Tetralogy of fallot and other congenital heart defects in Hey2 mutant mice (Q24310111)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12372254 AND SRC:MED&resulttype=core&format=json

13 December 2019

title

Tetralogy of fallot and other congenital heart defects in Hey2 mutant mice (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12372254 AND SRC:MED&resulttype=core&format=json

13 December 2019

main subject

congenital disorder

0 references

1 reference

Notch signaling involved in heart development

GOA release 2020-03-11

1 reference

Hairy/enhancer-of-split related with YRPW motif 2

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12372254 AND SRC:MED&resulttype=core&format=json

13 December 2019

author name string

Jena Donovan

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12372254 AND SRC:MED&resulttype=core&format=json

13 December 2019

Anna Kordylewska

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12372254 AND SRC:MED&resulttype=core&format=json

13 December 2019

Manuel F Utset

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12372254 AND SRC:MED&resulttype=core&format=json

13 December 2019

language of work or name

English

0 references

publication date

1 September 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12372254 AND SRC:MED&resulttype=core&format=json

13 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12372254 AND SRC:MED&resulttype=core&format=json

13 December 2019

volume

12

1 reference

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13 December 2019

issue

18

1 reference

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13 December 2019

page(s)

1605-1610

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12372254 AND SRC:MED&resulttype=core&format=json

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

13 December 2019

cites work

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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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Jagged1 mutations in patients ascertained with isolated congenital heart defects

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Familial Tetralogy of Fallot caused by mutation in the jagged1 gene

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Identification and expression of a novel family of bHLH cDNAs related to Drosophila hairy and enhancer of split

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Hey genes: a novel subfamily of hairy- and Enhancer of split related genes specifically expressed during mouse embryogenesis

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7 January 2021

HRT1, HRT2, and HRT3: a new subclass of bHLH transcription factors marking specific cardiac, somitic, and pharyngeal arch segments

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Cardiovascular basic helix loop helix factor 1, a novel transcriptional repressor expressed preferentially in the developing and adult cardiovascular system

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Members of the HRT family of basic helix-loop-helix proteins act as transcriptional repressors downstream of Notch signaling

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7 January 2021

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

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Analysis of HeyL expression in wild-type and Notch pathway mutant mouse embryos

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The basic helix-loop-helix transcription factor HESR1 regulates endothelial cell tube formation

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HERP, a new primary target of Notch regulated by ligand binding

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HERP, a novel heterodimer partner of HES/E(spl) in Notch signaling

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HERP1 is a cell type-specific primary target of Notch

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Genetic basis of syndromes associated with congenital heart disease

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Outcome of congenital heart defects--a population-based study

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Congenital heart disease: incidence and inheritance.

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Epidemiology of cardiovascular malformations: prevalence and risk factors

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7 January 2021

Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1

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7 January 2021

The myoD Gene Family: Nodal Point During Specification of the Muscle Cell Lineage

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HLH proteins, fly neurogenesis, and vertebrate myogenesis

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A subclass of bHLH proteins required for cardiac morphogenesis

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7 January 2021

Vertebrate hairy and Enhancer of split related proteins: transcriptional repressors regulating cellular differentiation and embryonic patterning

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Gridlock signalling pathway fashions the first embryonic artery

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7 January 2021

gridlock, a localized heritable vascular patterning defect in the zebrafish

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7 January 2021

The I.M.A.G.E. Consortium: an integrated molecular analysis of genomes and their expression

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7 January 2021

Oscillating expression of c-Hey2 in the presomitic mesoderm suggests that the segmentation clock may use combinatorial signaling through multiple interacting bHLH factors

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7 January 2021

Comparative analysis of the human and mouse Hey1 promoter: Hey genes are new Notch target genes

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7 January 2021

Null mutation of Dlx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain

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7 January 2021