نتایج جستجو برای: targeted gene delivery

تعداد نتایج: 1430970  

Ali Shakerizadeh Hossein Ghadiri, Mohammad Reza Ay, Neda Attaran Saeed Sarkar Sara Khademi Sharmin Kharrazi

Introduction: Head-and-neck cancer is the sixth most common cancer worldwide with the number of cases consistently increasing in developing countries. Successful development of effective, safe and cost effective nanoprobes for head-and-neck cancer targeting imaging is a big challenge. This study is aimed to develop cysteamine-folate conjugated gold nanoparticles (F-Cys-AuNPs) a...

Journal: :World Journal Of Advanced Research and Reviews 2022

Extracellular vesicles (EVs) are the substances that conveyed by most sorts of cell, which play a critical role in cell-to-cell communication. Exosomes among commonly explored EVs. contain lipids, RNAs and proteins. Many examinations have shown exosomes derived from cells different biological roles normal as well diseased condition. Recent investigations natural drug delivery vehicles, they abi...

Journal: :Gene 2013
Anthony Delalande Spiros Kotopoulis Michiel Postema Patrick Midoux Chantal Pichon

Microbubbles first developed as ultrasound contrast agents have been used to assist ultrasound for cellular drug and gene delivery. Their oscillation behavior during ultrasound exposure leads to transient membrane permeability of surrounding cells, facilitating targeted local delivery. The increased cell uptake of extracellular compounds by ultrasound in the presence of microbubbles is attribut...

2013
Azadeh Kia Teerapong Yata Nabil Hajji Amin Hajitou

Bacteriophage (phage), viruses that infect bacteria only, have become promising vectors for targeted systemic delivery of genes to cancer, although, with poor efficiency. We previously designed an improved phage vector by incorporating cis genetic elements of adeno-associated virus (AAV). This novel AAV/phage hybrid (AAVP) specifically targeted systemic delivery of therapeutic genes into tumors...

Journal: :Blood 2004
Anil Chandrashekran Myrtle Y Gordon Colin Casimir

Gene therapy for a wide variety of disorders would be greatly enhanced by the development of vectors that could be targeted for gene delivery to specific populations of cells. We describe here high-efficiency targeted transduction based on a novel targeting strategy that exploits the ability of retroviruses to incorporate host cell proteins into the surface of the viral particle as they bud thr...

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