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Vivo and ex vivo gene transfer into renal tissue using gutless adenovirus vectors
Vivo and ex vivo gene transfer into renal tissue using gutless adenovirus vectors
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机译:使用无肠腺病毒载体将体内和离体基因转移到肾组织中
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摘要
A method for treating a renal disease in a subject is disclosed. The method includes administering into a kidney of the subject with an effective amount of a gutless adenoviral vector containing a polynucleotide encoding a therapeutic agent. The gutless adenoviral vector contains the nucleotide sequence of SEQ ID NO:13 or SEQ ID NO:15 and expresses the therapeutic agent in a kidney tissue of the subject.
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机译:公开了一种用于治疗受试者的肾脏疾病的方法。该方法包括将有效量的含有编码治疗剂的多核苷酸的无肠腺病毒载体施用于受试者的肾脏。无肠腺病毒载体包含SEQ ID NO:13或SEQ ID NO:15的核苷酸序列,并在受试者的肾脏组织中表达治疗剂。
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