NKX2.5 mutations in patients with non-syndromic congenital heart disease-Reference-Cited by-同舟云学术

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NKX2.5 mutations in patients with non-syndromic congenital heart disease

Published:2010-02 Issue:3 Volume:138 Page:261-265
ISSN:0167-5273
Container-title:International Journal of Cardiology
language:en
Short-container-title:International Journal of Cardiology

Author:

Gioli-Pereira Luciana,Pereira Alexandre Costa,Mesquita Sônia M.,Xavier-Neto José,Lopes Antônio Augusto,Krieger José Eduardo

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference20 articles.

1. Congenital heart disease in adults. First of two parts;Brickner;N Engl J Med,2000

2. Congenital heart disease in adults. Second of two parts;Brickner;N Engl J Med,2000

3. Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways;Benson;J Clin Invest,1999

4. Intramolecular control of transcriptional activity by the NK2-specific domain in NK-2 homeodomain proteins;Watada;Proc Natl Acad Sci U S A,2000

5. Congenital heart disease caused by mutations in the transcription factor NKX2-5;Schott;Science,1998

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1. NKX2.5 coding exons sequencing reveals novel non-synonymous mutations in patients with sporadic congenital heart diseases among the Tanzanian population;Egyptian Journal of Medical Human Genetics;2024-07-31

2. The lncRNA Sweetheart regulates compensatory cardiac hypertrophy after myocardial injury in murine males;Nature Communications;2023-11-02

3. Whole-exome sequencing revealed novel genetic alterations in patients with tetralogy of Fallot;Translational Pediatrics;2023-10

4. Analysis of pathogenic variants in 605 Chinese children with non-syndromic cardiac conotruncal defects based on targeted sequencing;Genomics;2023-09

5. Altered contractility, Ca²⁺ transients, and cell morphology seen in a patient-specific iPSC-CM model of Ebstein’s anomaly with left ventricular noncompaction;American Journal of Physiology-Heart and Circulatory Physiology;2023-07-01

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