Zobrazeno 1 - 10
of 154
pro vyhledávání: '"A. V. Polikarpova"'
Publikováno v:
Московский журнал международного права, Vol 0, Iss 4, Pp 50-59 (2024)
INTRODUCTION. The swamps of Iraq are of great ecological, historical and cultural significance, however, a number of political, economic and anthropogenic reasons have caused the problem of draining the swamps, which negatively affects the economy
Externí odkaz:
https://doaj.org/article/9820051ac2d34ddca2eb26b7f7298e95
Publikováno v:
Арктика и Север, Vol 52, Iss 52, Pp 206-227 (2023)
The purpose of the article is to present to a wide range of readers the All-Russian scientific and educational project “Preserve the Nenets Language and Culture Together”, which is implemented at the Northern (Arctic) Federal University in cooper
Externí odkaz:
https://doaj.org/article/bc0a1c6eaca04b4ab3e1f96e08e0831f
Autor:
Tatiana V. Egorova, Anna V. Polikarpova, Svetlana G. Vassilieva, Marina A. Dzhenkova, Irina M. Savchenko, Oleg A. Velyaev, Anna A. Shmidt, Vladislav O. Soldatov, Mikhail V. Pokrovskii, Alexey V. Deykin, Maryana V. Bardina
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 30, Iss , Pp 161-180 (2023)
Duchenne muscular dystrophy (DMD) is a severe hereditary disease caused by a deficiency in the dystrophin protein. The most frequent types of disease-causing mutations in the DMD gene are frameshift deletions of one or more exons. Precision genome ed
Externí odkaz:
https://doaj.org/article/86a0dbc1beb14091855dc8b5f24c41bb
Publikováno v:
Research Results in Pharmacology, Vol 8, Iss 2, Pp 11-26 (2022)
Disease-causing genes have been identified for many severe muscular and neurological genetic disorders. Advances in the gene therapy field offer promising solutions for drug development to treat these life-threatening conditions. Depending on how the
Externí odkaz:
https://doaj.org/article/31c2eb50c5fb483f9491c11e61b85582
Autor:
Anna V. Polikarpova, Tatiana V. Egorova, Evgenii A. Lunev, Alexandra A. Tsitrina, Svetlana G. Vassilieva, Irina M. Savchenko, Yuliya Y. Silaeva, Alexey V. Deykin, Maryana V. Bardina
Publikováno v:
Frontiers in Genome Editing, Vol 5 (2023)
The development of personalized medicine for genetic diseases requires preclinical testing in the appropriate animal models. GNAO1 encephalopathy is a severe neurodevelopmental disorder caused by heterozygous de novo mutations in the GNAO1 gene. GNAO
Externí odkaz:
https://doaj.org/article/23346d150ced45478ada50824f70075c
Autor:
Alexander M. Polikarpov, Lyudmila M. Bondareva, Svetlana M. Kibardina, Elena V. Polikarpova, Evgeniya N. Zemtsovskaya
Publikováno v:
Арктика и Север, Vol 46, Iss 46, Pp 192-210 (2022)
The article studies lexical designations of the natural phenomenon of the Northern lights in scientific, literary, journalistic and advertising texts of German- and Russian-speaking authors. The purpose is to compare and contrast their implementation
Externí odkaz:
https://doaj.org/article/5a03dfed24484f5daa28084b856868c2
Autor:
Anna V. Starikova, Victoria V. Skopenkova, Anna V. Polikarpova, Denis A. Reshetov, Svetlana G. Vassilieva, Oleg A. Velyaev, Anna A. Shmidt, Irina M. Savchenko, Vladislav O. Soldatov, Tatiana V. Egorova, Maryana V. Bardina
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-13 (2022)
Abstract High expectations have been set on gene therapy with an AAV-delivered shortened version of dystrophin (µDys) for Duchenne muscular dystrophy (DMD), with several drug candidates currently undergoing clinical trials. Safety concerns with this
Externí odkaz:
https://doaj.org/article/e55381cec5004eccbc9982cbd02611bd
Autor:
Tatiana V. Egorova, Ivan I. Galkin, Oleg A. Velyaev, Svetlana G. Vassilieva, Irina M. Savchenko, Vyacheslav A. Loginov, Marina A. Dzhenkova, Diana S. Korshunova, Olga S. Kozlova, Dmitry N. Ivankov, Anna V. Polikarpova
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 11, p 9117 (2023)
Mutations that prevent the production of proteins in the DMD gene cause Duchenne muscular dystrophy. Most frequently, these are deletions leading to reading-frame shift. The “reading-frame rule” states that deletions that preserve ORF result in a
Externí odkaz:
https://doaj.org/article/3c824123831c446a8fd35bb5fc2799af
Autor:
Alexander A. Minin, Alexander A. Ananin, Yuri A. Buyvolov, Evgeniy G. Larin, Pavel A. Lebedev, Natalia V. Polikarpova, Irina V. Prokosheva, Marina I. Rudenko, Inna I. Sapelnikova, Violetta G. Fedotova, Elena A. Shuyskaya, Marina V. Yakovleva, Oksana V. Yantser
Publikováno v:
Nature Conservation Research: Заповедная наука, Vol 5, Iss 4, Pp 89-110 (2020)
In Russia, the methodics of phenological observation processing have been developing during many years. This aimed to unify the names of phenological phases and phenomena, uniform the signs of the onset of a particular phenological event. However, it
Externí odkaz:
https://doaj.org/article/a674599b10854fb780a9aa1dbc4aec6c
Autor:
A. M. Shulman, O. M. Lesnyak, I. Z. Gaidukova, L. P. Surmina, E. N. Ushakova, T. V. Polikarpova, E. V. Vasilyeva, O. V. Inamova
Publikováno v:
Klinicist, Vol 13, Iss 3-4, Pp 59-66 (2020)
Objective. To demonstrate the possibility of having a spondyloarthritic mask of osteomalacia in patients of both sexes.Materials and methods. Two clinical cases of osteomalacia occurring under the mask of spondyloarthritis in patients treated at the
Externí odkaz:
https://doaj.org/article/ea4825be646f484aac4e413b6c49a021