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Open AccessAuthor Correction: Allele specific repair of splicing mutations in cystic fibrosis through AsCas12a genome editing
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
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Article
Open AccessAllele specific repair of splicing mutations in cystic fibrosis through AsCas12a genome editing
Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the CFTR gene. The 3272–26A>G and 3849+10kbC>T CFTR mutations alter the correct splicing of the CFTR gene, generating new acceptor and...
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Article
A highly specific SpCas9 variant is identified by in vivo screening in yeast
Evolved SpCas9 variant evoCas9 has improved specificity and retains near wild-type on-target activity.
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Open AccessHit and go CAS9 delivered through a lentiviral based self-limiting circuit
In vivo application of the CRISPR-Cas9 technology is still limited by unwanted Cas9 genomic cleavages. Long-term expression of Cas9 increases the number of genomic loci non-specifically cleaved by the nuclease. H...
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Article
Open AccessAn epidemiological investigation to reconstruct a probable human immunodeficiency virus -1 transmission network: a case report
Recently published studies have highlighted the importance of phylogenetic and phylodynamic analyses in supporting epidemiological investigations to reconstruct the transmission network of human immunodeficien...
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Article
Open AccessAntiretroviral treatment and expression of the mRNA levels for Pgp, MRP1, MRP4 and MRP5 in HIV antiretroviral naïve patients. Follow-up at 48 weeks