Zobrazeno 1 - 10
of 56
pro vyhledávání: '"S., Gorbenko A."'
Autor:
I. A. Olkhovskiy, J. G. Garber, A. S. Gorbenko, M. A. Stolyar, O. M. Miller, E. S. Kostina, Yu. Yu. Komarovskiy, V. V. Potilitsina
Publikováno v:
Акушерство, гинекология и репродукция, Vol 13, Iss 3, Pp 204-210 (2019)
Aim: to assess the prevalence of V617F somatic mutation of the JAK2 gene in pregnant women.Materials and methods. This non-interventional study was performed in the framework of routine clinical practice and included 1532 samples of venous blood from
Externí odkaz:
https://doaj.org/article/fa14c52b65c34af88a8dd9ca9b9dd8f1
Publikováno v:
Терапевтический архив, Vol 91, Iss 7, Pp 25-28 (2019)
The JAK2 V617F somatic mutation is one of the most frequent markers of CHIP (clonal hematopoiesis of indeterminate potential). CHIP is characterized by the presence of a myeloid cells clone in peripheral blood in the absence of the sufficient reasons
Externí odkaz:
https://doaj.org/article/f042e6ea94fc4112a75653d758639630
Autor:
I. А. Olkhovskiy, M. A. Stolyar, Yu. Yu. Komarovskiy, A. S. Gorbenko, V. I. Korchagin, E. A. Dunaeva, K. O. Mironov, V. I. Bakhtina, T. I. Olkhovik, E. V. Vasiliev, M. A. Mikhalev
Publikováno v:
Russian journal of hematology and transfusiology. 67:377-387
Introduction. Haplotype JAK2 46/1 is associated with more frequent development of Ph-negative myeloproliferative neoplasms (MPN) and with an increased detection rate of the JAK2 V617F mutation. At the same time, the molecular mechanisms of such assoc
Autor:
S. V. Stolyar, S. V. Komogortsev, A. S. Gorbenko, Yu. V. Knyazev, R. N. Yaroslavtsev, I. A. Olkhovskiy, D. S. Neznakhin, A. V. Tyumentseva, O. A. Bayukov, R. S. Iskhakov
Publikováno v:
Journal of Superconductivity and Novel Magnetism. 35:1929-1936
Autor:
I. A. Olkhovskiy, A. S. Gorbenko, Yu. Yu. Komarovskiy, M. A. Stolyar, D. I. Vasil’eva, O. S. Epifanova, D. A. Khodov, S. A. Rudakova, N. V. Rudakov, I. P. Oskorbin, M. L. Filipenko
Publikováno v:
Russian Clinical Laboratory Diagnostics. 67:59-64
Early diagnosis of tick-borne borreliosis determines the indications for etiotropic therapy, and the detection of borrelia in a tick that has bitten you serves as the basis for antibiotic prophylaxis. To determine the causative agent of borreliosis,
Publikováno v:
Georgian Medical News; Jul/Aug2023, Vol. 340/341 Issue 7/8, p198-204, 7p
Autor:
I. A. Olkhovskiy, A. S. Gorbenko, M. A. Stolyar, V. I. Bakhtina, M. A. Mikhalev, T. I. Olkhovik, A. B. Sudarikov, Yu. S. Sidorova, T. I. Pospelova, M. A. Kolesnikova, T. S. Kaporskaya, V. A. Lyskova
Publikováno v:
Klinicheskaia laboratornaia diagnostika. 67(10)
Simultaneous quantitative measurement of mRNA of the WT1, BAALC, EVI1, PRAME and HMGA2 genes in whole blood samples reflects the specific pathological proliferative activity in acute leukemia and their ratio is promising as a diagnostic marker. The t
Autor:
M. A. Mikhalev, T I Olkhovik, M.A. Stolyar, E E Mochalova, K E Orlova, V I Bakhtina, E. V. Vasiliev, A. S. Gorbenko, I. A. Olkhovskiy
Publikováno v:
Russian Clinical Laboratory Diagnostics. 66:571-576
Abnormal mRNAs of the hybrid BCR-ABL gene in the majority of cases initiate the synthesis of proteins with a mass of 210 kDa (p210), 190 kDa (p190), and 230 kDa (p230). Expression of the p210 variant is most common in CML (95% of cases), while the p1
Autor:
A. S. Gorbenko, M. A. Stolyar, Yu. Yu. Komarovsky, M. A. Mikhalev, V. V. Potylitsyna, E. V. Vasilyev, I. A. Olkhovsky
Publikováno v:
Medical alphabet. 3:11-14
A large-scale study of DNA sequencing databases (Jorgenson E., et al., 2018) to search for hereditary susceptibility to early erectile dysfunction revealed an association with the rs17185536-T polymorphism regulating the expression of topologically a
Silica-Coated Iron Oxide Nanoparticles for DNA Isolation for Molecular Genetic Studies in Hematology
Autor:
M.A. Stolyar, Alina T. Saitova, Ekaterina S. Tyutrina, Alexey S. Gorbenko, I. A. Olkhovskiy, Sergey V. Stolyar, Anna V. Tyumentseva, R. N. Yaroslavtsev
Publikováno v:
Genetic testing and molecular biomarkers. 25(9)
Aim: To develop magnetic nanoparticles (MNPs) based on iron oxide for DNA isolation from blood cells for quantitative molecular genetic analyses of the V617F mutation in the Januskinase 2 (JAK2) ge...