The TBX1/miR-193a-3p/TGF-β2 Axis Mediates CHD by Promoting Ferroptosis

Congenital heart disease (CHD) is the most common noninfectious cause of death during the neonatal stage. T-box transcription factor 1 (TBX1) is the main genetic determinant of 22q11.2 deletion syndrome (22q11.2DS), which is a common cause of CHD. Moreover, ferroptosis is a newly discovered kind of...

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Detalles Bibliográficos
Autores principales: Zhong, Li, Yang, Huiqin, Zhu, Binlu, Zhao, Xueqi, Xie, Meijun, Cao, Meiling, Liu, Chang, Zhao, Danyang, Lyu, Yuan, Shang, Weiguang, Wang, Bo, Wu, Ying, Sun, Xiuju, Qiu, Guangrong, Fu, Weineng, Jiang, Hongkun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8759832/
https://www.ncbi.nlm.nih.gov/pubmed/35035663
http://dx.doi.org/10.1155/2022/5130546

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8759832/
https://www.ncbi.nlm.nih.gov/pubmed/35035663
http://dx.doi.org/10.1155/2022/5130546

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