Novel and deleterious nucleotide variations in the HAND1 gene probably affect miRNA target sites and protein function in pediatric patients with congenital heart disease-Reference-Cited by-同舟云学术

Novel and deleterious nucleotide variations in the HAND1 gene probably affect miRNA target sites and protein function in pediatric patients with congenital heart disease

Published:2024-03-29 Issue:1 Volume:51 Page:
ISSN:0301-4851
Container-title:Molecular Biology Reports
language:en
Short-container-title:Mol Biol Rep

Author:

Tabrizi Fateme^ORCID,Khatami Mehri^ORCID,Heidari Mohammad Mehdi^ORCID,Bragança José^ORCID,Tatari Hasan^ORCID,Namnabat Mohsen^ORCID,Hadadzadeh Mehdi^ORCID,Navabi Shirazi Mohammad Ali^ORCID

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s11033-024-09410-y.pdf

Reference41 articles.

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2. Liu W, Cheng L, Chen K, Wu J, Peng R, Tang Y-L, Chen J, Yang Y, Li P, Huang Z-P (2021) Identification of Novel single-nucleotide variants with potential of mediating malfunction of MicroRNA in congenital heart disease. Front Cardiovasc Med 8. https://doi.org/10.3389/fcvm.2021.739598

3. Fan D, Pang S, Chen J, Shan J, Cheng Q, Yan B (2021) Identification and functional study of GATA4 gene regulatory variants in atrial septal defects. BMC Cardiovasc Disord 21(1):321. https://doi.org/10.1186/s12872-021-02136-w

4. Saacks N, Spracklen T, Eales J, Shaboodien G, Keavney B, Zühlke L (2021) The genetics of congenital heart disease: the role of advanced genomic approaches. SA Heart 18(2). https://doi.org/10.24170/18-2-4886

5. Li L, Wang J, Liu XY, Liu H, Shi HY, Yang XX, Li N, Li YJ, Huang RT, Xue S, Qiu XB, Yang YQ (2017) HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle. Int J Mol Med 39(3):711–718. https://doi.org/10.3892/ijmm.2017.2865