4.6 Article

Genome-Wide DNA Methylation Analysis Identifies Novel Hypomethylated Non-Pericentromeric Genes with Potential Clinical Implications in ICF Syndrome

Related references

Note: Only part of the references are listed.
Review Genetics & Heredity

Mining cancer methylomes: prospects and challenges

Clare Stirzaker et al.

TRENDS IN GENETICS (2014)

Article Neurosciences

Non-coding RNAs in chromatin disease involving neurological defects

Floriana Della Ragione et al.

FRONTIERS IN CELLULAR NEUROSCIENCE (2014)

Article Multidisciplinary Sciences

A DERL3-associated defect in the degradation of SLC2A1 mediates the Warburg effect

Paula Lopez-Serra et al.

NATURE COMMUNICATIONS (2014)

Article Biochemistry & Molecular Biology

Heterogeneous clinical presentation in ICF syndrome: correlation with underlying gene defects

Corry M. R. Weemaes et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2013)

Article Biochemistry & Molecular Biology

Expression pattern of Boule in dairy goat testis and its function in promoting the meiosis in male germline stem cells (mGSCs)

Mingzhao Li et al.

JOURNAL OF CELLULAR BIOCHEMISTRY (2013)

Article Multidisciplinary Sciences

miR-221/222 Target the DNA Methyltransferase MGMT in Glioma Cells

Cristina Quintavalle et al.

PLOS ONE (2013)

Review Cell Biology

Cancer epigenomics: beyond genomics

Juan Sandoval et al.

CURRENT OPINION IN GENETICS & DEVELOPMENT (2012)

Article Biochemistry & Molecular Biology

Whole-genome bisulfite DNA sequencing of a DNMT3B mutant patient

Holger Heyn et al.

EPIGENETICS (2012)

Article Biochemistry & Molecular Biology

Validation of a DNA methylation microarray for 450,000 CpG sites in the human genome

Juan Sandoval et al.

EPIGENETICS (2011)

Article Biotechnology & Applied Microbiology

High density DNA methylation array with single CpG site resolution

Marina Bibikova et al.

GENOMICS (2011)

Article Biochemistry & Molecular Biology

ICF Syndrome Mutations Cause a Broad Spectrum of Biochemical Defects in DNMT3B-Mediated De Novo DNA Methylation

Amir H. Moarefi et al.

JOURNAL OF MOLECULAR BIOLOGY (2011)

Article Biochemistry & Molecular Biology

Epigenetic alteration of microRNAs in DNMT3B-mutated patients of ICF syndrome

Sole Gatto et al.

EPIGENETICS (2010)

Article Multidisciplinary Sciences

Dnmt3b recruitment through E2F6 transcriptional repressor mediates germ-line gene silencing in murine somatic tissues

Guillaume Velasco et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)

Review Medicine, General & Internal

Molecular origins of cancer: Epigenetics in cancer

Manel Esteller

NEW ENGLAND JOURNAL OF MEDICINE (2008)

Article Cell Biology

Multiple binding of methyl-CpG and polycomb proteins in long-term gene silencing events

M. R. Matarazzo et al.

JOURNAL OF CELLULAR PHYSIOLOGY (2007)

Review Genetics & Heredity

Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF)

Melanie Ehrlich et al.

ORPHANET JOURNAL OF RARE DISEASES (2006)

Review Oncology

Cancer/testis antigens, gametogenesis and cancer

AJG Simpson et al.

NATURE REVIEWS CANCER (2005)

Article Biochemistry & Molecular Biology

DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes

M Ehrlich et al.

HUMAN MOLECULAR GENETICS (2001)

Article Biochemistry & Molecular Biology

Escape from gene silencing in ICF syndrome:: evidence for advanced replication time as a major determinant

RS Hansen et al.

HUMAN MOLECULAR GENETICS (2000)

Article Biochemistry & Molecular Biology

Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2

T Kondo et al.

HUMAN MOLECULAR GENETICS (2000)