Vol.52 (6), p.363-372

De Sario, Albertina

2009

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Heterochromatic genes undergo epigenetic changes and escape silencing in immunodeficiency, centromeric instability, facial anomalies (ICF) syndrome

PloS one, 2011-04, Vol.6 (4), p.e19464-e19464

2011

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DNA replication is altered in Immunodeficiency Centromeric instability Facial anomalies (ICF) cells carrying DNMT3B mutations

European journal of human genetics : EJHG, 2012-10, Vol.20 (10), p.1044-1050

2012

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DNA methylation changes in cystic fibrosis: Cause or consequence?

Clinical genetics, 2020-07, Vol.98 (1), p.3-9

2020

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BAGE Hypomethylation Is an Early Event in Colon Transformation and Is Frequent in Histologically Advanced Adenomas

Cancers, 2009-11, Vol.1 (1), p.3-11

2009

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BAGE Hypomethylation, A New Epigenetic Biomarker for Colon Cancer Detection

Cancer epidemiology, biomarkers & prevention, 2008-06, Vol.17 (6), p.1374-1379

2008

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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

European journal of human genetics : EJHG, 2002-12, Vol.10 (12), p.833-840

2002

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The HDAC inhibitor SAHA does not rescue CFTR membrane expression in Cystic Fibrosis

The international journal of biochemistry & cell biology, 2017-07, Vol.88, p.124-132

2017

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DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosis

Clinical epigenetics, 2017-02, Vol.9 (1), p.19-19, Article 19

2017

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Frequent DNA hypomethylation of human juxtacentromericBAGE loci in cancer

Genes chromosomes & cancer, 2005-05, Vol.43 (1), p.11-24

2005

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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

Gene, 2002-02, Vol.284 (1-2), p.73-81

2002

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A balance between activating and repressive histone modifications regulates cystic fibrosis transmembrane conductance regulator (CFTR) expression in vivo

Epigenetics, 2014-07, Vol.9 (7), p.1007-1017

2014

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Mapping of the juxtacentromeric heterochromatin-euchromatin frontier of human chromosome 21

Genome Research, 2006-10, Vol.16 (10), p.1198-1207

2006

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Heterochromatic Genes Undergo Epigenetic Changes and Escape Silencing in Immunodeficiency

PloS one, 2011, Vol.6 (4)

2011

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DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosis

Clinical epigenetics, 2016-12, Vol.9 (1)

2016

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Heterochromatic Genes Undergo Epigenetic Changes and Escape Silencing in Immunodeficiency, Centromeric Instability, Facial Anomalies

PloS one, 2011-04, Vol.6 (4), p.e19464

2011

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Frequent DNA hypomethylation of human juxtacentromeric BAGE loci in cancer

Genes chromosomes & cancer, 2005-05, Vol.43 (1), p.11-24

2005

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The Highest Gene Concentrations in the Human Genome are in Telomeric Bands of Metaphase Chromosomes

Proceedings of the National Academy of Sciences - PNAS, 1992-06, Vol.89 (11), p.4913-4917

1992

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Characterization and expression analysis during embryo development of the mouse ortholog of MLL3

Gene, 2006-04, Vol.371 (1), p.25-33

2006

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Juxtacentromeric region of human chromosome 21: a boundary between centromeric heterochromatin and euchromatic chromosome arms

Gene, 2003-07, Vol.312, p.41-50

2003

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Correlations Between Isochores and Chromosomal Bands in the Human Genome

Proceedings of the National Academy of Sciences - PNAS, 1993-12, Vol.90 (24), p.11929-11933

1993

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Fundamental And Applied Biological Sciences. Psychology
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Blood co-expression modules identify potential modifier genes of diabetes and lung function in cystic fibrosis

Nasal epithelial cells: a tool to study DNA methylation in airway diseases

Dynamic changes of DNA methylation and lung disease in cystic fibrosis: lessons from a monogenic disease

DNA Methylation at ATP11A cg11702988 Is a Biomarker of Lung Disease Severity in Cystic Fibrosis: A Longitudinal Study

Clinical and molecular overview of inherited disorders resulting from epigenomic dysregulation

Heterochromatic genes undergo epigenetic changes and escape silencing in immunodeficiency, centromeric instability, facial anomalies (ICF) syndrome

DNA replication is altered in Immunodeficiency Centromeric instability Facial anomalies (ICF) cells carrying DNMT3B mutations

DNA methylation changes in cystic fibrosis: Cause or consequence?

BAGE Hypomethylation Is an Early Event in Colon Transformation and Is Frequent in Histologically Advanced Adenomas

BAGE Hypomethylation, A New Epigenetic Biomarker for Colon Cancer Detection

New BAGE (B melanoma antigen) genes mapping to the juxtacentromeric regions of human chromosomes 13 and 21 have a cancer/testis expression profile

The HDAC inhibitor SAHA does not rescue CFTR membrane expression in Cystic Fibrosis

DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosis

Frequent DNA hypomethylation of human juxtacentromericBAGE loci in cancer

MLL3, a new human member of the TRX/MLL gene family, maps to 7q36, a chromosome region frequently deleted in myeloid leukaemia

A balance between activating and repressive histone modifications regulates cystic fibrosis transmembrane conductance regulator (CFTR) expression in vivo

Mapping of the juxtacentromeric heterochromatin-euchromatin frontier of human chromosome 21

Heterochromatic Genes Undergo Epigenetic Changes and Escape Silencing in Immunodeficiency

DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosis

Heterochromatic Genes Undergo Epigenetic Changes and Escape Silencing in Immunodeficiency, Centromeric Instability, Facial Anomalies

Frequent DNA hypomethylation of human juxtacentromeric BAGE loci in cancer

The Highest Gene Concentrations in the Human Genome are in Telomeric Bands of Metaphase Chromosomes

Characterization and expression analysis during embryo development of the mouse ortholog of MLL3

Juxtacentromeric region of human chromosome 21: a boundary between centromeric heterochromatin and euchromatic chromosome arms

Correlations Between Isochores and Chromosomal Bands in the Human Genome

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