Zobrazeno 1 - 10
of 153
pro vyhledávání: '"Yu L, Orlov"'
Autor:
A. O. Bragin, O. V. Saik, I. V. Chadaeva, P. S. Demenkov, A. L. Markel, Yu. L. Orlov, E. I. Rogaev, I. N. Lavrik, V. A. Ivanisenko
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 21, Iss 8, Pp 911-919 (2018)
Aggressive behavior in animals plays an important role in protecting the territory, offspring, establishing social hierarchical relations, etc. Increased aggression is observed in a number of diseases ( schizophrenia, bipolar disorder, brain degenera
Externí odkaz:
https://doaj.org/article/92c985dc11af450f994b6bc5d39f73a9
Genetic polymorphisms and related risk factors of ischemic stroke in a Mongolian population in China
Autor:
Q. Wu, H. Wu, Yu. L. Orlov, G. Gegentana, W. Huo, A. O. Bragin, N. Wu, S. Suyalatu, F. Zhao, J. Zhao, L. E. Tabikhanova, M. Chen, H. Bai
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 21, Iss 5, Pp 581-587 (2017)
Ischemic stroke is caused by an interruption in the flow of blood to the brain and a risk factor for death and disability. Recent genome-wide association studies have identified more than 40 common sequence variants associated with ischemic stroke. H
Externí odkaz:
https://doaj.org/article/3539f1f1e0e6415988faee7ed7d3c8f2
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 19, Iss 3, Pp 303-309 (2015)
Microsatellites, or simple sequence repeats (SSRs), are ubiquitous in genomes of eukaryotes, including plant genomes. The structure and location of SSR loci determine their potential as molecular genetic markers and may have impact on the potential f
Externí odkaz:
https://doaj.org/article/a706d3f9c90341108ce3b64975c80cc0
Autor:
O. B. Dobrovol’skaya, P. Martinek, I. G. Adonina, E. D. Badaeva, Yu. L. Orlov, E. A. Salina, L. I. Laikova
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 18, Iss 4/1, Pp 672-680 (2015)
Four genetically independent bread wheat lines with altered spike morphology caused by development of supernumerary spikelets at rachis nodes were characterized by modern methods of karyotype analysis, Cbanding and FISH. Three lines carried rearrange
Externí odkaz:
https://doaj.org/article/34641158a2dd461f9bacecb4e47b9ef4
Autor:
Yu. L. Orlov
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 18, Iss 1, Pp 193-206 (2015)
The development of high-throughput sequencing technologies dramatically accelerated the accumulation of data on genome structure, distribution of gene regulatory regions in the genome and specific features of their interaction. Technologies associate
Externí odkaz:
https://doaj.org/article/84a6c87af36e4662ad4a68c1190fe32a
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 16, Iss 4/2, Pp 872-878 (2014)
The 3D organization of an eukaryotic genome plays an important role in nuclear gene expression. Until recently, studies of this organization were limited by light microscopy and electron microscopy methods. The development of chromosome conformation
Externí odkaz:
https://doaj.org/article/175e7a583d084090892d9aabe1640765
Autor:
Yu. L. Orlov, T. I. Pospelova, V. N. Maximov, Mikhail I. Voevoda, T. A. Ageeva, N. Cherdyntseva, E. N. Voropaeva
Publikováno v:
Russian Journal of Genetics. 55:1564-1568
The role of genetic susceptibility to the development of lymphoma is confirmed by the accumulating data on common genetic variants of the genes involved in lymphomogenesis. The varieties of disease variants, as well as the small effect of each of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::230c1b852155f125c0ac241dda5e5b83
https://doi.org/10.1134/s1022795419120123
https://doi.org/10.1134/s1022795419120123
Autor:
David P. Gold
Publikováno v:
Science. 200:1144-1144
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e8552074e2cb151b0d51e81dd170cb4
https://doi.org/10.1126/science.200.4346.1144-a
https://doi.org/10.1126/science.200.4346.1144-a
Autor:
R. A. Howie
Publikováno v:
Mineralogical Magazine. 42:565-565
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37bd6d549ee75b1e1754c517d53d95e5
https://doi.org/10.1180/minmag.1978.042.324.22
https://doi.org/10.1180/minmag.1978.042.324.22
Genetic polymorphisms and related risk factors of ischemic stroke in a Mongolian population in China
Autor:
Suyalatu Suyalatu, H. Wu, H. Bai, N. Wu, Ming Chen, J. Zhao, Q. Wu, W. Huo, G. Gegentana, Yu. L. Orlov, A. O. Bragin, F. Zhao, L. E. Tabikhanova
Publikováno v:
Vavilovskij Žurnal Genetiki i Selekcii, Vol 21, Iss 5, Pp 581-587 (2017)
Ischemic stroke is caused by an interruption in the flow of blood to the brain and a risk factor for death and disability. Recent genome-wide association studies have identified more than 40 common sequence variants associated with ischemic stroke. H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13ceee914b28d2fc279eea9fb874d2f0
https://vavilov.elpub.ru/jour/article/view/1144
https://vavilov.elpub.ru/jour/article/view/1144