4.7 Article

Association of promoter methylation statuses of congenital heart defect candidate genes with Tetralogy of Fallot

Related references

Note: Only part of the references are listed.
Article Biochemistry & Molecular Biology

A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot

Valentina Guida et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2013)

Article Biochemistry & Molecular Biology

Discovering high-resolution patterns of differential DNA methylation that correlate with gene expression changes

Nathan D. VanderKraats et al.

NUCLEIC ACIDS RESEARCH (2013)

Article Genetics & Heredity

LINE-1 methylation status and its association with tetralogy of fallot in infants

Wei Sheng et al.

BMC MEDICAL GENOMICS (2012)

Article Biochemistry & Molecular Biology

Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease

Scott Smemo et al.

HUMAN MOLECULAR GENETICS (2012)

Article Developmental Biology

Association of Common Variants in ERBB4 with Congenital Left Ventricular Outflow Tract Obstruction Defects

Kim L. McBride et al.

BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2011)

Article Genetics & Heredity

New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle

A. De Luca et al.

CLINICAL GENETICS (2011)

Article Genetics & Heredity

5.78 Mb terminal deletion of chromosome 15q in a girl, evaluation of NR2F2 as candidate gene for congenital heart defects

Eiki Nakamura et al.

EUROPEAN JOURNAL OF MEDICAL GENETICS (2011)

Article Genetics & Heredity

Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects

Marleny Salazar et al.

EUROPEAN JOURNAL OF MEDICAL GENETICS (2011)

Letter Cardiac & Cardiovascular Systems

CFC1 mutations in Chinese children with congenital heart disease

Binbin Wang et al.

INTERNATIONAL JOURNAL OF CARDIOLOGY (2011)

Article Multidisciplinary Sciences

Maternal Genome-Wide DNA Methylation Patterns and Congenital Heart Defects

Shimul Chowdhury et al.

PLOS ONE (2011)

Article Neurosciences

A role for DNA methylation in regulation of EphA5 receptor expression in the mouse retina

Tihomira D. Petkova et al.

VISION RESEARCH (2011)

Article Nutrition & Dietetics

Relation between hypomethylation of long interspersed nucleotide elements and risk of neural tube defects

Li Wang et al.

AMERICAN JOURNAL OF CLINICAL NUTRITION (2010)

Article Genetics & Heredity

Jagged1 (JAG1) Mutations in Patients with Tetralogy of Fallot or Pulmonic Stenosis

Robert C. Bauer et al.

HUMAN MUTATION (2010)

Review Biotechnology & Applied Microbiology

Epigenetic modifications and human disease

Anna Portela et al.

NATURE BIOTECHNOLOGY (2010)

Article Surgery

Tetralogy of Fallot: Yesterday and Today

Joanne P. Starr

WORLD JOURNAL OF SURGERY (2010)

Article Developmental Biology

Chromosomal Abnormalities among Children Born with Conotruncal Cardiac Defects

Edward J. Lammer et al.

BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2009)

Article Cardiac & Cardiovascular Systems

Structural Abnormalities of the Pulmonary Trunk in Tetralogy of Fallot and Potential Clinical Implications A Morphological Study

Elisabeth Bedard et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2009)

Article Multidisciplinary Sciences

Insulin Gene Expression Is Regulated by DNA Methylation

Akio Kuroda et al.

PLOS ONE (2009)

Review Cardiac & Cardiovascular Systems

Tetralogy of Fallot as a Model to Study Cardiac Progenitor Cell Migration and Differentiation During Heart Development

Valentina Di Felice et al.

TRENDS IN CARDIOVASCULAR MEDICINE (2009)

Article Biochemistry & Molecular Biology

NFATc2 is a necessary mediator of calcineurin-dependent cardiac hypertrophy and heart failure

Meriem Bourajjaj et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2008)

Article Multidisciplinary Sciences

Cytosine methylation profiling of cancer cell lines

Mathias Ehrich et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)

Article Multidisciplinary Sciences

Quantitative high-throughput analysis of DNA methylation patterns by base-specific cleavage and mass spectrometry

M Ehrich et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)

Article Developmental Biology

Ablation of the secondary heart field leads to tetralogy of Fallot and pulmonary atresia

C Ward et al.

DEVELOPMENTAL BIOLOGY (2005)

Article Cardiac & Cardiovascular Systems

Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies

LM Beauchesne et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2005)

Review Cardiac & Cardiovascular Systems

The incidence of congenital heart disease

JIE Hoffman et al.

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2002)

Article Cardiac & Cardiovascular Systems

NKX2.5 mutations in patients with tetralogy of Fallot

E Goldmuntz et al.

CIRCULATION (2001)

Article Biochemistry & Molecular Biology

Familial Tetralogy of Fallot caused by mutation in the jagged1 gene

ZA Eldadah et al.

HUMAN MOLECULAR GENETICS (2001)

Article Genetics & Heredity

Aberrant CpG-island methylation has non-random and tumour-type-specific patterns

JF Costello et al.

NATURE GENETICS (2000)