[Detection of complementary transcripts in intergenic region of the chicken α-globin gene domain] [0.03%]
鸡α-珠蛋白基因间区互补转录本的检测
E S Ioudinkova,A V Nefedochkina,O V Iarovaia et al.
E S Ioudinkova et al.
Using strand-specific reverse transcription followed by Real Time PCR analysis we have characterized the transcription profile of the segment of chicken α-globin gene domain harboring embryonic gene π, adult gene αD and spacer region sep...
O F Kandarakov,M V Kalashnikova,A A Vartanian et al.
O F Kandarakov et al.
Growth of malignant tumors occurs in three-dimensional space and depends on a presence of stromal component, which performs critical functions of tumor cell protection and growth support. Therefore, development and analysis of tumor models ...
[RPS4 and NAD5 sequences evidenced of polyphyly of ditrichaceae and parallelisms in the evolution of haplolepidous mosses] [0.03%]
[RPS4和NAD5序列表明了 Ditrichaceae的多系性以及无叶片苔藓进化过程中的趋同现象]
V E Fedosov,A V Fedorova,E A Ignatova et al.
V E Fedosov et al.
Molecular phylogenetic analysis of 66 representatives of haplolepidous mosses showed polyphylia of Ditrichaceae. According to the data obtained, the structure of the peristome, as well as features of the gametophyte on which a family tradit...
[Prevalence of gene polymorphisms associated with immune-dependent diseases in the populations of North Eurasia] [0.03%]
[北欧亚人群与免疫相关疾病易感基因多态性的分布规律研究]
A A Cherednichenko,E A Trifonova,K V Vagaitseva et al.
A A Cherednichenko et al.
The data on distribution of genetic diversity in gene polymorphisms associated with autoimmune and allergic diseases and with regulation of immunoglobulin E and cytokines levels in 26 populations of the Northern Eurasia is presented. Substa...
[Association of schizophrenia with variations in genes encoding transcription factors] [0.03%]
精神分裂症发病与转录因子基因多态性的关联研究进展
A S Boyajyan,S A Atshemyan,R V Zakharyan
A S Boyajyan
Alterations in neuronal plasticity and immune system play a key role in pathogenesis of schizophrenia. Identification of genetic factors contributing to these alterations will significantly encourage elucidation of molecular etiopathomechan...
[Mitochondrial DNA polymorphism association with myocardial infarction and prognostic signs for atherosclerosis] [0.03%]
线粒体DNA多态性与心肌梗塞及动脉硬化预后标志的关联性研究
M V Golubenko,R R Salakhov,O A Makeeva et al.
M V Golubenko et al.
We have performed association analysis for mtDNA most common variants and haplogroups with myocardial infarction and some prognostic characteristics in patients. Comparison of patients (N=406) and controls (N=183) has shown higher frequency...
[Brain neurotransmitter systems gene Polymorphism: the Search for pharmacogenetic markers of efficacy of haloperidol in Russians and Tatars] [0.03%]
脑神经递质系统基因多态性：氯丙嗪疗效药理遗传标志物的寻找（俄罗斯人和塔塔尔人）
A E Gareeva,K O Kinyasheva,D Yu Galaktionova et al.
A E Gareeva et al.
Antipsychotics are the main drugs for the treatment of severe mental illness--schizophrenia affects about 1% of the population. The mechanism of action of neuroleptics is still up to the end. Several studies in the field of pharmacogenetics...
[Bioluminescent assay to detect melanocortin-1 receptor (MC1R) polymorphisms (R160W, R151C, and D294H)] [0.03%]
检测黑色素皮质激素受体1型(MC1R)多态性的生物发光试验(R160W、R151C和D294H)
E E Bashmakova,V V Krasitskaya,A A Bondar et al.
E E Bashmakova et al.
Several polymorphisms in melanocortin-1 receptor (MC1R) gene are shown to have associations with melanoma risk. In particular, rs1805007, rs1805008, and rs1805009 mutations causing the corresponding R151C, R160W, and D294H changes and assoc...
[Significant association between nonsyndromic cleft lip with or without cleft palate and IRF6rs2235371 polymorphism in Iranian familiar population] [0.03%]
IRF6 rs2235371基因多态性与伊朗人群中非综合征唇裂(伴或不伴腭裂)的显著关联性研究
F Jafary,Z Nadeali,M Salehi et al.
F Jafary et al.
According to previous studies the IRF6rs2235371 polymorphism is a risk factor for NSCL/P in different populations. However our recent study revealed no correlation between IRF6rs642961 and NSCL/P in our population. In the present study we h...
[Molecular analysis of childhood B-acute lymphoblastic leukemia: Identification and prognosis of rare breakpoints] [0.03%]
儿童B细胞急性淋巴细胞白血病的分子特征及罕见断裂点的临床意义分析
D Kumar,M K Panigrahi,K K Saikia et al.
D Kumar et al.
Acute lymphoblastic leukaemia (ALL) is the most common subtype of childhood cancer. Detection of a specific gene rearrangement allows the identification of prognostically relevant subgroups in childhood B-ALL. There are four common gene rea...