Zobrazeno 1 - 10
of 86
pro vyhledávání: '"генная терапия"'
Autor:
V. V. Kalyuzhin, A. T. Teplyakov, I. D. Bespalova, E. V. Kalyuzhina, N. N. Terentyeva, E. V. Grakova, K. V. Kopeva, V. Yu. Usov, N. P. Garganeeva, O. A. Pavlenko, Yu. V. Gorelova, A. V. Teteneva
Publikováno v:
Бюллетень сибирской медицины, Vol 21, Iss 3, Pp 181-197 (2022)
Unprecedented advances of recent decades in clinical pharmacology, cardiac surgery, arrhythmology, and cardiac pacing have significantly improved the prognosis in patients with chronic heart failure (CHF). However, unfortunately, heart failure contin
Externí odkaz:
https://doaj.org/article/395ff86b53ec43f383e61188cb0c80d7
Publikováno v:
Архивъ внутренней медицины, Vol 12, Iss 5, Pp 363-369 (2022)
The article briefly summarizes recent advances in genetic medicine that paved the way for the further development of gene therapy and set the stage for the development of next generation technology. Issues related to the main obstacle for wider appli
Externí odkaz:
https://doaj.org/article/866f312ca6954901921e9ce90fae2ca4
Publikováno v:
Нервно-мышечные болезни, Vol 12, Iss 3, Pp 36-44 (2022)
Background. Proximal spinal muscular atrophy 5q (5q‑SMA) is one of the most common neuromuscular diseases, which is caused by mutations of the SMN1 gene. Despite the fact that most studies consider SMN1 “deletion” as the most common cause of 5q
Externí odkaz:
https://doaj.org/article/256111deb28f4884aebec07f19989666
Autor:
Yu. V. Chervyakov, I. A. Moskovskiy
Publikováno v:
Амбулаторная хирургия, Vol 19, Iss 1, Pp 51-59 (2022)
Introduction. An alternative way in the treatment of intermittent claudication is the use of genetic engineering technologies that lead to the stimulation of their own vasculogenesis in ischemic limbs. Treatment is carried out on an outpatient basis.
Externí odkaz:
https://doaj.org/article/8c198f81592e449893f3d3668516cc7c
Publikováno v:
Oftalʹmologiâ, Vol 19, Iss 1, Pp 22-32 (2022)
Currently, there is a wide range of antiglaucoma drugs. Ophthalmologists are faced with the task of choosing certain drugs and their combinations for specific patients. In this regard, studies aimed at studying the effectiveness of treatment, not onl
Externí odkaz:
https://doaj.org/article/da296ad222e8468caa445fd71d03995e
Publikováno v:
Российский офтальмологический журнал, Vol 14, Iss 3, Pp 78-82 (2021)
Inherited retinal dystrophies (IRD) is an extensive group of genetically heterogeneous diseases with significant clinical polymorphism. With the development of gene therapy, a new era in the treatment of hereditary human diseases has opened. To date,
Externí odkaz:
https://doaj.org/article/ec6b24b014894703822a2852f186d87f
Autor:
M. E. Ivanova, K. V. Gorgisheli, I. V. Zolnikova, D. S. Atarshchikov, D. Barh, Zh. M. Salmasi, L. M. Balashova
Publikováno v:
Российский офтальмологический журнал, Vol 12, Iss 3, Pp 77-84 (2019)
The complete form of X-linked congenital stationary night blindness (CSNB) is a rare genetic disease caused by a mutation in the NYX gene. CSNB is associated with the mutations taking place in 17 genes, whilst its CSNB1A form is caused by the mutatio
Externí odkaz:
https://doaj.org/article/01aeb942b8a8469a9671f5327953e5ec
Autor:
T. V. Budylskaya, D. V. Byrikhina, A. I. Gosudarev, V. D. Gusarova, F. M. Izhaeva, P. V. Mikhailov, D. A. Gusarov
Publikováno v:
Разработка и регистрация лекарственных средств, Vol 0, Iss 1, Pp 74-85 (2019)
Biopharmaceuticals intended for gene therapy are mostly presented by supercoiled plasmid DNA obtained with bacteria cell lines. The properties of their formulations, including stability under different storage conditions, are barely studied. This art
Externí odkaz:
https://doaj.org/article/76a0936eb59442f9b13f8218878d28d5
Publikováno v:
Разработка и регистрация лекарственных средств, Vol 0, Iss 2, Pp 86-92 (2019)
Today technologies stimulating growth and stabilization of new blood vessel, regulating trajectory of vascular growth are promising for the treatment of ischemia. These technologies represent a therapeutic angiogenesis. Its are essential in the rapid
Externí odkaz:
https://doaj.org/article/985745fe1eb747ecb0d5ff917f646284
Autor:
E. A. Nikolaeva, A. N. Semyachkina
Publikováno v:
Rossijskij Vestnik Perinatologii i Pediatrii, Vol 63, Iss 4, Pp 6-14 (2018)
In recent decades, the progressive development of medical genetics has led to significant advances in the diagnosis and therapy of hereditary pathology. As a result, the attitude of clinicians to hereditary diseases as to fatal and incurable, is grad
Externí odkaz:
https://doaj.org/article/9d353b98e58d4b81aab86a12e3d7ba4d