Figure 4
Figure 4. Bone marrow– or non–bone marrow–derived COMP in hemostasis and thrombosis. Chimeric mice were created by WT or COMP−/− (recipients) mice crosstransplanted with bone marrow from WT or COMP−/− mice (donors). (A-C) Tail-bleeding time (A), blood clotting time (B), and carotid artery occlusion time following FeCl3 injury (C) in chimeric mice. (D) TT was measured in the platelet-free plasma isolated from chimeric mice. n = 6 for each group. *P < .05; BM, bone marrow; NS, not significant.

Bone marrow– or non–bone marrow–derived COMP in hemostasis and thrombosis. Chimeric mice were created by WT or COMP−/− (recipients) mice crosstransplanted with bone marrow from WT or COMP−/− mice (donors). (A-C) Tail-bleeding time (A), blood clotting time (B), and carotid artery occlusion time following FeCl3 injury (C) in chimeric mice. (D) TT was measured in the platelet-free plasma isolated from chimeric mice. n = 6 for each group. *P < .05; BM, bone marrow; NS, not significant.

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