Zobrazeno 1 - 10
of 14
pro vyhledávání: '"N V, Sats"'
Autor:
L. A. Kuzmina, N. A. Petinati, V. A. Vasilieva, M. V. Dovydenko, M. Yu. Drokov, Yu. O. Davydova, N. M. Kapranov, N. V. Sats, Yu. A. Chabaeva, S. M. Kulikov, T. V. Gaponova, N. I. Drize, E. N. Parovichnikova, V. G. Savchenko
Publikováno v:
Терапевтический архив, Vol 92, Iss 7, Pp 23-30 (2020)
Aim.Analysis of the effectiveness of the MSCs aministration as the second- or third-line therapy of acute GVHD (aGVHD) resistant to glucocorticosteroid treatment. Materials and methods.The study included 35 patients who received MSCs obtained from
Externí odkaz:
https://doaj.org/article/3fe1d38921b144ad954c53dba2f489ee
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4158ff1f2952579e9708975b22415d4a
https://doi.org/10.1134/s1022795422070134
https://doi.org/10.1134/s1022795422070134
Autor:
A. I. Kostin, E. B. Orel, E. V. Yakovleva, P. S. Lavrova, A. M. Gasanov, I. V. Efimov, O. S. Pshenichnikova, N. I. Zozulya, V. L. Surin, N. V. Sats, M. Kh. Azimova, N. I. Konyashina
Publikováno v:
Russian journal of hematology and transfusiology. 66:79-87
Introduction. Among the most common congenital coagulopathies are haemophilia and Von Willebrand disease. These illnesses are often mimicked by orphan hereditary coagulopathies, including combined coagulation factor V and VIII deficiency.Aim — desc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cee501f9694fc7dc58a849b3f079e3d
https://doi.org/10.35754/0234-5730-2021-66-1-79-87
https://doi.org/10.35754/0234-5730-2021-66-1-79-87
Autor:
N A, Petinati, I N, Shipounova, E A, Fastova, A U, Magomedova, S K, Kravchenko, E Yu, Chelysheva, O A, Shukhov, A G, Turkina, N V, Sats, N I, Drize, E N, Parovichnikova, V G, Savchenko
Publikováno v:
Bulletin of experimental biology and medicine. 171(4)
Multipotent mesenchymal stromal cells (MSC) are the key regulators of hematopoiesis. We studied changes in MSC characteristics in patients with myeloid leukemia and patients with lymphoproliferative diseases. MSC were obtained from the bone marrow of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::da627663eea8a58257d6ea0593830cf4
https://pubmed.ncbi.nlm.nih.gov/34542753
https://pubmed.ncbi.nlm.nih.gov/34542753
Autor:
V. S. Komlev, N. V. Proskurina, N. I. Drize, N. V. Sats, E. M. Golubev, A. L. Berkovskiy, V. E. Mamonov, A. G. Chemis
Publikováno v:
Вестник травматологии и ортопедии имени Н.Н. Приорова, Vol 0, Iss 4, Pp 52-59 (2015)
Biological characteristics of bone substituting tissue engineering construction (TEC) that contained porous calcium phosphate ceramic granulate (CPC) of phase structure ((tricalcium phosphate (TCP)), fibrin hydrogel and autologous multipotent mesench
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::175c54d73fc178c17be63df3f25bacb0
https://doi.org/10.32414/0869-8678-2015-4-52-59
https://doi.org/10.32414/0869-8678-2015-4-52-59
Autor:
D. A. Svinareva, A. E. Bigildeev, Irina N. Shipounova, O. A. Zhironkina, N. V. Sats, Nina J. Drize
Publikováno v:
Bulletin of Experimental Biology and Medicine. 150:109-112
Mouse mesenchymal stromal precursor cells were labeled with lentiviral vector in long-term bone marrow culture. We studied the fate of labeled cells in the stromal sublayer of the long-term bone marrow culture and in ectopic hemopoiesis foci formed f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8896b0c84c70a0303c7ea8183893810
https://doi.org/10.1007/s10517-010-1082-1
https://doi.org/10.1007/s10517-010-1082-1
Publikováno v:
Bulletin of experimental biology and medicine. 145(1)
We developed a method for gene transfer into mesenchymal stromal cells. Lentivirus vector containing green fluorescent protein gene for labeling stromal and hemopoietic precursor cells was obtained using two plasmid sets from different sources. The v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bca85d2e5b5874ac091e215b8a639ae
https://pubmed.ncbi.nlm.nih.gov/19024021
https://pubmed.ncbi.nlm.nih.gov/19024021
Autor:
E V, Komissarova, V I, Pantin, L S, Pavlova, T V, Borovkova, M V, Soĭfer, M S, Shtutman, V F, Zarytova, E M, Ivanova, N V, Sats, N I, Grineva
Publikováno v:
Doklady Akademii nauk. 338(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a61f367aab49ab869cf53a5bf0e9b83c
https://pubmed.ncbi.nlm.nih.gov/7820079
https://pubmed.ncbi.nlm.nih.gov/7820079
Publikováno v:
Molekuliarnaia biologiia. 28(2)
In this investigation the primary structure of E1A and E1B regions of SA7 (C8) simian adenovirus integrated in malignant SH2 rat cell line was studied. Southern blotting revealed at least two copies of the SA7 oncogene integrated in the SH2 genome. P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d9dbaf5ee27db521a0ea24bd66bba08f
https://pubmed.ncbi.nlm.nih.gov/8183267
https://pubmed.ncbi.nlm.nih.gov/8183267
Publikováno v:
Molekuliarnaia biologiia. 28(2)
The SA7 (C8) simian adenovirus was sequenced from the 1478th to 3194th nucleotide. The region includes the 3'-terminal part of E1A and the major part of the E1B coding region. The sequence obtained was compared with the structure of SA7 (P) DNA previ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5be8fca5b25fe88ddbb57829b4ec069a
https://pubmed.ncbi.nlm.nih.gov/8183266
https://pubmed.ncbi.nlm.nih.gov/8183266