(Q33703791)

28 July 2017

title

Gene expression in pediatric heart disease with emphasis on conotruncal defects (English)

1 reference

28 July 2017

Douglas C Bittel

1

1 reference

28 July 2017

Nataliya Kibiryeva

2

1 reference

28 July 2017

James E O'Brien

3

1 reference

28 July 2017

Gary K Lofland

4

1 reference

28 July 2017

Merlin G Butler

5

1 reference

28 July 2017

publication date

9 June 2005

1 reference

Progress in pediatric cardiology

28 July 2017

published in

1 reference

28 July 2017

volume

20

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28 July 2017

issue

2

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28 July 2017

page(s)

127-141

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Gene expression profiles in children undergoing cardiac surgery for right heart obstructive lesions

28 July 2017

cites work

1 reference

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21 June 2018

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Dishevelled 2 is essential for cardiac outflow tract development, somite segmentation and neural tube closure

21 June 2018

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Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASD

21 June 2018

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21 June 2018

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HAND1 and HAND2 are expressed in the adult-rodent heart and are modulated during cardiac hypertrophy.

21 June 2018

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The essential role of Cited2, a negative regulator for HIF-1alpha, in heart development and neurulation

21 June 2018

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The Polycomb-group gene Rae28 sustains Nkx2.5/Csx expression and is essential for cardiac morphogenesis

21 June 2018

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Conditional mutation of the ErbB2 (HER2) receptor in cardiomyocytes leads to dilated cardiomyopathy

21 June 2018

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Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways

21 June 2018

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Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

21 June 2018

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Characterization of the TBX5 binding site and analysis of mutations that cause Holt-Oram syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Monitoring of the subtraction process in solid-phase representational difference analysis: characterization of a candidate drug

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Molecular determinants of left and right outflow tract obstruction

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

21 June 2018

1 reference

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Construction of a human cardiovascular cDNA microarray: portrait of the failing heart

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Congenital heart disease and genetic syndromes: specific correlation between cardiac phenotype and genotype.

21 June 2018

1 reference

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Functional analyses of three Csx/Nkx-2.5 mutations that cause human congenital heart disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

The expression of Jagged1 in the developing mammalian heart correlates with cardiovascular disease in Alagille syndrome

21 June 2018

1 reference

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Advances in the molecular genetics of congenital structural heart disease

21 June 2018

1 reference

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Defective angiogenesis in mice lacking endoglin

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Heart defects in connexin43-deficient mice

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Murine double nullizygotes of the angiotensin type 1A and 1B receptor genes duplicate severe abnormal phenotypes of angiotensinogen nullizygotes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Pathogenetic mechanisms of congenital cardiovascular malformations revisited

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Cardiac malformation in neonatal mice lacking connexin43.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Targeted disruption of the tyrosine hydroxylase gene reveals that catecholamines are required for mouse fetal development

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Cardiovascular malformations in Turner's and Noonan's syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

The Wnt/beta-catenin pathway regulates cardiac valve formation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Genome-wide array analysis of normal and malformed human hearts

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Distinct requirements for extra-embryonic and embryonic bone morphogenetic protein 4 in the formation of the node and primitive streak and coordination of left-right asymmetry in the mouse.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

PTPN11 mutations in Noonan syndrome type I: detection of recurrent mutations in exons 3 and 13.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

PTPN11 mutations in LEOPARD syndrome

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Genome-wide profiling of gene expression in 29 normal human tissues with a cDNA microarray

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Evidence for a single nucleotide polymorphism in the KCNQ1 potassium channel that underlies susceptibility to life-threatening arrhythmias

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

High-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the entire human DiGeorge syndrome critical region 2 (DGCR2) gene at 22q11.2.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

The hypoplastic heart in congenital diaphragmatic hernia: reduced expression of basic fibroblast growth factor and platelet-derived growth factor

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Analysis of human transcriptomes.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5436709

Cardiovascular genomics: estimating the total number of genes expressed in the human cardiovascular system

30 October 2018

1 reference

12 December 2020

Birth associated changes in pulmonary arterial connective tissue gene expression in the normal and hypertensive lung

1 reference

12 December 2020

[Congenital heart disease, heterotaxia and laterality]

1 reference

12 December 2020

Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patients

1 reference

12 December 2020

Analysis of cardiovascular phenotype and genotype-phenotype correlation in individuals with a JAG1 mutation and/or Alagille syndrome

1 reference

12 December 2020

10.1016/J.PPEDCARD.2005.04.004

Identifiers

DOI

1 reference

28 July 2017

1 reference

28 July 2017

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