The role of mural cells in hemorrhage of brain arteriovenous malformation
Brain Hemorrhages, ISSN: 2589-238X, Vol: 2, Issue: 1, Page: 49-56
2021
- 6Citations
- 9Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations6
- Citation Indexes6
- CrossRef6
- Captures9
- Readers9
Review Description
Brain arteriovenous malformation (bAVM) is the most common cause of intracranial hemorrhage (ICH), particularly in young patients. However, the exact cause of bAVM bleeding and rupture is not yet fully understood. In bAVMs, blood bypasses the entire capillary bed and directly flows from arteries to veins. The vessel walls in bAVMs have structural defects, which impair vascular integrity. Mural cells are essential structural and functional components of blood vessels and play a critical role in maintaining vascular integrity. Changes in mural cell number and coverage have been implicated in bAVMs. In this review, we discussed the roles of mural cells in bAVM pathogenesis. We focused on 1) the recent advances in human and animal studies of bAVMs; 2) the importance of mural cells in vascular integrity; 3) the regulatory signaling pathways that regulate mural cell function. More specifically, three signaling pathways that regulate mural cell-recruitment during vascular remodeling were discussed in detail, including the platelet-derived growth factor-B (PDGF-B)/PDGF receptor-β (PDGFR-β), EphrinB2/EphB4, and angiopoietins/tie2 signaling pathways.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S2589238X20300590; http://dx.doi.org/10.1016/j.hest.2020.10.005; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85121281874&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/34541474; https://linkinghub.elsevier.com/retrieve/pii/S2589238X20300590; https://dx.doi.org/10.1016/j.hest.2020.10.005
Elsevier BV
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