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New insights into form and function of fibronectin splice variants No conflicts of interest were declared.

dc.contributor.authorWhite, Eric S.en_US
dc.contributor.authorBaralle, F. E.en_US
dc.contributor.authorMuro, A. F.en_US
dc.date.accessioned2008-08-27T20:05:41Z
dc.date.available2009-11-06T18:12:57Zen_US
dc.date.issued2008-09en_US
dc.identifier.citationWhite, ES; Baralle, FE; Muro, AF (2008). "New insights into form and function of fibronectin splice variants No conflicts of interest were declared. ." The Journal of Pathology 216(1): 1-14. <http://hdl.handle.net/2027.42/60918>en_US
dc.identifier.issn0022-3417en_US
dc.identifier.issn1096-9896en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/60918
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18680111&dopt=citationen_US
dc.description.abstractThe extracellular matrix (ECM) is a highly dynamic structure that not only provides a physical framework for cells within connective tissues, but also imparts instructive signals for development, tissue homeostasis and basic cell functions through its composition and ability to exert mechanical forces. The ECM of tissues is composed of, in addition to proteoglycans and hyaluronic acid, a number of proteins, most of which are generated after alternative splicing of their pre-mRNA. However, the precise function of these protein isoforms is still obscure in most cases. Fibronectin (FN), one of the main components of the ECM, is also one of the best-known examples of a family of proteins generated by alternative splicing, having at least 20 different isoforms in humans. Over the last few years, considerable progress on elucidating the functions of the alternatively spliced FN isoforms has been achieved with the essential development of key engineered mouse strains. Here we summarize the phenotypes of the mouse strains having targeted mutations in the FN gene, which may lead to novel insights linking function of alternatively spliced isoforms of fibronectin to human pathologies. Copyright © 2008 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.en_US
dc.format.extent441230 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherJohn Wiley & Sons, Ltd.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCancer Research, Oncology and Pathologyen_US
dc.titleNew insights into form and function of fibronectin splice variants No conflicts of interest were declared.en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPathologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherInternational Centre for Genetic Engineering and Biotechnology, Trieste, Italyen_US
dc.contributor.affiliationotherInternational Centre for Genetic Engineering and Biotechnology, Trieste, Italy ; International Centre for Genetic Engineering and Biotechnology, Padriciano 99, I-34012 Trieste, Italy.en_US
dc.identifier.pmid18680111en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/60918/1/2388_ftp.pdf
dc.identifier.doihttp://dx.doi.org/10.1002/path.2388en_US
dc.identifier.sourceThe Journal of Pathologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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