(Q34096014)

31 July 2017

1 reference

title

Transcriptional regulation of cardiac development: implications for congenital heart disease and DiGeorge syndrome (English)

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31 July 2017

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congenital heart disease

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Epstein JA

1

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31 July 2017

Buck CA

series ordinal

2

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31 July 2017

language of work or name

English

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publication date

1 December 2000

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31 July 2017

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31 July 2017

volume

48

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31 July 2017

issue

6

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31 July 2017

page(s)

717-724

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https://scigraph.springernature.com/pub.10.1203/00006450-200012000-00003

31 July 2017

exact match

0 references

cites work

Molecular pathways controlling heart development

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https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Neural crest cells contribute to normal aorticopulmonary septation

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

GATA4 transcription factor is required for ventral morphogenesis and heart tube formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Requirement of the transcription factor GATA4 for heart tube formation and ventral morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

GATA transcription factors and cardiac development

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

The cardiac transcription factors Nkx2-5 and GATA-4 are mutual cofactors

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

GATA-4 and Nkx-2.5 coactivate Nkx-2 DNA binding targets: role for regulating early cardiac gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Wild-type endoderm abrogates the ventral developmental defects associated with GATA-4 deficiency in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

A calcineurin-dependent transcriptional pathway for cardiac hypertrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Prevention of cardiac hypertrophy by calcineurin inhibition: hope or hype?

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Calcineurin and human heart failure

21 January 2018

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https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Hox homeobox genes and regionalisation of the nervous system.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Regulation of chamber-specific gene expression in the developing heart by Irx4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

A subclass of bHLH proteins required for cardiac morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Regulation of cardiac mesodermal and neural crest development by the bHLH transcription factor, dHAND

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

The bHLH factors, dHAND and eHAND, specify pulmonary and systemic cardiac ventricles independent of left-right sidedness

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Csx: a murine homeobox-containing gene specifically expressed in the developing heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Myogenic and morphogenetic defects in the heart tubes of murine embryos lacking the homeo box gene Nkx2-5

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

NK-2 homeobox genes and heart development

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Congenital heart disease caused by mutations in the transcription factor NKX2-5

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

The transcription factor NF-ATc is essential for cardiac valve formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Role of the NF-ATc transcription factor in morphogenesis of cardiac valves and septum

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Defects in cardiac outflow tract formation and pro-B-lymphocyte expansion in mice lacking Sox-4

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

A role for smad6 in development and homeostasis of the cardiovascular system

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Requirement of type III TGF-beta receptor for endocardial cell transformation in the heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Tumour predisposition in mice heterozygous for a targeted mutation in Nf1

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Targeted disruption of the neurofibromatosis type-1 gene leads to developmental abnormalities in heart and various neural crest-derived tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Function of Rieger syndrome gene in left-right asymmetry and craniofacial development

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Pitx2 determines left-right asymmetry of internal organs in vertebrates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Sequential programs of retinoic acid synthesis in the myocardial and epicardial layers of the developing avian heart.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

FOG-2, a cofactor for GATA transcription factors, is essential for heart morphogenesis and development of coronary vessels from epicardium

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

RXR alpha deficiency confers genetic susceptibility for aortic sac, conotruncal, atrioventricular cushion, and ventricular muscle defects in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Role of Endothelin-1/Endothelin-A receptor-mediated signaling pathway in the aortic arch patterning in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Aortic arch malformations and ventricular septal defect in mice deficient in endothelin-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null alleles

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

21 January 2018

Closing time for CATCH22

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

DiGeorge syndrome: part of CATCH 22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Cloning and comparative mapping of the DiGeorge syndrome critical region in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

A common region of 10p deleted in DiGeorge and velocardiofacial syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

HIRA, a mammalian homologue of Saccharomyces cerevisiae transcriptional co-repressors, interacts with Pax3

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

HIRA, a DiGeorge syndrome candidate gene, is required for cardiac outflow tract septation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Cloning and comparative mapping of a gene from the commonly deleted region of DiGeorge and Velocardiofacial syndromes conserved in C. elegans

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Localization of the human mitochondrial citrate transporter protein gene to chromosome 22Q11 in the DiGeorge syndrome critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Cloning, genomic organization, and chromosomal localization of human citrate transport protein to the DiGeorge/velocardiofacial syndrome minimal critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Disruption of the clathrin heavy chain-like gene (CLTCL) associated with features of DGS/VCFS: a balanced (21;22)(p12;q11) translocation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Isolation of a new clathrin heavy chain gene with muscle-specific expression from the region commonly deleted in velo-cardio-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

The human homolog of Saccharomyces cerevisiae CDC45

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Identification, characterization, and precise mapping of a human gene encoding a novel membrane-spanning protein from the 22q11 region deleted in velo-cardio-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Alternative expression of platelet glycoprotein Ib(beta) mRNA from an adjacent 5' gene with an imperfect polyadenylation signal sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Isolation of a novel gene from the DiGeorge syndrome critical region with homology to Drosophila gdl and to human LAMC1 genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Isolation and characterization of a novel gene deleted in DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Isolation of a zinc finger gene consistently deleted in DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Prevention of Cardiac Hypertrophy in Mice by Calcineurin Inhibition

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

Engineering a broken heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200012000-00003

10.1203/00006450-200012000-00003

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

31 July 2017

1008325841

0 references

1 reference