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Small scale adeno-associated virusvector production for preclinical gene delivery based on chloroform precipitation
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作者 Marcus Davidsson andreas heuer 《Neural Regeneration Research》 SCIE CAS CSCD 2022年第1期99-100,共2页
Gene therapy aims to introduce genetic information into a cell-type of interest to replace,correct,silence,or modify defective genes.Gene therapy in its broadest sense can theoretically prevent,halt,or cure any condit... Gene therapy aims to introduce genetic information into a cell-type of interest to replace,correct,silence,or modify defective genes.Gene therapy in its broadest sense can theoretically prevent,halt,or cure any condition that affects mankind.In addition to that,the introduction and/or manipulation of genes is one of the major research areas in biological sciences,aimed to deepen our knowledge on how biological systems work.Scientific advances have made it possible to induce changes ranging from manipulations of large stretches of the genome to the change of single nucleotides.The gold-standard vehicles to bring this genetic information into the target cells are viral vectors. 展开更多
关键词 replace SMALL mankind
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