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The PDGF-BBPDGFR pathway and its downstream signaling mechanisms regulate BBB maintenance by promoting pericyte survival, proliferation, migration, differentiation, adherence to the vascular wall, and leukocyte trafficking [42, 73]
Skinner, and D
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14,15 Thus, interfering with the process of mitochondria-associated oxidative phosphorylation could lead to inhibition of O 2 consumption and ATP production
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