Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 6 de 6
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Genetika ; 48(6): 781-4, 2012 Jun.
Artigo em Russo | MEDLINE | ID: mdl-22946338

RESUMO

Time-dependent changes in reproductive parameters were analyzed using data on 203 female Uighurs. A decrease was observed for the total fertility (3.77 vs. 6.50 in females 45-55 or 56 and more years of age, respectively), live birth (3.3 vs. 5.14), stillbirth (0.045 vs. 0.41), and voluntary abortion (0.29 vs. 0.59) rates.


Assuntos
Etnicidade , Reprodução/fisiologia , Aborto Induzido , Coeficiente de Natalidade , Anticoncepção , Feminino , Humanos , Mortalidade Infantil , Recém-Nascido , Cazaquistão/epidemiologia , Pessoa de Meia-Idade , Gravidez
2.
Genetika ; 41(7): 973-80, 2005 Jul.
Artigo em Russo | MEDLINE | ID: mdl-16152803

RESUMO

Eight nuclear DNA loci, including six Alu insertions (ACE, APOA1, PV92, TPA25, Ya5NBC27, and Ya5NBC148), 32-bp deletion in the CCR5 gene, and VNTR locus at the eNOS gene, were examined in three ethnogeographic groups of Kazakhs (342 individuals). The individuals examined lived in southeastern, central, and southwestern regions of Kazakhstan, and according to their tribal attribution, belonged to the Senior, Middle, and Junior Zhuzes. The Alu insertions appeared to be polymorphic in all populations examined: the insertion frequency varied from 0.264 in the populations of the Senior and Middle Zhuzes at the Ya5NBC27 and Ya5NBC148 loci, to 0.827 in Kazakhs of the Middle Zhuz at the APOA1 locus. In Kazakh groups examined only two alleles of the eNOS VNTR locus were detected with the number of repeats constituting four (A) and five (B) copies. The highest frequency of A allele was found in Kazakhs from the Junior Zhuz (0.113), while the highest frequency of B allele was detected in population of the Senior Zhuz (0.893). The frequency of the 32-bp deletion in the chemokine receptor CCR5 gene varied from 0.027 in the Junior Zhuz to 0.045 in the Senior Zhuz. Kazakhs showed high genetic diversity (Hex = 0.376). In general, in three ethnogeographic groups of Kazakhs, the coefficient of gene differentiation (G(ST)) over eight diallelic markers of nuclear genome constituted 1.1%. The differences in the Alu insertions made the highest contribution to the among-population diversity (G(ST) = 1.2%).


Assuntos
Elementos Alu/genética , Deriva Genética , Genética Populacional , Polimorfismo Genético , Núcleo Celular/genética , DNA/genética , Etnicidade/genética , Frequência do Gene , Genoma Humano , Humanos , Cazaquistão/etnologia , Linhagem
3.
Mol Biol (Mosk) ; 39(3): 385-93, 2005.
Artigo em Russo | MEDLINE | ID: mdl-15981568

RESUMO

Allele frequency distribution of CTG-repeat in the 3'-flanking region of DMPK gene was analyzed in populations of Yakutia (three ethnogeographical groups of Yakuts, Evenks, Evens, Yukaghirs, Dolgans) and Central Asia (Kazakhs, Uzbeks, Uighurs). Frequencies of CTG alleles were found to be significantly different in two regions. Allele frequency distribution in populations of Yakutia was similar to Asian populations, whereas Central Asian populations showed similarity to European populations. The features of allele spectrum in Yakut populations were discussed in terms of high prevalence of myotonic dystrophy in Yakuts. Our result supports the hypothesis of founder effect in spread of myotonic dystrophy in Yakuts. The phylogenetic relationships between the investigated populations based on polymorphism of CTG-locus of the DMPK gene have been analyzed as well.


Assuntos
Distrofia Miotônica/genética , Polimorfismo Genético , Proteínas Serina-Treonina Quinases/genética , Repetições de Trinucleotídeos/genética , Alelos , Ásia Central , Povo Asiático , Feminino , Frequência do Gene , Humanos , Masculino , Distrofia Miotônica/epidemiologia , Miotonina Proteína Quinase , Filogenia , Prevalência , Sibéria
4.
Genetika ; 38(3): 376-82, 2002 Mar.
Artigo em Russo | MEDLINE | ID: mdl-11963566

RESUMO

A cytogenetic study was conducted for the first time on human populations neighboring the Semipalatinsk nuclear test site (STS) and exposed to ionizing radiation for a long period of time. In populations with the extreme and maximum radiation risks, high frequencies of radiation-induced chromosomal markers, including acentric fragments (1.99 +/- 0.10 per 100 cells), dicentrics (0.23 +/- 0.01), ring chromosomes (0.38 +/- 0.14), and stable chromosomal aberrations (1.17 +/- 0.02), were found. These frequencies significantly exceeded those in control populations. The spectrum of chromosomal aberrations and the frequencies of the aberrations of different types in persons living in the areas with the highest radionuclide contamination confirmed the mutagenic effect of radiation on chromosomes in the human populations studied.


Assuntos
Aberrações Cromossômicas , Exposição Ambiental , Radiogenética , Análise Citogenética , Genética Populacional , Humanos , Cazaquistão , Guerra Nuclear , Radiação Ionizante , Fatores de Risco
5.
Genetika ; 37(12): 1687-95, 2001 Dec.
Artigo em Russo | MEDLINE | ID: mdl-11785297

RESUMO

Rural populations neighboring the Semipalatinsk nuclear test site were used as a model to develop and test an integrated population-genetic approach to analysis of the medical genetic situation and environmental conditions in the areas studied. The contributions of individual factors of population dynamics into the formation of the genetic load were also assessed. The informative values of some genetic markers were estimated. Based on these estimates, a mathematical model was constructed that makes it possible to calculate numerical scores for analysis of the genetic loads in populations differing in environmental exposure.


Assuntos
Demografia , Genética Populacional , Guerra Nuclear , População Rural , Exposição Ambiental , Cazaquistão , Modelos Teóricos , Poluentes Radioativos
6.
Genetika ; 37(12): 1696-704, 2001 Dec.
Artigo em Russo | MEDLINE | ID: mdl-11785298

RESUMO

Information on the dynamics, frequency, and structure of congenital malformations (CMs) and chromosomal diseases in two generations of rural populations from the Semipalatinsk region was obtained for the first time. The tests performed in the Semipalatinsk nuclear test site (STS) for many years were demonstrated to deteriorate the genetic health of the populations of the zones of extreme and maximum radiation risks. Mutagenic and teratogenic effects of long-term ionizing irradiation were detected. These were mainly expressed as an increase in the frequencies of strictly registered CMs (SR CMs), including the Down syndrome, multiple malformations (MMs) and microcephaly (1.45 +/- 0.11, 1.39 +/- 0.01, and 0.77 +/- 0.05 per 1000 births, respectively). SR CMs exhibited linear trends toward higher frequencies in two generations of exposed persons after surface nuclear tests in 1949-1963. Their frequency was strongly correlated with the effective population dose of radiation; the main population genetic parameters (inbreeding coefficient, endogamy index, etc.) had less pronounced effects on Cms.


Assuntos
Anormalidades Múltiplas/etiologia , Síndrome de Down/etiologia , Microcefalia/etiologia , Radiação Ionizante , Anormalidades Múltiplas/genética , Humanos , Cazaquistão , Guerra Nuclear
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...