Zobrazeno 1 - 10
of 138
pro vyhledávání: '"T. V. Nasedkina"'
Autor:
V. O. Varachev, O. Yu. Susova, A. A. Mitrofanov, G. S. Krasnov, D. R. Naskhletashvili, Yu. I. Ammour, S. D. Bezhanova, N. V. Sevyan, E. V. Prozorenko, A. Kh. Bekyashev, T. V. Nasedkina
Publikováno v:
Успехи молекулярной онкологии, Vol 11, Iss 3, Pp 68-78 (2024)
Introduction. Epidermal growth factor receptor (EGFR) is a transmembrane protein of the receptor tyrosine kinase family that is activated in various cancers (non-small cell lung cancer, colorectal cancer, head and neck tumors). In glial brain tumors,
Externí odkaz:
https://doaj.org/article/c74688be09cf44c580704332ebb593c1
Autor:
T. V. Nasedkina
Publikováno v:
Онкогематология, Vol 0, Iss 1-2, Pp 25-37 (2022)
Externí odkaz:
https://doaj.org/article/4a989c66036148c8a68144d347b9a5f2
Autor:
E. V. Samochatova, D. D. Baidildina, M. A. Maschan, N. N. Savva, O. P. Khlebnikova, A. V. Shamardina, Yu. E. Mareiko, G. A. Tsaur, T. O. Riger, M. M. Shneider, Yu. V. Rumyantseva, T. V. Nasedkina, T. V. Savitskaya, A. A. Maschan
Publikováno v:
Онкогематология, Vol 0, Iss 3, Pp 8-17 (2022)
The use of all-trans retinoic acid (ATRA) drastically improved the results of therapy for acute promyelocytic leukeimia (APL). The high efficiency of the Russian protocol APL-93—98 applied to 62 children and adolescents with APL (event-free and ove
Externí odkaz:
https://doaj.org/article/a1999c503e6849b689ddc0507d049b22
Autor:
G. A. Tsaur, T. V. Nasedkina, A. M. Popov, O. V. Kalennik, A. G. Solodovnikov, T. O. Riger, Yu. A. Yakovleva, A. S. Ivanova, A. E. Druy, O. M. Plekhanova, E. V. Shorikov, L. I. Saveliev, L. G. Fechina
Publikováno v:
Онкогематология, Vol 0, Iss 2, Pp 46-54 (2022)
Early therapy response is one of the major prognostic factors influencing an outcome of acute lymphoblastic leukemia (ALL). The purpose of the given work was to define a time point (TP) of fusion gene transcript (FGt) monitoring by reverse-transcript
Externí odkaz:
https://doaj.org/article/bccdae5e6fb84086b30c2fa0980c4bf2
Autor:
E. N. Lukyanova, M. S. Fedorova, E. A. Pudova, T. V. Nasedkina, E. V. Stepanova, K. M. Nyushko, A. Y. Popov, N. V. Koroban, A. A. Dmitriev, M. V. Kiseleva, A. V. Lipatova, A. S. Zasedatelev, A. V. Kudryavtseva
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 21, Iss 8, Pp 925-931 (2018)
One of the most important branch of modern molecular genetics and biomedicine is the search for predictive markers that help choose the most effective way of treatment, drug and also determine its individual dosage. Among the markers, those that can
Externí odkaz:
https://doaj.org/article/ddfd0b34361947919ce85ff59c8cd8ff
Autor:
Yu. G. Payanidi, V. Yu. Selchuk, K. I. Zhordania, I. G. Komarov, T. P. Kazubskaya, T. V. Nasedkina, O. V. Fedorova, P. Z. Kutalia, I. A. Kislichko
Publikováno v:
Опухоли женской репродуктивной системы, Vol 0, Iss 1, Pp 51-54 (2014)
Prevention of cancer and its early diagnosis is today one of the promising lines of oncology. The identification of the hereditary forms of malignancies is particularly urgent, which prevents the development of tumor pathology in apparently healthy i
Externí odkaz:
https://doaj.org/article/cae7f84f7ded4678ba345b1ec5bc6226
Autor:
I. I. Kalinina, M. M. Shneyder, N. P. Kirsanova, D. D. Baydildina, E. V. Suntsova, O. V. Goronkova, L. A. Khachatryan, G. A. Novichkova, M. A. Maschan, R. I. Yutskevich, E. V. Volochnik, T. V. Savitskaya, N. V. Minakovskaya, I. V. Proleskovskaya, I. V. Emelyanova, O. V. Karas, N. V. Migal, Yu. E. Mareyko, A. G. Drekov, J. V. Rumyantseva, E. V. Fleyshman, T. V. Nasedkina, O. V. Aleynikova, A. A. Maschan
Publikováno v:
Онкогематология, Vol 6, Iss 1, Pp 11-19 (2014)
A t(8;21) is the most frequent abnormality in AML in children. Patients with this genetic abnormality are traditionally expected favorable prognosis with a probability of cure up to 80 %. Known additional cytogenetic abnormalities in AML with t(8;21)
Externí odkaz:
https://doaj.org/article/61550d5fd7a3461ea6fbd41aa62aeae6
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:
T. S. Belysheva, T. V. Nasedkina, V. V. Semenova, V. M. Kozlova, E. V. Sharapova, S. N. Mikhailova, T. T. Valiev, S. R. Varfolomeeva
Publikováno v:
Russian Journal of Pediatric Hematology and Oncology. 9:60-74
Genodermatoses are a heterogeneous group of hereditary diseases that are characterized by predominantly skin lesions. To date, there are more than 200 genetically determined skin diseases, representing about 35 % of all hereditary syndromes. In some
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1107e2b008691c8da041009302e596d3
https://doi.org/10.21682/2311-1267-2022-9-2-60-74
https://doi.org/10.21682/2311-1267-2022-9-2-60-74
Autor:
T. S. Belysheva, T. V. Nasedkina, T. T. Valiev, N. V. Matinyan, O. A. Malikhova, V. V. Semenova, V. M. Kozlova, T. P. Kazubskaya, Y. V. Vishnevskaya, S. N. Mikhailova, S. R. Varfolomeeva
Publikováno v:
Russian Journal of Pediatric Hematology and Oncology. 8:95-102
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e2a32cb1a676212354f98daf3db995d
https://doi.org/10.21682/2311-1267-2021-8-4-95-102
https://doi.org/10.21682/2311-1267-2021-8-4-95-102