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Autor:
Jonas Weinmann, Julia Söllner, Sarah Abele, Gudrun Zimmermann, Kai Zuckschwerdt, Christine Mayer, Jenny Danner-Liskus, Alexander Peltzer, Michael Schuler, Thorsten Lamla, Benjamin Strobel
Publikováno v:
Human gene therapy. 33(21-22)
Adeno-associated viruses (AAVs) represent highly attractive gene therapy vectors and potent research tools for the modulation of gene expression in animal models or difficult-to-transfect cell cultures. Engineered variants, comprising chimeric, mutat