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Marfan�s Syndrome Open Access Articles|OMICS International|Medical And Surgical Urology

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Marfan’s Syndrome Open Access Articles

Marfan’s syndrome is an autosomal dominant connective tissue disorder. Connective tissue strengthens the body structures. It is characterized by the mutations in gene FBN-1. Glycoprotein fibrillin-1 is encoded by FBN-1. Fibrillin-1 contributes to formation of elastin and the extracellular matrix. Blood vessels are commonly affected by this syndrome as connective tissue is present abundantly in them. Their elasticity gets altered which later results in aneurysm and rupture. Open access to the scientific literature means the removal of barriers (including price barriers) from accessing scholarly work. There are two parallel “roads” towards open access: Open Access articles and self-archiving. Open Access articles are immediately, freely available on their Web site, a model mostly funded by charges paid by the author (usually through a research grant). The alternative for a researcher is “self-archiving” (i.e., to publish in a traditional journal, where only subscribers have immediate access, but to make the article available on their personal and/or institutional Web sites (including so-called repositories or archives)), which is a practice allowed by many scholarly journals. Open Access raises practical and policy questions for scholars, publishers, funders, and policymakers alike, including what the return on investment is when paying an article processing fee to publish in an Open Access articles, or whether investments into institutional repositories should be made and whether self-archiving should be made mandatory, as contemplated by some funders.
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Last date updated on April, 2024