(Q38216312)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24880466%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

title

Novel and highly lethal NKX2.5 missense mutation in a family with sudden death and ventricular arrhythmia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24880466%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24880466%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

author name string

Jennifer L Perera

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24880466%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

Nicole M Johnson

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24880466%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

Jane E Crosson

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24880466%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

publication date

1 June 2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24880466%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24880466%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

volume

35

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24880466%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

issue

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24880466%20AND%20SRC:MED&resulttype=core&format=json

19 March 2020

page(s)

1206-1212

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24880466%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00246-014-0917-3

19 March 2020

exact match

0 references

cites work

Cardiac transcription factor Csx/Nkx2-5: Its role in cardiac development and diseases

1 reference

https://api.crossref.org/works/10.1007%2FS00246-014-0917-3

Genetic origins of pediatric heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-014-0917-3

Evolutionary conservation of Nkx2.5 autoregulation in the second heart field

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-014-0917-3

Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-014-0917-3

NKX2.5 mutations in patients with tetralogy of fallot

21 January 2018

2 references

https://api.crossref.org/works/10.1007%2FS00246-014-0917-3

21 January 2018

12 December 2020

Arrhythmia induced by spatiotemporal overexpression of calreticulin in the heart.

1 reference

https://api.crossref.org/works/10.1007%2FS00246-014-0917-3

A de novo mutation in NKX2.5 associated with atrial septal defects, ventricular noncompaction, syncope and sudden death

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-014-0917-3

An Nkx2-5/Bmp2/Smad1 negative feedback loop controls heart progenitor specification and proliferation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-014-0917-3

Clinical and molecular analysis of thyroid hypoplasia: a population-based approach in southern Brazil.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-014-0917-3

Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-014-0917-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-014-0917-3

Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00246-014-0917-3

Investigation of somatic NKX2-5 mutations in congenital heart disease

21 January 2018

1 reference

12 December 2020

Nkx-2.5: a novel murine homeobox gene expressed in early heart progenitor cells and their myogenic descendants.

1 reference

12 December 2020

Familial atrial septal defect and atrioventricular conduction disturbance associated with a point mutation in the cardiac homeobox gene CSX/NKX2-5 in a Japanese patient

1 reference

12 December 2020

Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations

1 reference

12 December 2020

NKX2.5mutations in patients with congenital heart disease

1 reference

12 December 2020

Changes in ionic currents and reduced conduction velocity in hypertrophied ventricular myocardium of Xin alpha-deficient mice.

1 reference

12 December 2020

Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease

1 reference

12 December 2020