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Targeting TGF-β and the extracellular matrix in Marfan's syndrome

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DEVELOPMENTAL CELL
卷 15, 期 1, 页码 1-2

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CELL PRESS
DOI: 10.1016/j.devcel.2008.06.005

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Marfan's syndrome is a genetic disorder affecting connective tissues, and it can lead to death due to aortic defects if left untreated. beta-blocker therapy has been used to slow the progression of this disease. Brooke et al. now report in this issue of Developmental Cell that combining angiotensin II receptor blockade by losartan with beta-blocker treatment is an effective treatment combination therapy for this disorder.

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