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C Adrian Shuttleworth

Showing results (21-30 of 30) with videos related to

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The Journal of Biological Chemistry|August 2, 2008
Heparan sulfate regulates fibrillin-1 N- and C-terminal interactionsStuart A Cain, Andrew K Baldwin, Yashithra Mahalingam, et al.
The Journal of Biological Chemistry|September 13, 2011
Collagen VI, conformation of A-domain arrays and microfibril architectureNicola Beecher, Alan M Roseman, Thomas A Jowitt, et al.
The Journal of Biological Chemistry|December 1, 2004
Homotypic fibrillin-1 interactions in microfibril assemblyAndrew Marson, Matthew J Rock, Stuart A Cain, et al.
Journal of Cell Science|August 12, 2010
Assembly of fibrillin microfibrils governs extracellular deposition of latent TGF betaTeresa Massam-Wu, Maybo Chiu, Rawshan Choudhury, et al.
Journal of Molecular Biology|August 30, 2003
Fibrillin microfibrils are stiff reinforcing fibres in compliant tissuesMichael J Sherratt, Clair Baldock, J Louise Haston, et al.
The Journal of Biological Chemistry|March 25, 2004
Molecular basis of elastic fiber formation. Critical interactions and a tropoelastin-fibrillin-1 cross-linkMatthew J Rock, Stuart A Cain, Lyle J Freeman, et al.
Circulation|August 16, 2006
Alpha2(VIII) collagen substrata enhance endothelial cell retention under acute shear stress flow via an alpha2beta1 integrin-dependent mechanism: an in vitro and in vivo studyNeill J Turner, Michael O Murphy, Cay M Kielty, et al.
Journal of Cell Science|March 22, 2007
Cell adhesion to fibrillin-1: identification of an Arg-Gly-Asp-dependent synergy region and a heparin-binding site that regulates focal adhesion formationDaniel V Bax, Yashithra Mahalingam, Stuart Cain, et al.
Human Molecular Genetics|January 14, 2010
A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfectaMartin J Barron, Steven J Brookes, Jennifer Kirkham, et al.
The Journal of Biological Chemistry|August 15, 2006
Marfan syndrome-causing mutations in fibrillin-1 result in gross morphological alterations and highlight the structural importance of the second hybrid domainKieran T Mellody, Lyle J Freeman, Clair Baldock, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
The Journal of Biological Chemistry|August 2, 2008
Heparan sulfate regulates fibrillin-1 N- and C-terminal interactionsStuart A Cain, Andrew K Baldwin, Yashithra Mahalingam, et al.
The Journal of Biological Chemistry|September 13, 2011
Collagen VI, conformation of A-domain arrays and microfibril architectureNicola Beecher, Alan M Roseman, Thomas A Jowitt, et al.
The Journal of Biological Chemistry|December 1, 2004
Homotypic fibrillin-1 interactions in microfibril assemblyAndrew Marson, Matthew J Rock, Stuart A Cain, et al.
Journal of Cell Science|August 12, 2010
Assembly of fibrillin microfibrils governs extracellular deposition of latent TGF betaTeresa Massam-Wu, Maybo Chiu, Rawshan Choudhury, et al.
Journal of Molecular Biology|August 30, 2003
Fibrillin microfibrils are stiff reinforcing fibres in compliant tissuesMichael J Sherratt, Clair Baldock, J Louise Haston, et al.
The Journal of Biological Chemistry|March 25, 2004
Molecular basis of elastic fiber formation. Critical interactions and a tropoelastin-fibrillin-1 cross-linkMatthew J Rock, Stuart A Cain, Lyle J Freeman, et al.
Circulation|August 16, 2006
Alpha2(VIII) collagen substrata enhance endothelial cell retention under acute shear stress flow via an alpha2beta1 integrin-dependent mechanism: an in vitro and in vivo studyNeill J Turner, Michael O Murphy, Cay M Kielty, et al.
Journal of Cell Science|March 22, 2007
Cell adhesion to fibrillin-1: identification of an Arg-Gly-Asp-dependent synergy region and a heparin-binding site that regulates focal adhesion formationDaniel V Bax, Yashithra Mahalingam, Stuart Cain, et al.
Human Molecular Genetics|January 14, 2010
A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfectaMartin J Barron, Steven J Brookes, Jennifer Kirkham, et al.
The Journal of Biological Chemistry|August 15, 2006
Marfan syndrome-causing mutations in fibrillin-1 result in gross morphological alterations and highlight the structural importance of the second hybrid domainKieran T Mellody, Lyle J Freeman, Clair Baldock, et al.
Pageof 3