Zobrazeno 1 - 10
of 59
pro vyhledávání: '"N A, Skryabin"'
Autor:
R. R. Savchenko, N. A. Skryabin
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 28, Iss 7, Pp 770-779 (2024)
Our understanding of human genes - particularly their structure, functions, and regulatory mechanisms - is still limited. The biological role of approximately 20 % of human proteins has not been established yet, and the molecular functions of the kno
Externí odkaz:
https://doaj.org/article/17ebabb3da394d81a8cce062f195c38b
Autor:
D. G. Tikhonov, A. N. Egorov, M. V. Golubenko, A. Yu. Molokov, V. A. Belyavskaya, P. A. Gervas, N. A. Skryabin
Publikováno v:
Сибирский онкологический журнал, Vol 22, Iss 6, Pp 74-82 (2024)
Background. The Sakha (Yakutia) population, the indigenous population of Siberia living in Yakutia, has one of the lowest rates of breast cancer (BC) incidence worldwide. The low BC incidence among the indigenous population of Yakutia has been report
Externí odkaz:
https://doaj.org/article/8755eb2f10bb415c8d97185552d1f2d2
Autor:
T. V. Karamysheva, I. N. Lebedev, L. I. Minaycheva, L. P. Nazarenko, A. A. Kashevarova, D. A. Fedotov, N. A. Skryabin, M. E. Lopatkina, A. D. Cheremnykh, E. A. Fonova, T. V. Nikitina, E. A. Sazhenova, M. M. Skleimova, N. A. Kolesnikov, G. V. Drozdov, Y. S. Yakovleva, G. N. Seitova, K. E. Orishchenko, N. B. Rubtsov
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Pallister-Killian syndrome (PKS) is a rare inherited disease with multiple congenital anomalies, profound intellectual disability, and the presence in the karyotype of sSMC - i(12)(p10). The frequency of PKS may be underestimated due to problems with
Externí odkaz:
https://doaj.org/article/88afa4cfc61a4a5da256eddbcc50ab10
Autor:
N. A. Skryabin, S. A. Vasilyev, T. V. Nikitina, D. I. Zhigalina, R. R. Savchenko, N. P. Babushkina, M. E. Lopatkina, A. A. Kashevarova, I. N. Lebedev
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 23, Iss 2, Pp 244-249 (2019)
Recurrent pregnancy loss (RPL) is a severe reproductive pathology with a significant component of unexplained etiology. Extended homozygous regions as a possible etiological factor for RPL were sought in the genomes of embryos. Twenty-two paired firs
Externí odkaz:
https://doaj.org/article/baac6f4e959c4f66ba4e0f71b76dcf5c
Autor:
A. A. Arkhipova, S. A. Zhuravitskii, N. N. Skryabin, I. V. D’yakonov, A. A. Kalinkin, S. P. Kulik, S. V. Chekalin, Ya. V. Kartashov, B. N. Zadkov, V. O. Kompanets
Publikováno v:
JETP Letters. 117:339-343
The features of nonlinear propagation of high-intensity pulses in the short-wavelength infrared range in extended one-dimensional waveguide arrays with different spatial periods, formed in fused silica by laser writing, are studied. More than tenfold
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa5dae55611644c70500013a89ff202a
https://doi.org/10.1134/s0021364023600179
https://doi.org/10.1134/s0021364023600179
Publikováno v:
Russian Journal of Genetics. 58:1208-1215
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd36a08949b2ed166c2ab8a29e176603
https://doi.org/10.1134/s1022795422100088
https://doi.org/10.1134/s1022795422100088
Publikováno v:
Russian Journal of Genetics. 58:1216-1227
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::586888594083d1bbf78af36f62dbec42
https://doi.org/10.1134/s1022795422100064
https://doi.org/10.1134/s1022795422100064
Autor:
M. V. Zavjalova, N. S. Telegina, S. V. Vtorushin, V. M. Perelmute, E. M. Slonimskaya, E. V. Denisov, N. V. Cherdyntseva, S. V. Patalyak, N. A. Skryabin, K. Yu. Khristenko
Publikováno v:
Сибирский онкологический журнал, Vol 0, Iss 2, Pp 41-44 (2016)
The present study has found significant heterogeneity of luminal A breast cancer group, which is manifested by differences in relationship between the frequency of lymphogenic metastasis and morphologic and molecular-biological parameters of the prim
Externí odkaz:
https://doaj.org/article/069f008dd8434ffab96e2a0347470a94
Publikováno v:
Сибирский онкологический журнал, Vol 1, Iss 6, Pp 64-69 (2016)
Abnormalities of DNA methylation play a significant role in initiation and progression of tumors. In this regard it is necessary to study these aberrations in order to better understand the malignant transformation pathogenesis. For this purpose the
Externí odkaz:
https://doaj.org/article/21eb46bcb53348218e36e68dd1865ebd
Autor:
O. V. Pankova, V. M. Perelmuter, E. V. Denisov, S. A. Tuzikov, S. V. Miller, S. A. Vasilyev, N. A. Skryabin
Publikováno v:
Сибирский онкологический журнал, Vol 1, Iss 6, Pp 26-30 (2016)
Comparative analysis of the relationship between the character of dysregeneratory changes occurring in the bronchial epithelium adjacent to the tumor and the development of recurrence of squamous cell and grandular carcinomas of the lung was carried
Externí odkaz:
https://doaj.org/article/69a6fa3528724e9789aeda0b232eedad