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Hemostatic gene polymorphisms in acute coronary syndrome with nonobstructive coronary atherosclerosis
Gomboeva, S. B., Ryabov, Vyacheslav V., Lugacheva, Y. G., Kulagina, I. V.
of homozygous genotypes for alleles predisposing to thromboses for all the studied polymorphic variants
Association of the Val158Met Polymorphism of the COMT Gene with Measures of Psychophysiological Status in Athletes
Valeeva E.V., Kashevarov G.S., Kasimova R.R., Ahmetov I.I., Kravtsova O.A.
are important for successful competitive activity in athletes. Polymorphism of the catechol
Association between polymorphic markers of gene IL-10 and chronic diseases of the upper respiratory tract in children living under technogenic pressure
Masnavieva L. B.
respiratory diseases were analyzed. It was found that allele C of polymorphic locus–592C/A is a marker
The clinical and genetic parallels of vitamin D provision and benign breast diseases
2060793 polymorphism on the level of VD. Subjects and methods. Genotyping for the locus -1559 T>C gene CYP
The Prognostic Value of Combinations of Genetic Polymorphisms in the ITGB3, ITGA2, and CYP2C19*2 Genes in Predicting Cardiovascular Outcomes After Coronary Bypass Grafting
Гринштейн, Ю. И., Косинова, А. А., Гринштейн, И. Ю., Субботина, Т. Н., Савченко, А. А.
polymorphisms (SNPs): rs2046934, rs1126643, rs5918, rs6065, rs4244285; rs4986893 and the occurrence
Association of polymorphisms near the FOXC2 gene with the risk of varicose veins in ethnic Russians
Shadrina A., Smetanina M., Sokolova E., Sevost’ianova K., Shevela A., Demekhova M., Shonov O., Ilyukhin E., Voronina E., Zolotukhin I., Kirienko A., Filipenko M.
© The Author(s) 2015.Objective: To investigate the association of polymorphisms located near
The polymorphism c677t of the gene MTHFR correlates with the complications of the coronary heart disease and arterial hypertension for the patients with dislipidaemia
Myandina G.I., Kasapova E.N., Zotova T.U., Frolov V.A.
. The distribution of the polymorphism C677T of the gene MTHFR among the 62 patients with dislipidaemia was studied
Allelic variants of NRF2 and TLR9 genes in critical illness
Chumachenko A.G.
Aim of the study. To elucidate the association of allelic variants of single nucleotide
Association of Interleukins Genes Polymorphic Markers with Speed of CGN’s Advance
Nekipelova, E. V., Sirotina, S. S., Proshchaev, K. I., Kalmykova, E. V., Churnosov, M. I.
The authors investigated associations of polymorphism of interleukins genes with nephritic
Fit genotypes and escape variants of subgroup III Neisseria meningitidis during three pandemics of epidemic meningitis
Zhu P.
The genetic variability at six polymorphic loci was examined within a global collection of 502

Страница 9 из 224

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