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Article
Intracellular generation of single-strand template increases the knock-in efficiency by combining CRISPR/Cas9 with AAV
Targeted integration of transgenes facilitates functional genomic research and holds prospect for gene therapy. The established microhomology-mediated end-joining (MMEJ)-based strategy leads to the precise gen...
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Article
CRISPR/Cas9-mediated somatic and germline gene correction to restore hemostasis in hemophilia B mice
Hemophilia B (HB) is an X-linked disorder caused by defects of F9 encoded coagulation factor IX, which is an ideal model for gene therapy. Most existing HB gene therapies are based on viral mediated gene suppleme...
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Article
esiRNAs purified with chromatography suppress homologous gene expression with high efficiency and specificity
Many preclinical studies have shown RNA interference (RNAi) as a new promising way to treat various human diseases including cancer and virus infection and there is an increasing demand for the large-scale pre...
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Article
Cloning of an alkaline lipase gene from Penicillium cyclopium and its expression in Escherichia coli
The gene encoding an alkaline lipase of Penicillium cyclopium PG37 was cloned with four steps of PCR amplification based on different principles. The cloned gene was 1,480 nucleotides in length, consisted of 94 b...