Zobrazeno 1 - 10
of 44
pro vyhledávání: '"E. I. Shvarts"'
Autor:
S N, Pchelina, O V, Sirotkina, A M, Sheĭdina, A E, Taraskina, T I, Rodygina, E P, Demina, A M, Zabotina, M I, Mitupova, E A, Bazhenova, O A, Berkovich, E V, Shliakhto, A L, Shvartsman, E I, Shvarts
Publikováno v:
Kardiologiia. 47(7)
With the aim to detect genetic factors of risk of development of early myocardial infarction (MI) we studied 29 allele variants of 19 genes in 206 men who had survived MI in the age before 45 years and in 195 men of similar age without cardiovascular
Publikováno v:
Genetika. 41(6)
Glycoprotein IIb/IIIa complex, a platelet surface fibrinogen receptor, plays a key role in producing primary hemostasis. At present, only a single mutation in the GPIIla gene, Leu33Pro, and a single mutation in the GPIIb gene, lle843Ser, has been des
Autor:
A M, Sheĭdina, S N, Pchelina, D V, Demidova, T I, Rodygina, A E, Taraskina, O B, Toperverg, O A, Berkovich, E V, Demina, E I, Shvarts, T V, Pogoda, E V, Generozov, V M, Govorun, Iu M, Lopukhin, Iu A, Shevchenko
Publikováno v:
Kardiologiia. 44(8)
Analysis of allele distribution of four single nucleotide polymorphisms (C-17G, C69T, G-191C and 319insG) of promoter and 5'-untranslated regions of the ABCA1 gene was carried out in a sample of 171 men, who had survived myocardial infarction before
Publikováno v:
Bulletin of experimental biology and medicine. 137(1)
The incidence of allele variants of glutathione-S transferase M1 xenobiotic detoxification gene and matrix metalloproteinase 9 gene was analyzed in patients with chronic obstructive pulmonary disease. A strict gene-gene interaction between these two
Publikováno v:
Vestnik otorinolaringologii. (1)
Hypoacusis is a common sensory defect in humans which creates problems in communication. Heredity is essential in etiology of hypoacusis and deafness. Genes PAX3 and MITF were studied in patients with Vaardenburg syndrome in 14 unrelated families. Fi
Autor:
O A, Berkovich, E A, Bazhenova, E A, Volkova, M Z, Alugishvili, I O, Kiselev, B I, Smirnov, E I, Shvarts, E V, Shliakhto
Publikováno v:
Rossiiskii fiziologicheskii zhurnal imeni I.M. Sechenova. 87(5)
The rate of D allele did not differ between patients with ischemic heart disease (IHD) who had myocardial infarction before the age 45, and healthy males. The DD genotype of the ACE gene was much more frequently encountered in the patients than in he
Publikováno v:
Molekuliarnaia biologiia. 34(3)
Publikováno v:
Voprosy meditsinskoi khimii. 45(1)
The interstrain differences in hepatic 7-pentoxyresorufin-O-dealkylase and 16 beta-androstendione hydroxylase activities specific for cytochrome P450 2B1 have been found in Sprague-Dawley, Brattleboro and Wistar rats treated with with phenobarbital,
Autor:
N A, Skobeleva, V I, Vasina, M V, Volkova, A M, Sverdlova, E V, Fomicheva, G I, Obraztsova, E I, Talalaeva, Kh, Shakir, M, Laasri, I M, Vorontsov, Iu P, Kovalev, E I, Shvarts
Publikováno v:
Molekuliarnaia genetika, mikrobiologiia i virusologiia. (4)
Polymorphisms of 3 apolipoprotein genes Xba I apoB, Sstl apoCIII, and apoE and the insertion-deletion polymorphism of the angiotensin-converting enzyme gene (I/D ACE) and lipid levels were studied in a random sample of 403 children and adolescents ag
Publikováno v:
Doklady Akademii nauk. 340(5)