Zobrazeno 1 - 10
of 103
pro vyhledávání: '"V. L. Surin"'
Autor:
E. A. Makunina, L. P. Mendeleeva, V. L. Surin, M. V. Soloviev, M. V. Firsova, A. M. Kovrigina, A. A. Sherstnev, I. V. Gal’tseva, Y. O. Davydova, S. M. Kulikov
Publikováno v:
Онкогематология, Vol 17, Iss 2, Pp 51-59 (2022)
Background. Nowadays, hematology is a dynamically developing science due to the in-depth study of the molecular mechanisms of a particular disease. A better understanding of oncohematological diseases biology makes it possible to synthesize new targe
Externí odkaz:
https://doaj.org/article/298f7058d1fc48a184d31cb66a58fea9
Autor:
K. I. Zarubina, E. N. Parovichnikova, V. L. Surin, O. S. Pshenichnikova, O. A. Gavrilina, G. A. Isinova, V. V. Troitskaia, A. N. Sokolov, I. V. Gal’tseva, N. M. Kapranov, Iu. O. Davydova, T. N. Obukhova, A. B. Sudarikov, V. G. Savchenko
Publikováno v:
Терапевтический архив, Vol 92, Iss 7, Pp 31-42 (2020)
Issue.The study of activating mutations (NRAS,KRAS,FLT3,JAK2,CRLF2genes) of RAS/RAF/MEK/ERK and JAK/STAT signaling pathways in B-cell acute lymphoblastic leukemia (B-ALL) in adult patients which are included in Russian multicenter clinical trials.
Externí odkaz:
https://doaj.org/article/9c2f567d281a4179aa2fc45866e4cb30
Autor:
L. L. Golovkina, R. S. Kalandarov, O. S. Pshenichnikova, V. L. Surin, A. G. Stremoukhova, T. D. Pushkina, G. V. Atroshchenko, O. S. Kalmykova, B. B. Khasigova
Publikováno v:
Онкогематология, Vol 16, Iss 4 (2021)
Background. One of the polymorphic antigens in the ABO system is antigen A, which includes many allelic variants with different expression. Immunological methods for determining the blood group of the ABO system have limitations in their use, includi
Externí odkaz:
https://doaj.org/article/28887e5bbe394390bf2a47f760843846
Autor:
L. L. Golovkina, R. S. Kalandarov, O. S. Pshenichnikova, V. L. Surin, A. G. Stremoukhova, T. D. Pushkina, G. V. Atroshchenko, O. S. Kalmykova, B. B. Khasigova
Publikováno v:
Онкогематология, Vol 16, Iss 4 (2021)
Background. 62 ABO*O alleles of the ABO system are known. Some ABO*O alleles may be accompanied by the presence of residual A-glycosyltransferase activity in people of group O, which may lead to errors in determining the blood group. This confirms th
Externí odkaz:
https://doaj.org/article/5327c8eb5eab447aae55062e3b8d06eb
Autor:
L. L. Golovkina, R. S. Kalandarov, O. S. Pshenichnikova, V. L. Surin, A. G. Stremoukhova, T. D. Pushkina, B. B. Khasigova
Publikováno v:
Онкогематология, Vol 14, Iss 3, Pp 52-59 (2019)
Background. Rhesus phenotype has been determined in 404 persons which have problems with blood groups identification. Genetic typing of antigen RhD variants was performed in 73 individuals. Objective of the work was to give molecular and serological
Externí odkaz:
https://doaj.org/article/982bca2a170845348a1f3e479d2ae729
Autor:
V. Yu. Zorenko, A. A. Koroleva, T. Yu. Polyanskaya, E. E. Karpov, O. S. Pshenichnikova, V. L. Surin
Publikováno v:
Russian journal of hematology and transfusiology. 68:80-87
Introduction. Hemophilia is an X-linked hereditary blood clotting disorder caused by insufficiency of blood clotting factor VIII or IX that affects mainly men. In extremely rare cases, the disease can be observed in women, which is most often associa
Autor:
D. M. Chernetskaya, V. L. Surin, V. V. Salomashkina, O. S. Pshenichnikova, E. V. Yakovleva, N. I. Zozulya, A. B. Sudarikov, E. A. Likhacheva, E. S. Shabanova, F. G. Perina
Publikováno v:
Russian journal of hematology and transfusiology. 67:172-180
Introduction. Von Willebrand disease (vWD) is caused by von Willebrand factor (vWF) dysfunction resulting from pathogenic variants in the vWF gene coding the vWF protein. vWD type 2N is of particular interest, as it is characterized by almost normal
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
Autor:
O. S. Pshenichnikova, V. L. Surin, N. V. Sats, E. V. Yakovleva, O. S. Dimitrieva, N. I. Zozulya
Publikováno v:
Russian Journal of Genetics. 58:829-834
Autor:
G. M. Galstyan, R. G. Shmakov, Е. Е. Klebanova, V. V. Troitskaya, V. N. Dvirnyk, V. L. Surin, O. S. Pshenichnikova, Yu. M. Pozdnyakova, E. S. Polushkina, T. V. Gaponova, S. Yu. Mamleeva, A. V. Pyregov, О. V. Rogachevskiy, E. P. Sysoeva, N. V. Tsvetaeva
Publikováno v:
Russian journal of hematology and transfusiology. 67:42-61
Introduction. Pregnancy is one of the most frequent triggers of congenital and acquired forms of thrombotic thrombocytopenic purpura (TTP).Aim — to develop tactics for the treatment of pregnant women with TTP.Results. TTP was associated with pregna