Zobrazeno 1 - 10
of 20
pro vyhledávání: '"O. V. Streneva"'
Autor:
M. Yu. Goroshkova, Yu. V. Rumyantseva, O. V. Aleinikova, S. A. Dudkin, L. G. Fechina, A. V. Shamardina, O. V. Streneva, K. L. Kondratchik, L. M. Minkina, E. S. Lapotentova, E. V. Inyushkina, O. B. Kozlova, E. V. Zhukovskaya, O. P. Khlebnikova, E. V. Basharova, V. N. Timofeeva, G. P. Pavlova, V. D. Zlobina, O. A. Utrobina, E. S. Banshchikova, K. S. Aslanyan, E. V. Kondakova, E. V. Tselousova, N. V. Myakova, T. V. Turobova, O. V. Ryskal, O. Yu. Fuks, V. V. Lebedev, N. F. Chipsanova, S. R. Varfolomeeva, A. I. Karachunsky
Publikováno v:
Онкогематология, Vol 0, Iss 3, Pp 25-33 (2022)
The paper presents the results of a multicenter randomized study of two-dose COLI-ASP regimens in therapy of consolidation of standard risk-group (SRG) children and adolescents with acute lymphoblastic leukemia (ALL) treated by the ALL-MB-2002 protoc
Externí odkaz:
https://doaj.org/article/273ffc5c215a492e9db3020d5e11e678
Autor:
J. V. Roumiantseva, A. I. Karachunsky, O. V. Aleinikova, L. G. Fechina, A. V. Schamardina, D. V. Litvinov, N. I. Ponomareva, E. G. Boichenko, L. V. Sidorenko, S. A. Dudkin, O. V. Streneva, K. L. Kondratchik, E. G. Mansurova, L. M. Minkina, E. S. Lapotentova, E. V. Inuschkina, N. B. Yudina, G. P. Pavlova, E. V. Zhukovskaya, O. P. Chlebnikova, S. N. Lagoiko, E. V. Bascharova, R. E. Denisov, V. D. Zlobina, E. S. Banschikova, K. S. Aslanyan, E. V. Kondakova, E. V. Celousova, N. V. Myakova, T. V. Turobova, O. V. Riskal, N. F. Chipsanova, S. R. Varfolomeeva, A. G. Rumiantsev
Publikováno v:
Онкогематология, Vol 0, Iss 1, Pp 37-49 (2022)
Проанализирована значимость прогностических факторов эффективности терапии у детей с острым лимфобластным лейкозом (ОЛЛ), получающих
Externí odkaz:
https://doaj.org/article/60da326014b14be09d19043fc252c8e4
Autor:
G. A. Tsaur, Т. О. Riger, A. M. Popov, T. Yu. Verzhbitskaya, L. V. Vakhonina, A. A. Vlasova, Yu. V. Olshanskaya, А. N. Kazakova, O. V. Streneva, O. V. Makarova, S. V. Tsvirenko, L. I. Saveliev, О. R. Arakaev, L. G. Fechina
Publikováno v:
Онкогематология, Vol 12, Iss 4, Pp 57-70 (2018)
Introduction. Translocation t(12;21)(p13;q22) is one of the most common structural genetic abnormalities in childhood acute lymphoblastic leukemia (ALL). It cannot be detected by conventional G-banding, so a reverse-transcriptase polymerase chain rea
Externí odkaz:
https://doaj.org/article/26a32e968772436993b26346444b3779
Autor:
A. M. Popov, Y. Yu. Verzhbitskaya, G. A. Tsaur, A. G. Solodovnikov, O. R. Arakaev, O. V. Streneva, O. P Khlebnikova, E. V. Shorikov, L. I. Saveliev, S. N. Lagoyko, Yu. V. Rumyantseva, A. I. Karachunskiy, L. G. Fechina
Publikováno v:
Онкогематология, Vol 10, Iss 4, Pp 44-55 (2015)
191 consecutive unselected children with acute lymphoblastic leukemia aged from 1 to 16 years were enrolled in the study. Bone marrow samples were obtained at the time of initial diagnostics as well as at days 15 (n = 188), 36 (n = 191), and 85 (n =
Externí odkaz:
https://doaj.org/article/0218a3540de14fb58723611f40943264
Autor:
G. A. Tsaur, A. M. Popov, O. V. Aleynikova, E. G. Boychenko, T. Yu. Verzhbitskaya, E. V. Volochnik, A. S. Ivanova, O. V. Kalennik, S. Yu. Kovalev, K. L. Kondtratchik, A. M. Kustanovich, E. S. Lapotentova, D. V. Litvinov, I. S. Martynkevich, N. V. Myakova, T. V. Nasedkina, V. A. Ovsepyan, Yu. V. Olshanskaya, O. M. Plehanova, A. V. Popa, T. O. Riger, L. I. Savelyev, O. V. Streneva, M. V. Strigaleva, I. V. Shmunk, E. V. Shorikov, L. G. Fechina
Publikováno v:
Онкогематология, Vol 6, Iss 3, Pp 57-64 (2014)
117 cases of infant acute lymphoblastic leukemia without Down syndrome (aged from 1 to 365 days) were included in the current study.Rearrangements of 11q23 (MLL) were revealed in 74 (63.2 %) patients. Among this group the most common rearrangement wa
Externí odkaz:
https://doaj.org/article/a38eecadd7c84ecc9537c84830839adc
Autor:
G. A. Tsaur, A. M. Popov, O. M. Plekhanova, A. M. Kustanovich, O. V. Aleynikova, T. L. Gindina, A. S. Demina, A. Ye. Druy, S. Yu. Kovalev, K. L. Kondratchik, A. V. Misyurin, N. V. Myakova, T. O. Riger, L. I. Savelyev, O. I. Sokova, O. V. Streneva, M. V. Suchkova, Yu. P. Finashutina, Ye. V. Fleyshman, Ye. V. Shorikov, R. I. Yutskevich, C. Meyer, R. Marschalek, L. G. Fechina
Publikováno v:
Онкогематология, Vol 8, Iss 1, Pp 17-32 (2014)
We performed clinical and laboratory characterization of patients with rare translocation t(1;11)(p32;q23) leading to MLL-EPS15 fusion gene formation. Study cohort consisted of 33 primary acute leukemia (AL) cases including 6 newly diagnosed and 27 p
Externí odkaz:
https://doaj.org/article/e9e8f963c1c2416d8aaa13d770f87300
Autor:
A. M. Popov, G. A. Tsaur, T. Yu. Verzhbitskaya, O. V. Streneva, E. V. Shorikov, L. I. Saveliev, L. G. Fechina
Publikováno v:
Онкогематология, Vol 7, Iss 2, Pp 14-24 (2014)
Aim of the study – immunophenotype description of infant acute lymphoblastic leukemia (ALL). 64 patients (29 boys and 35 girls) with acute leukemia (AL) aged from 0 to 11 months were included in the current study. ALL was found less frequently in i
Externí odkaz:
https://doaj.org/article/ec102b881d0f44e08af0f38f9dacf9ad
Autor:
A. M. Popov, G. A. Tsaur, T. Yu. Verzhbitskaya, O. V. Streneva, E. V. Shorikov, L. I. Saveliev, L. G. Fechina
Publikováno v:
Онкогематология, Vol 8, Iss 1, Pp 33-39 (2014)
Aim of the study – characterization of immunophenotype in infant acute myeloid leukemia (AML). 90 patients (40 boys and 50 girls) with acute leukemia (AL) aged up to 365 days were included in the current study. AML was found more frequently in infa
Externí odkaz:
https://doaj.org/article/ecdea07ef7e142fd86128cd15e46cedd
Autor:
Riger To, C Meyer, E.A. Matveeva, A.E. Drui, R Marschalek, Grigory Tsaur, O. R. Arakaev, OI Sokova, SA Rumyantsev, Larisa Fechina, EV Fleischman, O. V. Streneva, Egor Shorikov, Solodovnikov Ag, Savel'ev Li, AM Kustanovich, YuV Ol’shanskaya, Alexander Popov, O. V. Nikulina
Publikováno v:
Kliničeskaâ onkogematologiâ, Vol 9, Iss 1, Pp 22-29 (2016)
Aim. To evaluate the relation between genomic DNA breakpoints in MLL and translocation partner genes (TPG) and clinical parameters of infant AL. Methods. 68 infants (29 boys and 39 girls with median age of 4.8 mo) with MLL-rearranged acute lymphoblas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e4f49337fd2669115a53e5a5cc1d0a5
http://bloodjournal.ru/en/relation-between-genomic-dna-breakpoints-in-mll-gene-and-treatment-outcome-in-infants-with-acute-leukemia/
http://bloodjournal.ru/en/relation-between-genomic-dna-breakpoints-in-mll-gene-and-treatment-outcome-in-infants-with-acute-leukemia/
Autor:
G. A. Tsaur, A. M. Popov, O. V. Aleynikova, E. G. Boychenko, T. Yu. Verzhbitskaya, E. V. Volochnik, A. S. Ivanova, O. V. Kalennik, S. Yu. Kovalev, K. L. Kondtratchik, A. M. Kustanovich, E. S. Lapotentova, D. V. Litvinov, I. S. Martynkevich, N. V. Myakova, T. V. Nasedkina, V. A. Ovsepyan, Yu. V. Olshanskaya, O. M. Plehanova, A. V. Popa, T. O. Riger, L. I. Savelyev, O. V. Streneva, M. V. Strigaleva, I. V. Shmunk, E. V. Shorikov, L. G. Fechina
Publikováno v:
Onkogematologiâ, Vol 6, Iss 3, Pp 57-64 (2014)
117 cases of infant acute lymphoblastic leukemia without Down syndrome (aged from 1 to 365 days) were included in the current study. Rearrangements of 11q23 (MLL) were revealed in 74 (63.2 %) patients. Among this group the most common rearrangement w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::faf3644e23b2106acd7e4dd199cad56d
http://cyberleninka.ru/article/n/detection-of-11q23-mll-rearrangements-in-infant-acute-lymphoblastic-leukemia
http://cyberleninka.ru/article/n/detection-of-11q23-mll-rearrangements-in-infant-acute-lymphoblastic-leukemia