Pages that link to "Q36302317"
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The following pages link to Precise hit: adeno-associated virus in gene targeting (Q36302317):
Displaying 45 items.
- Engineered Viruses as Genome Editing Devices (Q26785927) (← links)
- AAV-dominant negative tumor necrosis factor (DN-TNF) gene transfer to the striatum does not rescue medium spiny neurons in the YAC128 mouse model of Huntington's disease (Q27334472) (← links)
- The catalytic subunit of DNA-dependent protein kinase regulates proliferation, telomere length, and genomic stability in human somatic cells (Q28115800) (← links)
- Focal Delivery of AAV2/1-transgenes Into the Rat Brain by Localized Ultrasound-induced BBB Opening. (Q30457601) (← links)
- Indexing TNF-alpha gene expression using a gene-targeted reporter cell line (Q33409740) (← links)
- Engineering of human pluripotent stem cells by AAV-mediated gene targeting (Q33930075) (← links)
- Formation of AAV single stranded DNA genome from a circular plasmid in Saccharomyces cerevisiae (Q33997202) (← links)
- In vivo genome editing using Staphylococcus aureus Cas9 (Q34043628) (← links)
- Human gene targeting favors insertions over deletions (Q34132693) (← links)
- Adeno-associated virus: a key to the human genome? (Q34459999) (← links)
- Intraganglionic AAV6 results in efficient and long-term gene transfer to peripheral sensory nervous system in adult rats. (Q34684229) (← links)
- Adeno-associated virus gene repair corrects a mouse model of hereditary tyrosinemia in vivo. (Q35105022) (← links)
- The mechanism of gene targeting in human somatic cells (Q35139201) (← links)
- Targeting the absence: homozygous DNA deletions as immutable signposts for cancer therapy (Q36002501) (← links)
- Strategies to circumvent humoral immunity to adeno-associated viral vectors (Q36398678) (← links)
- Neurotrophin-3 gene transduction of mouse neural stem cells promotes proliferation and neuronal differentiation in organotypic hippocampal slice cultures (Q36516349) (← links)
- Development of human gene reporter cell lines using rAAV mediated homologous recombination (Q36642451) (← links)
- A dual AAV system enables the Cas9-mediated correction of a metabolic liver disease in newborn mice (Q36673956) (← links)
- Efficient modification of CCR5 in primary human hematopoietic cells using a megaTAL nuclease and AAV donor template (Q36684377) (← links)
- Modifying the Mitochondrial Genome (Q36894373) (← links)
- Immunity to adeno-associated virus vectors in animals and humans: a continued challenge (Q37127246) (← links)
- The CRISPR/Cas9 system for gene editing and its potential application in pain research (Q37148023) (← links)
- Viral vectors: from virology to transgene expression (Q37262766) (← links)
- Viral manipulation of DNA repair and cell cycle checkpoints (Q37301053) (← links)
- Stimulation of homology-directed gene targeting at an endogenous human locus by a nicking endonuclease. (Q37385910) (← links)
- An update on targeted gene repair in mammalian cells: methods and mechanisms (Q37834094) (← links)
- Combining CRISPR/Cas9 and rAAV Templates for Efficient Gene Editing (Q38626061) (← links)
- Site-Specific PEGylated Adeno-Associated Viruses with Increased Serum Stability and Reduced Immunogenicity (Q38684383) (← links)
- Somatic correction of junctional epidermolysis bullosa by a highly recombinogenic AAV variant. (Q38692453) (← links)
- In vivo and in vitro disease modeling with CRISPR/Cas9. (Q38920337) (← links)
- Probing the Link among Genomic Cargo, Contact Mechanics, and Nanoindentation in Recombinant Adeno-Associated Virus 2. (Q38988629) (← links)
- May I Cut in? Gene Editing Approaches in Human Induced Pluripotent Stem Cells (Q39126523) (← links)
- Efficient growth suppression and apoptosis in human laryngeal carcinoma cell line HEP-2 induced by an adeno-associated virus expressing human FAS ligand (Q39408042) (← links)
- AAV-based dual-reporter circuit for monitoring cell signaling in living human cells (Q40168039) (← links)
- Homologous recombination is required for AAV-mediated gene targeting (Q40258601) (← links)
- Integration of a CD19 CAR into the TCR Alpha Chain Locus Streamlines Production of Allogeneic Gene-Edited CAR T Cells (Q40318331) (← links)
- SgRNA Expression of CRIPSR-Cas9 System Based on MiRNA Polycistrons as a Versatile Tool to Manipulate Multiple and Tissue-Specific Genome Editing. (Q41061980) (← links)
- Inverted terminal repeats of adeno-associated virus decrease random integration of a gene targeting fragment in Saccharomyces cerevisiae. (Q41936505) (← links)
- Introduction of tau mutation into cultured Rat1-R12 cells by gene targeting, using recombinant adeno-associated virus vector (Q45385799) (← links)
- Streamlined ex vivo and in vivo genome editing in mouse embryos using recombinant adeno-associated viruses. (Q47548145) (← links)
- Targeted gene modification in mouse ES cells using integrase-defective lentiviral vectors. (Q51828637) (← links)
- Mapping and Engineering Functional Domains of the Assembly Activating Protein of Adeno-Associated Viruses. (Q52563022) (← links)
- The classification, genetic diagnosis and modelling of monogenic autoinflammatory disorders (Q57160539) (← links)
- Genome editing by natural and engineered CRISPR-associated nucleases (Q89144123) (← links)
- A non-invasive far-red light-induced split-Cre recombinase system for controllable genome engineering in mice (Q97692696) (← links)