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pro vyhledávání: '"A A, Bukaeva"'
Раздел 2. Сопоставительные и диахронические исследования языковых единиц и категорий Статья посвящена вопросу классификации композитн
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1594::61489ec9f4c5d74d19ecfe54328b9b8a
http://elib.bsu.by/handle/123456789/189626
http://elib.bsu.by/handle/123456789/189626
Publikováno v:
Медицинская иммунология, Vol 23, Iss 5, Pp 1017-1030 (2021)
This review describes principles of action and the method of delivery of mRNA molecules into cells, as well as some of developed RNA vaccines and the results obtained in their study, though they have not been authorized for use yet. In addition, the
Externí odkaz:
https://doaj.org/article/d260a86bf48a42c1bac4c48f6a9f241e
Optimal voluntary waiting period for highly productive cows in herds of more than 3000 milking heads
Autor:
Garanin Maksim, Pereryadkina Svetlana, Lisichenko Galina, Kocharyan Valentina, Bukaeva Yuliya
Publikováno v:
E3S Web of Conferences, Vol 463, p 01042 (2023)
The study showed that fertility at the first artificial insemination (AI) is 9% higher if the voluntary waiting period (VWP) is 80 days compared to 60 days. However, in the second IO, the level of fertilization in both cases remains the same and is 4
Externí odkaz:
https://doaj.org/article/c878ba3a77ab40c183c1c5a21965f093
Autor:
R. P. Myasnikov, A. A. Bukaeva, O. V. Kulikova, A. I. Ershova, A. V. Petukhova, E. D. Zotova, A. N. Meshkov, E. A. Mershina, A. V. Kiseleva, M. G. Divashuk, P. S. Pilyus, M. S. Kharlap, V. M. Mikova, S. N. Koretsky, L. A. Gandaeva, V. E. Sinitsyn, E.. N. Basargina, S. A. Boytsov, E. A. Snigir, A. I. Akinshina, D. A. Kashtanova, V. V. Makarov, V. S. Yudin, O. M. Drapkina
Publikováno v:
Российский кардиологический журнал, Vol 26, Iss 1S (2021)
The article presents the examination of three generations of a family with diagnosed left ventricular noncompaction (LVNC) and various phenotypic manifestations of the disease (isolated, hypertrophic and dilated type of LVNC). As a result of a molecu
Externí odkaz:
https://doaj.org/article/0ce62cb7901e4c04af8ca2327cf631cb
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Primary cardiomyopathies (CMPs) are monogenic but multi-allelic disorders with dozens of genes involved in pathogenesis. The implementation of next-generation sequencing (NGS) approaches has resulted in more time- and cost-efficient DNA diagnostics o
Externí odkaz:
https://doaj.org/article/5f94ddc6645a4c35bb89dda3f856cd70
Publikováno v:
International Journal of Biomedicine, Vol 9, Iss Suppl_1, Pp S33-S33 (2019)
Background: The differential diagnosis between renal oncocytoma (RO) and chromophobe renal cell carcinoma (chRCC) is clinically significant because of their different biological behavior: the former widely accepted as a benign neoplasm and the latter
Externí odkaz:
https://doaj.org/article/b9c2059977c1479aa2c037ecdee788b5
Akademický článek
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Autor:
M. E. Polyak, A. A. Bukaeva, A. G. Shestak, O. V. Blagova, A. V. Sveshnikov, Yu. A. Lutokhina, A. V. Nedostup, E. V. Zaklyazminakaya
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 98-104 (2016)
Non-compaction myocardium syndrome of the left ventricle (NCM) is relatively new diagnosis. There is no consensual approach to classification, diagnostics, as treatment and management of patients with NCM till recently. Predictive value of the observ
Externí odkaz:
https://doaj.org/article/4720e8f75c0b43ac94a48fb8113bd4d4
Autor:
V. A. Rumyantseva, Yu. A. Rogozhina, A. A. Bukaeva, D. V. Bazarov, E. R. Charchyan, E. V. Zaklyazminskaya
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 7-14 (2016)
Aim. To invent a complex approach to patients with “marfanoid phenotype” undergoing surgery, applying the DNA-diagnostics of the gene FBN1 and medical genetic counseling.Material and methods. In the group of 37 patients with suspected Marfan synd
Externí odkaz:
https://doaj.org/article/71eb75d8bfa54a8a8dae90231d2625d6
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 10, Pp 93-97 (2016)
Noonan syndrome is clinically and genetically heterogenic disease caused by mutations in genes coding the proteins of universal cascade of cellular signalling Ras-MAPK. Recently, about 10 genes known, with mutations leading to the disease development
Externí odkaz:
https://doaj.org/article/a1bc6f9222834de1a3a1915f07793da9