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Molecular and Genetic Profiling for Precision Medicines in Pulmonary Arterial Hypertension
Pulmonary arterial hypertension (PAH) is a rare and chronic lung disease characterized by progressive occlusion of the small pulmonary arteries, which is associated with structural and functional alteration of the smooth muscle cells and endothelial cells within the pulmonary vasculature. Excessive...
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| Vydáno v: | Cells |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
MDPI
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7999465/ https://ncbi.nlm.nih.gov/pubmed/33805595 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells10030638 |
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