Zobrazeno 1 - 10
of 14
pro vyhledávání: '"N V Makeeva"'
Autor:
A. Yu. Salomatin, N. V. Makeeva
Publikováno v:
Известия высших учебных заведений. Поволжский регион: Общественные науки, Iss 2 (2020)
Background. In the conditions of increasing influence of complex organized states and noticeable erosion of the foundations of unitarianism in the era of changing technological structures and globalizing political turbulence, federalism remains re
Externí odkaz:
https://doaj.org/article/5d50e05b7a304f0e8a15623dc17ee35c
Autor:
N. V. Makeeva
Publikováno v:
Pravo: istoriya i sovremennost'. :064-068
Publikováno v:
Modern Technologies in Medicine
The aim of the study is to determine the diagnostic utility of several islet autoantibodies and their combinations in order to identify individuals susceptible to type 1 diabetes mellitus (T1DM) among healthy siblings in the pediatric population with
Autor:
Z. A. Miryaeva, N. V. Makeeva
Publikováno v:
University proceedings. Volga region. Social sciences.
Autor:
Anna Pestova, Rachel E. Ibbotson, Ancha Baranova, Francesco Gorreta, N. V. Makeeva, Stefan Einhorn, Marianne Hammarsund, Tariq Alsheddi, Martin Corcoran, Dmitry A. Shagin, Eugene R. Zabarovsky, T. V. Tyazhelova, Nikitin Ea, Andrey Ivanovich Vorobiev, Dmitry Ivanov, Kapanadze Bi, Mikhail Skoblov, N. K. Yankovsky, Karen Schlauch, Olle Sangfelt, Tatiana Borodina, Vikas Chandhoke, A. B. Poltaraus, Dan Grandér, Svetlana Nazarenko, David Oscier, Sergey Lukianov
Publikováno v:
Gene. 321:103-112
In the present study, we describe the human and mouse RFP2 gene structure, multiple RFP2 mRNA isoforms in the two species that have different 5' UTRs and a human-specific antisense transcript RFP2OS. Since the human RFP2 5' UTR is not conserved in mo
Autor:
E. V. Stepanova, Ancha Baranova, Dmitry Ivanov, D. A. Madera, A. A. Pestova, N. V. Makeeva, T. A. Borodina
Publikováno v:
Russian Journal of Genetics. 39:973-985
The Human Genome Project stimulated the development of efficient strategies and relevant hardware for complete genome sequencing. The comparative genomic approach extends the possibilities of using the sequencing data to identify new genes or conserv
Autor:
Stefan Einhorn, T. V. Tyazhelova, Kapanadze Bi, Dmitry Ivanov, E. A. Nikitin, Ancha Baranova, A. I. Vorobiev, N. V. Makeeva, N. K. Yankovsky, Dan Grandér, Olle Sangfelt, A. B. Semov
Publikováno v:
Russian Journal of Genetics. 37:1286-1292
Deletions in the region located between the STS markers D13S1168 and D13S25 on chromosome 13 are the most frequent genomic changes in patients with B-cell chronic lymphocytic leukemia (B-CLL). After sequencing of this region, two novel candidate gene
Autor:
Glinshchikova Oa, Dmitry Ivanov, A. B. Poltaraus, N. V. Makeeva, E. A. Nikitin, David Oscier, Ancha Baranova, A. B. Soudarikov, Martin Corcoran, N. K. Yankovsky, T. A. Borodina
Publikováno v:
Molecular Biology. 34:232-236
ING1, a supposed tumor suppressor gene, codes for a p33 protein involved in cell proliferation control and regulation of apoptosis. A GenBank search revealed two groups of expressed sequence tags corresponding toING1 mRNA forms. The 3′ exon 2 is th
Autor:
N V, Makeeva, A A, Pestova, T A, Borodina, D A, Madera, D V, Ivanov, E V, Stepanova, A V, Baranova
Publikováno v:
Genetika. 39(9)
The Human Genome Project stimulated the development of efficient strategies and relevant hardware for complete genome sequencing. The comparative genomic approach extends the possibilities of using the sequencing data to identify new genes or conserv
Autor:
T V, Tiazhelova, D V, Ivanov, N V, Makeeva, B I, Kapanadze, E A, Nikitin, A B, Semov, O, Sangfeldt, D, Grander, A I, Vorob'ev, S, Einhorn, N K, Iankovskiĭ, A V, Baranova
Publikováno v:
Genetika. 37(11)
Deletions in the region located between the STS markers D13S1168 and D13S25 on chromosome 13 are the most frequent genomic changes in patients with B-cell chronic lymphocytic leukemia (B-CLL). After sequencing of this region, two novel candidate gene