9.2 DELETION OF CHROMOSOME 9P21 NONCODING CARDIOVASCULAR RISK INTERVAL IN MICE INDUCES A PROTHROMBOTIC PHENOTYPE
Background: SNPs on chromosome 9p21.3 risk locus have been associated with cardiovascular diseases. We have established a direct mechanistic link between 9p21 noncoding risk interval and susceptibility to aneurysm in a mouse model with a targeted deletion of the 9p21 noncoding cardiovascular disease...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Atlantis Press
2016-11-01
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Series: | Artery Research |
Online Access: | https://www.atlantis-press.com/article/125930444/view |