| 1 |
19802897 | Missense mutations of conserved glycine residues in fibrillin-1 highlight a potential subtype of cb-EGF-like domains. | 2010 Jan |
3 |
| 2 |
20375004 | Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome. | 2010 Mar 17 |
1 |
| 3 |
20686071 | Microfibrils and fibrillin-1 induce integrin-mediated signaling, proliferation and migration in human endothelial cells. | 2010 Nov |
1 |
| 4 |
18789468 | Integrin alphavbeta3 regulates microfibril assembly in human periodontal ligament cells. | 2009 Apr |
1 |
| 5 |
18006876 | Arg-Gly-Asp-containing domains of fibrillins-1 and -2 distinctly regulate lung fibroblast migration. | 2008 Apr |
1 |
| 6 |
17374638 | Cell adhesion to fibrillin-1: identification of an Arg-Gly-Asp-dependent synergy region and a heparin-binding site that regulates focal adhesion formation. | 2007 Apr 15 |
1 |
| 7 |
15517394 | RGD-containing fibrillin-1 fragments upregulate matrix metalloproteinase expression in cell culture: a potential factor in the pathogenesis of the Marfan syndrome. | 2005 Jan |
2 |
| 8 |
15733436 | [Novel mutation of fibrillin 1 gene cause ectopia lentis in a Chinese family]. | 2004 Dec |
1 |
| 9 |
12807887 | Cell adhesion to fibrillin-1 molecules and microfibrils is mediated by alpha 5 beta 1 and alpha v beta 3 integrins. | 2003 Sep 5 |
4 |
| 10 |
9525872 | A Gly --> Ser change causes defective folding in vitro of calcium-binding epidermal growth factor-like domains from factor IX and fibrillin-1. | 1998 Apr 3 |
3 |
| 11 |
7762551 | A Gly1127Ser mutation in an EGF-like domain of the fibrillin-1 gene is a risk factor for ascending aortic aneurysm and dissection. | 1995 Jun |
1 |