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Keywords: fibronectin
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Biochem J (2014) 464 (3): 301–313.
Published: 05 December 2014
... have investigated the interaction of four different RGD-binding integrins (α5β1, αVβ1, αVβ3 and αVβ6) with fibronectin (FN) using surface plasmon resonance. The ability of inhibitors to reverse ligand binding was assessed by their capacity to increase the dissociation rate of pre-formed integrin–FN...
Includes: Supplementary data
Articles
Biochem J (2014) 464 (1): 99–108.
Published: 23 October 2014
... cell attachment to fibronectin recruits MEKK2 to focal adhesion complexes, and that MEKK2 knockdown is associated with stabilized focal adhesions and significant inhibition of tumour cell migration. In the present study we investigate MEKK2 function in focal adhesions and we report that MEKK2...
Includes: Supplementary data
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Biochem J (2014) 459 (2): 313–322.
Published: 28 March 2014
...Christine Y. Chuang; Georg Degendorfer; Astrid Hammer; John M. Whitelock; Ernst Malle; Michael J. Davies ECM (extracellular matrix) materials, such as laminin, perlecan, type IV collagen and fibronectin, play a key role in determining the structure of the arterial wall and the properties of cells...
Includes: Supplementary data
Articles
Biochem J (2013) 456 (2): 283–295.
Published: 08 November 2013
... into microfibrils and their homoeostasis is poorly understood and is often compromised in connective tissue disorders such as Marfan syndrome and other fibrillinopathies. Using interaction mapping studies, we demonstrate that fibrillins require the complete gelatin-binding region of fibronectin for interaction...
Includes: Supplementary data
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Biochem J (2011) 435 (3): 563–568.
Published: 13 April 2011
...Montserrat Porta-de-la-Riva; Jelena Stanisavljevic; Josue Curto; Clara Francí; Víctor Manuel Díaz; Antonio García de Herreros; Josep Baulida Fibronectins are cell-secreted glycoproteins that modulate cell attachment, spreading, migration, morphology, differentiation and oncogenic transformation...
Includes: Supplementary data
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Biochem J (2011) 435 (3): 651–660.
Published: 13 April 2011
... (fibronectin type III) domains or one REJ (receptor of egg jelly protein) module in the same portion of polypeptide. Stimulated by recent atomic force microscopy work, we re-examined the similarity of these four domains with a FNIII sequence profile showing the evolutionary relationship. Two of the predicted...
Includes: Supplementary data
Articles
Biochem J (2009) 424 (2): 179–189.
Published: 11 November 2009
...A. Paul Mould; Ewa J. Koper; Adam Byron; Grit Zahn; Martin J. Humphries Integrin α5β1 is a key receptor for the extracellular matrix protein fibronectin. Antagonists of human integrin α5β1 have therapeutic potential as anti-angiogenic agents in cancer and diseases of the eye. However, the structure...
Includes: Supplementary data
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Biochem J (2006) 393 (1): 43–50.
Published: 12 December 2005
... in vitro with a number of extracellular matrix proteins, e.g. Fn (fibronectin). In view of its strong binding to Fn, we examined in the present study whether the released soluble ectodomain can bind to the fibrillar Fn matrix under cell-culture conditions and, if so, influence its assembly. In this study...
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Biochem J (2003) 369 (3): 603–610.
Published: 01 February 2003
... compatible with tryptase monomers in complex with heparin. The monomers were, in contrast to tryptase in the tetrameric form, inhibited by bovine pancreatic trypsin inhibitor. Further, the monomers, but not the tetramers, degraded fibronectin. Formation of active monomers was more pronounced at pH7.5 than...
Articles
Biochem J (2003) 369 (2): 311–318.
Published: 15 January 2003
... b $ and TGFb, which may have implications in cancer and a number of inflammatory and fibrotic diseases where expression of both proteins has been documented. Key words: adhesion, binding, cell, fibronectin, vitronectin. (MMP-2 and MMP-9) [9] and cathepsin [10], which elicit effects by proteolytic...
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Biochem J (2002) 367 (3): 715–721.
Published: 01 November 2002
... and collagen I was studied in greater detail and could be shown to occur at distinct sites on the collagen I molecule and to have a K D of about 3×10 -8 M. Interactions with some non-collagenous protein ligands were even stronger, with matrilin-2 binding to fibrillin-2, fibronectin and laminin-1—nidogen-1...
Articles
Biochem J (2002) 364 (3): 739–746.
Published: 15 June 2002
... of triglyceride accumulation. Inhibitor treatment prevented the fibronectin-network degradation, as well as the induction of the genes for peroxisome-proliferator-activated receptor γ and adipsin, two adipocyte phenotype markers. Inhibitor treatment was effective when applied during the early stages of adipocytic...
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Biochem J (2001) 359 (1): 77–87.
Published: 24 September 2001
... days. CTGF protein is also present in glomeruli of human patients with diabetic nephropathy. No CTGF was detected in either normal murine or human glomeruli. Transient transfection of a transformed human mesangial cell line with a CTGF–V5 epitope fusion protein markedly increased fibronectin...
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