Simple Summary Gene therapy is one of the most promising approaches to treating various inherited and acquired diseases by delivering genetic constructs into the cells and tissues of …
A Egorova, S Shtykalova, M Maretina, A Selutin… - International Journal of …, 2022 - mdpi.com
Suicide gene therapy was suggested as a possible strategy for the treatment of uterine fibroids (UFs), which are the most common benign tumors inwomen of reproductive age. For …
В книге рассматриваются современные взгляды о роли генетических, эндокринных и иммунологических факторов в патогенезе генитального эндометриоза, обсуждаются …
A Egorova, A Selutin, M Maretina, S Selkov, A Kiselev - Molecules, 2022 - mdpi.com
Uterine leiomyoma is the most common benign tumor of the reproductive system. Current therapeutic options do not simultaneously meet the requirements of long-term efficiency and …
A Egorova, A Shubina, D Sokolov, S Selkov… - International journal of …, 2016 - Elsevier
The application of small interfering RNA (siRNA) for specific gene inhibition is a promising strategy in gene therapy treatments. The efficient cellular delivery of therapeutic siRNA is a …
A Egorova, A Selutin, M Maretina, S Selkov, V Baranov… - Pharmaceuticals, 2020 - mdpi.com
Efficient and specific delivery of nucleic acid (NA) therapeutics to tumor cells is extremely important for cancer gene therapy. Various therapeutic strategies include delivery of DNA …
A Egorova, M Petrosyan, M Maretina, N Balashova… - Gene Therapy, 2018 - nature.com
Abstract Development of gene therapy for endometriosis requires inhibition of vascularization in endometrial lesions. We have previously developed CXCR4 receptor …
Gene therapy using siRNA molecules is nowadays considered as a promising approach. For successful therapy, development of a stable and reliable vector for siRNA is crucial. Non …
M Bogacheva, A Egorova, A Slita, M Maretina… - Bioorganic & Medicinal …, 2017 - Elsevier
The major barriers for intracellular DNA transportation by cationic polymers are their toxicity, poor endosomal escape and inefficient nuclear uptake. Therefore, we designed novel …