Zobrazeno 1 - 10
of 23
pro vyhledávání: '"F A Zakharova"'
Autor:
V. A. Korneva, M. Yu. Mandelshtam, A. V. Orlov, V. B. Vasiliev, T. Yu. Kuznetsova, F. M. Zakharova
Publikováno v:
Кардиоваскулярная терапия и профилактика, Vol 22, Iss 7 (2023)
Familial hypercholesterolemia (FH) is one of the most common monogenic diseases that leads to the early development of atherosclerosis and is characterized by a poor prognosis. However, only about 1% of FH cases are diagnosed in Russia. The aim of th
Externí odkaz:
https://doaj.org/article/9d408cd1784d4fd187413f638030de25
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 26, Iss 3, Pp 319-326 (2022)
Familial hypercholesterolemia (FH) is a very common human hereditary disease in Russia and in the whole world with most of mutations localized in the gene coding for the low density lipoprotein receptor (LDLR). The object of this review is to systema
Externí odkaz:
https://doaj.org/article/12efa716ef884ebfbeaa8c037afd057a
Publikováno v:
"Arterial’naya Gipertenziya" ("Arterial Hypertension"). 27:671-682
Objective. To assess cardiovascular functional adaptation in athletes with different levels of blood pressure (BP) in the Republic of Sakha (Yakutia).Design and methods. We examined 147 professional athletes of high sportsmanship (average age 22 (18;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3572efa16b5b4acb73117967bad0532b
https://doi.org/10.18705/1607-419x-2021-27-6-671-682
https://doi.org/10.18705/1607-419x-2021-27-6-671-682
Publikováno v:
"Medical & pharmaceutical journal "Pulse". :176-182
Currently, due to the intensive development of high-tech science-intensive medical and research devices, more and more attention is paid to the development of diagnostics of rare and difficult to diagnose diseases. It is known that among numerous nep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dedfe5c42e199c9667119cf96648b28a
https://doi.org/10.26787/nydha-2686-6838-2020-22-12-176-182
https://doi.org/10.26787/nydha-2686-6838-2020-22-12-176-182
Publikováno v:
Vavilovskii zhurnal genetiki i selektsii. 26(3)
Familial hypercholesterolemia (FH) is a very common human hereditary disease in Russia and in the whole world with most of mutations localized in the gene coding for the low density lipoprotein receptor (LDLR). The object of this review is to systema
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1de5afb1e4ee2a43c7ae6988bf34454a
https://pubmed.ncbi.nlm.nih.gov/35774363
https://pubmed.ncbi.nlm.nih.gov/35774363
Autor:
V. V. Zakharov, F. M. Zakharova
Publikováno v:
Russian Journal of Developmental Biology. 48:159-168
The similarity between the calcium-activated signaling systems of oocytes and neuronal axon terminals has prompted us to test whether BASP1 and GAP-43 proteins, highly expressed in brain neurons, are present in oocytes. Using immunocytochemical techn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::376b7f75ee79a343fc4d73e3daa93e4d
https://doi.org/10.1134/s1062360417030110
https://doi.org/10.1134/s1062360417030110
Autor:
F. M. Zakharova, M. G. Bass, Vadim B. Vasilyev, V. A. Sokolova, O. V. Kidgotko, M. E. Kustova
Publikováno v:
Cell and Tissue Biology. 9:208-216
Transmission of foreign mtDNA of paternal origin to the offspring of F0 males, as well as its distribution in early embryos, was studied in a mouse model. It was shown that F0 male mice obtained by microinjection of human mitochondria into a mouse zy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ada6d91eb8fa4df0d1c7032ffad349a1
https://doi.org/10.1134/s1990519x15030098
https://doi.org/10.1134/s1990519x15030098
Autor:
A. S. Golovina, B. M. Lipovetskii, Vadim B. Vasilyev, M. P. Serebrenitskaya, M. Yu. Mandelshtam, F. M. Zakharova, N. A. Grudinina, V. O. Konstantinov, V. A. Korneva, T. Yu. Komarova
Publikováno v:
Bulletin of Experimental Biology and Medicine. 155:380-383
The search for two mutations, FH-Helsinki and FH-North Karelia, in LDL receptor gene was carried out in patients with familial hypercholesterolemia from St. Petersburg (80 families) and Petrozavodsk (80 families) using allele-specific PCR and analysi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d5e0d88c786c35187b13feae247b403
https://doi.org/10.1007/s10517-013-2159-4
https://doi.org/10.1007/s10517-013-2159-4
Publikováno v:
Cell and Tissue Biology. 2:609-613
The distribution of human mitochondrial DNA (mtDNA) among single murine blastomeres was analyzed during the splitting of embryos injected with a suspension of human mitochondria at the one- or two-cell stage. Human mtDNA was detected by PCR with spec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6a571209c3c6aad0f93b53911a69ad3
https://doi.org/10.1134/s1990519x08060072
https://doi.org/10.1134/s1990519x08060072
Publikováno v:
Tsitologiia. 57(1)
Transmission of foreign mtDNA along the paternal lineage founded by male mice (F0), and distribution of that mtDNA in their progeny at early stages of prenatal development were studied. Transmitochondrial males of F0 obtained after injection of human
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1f2aca1866e5dafdd71bea8e786ee76c
https://pubmed.ncbi.nlm.nih.gov/25872374
https://pubmed.ncbi.nlm.nih.gov/25872374