Zobrazeno 1 - 8
of 8
pro vyhledávání: '"D S Selivanova"'
Autor:
E V Yakovleva, V L Surin, D S Selivanova, A M Sergeeva, M V Gonсharova, E Yu Demidova, N P Soboleva, S A Makhinya, A V Dezhenkova, E A Likhacheva, N I Zozulya
Publikováno v:
Терапевтический архив, Vol 88, Iss 12, Pp 120-125 (2016)
Afibrinogenemia is a rare congenital coagulopathy that leads to life-threatening bleeding. In afibrinogenemia, plasma fibrinogen levels are less than 0.1 g/L. The clinical manifestations of the disease can be both bleeding and thromboses of different
Externí odkaz:
https://doaj.org/article/58e020fe91b649adaaa22291503cf6bb
Autor:
E. V. Yakovleva, V. V. Salomashkina, V. L. Surin, D. S. Selivanova, P. S. Lavrova, L. A. Gorgidze, N. P. Soboleva, N. I. Zozulya
Publikováno v:
Russian journal of hematology and transfusiology. 67:193-201
Introduction. In most cases, in patients with hereditary fibrinogen deficiency, clinical manifestations are represented by bleeding of varying intensity and localization. However, the clinical picture of hereditary fibrinogen deficiency can also be r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55890c08e404e046ae7c7e543eec5924
https://doi.org/10.35754/0234-5730-2022-67-2-193-201
https://doi.org/10.35754/0234-5730-2022-67-2-193-201
Autor:
D S Selivanova, E Yu Demidova, N P Soboleva, A M Sergeeva, A V Dezhenkova, M V Gonсharova, E. A. Likhacheva, E. V. Yakovleva, N I Zozulya, V. L. Surin, S A Makhinya
Publikováno v:
Терапевтический архив, Vol 88, Iss 12, Pp 120-125 (2016)
Afibrinogenemia is a rare congenital coagulopathy that leads to life-threatening bleeding. In afibrinogenemia, plasma fibrinogen levels are less than 0.1 g/L. The clinical manifestations of the disease can be both bleeding and thromboses of different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::900c335d65d2d6d74ad79fdb75cfa16d
https://doi.org/10.17116/terarkh20168812120-125
https://doi.org/10.17116/terarkh20168812120-125
Autor:
E Yu Demidova, V. V. Salomashkina, E. A. Likhacheva, O. S. Pshenichnikova, Yu. A. Luchinina, V. L. Surin, D. S. Selivanova
Publikováno v:
Scopus-Elsevier
Hemophilia B is a hereditary X-linked coagulation disorder. This pathology is caused by various defects in the factor IX gene, which is, being about 34 kb long and consisting of eight exons, localized in the Xq27 locus of the X-chromosome long arm. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d10173da66b7affa1ded285d4a11e050
https://doi.org/10.1134/s1022795416040116
https://doi.org/10.1134/s1022795416040116
Autor:
P. A. Medvedeva, Yu. N. Kupriyanovich, Boris G. Sukhov, A. A. Pristavka, S. M. Popkova, Boris A. Trofimov, E. B. Rakova, Yu. P. Dzhioev, D. S. Selivanova, G. V. Yurinova, S. V. Kuznetsov, N. N. Pogodaeva
Publikováno v:
Russian Chemical Bulletin. 63:2189-2194
Arabinogalactan extracted from Siberian larch on an industrial scale was found to exist as noncovalent glycoconjugates with a group of wood extractive substances (their content in arabinogalactan is ~3%). The flavonoids dihydroquercetin (prevailing i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2088ceadc4332760cdd7bc075a1910eb
https://doi.org/10.1007/s11172-014-0718-0
https://doi.org/10.1007/s11172-014-0718-0
Autor:
V L, Surin, E Yu, Demidova, D S, Selivanova, Yu A, Luchinina, V V, Salomashkina, O S, Pshenichnikova, E A, Likhacheva
Publikováno v:
Genetika. 52(4)
Hemophilia B is a hereditary X-linked coagulation disorder. This pathology is caused by various defects in the factor IX gene, which is, being about 34 kb long and consisting of eight exons, localized in the Xq27 locus of the. X-chromosome long arm.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::da7e86a61c4a36fd4dcef6109eeaf9ad
https://pubmed.ncbi.nlm.nih.gov/27529981
https://pubmed.ncbi.nlm.nih.gov/27529981
Publikováno v:
Biology Bulletin. 38:912-926
The history of ranges of the great tit (Parus major) and Japanese tit (P. minor) in the Amur River basin is described on the basis of original data collected between 1970 and 2010 and published data. The main factor accounting for the expansion of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::daf0b6374f10bf6604a6929cb202e50e
https://doi.org/10.1134/s1062359011090044
https://doi.org/10.1134/s1062359011090044
Autor:
Yu. A. Luchinina, I. V. Karpova, D. S. Selivanova, Kravchenko Sk, A V Luk'ianenko, Ya. S. Pustovoit, Pivnik Av, V. L. Surin
Publikováno v:
Russian Journal of Genetics. 46:476-487
Acute intermittent porphyria (AIP) is an autosomal dominant hereditary disease, caused by partial deficiency of porphobilinogen deaminase (PBGD), one of the key enzymes ofheme biosynthesis. This study describes molecular genetics of AIP in Russia. Mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a186a6f22b26fbb5f1fdb5015d1ad283
https://doi.org/10.1134/s1022795410040149
https://doi.org/10.1134/s1022795410040149