239 research outputs found

    Використання снайпера в спеціальній операції

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    Хряк, А. П. Використання снайпера в спеціальній операції / А. П. Хряк, Д. О. Акіменко // Вісник Національного університету внутрішніх справ. - 2004. - Вип. 25. - С. 77-80.Розкрито використання снайперів у спеціальних операціях. Раскрыто использование снайперов в специальных операциях. The use of snipers in special operations is disclosed

    Особливості техніки пересування штурмових груп в умовах антитерористичних заходів та при звільненні заручників

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    Акіменко, Д. О. Особливості техніки пересування штурмових груп в умовах антитерористичних заходів та при звільненні заручників / Д. О. Акіменко, А. П. Хряк // Вісник Харківського національного університету внутрішніх справ.- 2006.- Вип. 32.- С. 343 - 346Розглядаються особливості техніки пересування штурмових груп в умовах антитерористичних заходів та при звільненні заручників. Рассматриваются особенности техники передвижения штурмовых групп в условиях антитеррористических мероприятий и при освобождении заложников. The peculiarities of the technique of moving assault groups in the context of anti-terrorist activities and the release of hostages are considered

    Experimental Study of the Radiative Decays K+ -> mu+ nu e+e- and K+ -> e+ nu e+e-

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    Experiment 865 at the Brookhaven AGS obtained 410 K+ -> e+ nu e+e- and 2679 K+ -> mu+ nu e+e- events including 10% and 19% background. The branching ratios were measured to be (2.48+-0.14(stat.)+-0.14(syst.))x10^-8 (m_ee>150 MeV) and (7.06+-0.16+-0.26)x10^-8 (m_ee>145 MeV), respectively. Results for the decay form factors are presented.Comment: 4 pages, 3 figures, RevTeX

    Measurement of the K+μ+νμγK^+\rightarrow{\mu^+}{\nu_{\mu}}{\gamma} decay form factors in the OKA experiment

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    A precise measurement of the vector and axial-vector form factors difference FVFAF_V-F_A in the K+μ+νμγK^+\rightarrow{\mu^+}{\nu_{\mu}}{\gamma} decay is presented. About 95K events of K+μ+νμγK^+\rightarrow{\mu^+}{\nu_{\mu}}{\gamma} are selected in the OKA experiment. The result is FVFA=0.134±0.021(stat)±0.027(syst)F_V-F_A=0.134\pm0.021(stat)\pm0.027(syst). Both errors are smaller than in the previous FVFAF_V-F_A measurements.Comment: 9 pages, 8 figure

    Test of exotic scalar and tensor interactions in K_e3 decay using stopped positive kaons

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    The form factors of the decay K+ --> pi0 e+ nu (K_e3) have been determined from the comparison of the experimental and Monte Carlo Dalitz distributions containing about 10^5 K_e3 events. The following values of the parameters were obtained: lambda_+ = 0.0278 +- 0.0017(stat) +- 0.0015(syst), f_S/f_+(0) = 0.0040 +- 0.0160(stat) +- 0.0067(syst) and f_T/f_+(0) = 0.019 +- 0.080(stat) +- 0.038(syst). Both scalar f_S and tensor f_T form factors are consistent with the Standard Model predictions of zero values.Comment: 10 pages, 5 figures, contributed to the proceedings of NANP Conference, Dubna, June 19-23, 200

    Experimental study of direct photon emission in K- --> pi- pi0 gamma decay using ISTRA+ detector

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    The branching ratio in the charged-pion kinetic energy region of 55 to 90 MeV for the direct photon emission in the K- --> pi- pi0 gamma decay has been measured using in-flight decays detected with the ISTRA+ setup operating in the 25 GeV/c negative secondary beam of the U-70 PS. The value Br(DE)=[0.37+-0.39(stat)+-0.10(syst)]*10^(-5) obtained from the analysis of 930 completely reconstructed events is consistent with the average value of two stopped-kaon experiments, but it differs by 2.5 standard deviations from the average value of three in-flight-kaon experiments. The result is also compared with recent theoretical predictions.Comment: 13 pages, 8 figure

    Intellectual disability associated with a homozygous missense mutation in THOC6

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    BACKGROUND: We recently described a novel autosomal recessive neurodevelopmental disorder with intellectual disability in four patients from two related Hutterite families. Identity-by-descent mapping localized the gene to a 5.1 Mb region at chromosome 16p13.3 containing more than 170 known or predicted genes. The objective of this study was to identify the causative gene for this rare disorder. METHODS AND RESULTS: Candidate gene sequencing followed by exome sequencing identified a homozygous missense mutation p.Gly46Arg, in THOC6. No other potentially causative coding variants were present within the critical region on chromosome 16. THOC6 is a member of the THO/TREX complex which is involved in coordinating mRNA processing with mRNA export from the nucleus. In situ hybridization showed that thoc6 is highly expressed in the midbrain and eyes. Cellular localization studies demonstrated that wild-type THOC6 is present within the nucleus as is the case for other THO complex proteins. However, mutant THOC6 was predominantly localized to the cytoplasm, suggesting that the mutant protein is unable to carry out its normal function. siRNA knockdown of THOC6 revealed increased apoptosis in cultured cells. CONCLUSION: Our findings associate a missense mutation in THOC6 with intellectual disability, suggesting the THO/TREX complex plays an important role in neurodevelopment
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