Endothelial and smooth muscle cell interactions with a PCL-PU composite vascular scaffold with potential for bioactive release [PDF]
Paper discussing endothelial and smooth muscle cell interactions with a PCL-PU composite vascular scaffold with potential for bioactive ...
Black, Richard +2 more
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Acromicric dysplasia caused by a mutation of fibrillin 1 in a family: A case report. [PDF]
Shen R, Feng JH, Yang SP.
europepmc +1 more source
Letter by Groth et al Regarding Article, “Impact of Pathogenic FBN1 (Fibrillin-1) Variant Types on the Progression of Aortic Disease in Patients With Marfan Syndrome” [PDF]
Kristian A. Groth +2 more
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Fibrillin-1 mutation contributes to Marfan syndrome by inhibiting Cav1.2-mediated cell proliferation in vascular smooth muscle cells. [PDF]
Lin W +7 more
europepmc +1 more source
NMR studies of cbEFG-like domains from human fibrillin-1
Rachel Smallridge +1 more
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Case Report: A FBN1 frameshift-and-nonsense mutation and aortic dissection in Marfan syndrome
BackgroundMarfan syndrome (MFS) is an autosomal dominant connective tissue disorder primarily affecting the cardiovascular, ocular, and skeletal systems. Cardiovascular complications are the leading cause of mortality in MFS.
Chao Su +4 more
doaj +1 more source
Nanoscale Structural Comparison of Fibrillin-1 Microfibrils Isolated from Marfan and Non-Marfan Syndrome Human Aorta. [PDF]
Șulea CM +9 more
europepmc +1 more source
The Multiple Functions of Fibrillin-1 Microfibrils in Organismal Physiology. [PDF]
Asano K +3 more
europepmc +1 more source
POGLUT2 and POGLUT3 O-glucosylate multiple EGF repeats in fibrillin-1, -2, and LTBP1 and promote secretion of fibrillin-1. [PDF]
Williamson DB +3 more
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