发明名称 Polymorphisms in the human genes for OCT1 and their use in diagnostic and therapeutic applications
摘要 <p>The present invention relates to a polymorphic OCT1 polynucleotide. Moreover, the invention relates to genes or vectors comprising the polynucleotides of the invention and to a host cell genetically engineered with the polynucleotide or gene of the invention. Further, the invention relates to methods for producing molecular variant polypeptides or fragments thereof, methods for producing cells capable of expressing a molecular variant polypeptide and to a polypeptide or fragment thereof encoded by the polynucleotide or the gene of the invention or which is obtainable by the method or from the cells produced by the method of the invention. Furthermore, the invention relates to an antibody which binds specifically the polypeptide of the invention. Moreover, the invention relates to a transgenic non-human animal. The invention also relates to a solid support comprising one or a plurality or the above mentioned polynucleotides, genes, vectors, polypeptides, antibodies or host cells. Furthermore, methods of identifying a polymorphism, identifying and obtaining a pro-drug or drug or an inhibitor are also encompassed by the present invention. In addition, the invention relates to methods for producing of a pharmaceutical composition and to methods of diagnosing a disease. Further, the invention relates to a method of detection of the polynucleotide of the invention. Furthermore, comprised by the present invention are a diagnostic and a pharmaceutical composition. Even more, the invention relates to uses of the polynucleotides, genes, vectors, polypeptides or antibodies of the invention. Finally, the invention relates to a diagnostic kit.</p>
申请公布号 EP2319866(A2) 申请公布日期 2011.05.11
申请号 EP20100185649 申请日期 2003.08.22
申请人 PGXHEALTH, LLC 发明人 KERB, REINHOLD;KOEPSELL, HERMANN;BRINKMANN, ULRICH
分类号 C07K14/47;A01K67/027;A61K38/00;A61K38/17;A61K48/00;C07K16/18;C12N15/12;C12Q1/68;G01N33/50;G01N33/53 主分类号 C07K14/47
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