Genetic transduction articles from across Nature Portfolio

Genetic transduction is the transfer of DNA from a virus to its bacterial or eukaryotic host cell. Transduction with viral vectors is a common method for gene delivery.

Latest Research and Reviews

Research
09 February 2023 | Open Access

Characterization of antibiotic resistomes by reprogrammed bacteriophage-enabled functional metagenomics in clinical strains

Application of reprogrammed bacteriophage to functional metagenomics in clinically relevant bacterial strains improves identification of antibiotic resistance genes, including those against recently developed or approved antibiotics.
- Gábor Apjok
- , Mónika Számel
- & Bálint Kintses
Nature Microbiology 8, 410-423
Research
13 January 2023 | Open Access

Improving adeno-associated viral (AAV) vector-mediated transgene expression in retinal ganglion cells: comparison of five promoters
- Bart Nieuwenhuis
- , Elise Laperrousaz
- & Andrew Osborne
Gene Therapy, 1-17
Research
13 December 2022 | Open Access

Efficient simultaneous double DNA knock-in in murine embryonic stem cells by CRISPR/Cas9 ribonucleoprotein-mediated circular plasmid targeting for generating gene-manipulated mice
- Manabu Ozawa
- , Jumpei Taguchi
- & Masahito Ikawa
Scientific Reports 12, 21558
Research
11 November 2022 | Open Access

Development of microglia-targeting adeno-associated viral vectors as tools to study microglial behavior in vivo

Microglia-targeting AAV vectors are created which can be utilized to study microglial pathophysiology and microglia-targeted therapies in mice, especially in the regions of striatum and cerebellar cortex.
- Yukihiro Okada
- , Nobutake Hosoi
- & Hirokazu Hirai
Communications Biology 5, 1224
Research
04 November 2022 | Open Access

Site-specific CRISPR-based mitochondrial DNA manipulation is limited by gRNA import
- Ludwig Schmiderer
- , David Yudovich
- & Jonas Larsson
Scientific Reports 12, 18687
Research
25 October 2022 | Open Access

An efficient rAAV vector for protein expression in cortical parvalbumin expressing interneurons
- Tatiana Tkatch
- , Kristina Rysevaite-Kyguoliene
- & Gytis Baranauskas
Scientific Reports 12, 17851

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News and Comment

Correspondence | 18 July 2012

Lentiviral marking of patient-derived acute lymphoblastic leukaemic cells allows in vivo tracking of disease progression
- S Bomken
- , L Buechler
- & O Heidenreich
Leukemia 27, 718-721

All News & Comment

Genetic transduction articles from across Nature Portfolio

Latest Research and Reviews

Characterization of antibiotic resistomes by reprogrammed bacteriophage-enabled functional metagenomics in clinical strains

Improving adeno-associated viral (AAV) vector-mediated transgene expression in retinal ganglion cells: comparison of five promoters

Efficient simultaneous double DNA knock-in in murine embryonic stem cells by CRISPR/Cas9 ribonucleoprotein-mediated circular plasmid targeting for generating gene-manipulated mice

Development of microglia-targeting adeno-associated viral vectors as tools to study microglial behavior in vivo

Site-specific CRISPR-based mitochondrial DNA manipulation is limited by gRNA import

An efficient rAAV vector for protein expression in cortical parvalbumin expressing interneurons

News and Comment

Lentiviral marking of patient-derived acute lymphoblastic leukaemic cells allows in vivo tracking of disease progression

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