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Arterial endoglin does not protect against arteriovenous malformations
INTRODUCTION: Endoglin (ENG) forms a receptor complex with ALK1 in endothelial cells (ECs) to promote BMP9/10 signalling. Loss of function mutations in either ENG or ALK1 genes lead to the inherited vascular disorder hereditary haemorrhagic telangiectasia (HHT), characterised by arteriovenous malfor...
Gorde:
| Argitaratua izan da: | Angiogenesis |
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| Egile Nagusiak: | , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Springer Netherlands
2020
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7524831/ https://ncbi.nlm.nih.gov/pubmed/32506200 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10456-020-09731-z |
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