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Ultrasonic particles: An approach for targeted gene delivery

Study of MiR-451 in the Treatment of Human Gliomas through Regulating the AMPK Pathway Mediated by Bone Mesenchymal Stem Cells

An artificial virus-like triblock protein shows low in vivo humoral immune response and high stability.

Gene therapy in the anterior eye segment.

PiggyBac transposase and transposon derivatives for gene transfer targeting the ribosomal DNA loci of CHO cells.

Chitosan Oleate Coated PLGA Nanoparticles as siRNA Drug Delivery System

Novel α-tocopherol-ferrocene conjugates for the specific delivery of transgenes in liver cancer cells under high serum conditions.

Bioengineering Technologies for Cardiac Regenerative Medicine

Systemic delivery of mRNA and DNA to the lung using polymer-lipid nanoparticles.

Using CRISPR-Cas9 for Therapeutic Protein Production (Review Article)

How Far Are Non-Viral Vectors to Come of Age and Reach Clinical Translation in Gene Therapy?

Non-viral Vectors in Gene Therapy: Recent Development, Challenges, and Prospects

An Overview of Nanocarrier-Based Adjuvants for Vaccine Delivery


Membrane-destabilizing ionizable phospholipids: Novel components for organ-selective mRNA delivery and CRISPR–Cas gene editing

Transfected plasmid DNA is incorporated into the nucleus via nuclear envelope reformation at telophase

New Approaches to Moderate CRISPR-Cas9 Activity: Addressing Issues of Cellular Uptake and Endosomal Escape.

Peptide-Based Nanoparticles for Therapeutic Nucleic Acid Delivery

CRISPR/Cas9 Delivery System Engineering for Genome Editing in Therapeutic Applications

Gene Therapy Approaches

Lipid Nanoparticles as Delivery Systems for RNA-Based Vaccines

Key considerations in formulation development for gene therapy.

Strategies for cancer gene-delivery improvement by non-viral vectors.

Gene Therapy Approach with an Emphasis on Growth Factors: Theoretical and Clinical Outcomes in Neurodegenerative Diseases

In vitro vascularization of tissue engineered constructs by non-viral delivery of pro-angiogenic genes.

DNA-binding Cell-penetrating Peptide-based TRAIL Over-expression in Adipose Tissue-derived Mesenchymal Stem Cells Inhibits Glioma U251MG Growth

Nanotechnology-based siRNA delivery strategies for treatment of triple negative breast cancer.

Trends and Frontiers of Research on Cancer Gene Therapy From 2016 to 2020: A Bibliometric Analysis

Effect of Plasmid DNA Size on Chitosan or Polyethyleneimine Polyplexes Formulation

Prospects of Cationic Carbosilane Dendronized Gold Nanoparticles as Non-viral Vectors for Delivery of Anticancer siRNAs siBCL-xL and siMCL-1


Current Non-Viral Gene Therapy Strategies for the Treatment of Glioblastoma.

Novel vectors and approaches for gene therapy in liver diseases

Application of Non-Viral Vectors in Drug Delivery and Gene Therapy

Nanotechnology-Based Strategies to Overcome Current Barriers in Gene Delivery

Advances in the Development and the Applications of Non-viral, Episomal Vectors for Gene Therapy.

Robust induction of TRMs by combinatorial nanoshells confers cross-strain sterilizing immunity against lethal influenza viruses

Minicircles for Investigating and Treating Arthritic Diseases

The future of retinal gene therapy: evolving from subretinal to intravitreal vector delivery

Generation of Recombinant Primary Human B Lymphocytes Using Non-Viral Vectors

Lipophilic Peptide Dendrimers for Delivery of Splice-Switching Oligonucleotides

Exosome/Liposome-like Nanoparticles: New Carriers for CRISPR Genome Editing in Plants

Estimating the Two Graph Dextran-Stearic Acid-Spermine Polymers Based on Iron Oxide Nanoparticles as Carrier for Gene Delivery

Current Designs of Polymeric Platforms towards the Delivery of Nucleic Acids inside the Cells with Focus on Polyethylenimine.

Current and novel therapeutic strategies for the management of cystic fibrosis

Nucleic acids delivered by PEGylated cationic liposomes in systemic lupus erythematosus-prone mice: a possible exacerbation of lupus nephritis in the presence of pre-existing anti-nucleic acid antibodies.

Non-Viral Vector-Mediated Gene Therapy for ALS: Challenges and Future Perspectives.

β-Cyclodextrins-based nano carriers for cancer therapy

Dysregulation of miRNAs in DLBCL: Causative Factor for Pathogenesis, Diagnosis and Prognosis

Gene therapy for critical limb ischemia: Per aspera ad astra.

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Non Viral Vectors 비바이러스성 벡터
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