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  xmlns:dcterms="http://purl.org/dc/terms/"><dc:Title>Fusion protein technologies for biopharmaceuticals : applications and challenges / edited by Stefan R. Schmidt. [electronic resource]</dc:Title>
<dc:Creator>Schmidt, Stefan R.</dc:Creator>
<dc:Subject>Biopharmaceutics.</dc:Subject>
<dc:Subject>Pharmaceutical biotechnology.</dc:Subject>
<dc:Subject>Recombinant Fusion Proteins therapeutic use.</dc:Subject>
<dc:Subject>Drug Carriers.</dc:Subject>
<dc:Subject>Immunotoxins pharmacokinetics.</dc:Subject>
<dc:Subject>Immunotoxins therapeutic use.</dc:Subject>
<dc:Subject>Protein Engineering.</dc:Subject>
<dc:Subject>Recombinant Fusion Proteins pharmacokinetics.</dc:Subject>
<dc:Subject>RM301.4 .F87 2013</dc:Subject>
<dc:Subject>615.7 23</dc:Subject>
<dc:Description>Includes bibliographical references and index.</dc:Description>
<dc:Description>Print version record and CIP data provided by publisher.</dc:Description>
<dc:Description>The state of the art in biopharmaceutical FUSION PROTEIN DESIGN Fusion proteins belong to the most lucrative biotech drugs-with Enbrel® being one of the best-selling biologics worldwide. Enbrel® represents a milestone of modern therapies just as Humulin®, the first therapeutic recombinant protein for human use, approved by the FDA in 1982 and Orthoclone® the first monoclonal antibody reaching the market in 1986. These first generation molecules were soon followed by a plethora of recombinant copies of natural human proteins, and in 1998, the first de novo designed fusion protei.</dc:Description>
<dc:Publisher>Hoboken, New Jersey : John Wiley & Sons,</dc:Publisher>
<dc:Date>©2013.</dc:Date>
<dc:Date>©2013.</dc:Date>
<dc:Date>2013</dc:Date>
<dc:Type>Text</dc:Type>
<dc:Format>1 online resource.</dc:Format>
<dc:Identifier>http://onlinelibrary.wiley.com/book/10.1002/9781118354599</dc:Identifier>
<dc:Language>eng</dc:Language>
<dc:Relation>Fusion protein technologies for biopharmaceuticals.</dc:Relation>
<dc:Relation>Fusion protein technologies for biopharmaceuticals.</dc:Relation>

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