(Q34042368)

30 July 2017

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title

A genetic blueprint for cardiac development (English)

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30 July 2017

Srivastava D

1

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30 July 2017

Olson EN

series ordinal

2

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30 July 2017

language of work or name

English

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publication date

1 September 2000

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30 July 2017

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30 July 2017

volume

407

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30 July 2017

issue

6801

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30 July 2017

page(s)

221-226

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NK-2 homeobox genes and heart development

30 July 2017

cites work

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7 January 2021

D-mef2 is a target for Tinman activation during Drosophila heart development

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7 January 2021

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

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7 January 2021

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.

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Gata5 is required for the development of the heart and endoderm in zebrafish.

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7 January 2021

Mechanisms of left-right determination in vertebrates

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7 January 2021

Induction of Purkinje fiber differentiation by coronary arterialization

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7 January 2021

A subclass of bHLH proteins required for cardiac morphogenesis

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7 January 2021

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

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7 January 2021

Heart and extra-embryonic mesodermal defects in mouse embryos lacking the bHLH transcription factor Hand1

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7 January 2021

The Hand1 bHLH transcription factor is essential for placentation and cardiac morphogenesis

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7 January 2021

Homeodomain factor Nkx2-5 controls left/right asymmetric expression of bHLH gene eHand during murine heart development

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7 January 2021

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

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7 January 2021

Cardiac expression of the ventricle-specific homeobox gene Irx4 is modulated by Nkx2-5 and dHand

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7 January 2021

Control of mouse cardiac morphogenesis and myogenesis by transcription factor MEF2C

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7 January 2021

The orphan nuclear receptor COUP-TFII is required for angiogenesis and heart development

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7 January 2021

Atrial-like phenotype is associated with embryonic ventricular failure in retinoid X receptor alpha -/- mice.

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7 January 2021

Requirement for neuregulin receptor erbB2 in neural and cardiac development

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7 January 2021

Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele

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7 January 2021

Requisite role of angiopoietin-1, a ligand for the TIE2 receptor, during embryonic angiogenesis

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Neural crest and cardiovascular patterning.

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

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7 January 2021

Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations

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7 January 2021

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

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7 January 2021

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

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7 January 2021

Jagged1 mutations in patients ascertained with isolated congenital heart defects

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7 January 2021

The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis

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7 January 2021

Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene

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7 January 2021

Identifiers

DOI

10.1038/35025190

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Dimensions Publication ID

30 July 2017

1037669820

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