Engineering adeno-associated virus vectors for gene therapy
C Li, RJ Samulski - Nature Reviews Genetics, 2020 - nature.com
Adeno-associated virus (AAV) vector-mediated gene delivery was recently approved for the
treatment of inherited blindness and spinal muscular atrophy, and long-term therapeutic …
treatment of inherited blindness and spinal muscular atrophy, and long-term therapeutic …
Adeno-associated virus vector as a platform for gene therapy delivery
Adeno-associated virus (AAV) vectors are the leading platform for gene delivery for the
treatment of a variety of human diseases. Recent advances in developing clinically …
treatment of a variety of human diseases. Recent advances in developing clinically …
Exercise training maintains cardiovascular health: signaling pathways involved and potential therapeutics
Exercise training has been widely recognized as a healthy lifestyle as well as an effective
non-drug therapeutic strategy for cardiovascular diseases (CVD). Functional and …
non-drug therapeutic strategy for cardiovascular diseases (CVD). Functional and …
The interplay between adeno-associated virus and its helper viruses
AF Meier, C Fraefel, M Seyffert - Viruses, 2020 - mdpi.com
The adeno-associated virus (AAV) is a small, nonpathogenic parvovirus, which depends on
helper factors to replicate. Those helper factors can be provided by coinfecting helper …
helper factors to replicate. Those helper factors can be provided by coinfecting helper …
Artificially cloaked viral nanovaccine for cancer immunotherapy
M Fusciello, F Fontana, S Tähtinen, C Capasso… - Nature …, 2019 - nature.com
Virus-based cancer vaccines are nowadays considered an interesting approach in the field
of cancer immunotherapy, despite the observation that the majority of the immune responses …
of cancer immunotherapy, despite the observation that the majority of the immune responses …
Biology of tissue inhibitor of metalloproteinase 3 (TIMP3), and its therapeutic implications in cardiovascular pathology
D Fan, Z Kassiri - Frontiers in Physiology, 2020 - frontiersin.org
Tissue inhibitor of metalloproteinase 3 (TIMP3) is unique among the four TIMPs due to its
extracellular matrix (ECM)-binding property and broad range of inhibitory substrates that …
extracellular matrix (ECM)-binding property and broad range of inhibitory substrates that …
Ionizable lipid nanoparticle-mediated delivery of plasmid DNA in cardiomyocytes
Introduction Gene therapy is a promising approach to be applied in cardiac regeneration
after myocardial infarction and gene correction for inherited cardiomyopathies. However …
after myocardial infarction and gene correction for inherited cardiomyopathies. However …
[HTML][HTML] Nucleic acid-based therapy for brain cancer: Challenges and strategies
Nucleic acid-based therapy emerges as a powerful weapon for the treatment of tumors
thanks to its direct, effective, and lasting therapeutic effect. Encouragingly, continuous …
thanks to its direct, effective, and lasting therapeutic effect. Encouragingly, continuous …
Gene therapy for ischaemic heart disease and heart failure
H Korpela, N Järveläinen, S Siimes… - Journal of Internal …, 2021 - Wiley Online Library
Gene therapy has been expected to become a novel treatment method since the structure of
DNA was discovered in 1953. The morbidity from cardiovascular diseases remains …
DNA was discovered in 1953. The morbidity from cardiovascular diseases remains …
[HTML][HTML] IGF1–PI3K-induced physiological cardiac hypertrophy: Implications for new heart failure therapies, biomarkers, and predicting cardiotoxicity
S Bass-Stringer, CMK Tai, JR McMullen - Journal of sport and health …, 2021 - Elsevier
Heart failure represents the end point of a variety of cardiovascular diseases. It is a growing
health burden and a leading cause of death worldwide. To date, limited treatment options …
health burden and a leading cause of death worldwide. To date, limited treatment options …