A disease-associated mutation in fibrillin-1 differentially regulates integrin-mediated cell adhesion

Integrin-modulating therapy prevents fibrosis and autoimmunity in mouse models of scleroderma

(2013) Elizabeth E. Gerber et al.   NATURE

Structure of the Fibrillin-1 N-Terminal Domains Suggests that Heparan Sulfate Regulates the Early Stages of Microfibril Assembly

(2013) David A. Yadin et al.   STRUCTURE

Dissecting the Fibrillin Microfibril: Structural Insights into Organization and Function

(2012) Sacha A. Jensen et al.   STRUCTURE

TB domain proteins: evolutionary insights into the multifaceted roles of fibrillins and LTBPs

(2010) Ian Robertson et al.   BIOCHEMICAL JOURNAL

Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome

(2010) B. L. Loeys et al.   Science Translational Medicine

Fibrillin–integrin interactions in health and disease

(2008) Jelena Jovanović et al.   BIOCHEMICAL SOCIETY TRANSACTIONS