(Q35060426)

6 August 2017

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title

Building a heart: implications for congenital heart disease (English)

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6 August 2017

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Deepak Srivastava

1

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6 August 2017

publication date

1 January 2003

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Journal of Nuclear Cardiology

6 August 2017

published in

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6 August 2017

volume

10

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6 August 2017

issue

1

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6 August 2017

page(s)

63-70

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A requirement for neuropilin-1 in embryonic vessel formation.

6 August 2017

cites work

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12 December 2020

Tinman function is essential for vertebrate heart development: elimination of cardiac differentiation by dominant inhibitory mutants of the tinman-related genes, XNkx2-3 and XNkx2-5.

1 reference

12 December 2020

A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome

1 reference

12 December 2020

A molecular pathway determining left-right asymmetry in chick embryogenesis

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12 December 2020

Incidence of congenital heart disease: II. Prenatal incidence

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12 December 2020

The gene tinman is required for specification of the heart and visceral muscles in Drosophila

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12 December 2020

Cardiac septal and valvular dysmorphogenesis in mice heterozygous for mutations in the homeobox gene Nkx2-5

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12 December 2020

NK-2 homeobox genes and heart development

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12 December 2020

Disruption of hyaluronan synthase-2 abrogates normal cardiac morphogenesis and hyaluronan-mediated transformation of epithelium to mesenchyme

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

1 reference

12 December 2020

A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

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12 December 2020

Pitx2 participates in the late phase of the pathway controlling left-right asymmetry

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12 December 2020

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

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12 December 2020

Inhibition of Wnt activity induces heart formation from posterior mesoderm

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12 December 2020

Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease

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12 December 2020

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

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12 December 2020

Control of vertebrate left-right asymmetry by a snail-related zinc finger gene

1 reference

12 December 2020

A syndrome of tricuspid atresia in mice with a targeted mutation of the gene encoding Fog-2

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12 December 2020

Targeted deletion of the ATP binding domain of left-right dynein confirms its role in specifying development of left-right asymmetries

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12 December 2020

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

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12 December 2020

Conservation of sequence and expression of Xenopus and zebrafish dHAND during cardiac, branchial arch and lateral mesoderm development.

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12 December 2020

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

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12 December 2020

Congenital heart disease in mice deficient for the DiGeorge syndrome region

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12 December 2020

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

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12 December 2020

Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region

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12 December 2020

Gridlock signalling pathway fashions the first embryonic artery

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12 December 2020

Linkage mapping of a mouse gene, iv, that controls left-right asymmetry of the heart and viscera

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12 December 2020

gridlock, an HLH gene required for assembly of the aorta in zebrafish

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12 December 2020

A subclass of bHLH proteins required for cardiac morphogenesis

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12 December 2020

The cardiac homeobox gene Csx/Nkx2.5 lies genetically upstream of multiple genes essential for heart development

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12 December 2020

D-mef2: a Drosophila mesoderm-specific MADS box-containing gene with a biphasic expression profile during embryogenesis

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12 December 2020

A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease

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12 December 2020

Left-right asymmetry and cardiac looping: implications for cardiac development and congenital heart disease

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12 December 2020

The 22q11 deletion syndromes

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12 December 2020

Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome

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12 December 2020

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

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12 December 2020

Mutation of an axonemal dynein affects left-right asymmetry in inversus viscerum mice

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12 December 2020

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

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12 December 2020

Control of mouse cardiac morphogenesis and myogenesis by transcription factor MEF2C

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12 December 2020

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

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12 December 2020

The combinatorial activities of Nkx2.5 and dHAND are essential for cardiac ventricle formation

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12 December 2020

Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome

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12 December 2020

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

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12 December 2020

Requirement of MADS domain transcription factor D-MEF2 for muscle formation in Drosophila

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12 December 2020

A heart segmental defect in the anterior-posterior axis of a transgenic mutant mouse

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12 December 2020

Jagged1 mutations in patients ascertained with isolated congenital heart defects

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12 December 2020

Mouse trisomy 16 as an animal model of human trisomy 21 (Down syndrome): Production of viable trisomy 16 ↔ diploid mouse chimeras

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12 December 2020

The basic helix-loop-helix transcription factor, dHAND, is required for vascular development

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12 December 2020

Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus

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12 December 2020

Wnt antagonism initiates cardiogenesis in Xenopus laevis

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12 December 2020

The bHLH transcription factor hand2 plays parallel roles in zebrafish heart and pectoral fin development

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12 December 2020

Vertebrate tinman homologues XNkx2-3 and XNkx2-5 are required for heart formation in a functionally redundant manner.

1 reference

12 December 2020

Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein

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12 December 2020

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

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12 December 2020

Induction of avian cardiac myogenesis by anterior endoderm

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12 December 2020

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Bop encodes a muscle-restricted protein containing MYND and SET domains and is essential for cardiac differentiation and morphogenesis

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12 December 2020

Cranial and cardiac neural crest defects in endothelin-A receptor-deficient mice

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12 December 2020

A signaling cascade involving endothelin-1, dHAND and msx1 regulates development of neural-crest-derived branchial arch mesenchyme

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12 December 2020

Identifiers

DOI

10.1067/MNC.2003.25

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Dimensions Publication ID

6 August 2017

1022365721

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