(Q35030608)

5 August 2017

title

DNA methylation status of NKX2-5, GATA4 and HAND1 in patients with tetralogy of fallot (English)

1 reference

5 August 2017

0 references

1 reference

Wei Sheng

1

1 reference

5 August 2017

Yanyan Qian

2

1 reference

5 August 2017

Huijun Wang

3

1 reference

5 August 2017

Xiaojing Ma

4

1 reference

5 August 2017

Ping Zhang

5

1 reference

5 August 2017

Lianwei Diao

6

1 reference

5 August 2017

Quan An

7

1 reference

5 August 2017

Long Chen

8

1 reference

5 August 2017

Duan Ma

9

1 reference

5 August 2017

Guoying Huang

10

1 reference

5 August 2017

publication date

1 November 2013

1 reference

5 August 2017

1 reference

5 August 2017

volume

6

1 reference

5 August 2017

page(s)

46

1 reference

GATA4 and DcR1 methylation in glioblastomas

5 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Epigenetic regulation of cardiovascular differentiation

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Gene expression in cardiac tissues from infants with idiopathic conotruncal defects

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Jagged1 (JAG1) mutations in patients with tetralogy of Fallot or pulmonic stenosis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Structural abnormalities of the pulmonary trunk in tetralogy of Fallot and potential clinical implications: a morphological study

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Comparison of bisulfite sequencing PCR with pyrosequencing for measuring differences in DNA methylation

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Tetralogy of fallot as a model to study cardiac progenitor cell migration and differentiation during heart development

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

A functional genetic study identifies HAND1 mutations in septation defects of the human heart

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

A pipeline for the quantitative analysis of CG dinucleotide methylation using mass spectrometry

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Investigation of somatic NKX2-5 mutations in congenital heart disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

DNA methylation profile of tissue-dependent and differentially methylated regions (T-DMRs) in mouse promoter regions demonstrating tissue-specific gene expression

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Gene-environment interactions and epigenetic basis of human diseases

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Cytosine methylation profiling of cancer cell lines.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

The developmental genetics of congenital heart disease.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pedia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

The epigenomics of cancer

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Gene regulatory networks in the evolution and development of the heart

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Differential DNA methylation patterns of small B-cell lymphoma subclasses with different clinical behavior

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

EUKARYOTIC CYTOSINE METHYLTRANSFERASES

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

In vitro mutation artifacts after formalin fixation and error prone translesion synthesis during PCR

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Clinical update on adults with congenital heart disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Cardiac T-box factor Tbx20 directly interacts with Nkx2-5, GATA4, and GATA5 in regulation of gene expression in the developing heart

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Familial Tetralogy of Fallot caused by mutation in the jagged1 gene

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3819647

Noncoding RNA expression in myocardium from infants with tetralogy of Fallot.

8 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-6-46

Two novel HAND1 mutations in Chinese patients with ventricular septal defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-6-46

Detection of hypermethylated genes in women with and without cervical neoplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-6-46

DNA methylation analysis of multiple tissues from newborn twins reveals both genetic and intrauterine components to variation in the human neonatal epigenome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1755-8794-6-46

Somatic mutations in NKX2–5, GATA4, and HAND1 are not a common cause of tetralogy of Fallot or hypoplastic left heart

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24182332

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Advances in molecular genetics of congenital heart disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24182332

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Investigation of somatic NKX2-5, GATA4 and HAND1 mutations in patients with tetralogy of Fallot

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24182332

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1755-8794-6-46

1 reference

Dimensions Publication ID

5 August 2017

0 references

1 reference

5 August 2017

1 reference