Zobrazeno 1 - 10
of 49
pro vyhledávání: '"N R, Maksimova"'
Autor:
N. S. Demikova, M. A. Podol’naya, A. L. Sukhomyasova, A. S. Lapina, A. N. Sleptsov, A. I. Fedorov, N. R. Maksimova
Publikováno v:
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 67:47-51
Purpose. The study aims at assessing and analyzing the prevalence of congenital malformations in the Republic of Sakha (Yakutia) based on the data from birth defects surveillance from 2012 to 2019.Material and methods. The data of congenital malforma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4da0d5f40a2299d712291d0999d6af29
https://doi.org/10.21508/1027-4065-2022-67-1-47-51
https://doi.org/10.21508/1027-4065-2022-67-1-47-51
Autor:
N. A. Kolesnikov, V. N. Kharkov, A. A. Zarubin, M. I. Voevoda, M. A. Gubina, O. V. Shtygasheva, N. R. Maksimova, A. L. Sukhomyasova, V. A. Stepanov
Publikováno v:
Russian Journal of Genetics. 58:473-477
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de686e5193c85ead1148adeda02c0c22
https://doi.org/10.1134/s102279542204007x
https://doi.org/10.1134/s102279542204007x
Publikováno v:
Инфекция и иммунитет, Vol 5, Iss 4, Pp 297-302 (2016)
Abstract. Hepatitis B virus is a serious issue of public health services all over the world, particularly in Russia and its regions. The cause can be determined due to its higher incidence rate in different ethnic and geographical groups, variety of
Externí odkaz:
https://doaj.org/article/b7391027a6df4b87830f81452547be67
Autor:
N. V. Ekomasova, Vadim Stepanov, Mikhail I. Voevoda, A. A. Zarubin, S. S. Litvinov, N. A. Kolesnikov, E. K. Khusnutdinova, N. R. Maksimova, A. L. Sukhomyasova, V. N. Kharkov, O. V. Shtygasheva, Marina Gubina, M. O. Radzhabov
Publikováno v:
Russian Journal of Genetics. 57:1271-1284
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9ad3237b88fa73af53c7ceb92c5dd66
https://doi.org/10.1134/s1022795421110053
https://doi.org/10.1134/s1022795421110053
Publikováno v:
Ekologiya cheloveka (Human Ecology). 28:12-20
Introduction: Natural selection in humans is influenced by genetic and environmental factors. It can be assessed using selected genetic and demographic parameters, namely, vital statistics, the Crow index, or the total selection index and its compone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3641e0a818a872b87cdaf5ac6d6f570
https://doi.org/10.33396/1728-0869-2021-6-12-20
https://doi.org/10.33396/1728-0869-2021-6-12-20
Autor:
Sergey Litvinov, Irina Khitrinskaya, Elza Khusnutdinova, Vadim Stepanov, V. N. Kharkov, N. A. Kolesnikov, Aitalina Sukhomyasova, A.V. Markov, M. G. Swarovskaya, N. R. Maksimova, Natalia Ekomasova, Murat Dzhaubermezov, A. V. Marusin, Magomed Radjabov, Aleksei A. Zarubin, O. V. Shtygasheva
Publikováno v:
Genes, Vol 12, Iss 19, p 19 (2021)
Genes
Volume 12
Issue 1
Genes
Volume 12
Issue 1
The human serine protease serine 2 TMPRSS2 is involved in the priming of proteins of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and represents a possible target for COVID-19 therapy. The TMPRSS2 gene may be co-expressed with SAR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::733edcc33b5fe4808fd900198c37b489
https://www.mdpi.com/2073-4425/12/1/19
https://www.mdpi.com/2073-4425/12/1/19
Autor:
R N Ivanova, T. Ya. Nikolaeva, D. A. Petukhova, N. R. Maksimova, Aitalina Sukhomyasova, E. E. Gurinova, P I Golikova
Publikováno v:
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. 121(8)
Neuronal ceroid lipofuscinosis type 6 (NCL 6) is a rare progressive neurodegenerative disease that belongs to the group of lysosomal storage diseases. A clinical and genetic description of NCL 6 in a Yakut family was carried out. The proband and her
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dd75eabcb025ac996c945263dadd26d
https://pubmed.ncbi.nlm.nih.gov/34481439
https://pubmed.ncbi.nlm.nih.gov/34481439
Autor:
Dmitrii Ivanov, Natalia Dvoynova, Olesya N. Bespalova, Olga A Tarasenko, N. R. Maksimova, Polina Y. Kozyulina, T. E. Ivashchenko, Alexander Koroteev, Igor Yu. Kogan, Elena S Vashukova, Anastasia Chentsova, Elena A. Serebryakova, Olga E. Talantova, Aitalina Sukhomyasova, Alisa Morshneva, Andrey S. Glotov, Vladislav S Baranov
Publikováno v:
Genes, Vol 12, Iss 743, p 743 (2021)
Genes
Volume 12
Issue 5
Genes
Volume 12
Issue 5
Clinical tests based on whole-genome sequencing are generally focused on a single task approach, testing one or several parameters, although whole-genome sequencing (WGS) provides us with large data sets that can be used for many supportive analyses.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c270eb2ff5cc67640dd35c53087667e7
https://www.mdpi.com/2073-4425/12/5/743
https://www.mdpi.com/2073-4425/12/5/743
Publikováno v:
Bioinformatics Research and Applications ISBN: 9783030578206
ISBRA
ISBRA
Biallelic mutations in the NBAS gene have been reported to cause three different clinical signs: short stature with optic nerve atrophy and Pelger-Huet anomaly (SOPH) syndrome, infantile liver failure syndrome 2 (ILFS2) and a combined severe phenotyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::986d3d9c9878f2c5f870c2ca3ae0f766
https://doi.org/10.1007/978-3-030-57821-3_4
https://doi.org/10.1007/978-3-030-57821-3_4
Autor:
Zoya A. Rudykh, Dmitriy A. Sychev, D. V. Ivashchenko, Ilyas I. Temirbulatov, Nyurguiana V. Popova, Denis S Fedorinov, Ksenia S. Tayurskaya, Jana Valer'evna Chertovskih, N. R. Maksimova, K. B. Mirzaev
Publikováno v:
Drug Metabolism and Personalized Therapy. 33:91-98
Background: The focus of the study is to determine the prevalence of CYP2C19 alleles, associated with the risk of changes in the pharmacological response to clopidogrel and proton pump inhibitors in patients with acute coronary syndrome (ACS) and gas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a334f0f25a2c7bdf2184fcb36d1ceb02
https://doi.org/10.1515/dmpt-2018-0004
https://doi.org/10.1515/dmpt-2018-0004