Zobrazeno 1 - 10
of 54
pro vyhledávání: '"O. L. Kolomiets"'
Autor:
O. L. Kolomiets, E. E. Bragina, A. A. Kashintsova, V. E. Spangenberg, L. A. Nikulina, Yu. N. Korolev, L. V. Mikhailik
Publikováno v:
Андрология и генитальная хирургия, Vol 21, Iss 4, Pp 76-88 (2021)
Introduction. Metabolic syndrome (MS) can cause impaired spermatogenesis and a decrease in sperm counts. However, the details of the effect of MS on developing spermatogenic cells remain unclear. Difficulties in solving this problem, the inconsistenc
Externí odkaz:
https://doaj.org/article/3231de42a41347d786699846e335c95a
Autor:
E. E. Bragina, I. I. Vityazeva, M. A. Lelekova, A. A. Kashintsova, S. V. Bogolyubov, M. Yu. Gabliya, I. V. Vinogradov, V. E. Spanberg, O. L. Kolomiets
Publikováno v:
Андрология и генитальная хирургия, Vol 20, Iss 1, Pp 43-54 (2019)
The study objective is to determine the connection between meiosis abnormalities and changes in the basement membrane (BM) ultrastructure of the seminiferous tubules in patients with spermatogenesis disorders: azoospermia or severe oligospermia.Mater
Externí odkaz:
https://doaj.org/article/8ad14c62024b4cc2aadd0c10fc1da639
Autor:
V. G. Tambovtseva, S. N. Matveevsky, A. A. Kashintsova, A. V. Tretiakov, O. L. Kolomiets, I. Yu. Bakloushinskaya
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 23, Iss 2, Pp 239-243 (2019)
Chromosomal rearrangements can lead to the formation of new stable karyotypes, nevertheless changing the architectonics of the nucleus. The differences in locations might promote Robertsonian (Rb) translocations and encourage meiotic drive in favour
Externí odkaz:
https://doaj.org/article/d0cd2386da374d72aea2ca0b9491217c
Autor:
O. L. Kolomiets, M. A. Lelekova, A. A. Kashintsova, L. F. Kurilo, E. E. Bragina, V. B. Chernykh, M. Yu. Gabliya, I. V. Vinogradov, I. I. Vityazeva, S. V. Bogolyubov, V. E. Spangenberg
Publikováno v:
Андрология и генитальная хирургия, Vol 19, Iss 1, Pp 24-35 (2018)
Introduction. Infertility is diagnosed in 10–15 % of couples wishing to have children. In about half cases, the cause is a disorders of male fertility. Defects of spermatogenesis are often caused by the damages of key events of prophase I meiosis
Externí odkaz:
https://doaj.org/article/11e3b1be8b9a44a4869310354ce4d26c
Autor:
E. E. Bragina, E. A. Arifulin, E. M. Lazareva, M. A. Lelekova, O. L. Kolomiets, A. G. Chogovadze, T. M. Sorokina, L. F. Kurilo, V. Yu. Polyakov
Publikováno v:
Андрология и генитальная хирургия, Vol 18, Iss 1, Pp 48-61 (2017)
Externí odkaz:
https://doaj.org/article/90d31d38491a493488f823bbfa72fa15
Autor:
L. F. Kurilo, M. V. Andreeva, O. L. Kolomiets, T. M. Sorokina, V. B. Chernykh, L. V. Schileiko, S. Sh. Hayat, N. S. Demikova, S. I. Kozlova
Publikováno v:
Андрология и генитальная хирургия, Vol 14, Iss 4, Pp 17-27 (2014)
Classification of congenital disorders, their frequency of occurrence in populations, and some terminology questions discussed in the review. Genetically caused congenital anomalies of reproductive system are outlined. Full information about genetic
Externí odkaz:
https://doaj.org/article/3061f31bf8594ac286ad3de6e17acd29
Autor:
S N, Matveevsky, O L, Kolomiets
Publikováno v:
Tsitologiia. 58(4)
We present here the classification of synaptonemal complex (SC) configurations in meiotic prophase I in animals heterozygous for Robertsonian (Rb) translocations on the basis of own studies and literature data. Configurations of SC multivalents, due
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f1110e306d77b3789ce0698af90cd986
https://pubmed.ncbi.nlm.nih.gov/30191700
https://pubmed.ncbi.nlm.nih.gov/30191700
Autor:
O. L. Kolomiets, M. M. Atsaeva, S. Ya. Dadashev, S. K. Abilev, V. E. Spangenberg, S. N. Matveevsky
Publikováno v:
Russian Journal of Genetics. 49:1098-1106
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48f18d81d2efc1f41eb87f839335e730
https://doi.org/10.1134/s1022795413110100
https://doi.org/10.1134/s1022795413110100