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Supplementation with Tex261 provides a possible preventive treatment for hypoxic pulmonary artery hypertension
Objectives: Pulmonary artery hypertension (PAH) is a serious disease for which there is no effective treatment. Its pathogenesis is complex and has not yet been clarified. Tex261 is a protein-coding gene whose functional enrichment nodes include the transporter activity of COP II. However, the role...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669906/ https://www.ncbi.nlm.nih.gov/pubmed/36408272 http://dx.doi.org/10.3389/fphar.2022.1028058 |