Search Results - "gene therapy"
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Intraperitoneal delivery of nanoparticles for cancer gene therapy
Published 2013Subjects: Get full text
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Gene therapy in oral cancer: a promising prospect
Published 2016“…Although still in its early stages, gene therapy holds great promise for the treatment of oral cancer. …”
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Gene therapy in treating sickle cell anemia disease
Published 2022“…In this research which is based on application of biotechnology, it will be focusing on gene therapy. Gene therapy is also one of the best treatments for this disease. …”
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Gene therapy in treating sickle cell anemia disease
Published 2022“…In this research which is based on application of biotechnology, it will be focusing on gene therapy. Gene therapy is also one of the best treatments for this disease. …”
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Current progress in non-viral vectors for cancer gene therapy
Published 2017“…The success of gene therapy is dependent on the choice of the gene delivery system, which is either viral or non-viral vector. …”
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Functionalising and Preserving Blood Platelets for Biologically Targeted Gene Therapies
Published 2025Subjects: Get full text
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Differences between CTAB and chitosan in modifying PLGA nanoparticles for gene therapy
Published 2015“…This study highlights the significant differences between CTAB and chitosan in modifying nanoparticles for gene therapy.…”
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PEGylated enhanced cell penetrating peptide nanoparticles for lung gene therapy
Published 2018Subjects: “…Glycosaminoglycan-binding enhanced transduction (GET); Lung; Transfection; Gene therapy; Cell-penetrating peptide (CPP); Plasmid DNA (pDNA)…”
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Adenoviral based gene therapy for cancer in human and animals: a review
Published 2011“…Tissue- or disease-specific approach has been used to improve the specificity of adenoviral vector for cancer gene therapy. This review summarizes some adenoviral gene therapy and targeting approaches available for human cancer as well as animal cancer.…”
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Advantage of delivering the gene therapy tool (Cas9) as purified protein formulation
Published 2017“…Gene editing permits the alteration of genomic sequences in vitro and in vivo, which could serve as a powerful tool in basic research and human gene therapy. The recent clustered regularly interspaced short palindromic repeat (CRISPR) system has revolutionized the way of gene editing. …”
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Hunting for a cure: the therapeutic potential of gene therapy in Duchenne muscular dystrophy
Published 2014“…With better understanding of the molecular mechanism, gene therapy has improved with regard to the key areas of gene stability, safety, and route of delivery. …”
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Enhancement Of Tumour Regression In Vp3-Based Gene Therapy In Combination With Immunomodulators
Published 2009“…In conclusion, recombinant VP3 gene is best combined with cellular immune modulators (IL12/GM-CSF) for a more effective anti-cancer gene therapy.…”
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Hunting for a cure: the therapeutic potential of gene therapy in Duchenne muscular dystrophy
Published 2014“…With better understanding of the molecular mechanism, gene therapy has improved with regard to the key areas of gene stability, safety, and route of delivery. …”
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Targeted delivery of short hairpin RNA expressing plasmid using hepatitis B virus-like particle for bcl-2 gene silencing in cervical cancer cells
Published 2021Subjects: “…Gene therapy…”
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