E2F1 Mediates SOX17 Deficiency-Induced Pulmonary Hypertension

RATIONALE: Rare genetic variants and genetic variation at loci in an enhancer in SRY-Box Transcription Factor 17 (SOX17) are identified in patients with idiopathic pulmonary arterial hypertension (PAH) and PAH with congenital heart disease. However, the exact role of genetic variants or mutation in...

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Detalles Bibliográficos
Autores principales: Yi, Dan, Liu, Bin, Ding, Hongxu, Li, Shuai, Li, Rebecca, Pan, Jiakai, Ramirez, Karina, Xia, Xiaomei, Kala, Mrinalini, Singh, Indrapal, Ye, Qinmao, Lee, Won Hee, Frye, Richard E., Wang, Ting, Zhao, Yutong, Knox, Kenneth S., Glembotski, Christopher C., Fallon, Michael B., Dai, Zhiyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949178/
https://www.ncbi.nlm.nih.gov/pubmed/36824855
http://dx.doi.org/10.1101/2023.02.15.528740

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949178/
https://www.ncbi.nlm.nih.gov/pubmed/36824855
http://dx.doi.org/10.1101/2023.02.15.528740

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