Creld1 regulates myocardial development and function-Reference-Cited by-同舟云学术

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Creld1 regulates myocardial development and function

Published:2021-07 Issue: Volume:156 Page:45-56
ISSN:0022-2828
Container-title:Journal of Molecular and Cellular Cardiology
language:en
Short-container-title:Journal of Molecular and Cellular Cardiology

Author:

Beckert Vera,Rassmann Sebastian,Kayvanjoo Amir Hossein,Klausen Christina,Bonaguro Lorenzo,Botermann Dominik Simon,Krause Melanie,Moreth Kristin,Spielmann Nadine,da Silva-Buttkus Patricia,Fuchs Helmut,Gailus-Durner Valerie,de Angelis Martin Hrabě,Händler Kristian,Ulas Thomas,Aschenbrenner Anna C.,Mass Elvira,Wachten Dagmar

Funder

Fritz Thyssen Stiftung

Daimler und Benz Stiftung

BMBF Berlin

Deutsche Forschungsgemeinschaft

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Molecular Biology

Reference59 articles.

1. Missense mutations in CRELD1 are associated with cardiac atrioventricular septal defects;Robinson;Am. J. Hum. Genet.,2003

2. CRELD1 gene variants and atrioventricular septal defects in Down syndrome;Asim;Gene,2018

3. Polymorphic haplotypes of CRELD1 differentially predispose Down syndrome and euploids individuals to atrioventricular septal defect;Ghosh;Am. J. Med. Genet. A,2012

4. Novel CRELD1 gene mutations in patients with atrioventricular septal defect;Guo;World J. Pediatr.,2010

5. A maiden report on CRELD1 single-nucleotide polymorphism association in congenital heart disease patients of Mysore, South India, Genet;Kusuma;Test. Mol. Biomarkers,2011

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections;Genetics in Medicine;2024-02

2. Functions of cilia in cardiac development and disease;Annals of Human Genetics;2023-10-23

3. Genetic Alterations of Transcription Factors and Signaling Molecules Involved in the Development of Congenital Heart Defects—A Narrative Review;Children;2023-04-29

4. CRELD1 variants are associated with bicuspid aortic valve in Turner syndrome;Human Genetics;2023-03-16

5. CRELD2, endoplasmic reticulum stress, and human diseases;Frontiers in Endocrinology;2023-03-02

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