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注意:仅列出部分参考文献,下载原文获取全部文献信息。Recent insights into cerebral cavernous malformations: the molecular genetics of CCM
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Combinatorial interaction between CCM pathway genes precipitates hemorrhagic stroke
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santa and valentine pattern concentric growth of cardiac myocardium in the zebrafish
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Patterns of expression of the three cerebral cavernous malformation (CCM) genes during embryonic and postnatal brain development
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Neuronal expression of the Ccm2 gene in a new mouse model of cerebral cavernous malformations
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Cerebral venous malformations have distinct genetic origin from cerebral cavernous malformations
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Regulation of vascular endothelial barrier function by Epac, a cAMP-activated exchange factor for Rap GTPase
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Mutations within the programmed cell death 10 gene cause cerebral cavernous malformations
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Ccm1 is required for arterial morphogenesis:: implications for the etiology of human cavernous malformations
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Mutations within the MGC4607 gene cause cerebral cavernous malformations
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Loss of p53 sensitizes mice with a mutation in Ccm1 (KRIT1) to development of cerebral vascular malformations
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Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformations
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Krit1/cerebral cavernous malformation 1 mRNA is preferentially expressed in neurons and epithelial cells in embryo and adult
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