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Paper Details

Fibronectin rescues aberrant phenotype of endothelial cells lacking either CCM1, CCM2 or CCM3.
FASEB Journal
5
2020
CCM1, CCM1-, CCM2-, and CCM3-deficient ECs, CCM2, CCM3, CCM3-/, CCM3-/- ECs, CCMs, Cas9, EC, ECs, Fibronectin, KRIT1, PDCD10, actin, autosomal dominant cerebral cavernous malformations, endothelial cells, fibronectin, fibronectin fibrils, human, human endothelial cells, spheroid
Author NameAffiliation
Tim M StromInstitute of Human Genetics, Technische Universitat Munchen
Tim M StromInstitute of Human Genetics
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Release 1.2