(Q61650596)

English

Familial congenital heart disease, progressive atrioventricular block and the cardiac homeobox transcription factor gene NKX2.5:

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scholarly article

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27 December 2019

Familial congenital heart disease, progressive atrioventricular block and the cardiac homeobox transcription factor gene NKX2.5: identification of a novel mutation (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16845574%20AND%20SRC:MED&resulttype=core&format=json

27 December 2019

atrioventricular block

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based on heuristic

inferred from title

congenital heart disease

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based on heuristic

inferred from title

3

1 reference

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27 December 2019

author name string

K König

1

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27 December 2019

J C Will

2

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27 December 2019

D Müller

4

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27 December 2019

D W Benson

5

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27 December 2019

publication date

20 July 2006

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27 December 2019

Clinical Research in Cardiology

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27 December 2019

95

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9

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27 December 2019

499-503

1 reference

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27 December 2019

https://scigraph.springernature.com/pub.10.1007/s00392-006-0412-9

0 references

Novel point mutation in the cardiac transcription factor CSX/NKX2.5 associated with congenital heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical analyses of eight NKX2.5 homeodomain missense mutations causing atrioventricular block and cardiac anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect

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https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NK-2 homeobox genes and heart development

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcription factors and congenital heart defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nkx2-5 pathways and congenital heart disease; loss of ventricular myocyte lineage specification leads to progressive cardiomyopathy and complete heart block

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parsing the heart: genetic modules for organ assembly

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two novel frameshift mutations in NKX2.5 result in novel features including visceral inversus and sinus venosus type ASD

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular pathways controlling heart development

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Advances in cardiovascular genetics and embryology: role of transcription factors in congenital heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The incidence of congenital heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive AV-block and anomalous venous return among cardiac anomalies associated with two novel missense mutations in the CSX/NKX2-5 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NKX2.5 mutations in patients with tetralogy of fallot

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NKX2.5mutations in patients with congenital heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

tinman and bagpipe: two homeo box genes that determine cell fates in the dorsal mesoderm of Drosophila

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pregnancy and congenital heart defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/16845574

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00392-006-0412-9

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16845574%20AND%20SRC:MED&resulttype=core&format=json

27 December 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16845574%20AND%20SRC:MED&resulttype=core&format=json

27 December 2019

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