Access the full text.
Sign up today, get DeepDyve free for 14 days.
V. Akhmetova, Viktorova Tv, E. Khusnutdinova (2000)
Molecular genetic analysis of the VNTR polymorphism at the phenylalanine hydroxylase gene in populations of the Volga-Ural region, 36
V. Akhmetova, T. Viktorova, E. Khusnutdinova (2000)
[Molecular-genetic analysis of VNTR polymorphism in alleles of the phenylalanine hydroxylase gene in inhabitants of the Volga-Urals region].Genetika, 36 8
S. Ichihara, Yoshiji Yamada, T. Fujimura, N. Nakashima, M. Yokota (1998)
Association of a Polymorphism of the Endothelial Constitutive Nitric Oxide Synthase Gene With Myocardial Infarction in the Japanese PopulationAmerican Journal of Cardiology, 81
P. Slominskii, M. Shadrina, V. Spitsyn, V. Mikulich, E. Khusnutdinova, S. Limborskaia (1997)
[A simple and rapid method for determining a 32-bp deletion in the gene for the chemokine receptor CCR5].Genetika, 33 11
(1999)
Clinical Genetic Analysis of the Factors Predisposing to Essential Hypertension and Idiopathic Hypertrophic Cardiomyopathy, Cand
Nejat Akar, E. Akar, Ș. Cin, G. Deda, F. Avcu, Atilla Yalçin (1999)
Endothelial nitric oxide synthase intron 4, 27 bp repeat polymorphism in Turkish patients with deep vein thrombosis and cerebrovascular accidents.Thrombosis research, 94 1
W. Hooper, C. Lally, H. Austin, J. Benson, A. Dilley, Nanette Wenger, C. Whitsett, Peggy Rawlins, Bruce Evatt (1999)
The relationship between polymorphisms in the endothelial cell nitric oxide synthase gene and the platelet GPIIIa gene with myocardial infarction and venous thromboembolism in African Americans.Chest, 116 4
Galeeva Ar, E. Khusnutdinova, P. Slominsky, S. Limborska (1998)
DISTRIBUTION OF THE CCR5 CHEMOKINE RECEPTOR-GENE 32-BP DELETION IN POPULATIONS OF THE VOLGA-URAL REGIONRussian Journal of Genetics, 34
(1960)
Narody Kavkaza
O. Mustafina, E. Shagisultanova, T. Nasibullin, I. Tuktarova, A. Bikmeeva, O. Poliudova, E. Khusnutdinova (2001)
[Endothelial nitric oxide synthase gene minisatellite polymorphism: study in populations of the Volga-Ural region and analysis of associations with myocardial infarct and essential hypertension].Genetika, 37 5
Xing-li Wang, A. Sim, R. Badenhop, R. Mccredie, D. Wilcken (1996)
A smoking–dependent risk of coronary artery disease associated with a polymorphism of the endothelial nitric oxide synthase geneNature Medicine, 2
A. Galeeva, E. Khusnutdinova, P. Slominskii, S. Limborskaia (1998)
[Distribution of the 32 bp deletion in the CCR5 chemokine receptor gene in populations of the Volga-Ural region].Genetika, 34 8
J. Martinson, N. Chapman, D. Rees, Yantan Liu, J. Clegg (1997)
Global distribution of the CCR5 gene 32-basepair deletionNature Genetics, 16
R. Eisensmith, Yoshiyuki Okano, M. Dasovich, Tao Wang, Flemming Güttler, Hans Lou, P. Guldberg, U. Lichter-Konecki, David Konecki, E. Svensson (1992)
Multiple origins for phenylketonuria in Europe.American journal of human genetics, 51 6
J. Reynolds, B. Weir, C. Cockerham (1983)
Estimation of the coancestry coefficient: basis for a short-term genetic distance.Genetics, 105 3
K.V. Puzyrev (1999)
Cand. Sci. (Med.) Dissertation
Alexei Goltsov, R. Eisensmith, D. Konecki, U. Lichter-Konecki, S. Woo (1992)
Associations between mutations and a VNTR in the human phenylalanine hydroxylase gene.American journal of human genetics, 51 3
VNTR allelic polymorphism at the phenylalanine hydroxilase (PAH) and endothelial constitutive nitric oxide synthase (eNOS) genes and the prevalence of the CCR5 chemokine receptor gene 32-bp deletion were examined in four populations of Northern Caucasus: Adygs, Kumyks, Karachais, and Nogais (Kuban and Karanogais). Population-specific features of the allele and genotype frequency distribution patterns of the polymorphisms examined were described. The data obtained were compared to those obtained from literature. The results of the study confirmed that the frequency and occurrence of the PAH polymorphic alleles exhibit substantial interpopulation differences. In the populations of Northern Caucasus, the eNOS minisatellite polymorphism alleles and genotypes frequency distribution patterns were close to those described earlier for populations of the Volga–Ural region (VUR), and also for the Australian Caucasoids, Japanese, and Turks. In the populations examined, the mean frequency of the CCR5 gene deletion was 0.055, which was somewhat lower than in the populations of VUR (0.070) and Europe (0.081), and practically identical to that in Asian populations (0.050). For each population observed and expected heterozygosities at each locus were calculated. In general, the gene pool of Northern Caucasian populations showed substantial differentiation at the loci examined: the G ST value was 0.0274. The data for individual loci showed that the greater contribution to the interpopulation diversity was made by the differences in the PAH VNTR allele frequencies (G ST = 0.04), while the differences at the eNOSand CCR5 loci were small (G ST = 0.0025 and G ST = 0.0039, respectively).
Russian Journal of Genetics – Springer Journals
Published: Oct 18, 2004
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.