Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Igor V, Morozov"'
Autor:
Tuyara V. Borisova, Aleksandra M. Cherdonova, Vera G. Pshennikova, Fedor M. Teryutin, Igor V. Morozov, Alexander A. Bondar, Olga A. Baturina, Marsel R. Kabilov, Georgii P. Romanov, Aisen V. Solovyev, Sardana A. Fedorova, Nikolay A. Barashkov
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Mitochondrial forms account approximately 1–2% of all nonsyndromic cases of hearing loss (HL). One of the most common causative variants of mtDNA is the m.1555A > G variant of the MT-RNR1 gene (OMIM 561000). Currently the detection of the
Externí odkaz:
https://doaj.org/article/e857d32e5fce41179211500a006e9097
Autor:
Andrey I. Shilov, Evgeny O. Rakhmanov, Konstantin A. Lyssenko, Alexey N. Kuznetsov, Igor V. Morozov, Andrei V. Shevelkov
Publikováno v:
Crystals, Vol 14, Iss 2, p 155 (2024)
Recently discovered bismuthides with the BaAu2Sb2 structure type demonstrate interesting properties and electronic structures. Here, we report successful crystal growth, crystal structure, band structure calculations, and DOS for BaAg1.8Bi2 and BaAu1
Externí odkaz:
https://doaj.org/article/182a5a9d2359407d8429eebd686407fd
Autor:
Andrey E. Vertepov, Anna A. Fedorova, Alexander M. Batkin, Alexander V. Knotko, Konstantin I. Maslakov, Vladimir D. Doljenko, Alexander V. Vasiliev, Gennadiy I. Kapustin, Tatyana B. Shatalova, Nadezhda M. Sorokina, Leonid M. Kustov, Igor V. Morozov, Alexander L. Kustov
Publikováno v:
Catalysts, Vol 13, Iss 9, p 1231 (2023)
A series of mixed copper (II)—zinc oxide catalysts supported on unmodified and ceria-modified silica supports were synthesized using β-cyclodextrin as a template. The novelty of this work lies in the use of cyclosextrins for the template synthesis
Externí odkaz:
https://doaj.org/article/279ea6c5a6544130bfd5dba6bf16bd29
Autor:
Stanislav V. Dryomov, Elena B. Starikovskaya, Azhar M. Nazhmidenova, Igor V. Morozov, Rem I. Sukernik
Publikováno v:
BMC Evolutionary Biology, Vol 20, Iss 1, Pp 1-8 (2020)
Abstract Background We have described the diversity of complete mtDNA sequences from ‘relic’ groups of the Russian Far East, primarily the Nivkhi (who speak a language isolate with no clear relatedness to any others) and Oroki of Sakhalin, as wel
Externí odkaz:
https://doaj.org/article/74067ce749164277bc96d9337a0afab3
Autor:
Anna A. Vorobyova, Igor L. Danilovich, Igor V. Morozov, Alexander N. Vasiliev, Olga S. Volkova, Asif Iqbal, Badiur Rahaman, Tanusri Saha-Dasgupta
Publikováno v:
Materials, Vol 15, Iss 20, p 7066 (2022)
The appearance of electrically neutral water molecules in the structure of cobalt dinitrate dihydrate, Co(NO3)2⋅2H2O, drastically changes its magnetic properties as compared to its waterless counterpart, Co(NO3)2. The title compound shows Ising-lik
Externí odkaz:
https://doaj.org/article/dd44bfce1bfe45caba7c29fc56d9a629
Autor:
Mikhail Yu. Mashkin, Marina A. Tedeeva, Anna A. Fedorova, Evgeniya R. Fatula, Alexander V. Egorov, Stanislav V. Dvoryak, Konstantin I. Maslakov, Alexander V. Knotko, Alexander E. Baranchikov, Gennadii I. Kapustin, Dmitrii I. Petukhov, Tatyana B. Shatalova, Igor V. Morozov, Leonid M. Kustov, Alexander L. Kustov
Publikováno v:
Journal of Chemical Technology & Biotechnology. 98:1247-1259
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75bd57d2838fa53ee91f44c8007a3dcc
https://doi.org/10.1002/jctb.7339
https://doi.org/10.1002/jctb.7339
Publikováno v:
Journal of Computational Chemistry. 44:1189-1198
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1aed8df2285a6976dcedd84c23a1e042
https://doi.org/10.1002/jcc.27078
https://doi.org/10.1002/jcc.27078
Autor:
Marina V. Zytsar, Nikolay A. Barashkov, Marita S. Bady-Khoo, Olga A. Shubina-Olejnik, Nina G. Danilenko, Alexander A. Bondar, Igor V. Morozov, Aisen V. Solovyev, Valeriia Yu. Danilchenko, Vladimir N. Maximov, Olga L. Posukh
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-9 (2018)
Abstract Background Mutations in GJB2 gene are a major causes of deafness and their spectrum and prevalence are specific for various populations. The well-known mutation c.35delG is more frequent in populations of Caucasian origin. Data on the c.35de
Externí odkaz:
https://doaj.org/article/b6738adfe8d943aa907dab8a1b0ae287
Autor:
Valeriia Yu. Danilchenko, Marina V. Zytsar, Ekaterina A. Maslova, Marita S. Bady-Khoo, Nikolay A. Barashkov, Igor V. Morozov, Alexander A. Bondar, Olga L. Posukh
Publikováno v:
Diagnostics, Vol 11, Iss 12, p 2378 (2021)
Hereditary hearing loss (HL) is known to be highly locus/allelic heterogeneous, and the prevalence of different HL forms significantly varies among populations worldwide. Investigation of region-specific landscapes of hereditary HL is important for l
Externí odkaz:
https://doaj.org/article/4800eab104624524956d659e19c4d0b7
Autor:
Nikolay A. Barashkov, Georgii P. Romanov, Uigulaana P. Borisova, Aisen V. Solovyev, Vera G. Pshennikova, Fedor M. Teryutin, Alexander A. Bondar, Igor V. Morozov, Elza K. Khusnutdinova, Olga L. Posukh, Tatiana E. Burtseva, Jon Øyvind Odland, Sardana A. Fedorova
Publikováno v:
International Journal of Circumpolar Health, Vol 78, Iss 1 (2019)
Waardenburg syndrome (WS) is an orphan genetic disease with autosomal dominant pattern of inheritance characterised by varying degrees of hearing loss accompanied by skin, hair and iris pigmentation abnormalities. Four types of WS differing in phenot
Externí odkaz:
https://doaj.org/article/9ce92d50cdb7413bbd9b6090097ffef5