Results 21 to 30 of about 212,876 (206)

CRISPR/Cas systems: Delivery and application in gene therapy

open access: yesFrontiers in Bioengineering and Biotechnology, 2022
The CRISPR/Cas systems in prokaryotes such as bacteria and archaea are the adaptive immune system to prevent infection from viruses, phages, or other foreign substances. When viruses or phages first invade the bacteria, Cas proteins recognize and cut the
Jie Huang   +8 more
doaj   +1 more source

Current Approaches for Glioma Gene Therapy and Virotherapy

open access: yesFrontiers in Molecular Neuroscience, 2021
Glioblastoma (GBM) is the most common and aggressive primary brain tumor in the adult population and it carries a dismal prognosis. Inefficient drug delivery across the blood brain barrier (BBB), an immunosuppressive tumor microenvironment (TME) and ...
Kaushik Banerjee   +22 more
doaj   +1 more source

Gene Therapy for Acute Respiratory Distress Syndrome

open access: yesFrontiers in Physiology, 2022
Acute respiratory distress syndrome (ARDS) is a devastating clinical syndrome that leads to acute respiratory failure and accounts for over 70,000 deaths per year in the United States alone, even prior to the COVID-19 pandemic.
Jing Liu   +3 more
doaj   +1 more source

Barriers and recent advances in non-viral vectors targeting the lungs for cystic fibrosis gene therapy [PDF]

open access: yesNanomedicine Journal, 2019
Cystic fibrosis (CF) is an autosomal recessive disorder caused by mutations in CFTR genes that affect chloride ion channel. The CF is a good nominee for gene therapy as the asymptomatic carriers are phenotypically normal, and the desired cells are ...
Faisal Qaisar   +3 more
doaj   +1 more source

Applications and developments of gene therapy drug delivery systems for genetic diseases

open access: yesAsian Journal of Pharmaceutical Sciences, 2021
Genetic diseases seriously threaten human health and have always been one of the refractory conditions facing humanity. Currently, gene therapy drugs such as siRNA, shRNA, antisense oligonucleotide, CRISPR/Cas9 system, plasmid DNA and miRNA have shown ...
Xiuhua Pan   +6 more
doaj   +1 more source

Gene Therapy for Regenerative Medicine

open access: yesPharmaceutics, 2023
The development of biological methods over the past decade has stimulated great interest in the possibility to regenerate human tissues. Advances in stem cell research, gene therapy, and tissue engineering have accelerated the technology in tissue and ...
Hossein Hosseinkhani   +3 more
doaj   +1 more source

Advances of non-viral nanometer vectors delivery systemfor siRNA

open access: yes生物医学转化, 2021
The delivery of small interfering RNA is now mainly through viral vector delivery, chemicalmodification delivery, microinjection delivery, and non-viral nanometer vector delivery.
Geng Xiang, Huang Meizhou, Li Jianyong
doaj   +1 more source

Aminoglycosides: From Antibiotics to Building Blocks for the Synthesis and Development of Gene Delivery Vehicles

open access: yesAntibiotics, 2020
Aminoglycosides are a class of naturally occurring and semi synthetic antibiotics that have been used for a long time in fighting bacterial infections.
Maria Cristina Bellucci   +1 more
doaj   +1 more source

Vectors for Glioblastoma Gene Therapy: Viral & Non-Viral Delivery Strategies

open access: yesNanomaterials, 2019
Glioblastoma multiforme is the most common and aggressive primary brain tumor. Even with aggressive treatment including surgical resection, radiation, and chemotherapy, patient outcomes remain poor, with five-year survival rates at only 10%.
Breanne Caffery   +2 more
doaj   +1 more source

Beyond Gene Delivery: Strategies to Engineer the Surfaces of Viral Vectors

open access: yesBiomedicines, 2013
Viral vectors have been extensively studied due to their great transduction efficiency compared to non-viral vectors. These vectors have been used extensively in gene therapy, enabling the comprehension of, not only the advantages of these vectors, but ...
Cristian Capasso   +2 more
doaj   +1 more source

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