1,274 research outputs found

    A Highly Sensitive Plant Hybrid Protein Assay System Based on the \u3cem\u3eSpm\u3c/em\u3e Promoter and TnpA Protein for Detection and Analysis of Transcription Activation Domains

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    TnpA is a multifunctional DNA binding protein encoded by the maize Suppressor-mutator (Spm) transposable element. TnpA is required for transposition and is a repressor of the unmethylated Spm promoter. While analyzing protein domains using a yeast GAL4-based hybrid system in transiently transformed tobacco cells, we found that TnpA represses the \u3e10-fold transcriptional activation observed when the GAL4 DNA-binding domain is used alone. By contrast, compared to the backgroundless TnpA DNA-binding domain alone, 33- to 45-fold activation of the Spm promoter was observed when the VP16 activation domain was fused to it. TnpA-binding sites, but no TATA box, were required for transcription activation. Among the TnpA deletion derivatives tested, those retaining the coding sequences for the DNA-binding and protein dimerization domains gave the highest level of transcription activation when fused with the VP16 activation domain. The TnpA gene and TnpA-binding sites in the short Spm promoter therefore provide a novel, highly sensitive single-hybrid system for identifying and studying plant transcription activation domains in plant cells

    Concerted Formation of Macromolecular \u3cem\u3eSuppressor-mutator\u3c/em\u3e Transposition Complexes

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    Transposition of the maize Suppressor-mutator (Spm) transposon requires two element-encoded proteins, TnpA and TnpD. Although there are multiple TnpA binding sites near each element end, binding of TnpA to DNA is not cooperative, and the binding affinity is not markedly affected by the number of binding sites per DNA fragment. However, intermolecular complexes form cooperatively between DNA fragments with three or more TnpA binding sites. TnpD, itself not a sequence-specific DNA-binding protein, binds to TnpA and stabilizes the TnpA-DNA complex. The high redundancy of TnpA binding sites at both element ends and the protein-protein interactions between DNA-bound TnpA complexes and between these and TnpD imply a concerted transition of the element from a linear to a protein crosslinked transposition complex within a very narrow protein concentration range

    Primary Amoebic (Naegleria fowleri) Meningoencephalitis Presenting as Status Epilepticus

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    Primary amebic meningoencephalitis (PAM) is a rare entity. Usual presenting features are fever, headache and seizures with meningeal signs and this disease carries high mortality rate. We present a case report of PAM presenting as status epilepticus

    Universal adversarial attacks on spoken language assessment systems

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    There is an increasing demand for automated spoken language assessment (SLA) systems, partly driven by the performance improvements that have come from deep learning based approaches. One aspect of deep learning systems is that they do not require expert derived features, operating directly on the original signal such as a speech recognition (ASR) transcript. This, however, increases their potential susceptibility to adversarial attacks as a form of candidate malpractice. In this paper the sensitivity of SLA systems to a universal black-box attack on the ASR text output is explored. The aim is to obtain a single, universal phrase to maximally increase any candidate's score. Four approaches to detect such adversarial attacks are also described. All the systems, and associated detection approaches, are evaluated on a free (spontaneous) speaking section from a Business English test. It is shown that on deep learning based SLA systems the average candidate score can be increased by almost one grade level using a single six word phrase appended to the end of the response hypothesis. Although these large gains can be obtained, they can be easily detected based on detection shifts from the scores of a “traditional” Gaussian Process based grader

    The efficiency and efficacy of tranexamic acid in prevention of blood loss during or after caesarean delivery: a comparative study

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    Background: The practice of caesarean section is increasing day by day. Delivery by caesarean section can cause more complications than normal vaginal delivery and one of the most common complications is primary or secondary postpartum hemorrhage. The aim of present study was to study the efficacy and safety of tranexamic acid in reducing blood loss during and after caesarean section.Methods: This study was conducted at Deccan College of Medical Sciences, Hyderabad. It was a prospective randomized double blind placebo controlled study. This study includes 60 pregnant women divided in to two groups. Just before the induction of anesthesia 1 gm of tranexamic acid in 20 ml of normal saline was given over 10 minutes in test group and 20 ml of normal saline was infused in control group.Results: The demographic characters of patients in two groups were comparable. There was no statistically significant difference in the heart rates, respiratory rates and blood pressures in the two groups. There was statistically significant difference in the quantity of the blood loss from during the operation and 2 hours postpartum (p=0.003). Total mean blood loss in control group was 718.80±233.1 ml and in study group was 554.28±207.8 ml. The drop in hemoglobin after caesarean section in study group was not significant where as in control group was significant. There was no significant difference in the prothrombin time and partial thromboplastin time in the groups, pre and post operatively. In this study the use of tranexamic acid reduced the dose of other uterotonics like syntocin in study group.Conclusions: Tranexamic acid significantly reduced the amount of blood loss during the caesarean section and also reduced the use of other uterotonics. Thus, tranexamic acid can be used safely and effectively in subjects undergoing caesarean section

    Nuclear deformation and neutrinoless double-β\beta decay of 94,96^{94,96}Zr, 98,100^{98,100}Mo, 104^{104}Ru, 110^{110}Pd, 128,130^{128,130}Te and 150^{150}Nd nuclei in mass mechanism

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    The (ββ)0ν(\beta ^{-}\beta ^{-})_{0\nu} decay of 94,96^{94,96}Zr, 98,100^{98,100}Mo, 104^{104}Ru, 110^{110}Pd, 128,130^{128,130}Te and 150^{150}Nd isotopes for the 0+0+0^{+}\to 0^{+} transition is studied in the Projected Hartree-Fock-Bogoliubov framework. In our earlier work, the reliability of HFB intrinsic wave functions participating in the ββ\beta ^{-}\beta ^{-} decay of the above mentioned nuclei has been established by obtaining an overall agreement between the theoretically calculated spectroscopic properties, namely yrast spectra, reduced B(E2B(E2:0+2+)0^{+}\to 2^{+}) transition probabilities, quadrupole moments Q(2+)Q(2^{+}), gyromagnetic factors g(2+)g(2^{+}) as well as half-lives T1/22νT_{1/2}^{2\nu} for the 0+0+0^{+}\to 0^{+} transition and the available experimental data. In the present work, we study the (ββ)0ν(\beta ^{-}\beta ^{-})_{0\nu} decay for the 0+0+0^{+}\to 0^{+} transition in the mass mechanism and extract limits on effective mass of light as well as heavy neutrinos from the observed half-lives T1/20ν(0+0+)T_{1/2}^{0\nu}(0^{+}\to 0^{+}) using nuclear transition matrix elements calculated with the same set of wave functions. Further, the effect of deformation on the nuclear transition matrix elements required to study the (ββ)0ν(\beta ^{-}\beta ^{-})_{0\nu} decay in the mass mechanism is investigated. It is noticed that the deformation effect on nuclear transition matrix elements is of approximately same magnitude in (ββ)2ν(\beta ^{-}\beta ^{-})_{2\nu} and (ββ)0ν(\beta ^{-}\beta ^{-})_{0\nu} decay.Comment: 15 pages, 1 figur

    Thermo-Optical Studies of Nematic Liquid Crystal Mixtures

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