Zobrazeno 1 - 10
of 52
pro vyhledávání: '"A. Yu. Skoblov"'
Autor:
Irina A. Krivosheeva, Alexandra Yu. Filatova, Sergei A. Moshkovskii, Ancha V. Baranova, Mikhail Yu. Skoblov
Publikováno v:
Cancer Cell International, Vol 20, Iss 1, Pp 1-8 (2020)
Abstract Introduction Cancers may be treated by selective targeting of the genes vital for their survival. A number of attempts have led to discovery of several genes essential for surviving of tumor cells of different types. In this work, we tried t
Externí odkaz:
https://doaj.org/article/7c39ab76f05b4ceda2881bcd5ef58b6e
Publikováno v:
BMC Medical Genomics, Vol 13, Iss S8, Pp 1-7 (2020)
Abstract Background Single nucleotide variants account for approximately 90% of all known pathogenic variants responsible for human diseases. Recently discovered CRISPR/Cas9 base editors can correct individual nucleotides without cutting DNA and indu
Externí odkaz:
https://doaj.org/article/4cd986950ed74e388ff9b8a158fb0ba5
Publikováno v:
BMC Genomics, Vol 20, Iss S3, Pp 1-7 (2019)
Abstract Background It was shown that the major part of human genome is transcribed and produces a large number of long noncoding RNAs (lncRNAs). Today there are many evidences that lncRNAs play important role in the regulation of gene expression dur
Externí odkaz:
https://doaj.org/article/7a31ac49cd924f1aa77e6bbf372d2151
Autor:
Ancha V. Baranova, Mikhail Yu. Skoblov, Elena N. Voropaeva, Piramanayagam Shanmughavel, Yuriy L. Orlov
Publikováno v:
BMC Medical Genetics, Vol 20, Iss S1, Pp 1-3 (2019)
Externí odkaz:
https://doaj.org/article/38028926c04a4e0f97604ab7ba678d74
Autor:
Liubov O. Skorodumova, Ksenia A. Davydenko, Alexandra Y. Filatova, Mikhail Yu Skoblov, Nikolay A. Kulemin, Maryam B. Khadzhieva, Elena S. Zakharova, Veronika D. Gordeeva, Nataliya S. Smetanina, Irina V. Fedyushkina, Lyudmila A. Anastasevich, Sergey S. Larin
Publikováno v:
Clinical Genetics. 103:93-96
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b09e36545dc579b77e992b29446043d0
https://doi.org/10.1111/cge.14221
https://doi.org/10.1111/cge.14221
Induction of osteogenic differentiation of MSCs by GSK3β knockdown through GSK3β siRNAs transfection
Autor:
Elena V. Galitsyna, Anastasiia A. Buianova, Tatiana B. Bukharova, Irina A. Krivosheeva, Mikhail Yu. Skoblov, Dmitriy V. Goldshtein
The development of effective strategies for the treatment of bone defects is based on gene therapy methods aimed at regulating the differentiation of osteoprogenitor cells. One approach is the development of knockdown systems of inhibitory genes of o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b8ee28ade7e0a39eebd294b6d94a70b
https://doi.org/10.1101/2023.03.21.533598
https://doi.org/10.1101/2023.03.21.533598
Autor:
Liubov O, Skorodumova, Ksenia A, Davydenko, Alexandra Y, Filatova, Mikhail Yu, Skoblov, Nikolay A, Kulemin, Maryam B, Khadzhieva, Elena S, Zakharova, Veronika D, Gordeeva, Nataliya S, Smetanina, Irina V, Fedyushkina, Lyudmila A, Anastasevich, Sergey S, Larin
Publikováno v:
Clinical geneticsREFERENCES. 103(1)
Diamond-Blackfan anemia (DBA) is an inherited bone marrow failure syndrome characterized by erythroid aplasia. Pathogenic variants in ribosomal protein (RP) genes, GATA1, TSR2, and EPO, are considered to be the etiology of DBA. Variants in 5'-untrans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b4aab7e615039ab85705e8baa7947b2
https://pubmed.ncbi.nlm.nih.gov/36057918
https://pubmed.ncbi.nlm.nih.gov/36057918
Publikováno v:
Bulletin of Experimental Biology and Medicine. 164:536-542
We analyzed cultures of 5 independent myoblast lines from human skeletal muscles. It was shown that the content of desmin-positive cells in cultures at early passages exceeds 90%. Typical morphofunctional signs of myogenic differentiation disturbance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01535a87b0bdef9eae118f2b1b1b3aed
https://doi.org/10.1007/s10517-018-4028-7
https://doi.org/10.1007/s10517-018-4028-7
Publikováno v:
Russian Journal of Genetics. 54:45-56
Voltage-gated sodium channels are heteromeric transmembrane proteins involved in the conduction of sodium ion currents in response to membrane depolarization. In humans, nine homologous genes, SCN1A–11A, which encode different isoforms of the volta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0eb0c15e33591fece29457f8399e699f
https://doi.org/10.1134/s102279541801009x
https://doi.org/10.1134/s102279541801009x
Autor:
J. V. Vyakhireva, M. Yu. Skoblov, A. A. Gus’kova, Elena L. Dadali, Andrey V. Marakhonov, Nikolay V. Zernov
Publikováno v:
Russian Journal of Genetics. 53:640-650
Landouzy–Dejerine facioscapulohumeral muscular dystrophy (FSHD) is one of the most common hereditary myodystrophies. A study of the genetic nature of the disease, which has an autosomal dominant mode of inheritance, is extremely interesting and rev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0960f9f5c43f7dd959b42c32cda69d40
https://doi.org/10.1134/s102279541706014x
https://doi.org/10.1134/s102279541706014x