Zobrazeno 1 - 10
of 16
pro vyhledávání: '"F. M. 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:
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
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
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
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
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
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
Autor:
M. D. Kvasova, M. Yu. Mandelshtam, Yu. S. Astakhov, F. M. Zakharova, Vadim B. Vasilyev, V. V. Rakhmanov, N. Ya. Nikitina, V. I. Golubkov
Publikováno v:
Russian Journal of Genetics. 41:1295-1301
A collection of DNA samples obtained from primary open-angle glaucoma (POAG) patients from St. Petersburg was analyzed for single-strand conformation polymorphism (SSCP) to reveal sequence variants in exon 3 of the myocilin gene (MYOC/TIGR) and in ex
Autor:
T Yu, Komarova, A S, Golovina, N A, Grudinina, F M, Zakharova, V A, Korneva, B M, Lipovetsky, M P, Serebrenitskaya, V O, Konstantinov, V B, Vasilyev, M Yu, Mandelshtam
Publikováno v:
Genetika. 49(6)
Using an automated fluorescent single-strand conformation polymorphism (SSCP) analysis of the entire coding region, promoter zone, and exon-intron junctions of the low-density lipoprotein (LDL) receptor gene, we examined 80 DNA samples of patients wi