(Q46257517)

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The effect of p.Arg25Cys alteration in NKX2-5 on conotruncal heart anomalies: mutation or polymorphism?

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scholarly article

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/17891434

The effect of p.Arg25Cys alteration in NKX2-5 on conotruncal heart anomalies: mutation or polymorphism? (English)

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/17891434

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M Tekin

7

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author name string

M I Akçaboy

1

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/17891434

F B Cengiz

2

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/17891434

B Inceoğlu

3

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/17891434

T Uçar

4

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/17891434

S Atalay

5

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/17891434

E Tutar

6

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Europe PubMed Central

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20 December 2017

http://europepmc.org/abstract/MED/17891434

publication date

22 September 2007

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/17891434

Pediatric Cardiology

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/17891434

29

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/17891434

1

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/17891434

126-129

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Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/17891434

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17891434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/17891434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17891434

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/17891434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17891434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17891434

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/17891434

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/17891434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Csx: a murine homeobox-containing gene specifically expressed in the developing heart

1 reference

https://pubmed.ncbi.nlm.nih.gov/17891434

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/17891434

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/17891434

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/17891434

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/17891434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00246-007-9058-2

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/17891434

release_26js3ftsbnhofidbuksuwtxeqa

1 reference

https://api.fatcat.wiki/v0/release/26js3ftsbnhofidbuksuwtxeqa

24 November 2022

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 December 2017

http://europepmc.org/abstract/MED/17891434

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