5,724 research outputs found

    Reply to ``Comment on `Insulating Behavior of λ\lambda-DNA on the Micron Scale' "

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    In our experiment, we found that the resistance of vacuum-dried λ\lambda-DNA exceeds 1014Ω10^{14} \Omega at 295 K. Bechhoefer and Sen have raised a number of objections to our conclusion. We provide counter arguments to support our original conclusion.Comment: 1 page reply to comment, 1 figur

    Small Energy Scale for Mixed-Valent Uranium Materials

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    We investigate a two-channel Anderson impurity model with a 5f15f^1 magnetic and a 5f25f^2 quadrupolar ground doublet, and a 5f25f^2 excited triplet. Using the numerical renormalization group method, we find a crossover to a non-Fermi liquid state below a temperature T∗T^* varying as the 5f25f^2 triplet-doublet splitting to the 7/2 power. To within numerical accuracy, the non-linear magnetic susceptibility and the 5f15f^1 contribution to the linear susceptibility are given by universal one-parameter scaling functions. These results may explain UBe13_{13} as mixed valent with a small crossover scale T∗T^*.Comment: 4 pages, 3 figures, REVTeX, to appear in Phys. Rev. Let

    Enhancing the management of anorexia of ageing to counteract malnutrition : are physical activity guidelines optimal?

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    Funding Information: NJC and SERL receive funding from by The National Institute for Health Research (NIHR). The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health and Social Care.Peer reviewedPublisher PD

    Synthetic Biology Driven Biosynthesis of Unnatural Tropolone Sesquiterpenoids

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    Tropolone sesquiterpenoids (TS) are an intriguing family of biologically active fungal meroterpenoids that arise through a unique intermolecular hetero Diels–Alder (hDA) reaction between humulene and tropolones. Here, we report on the combinatorial biosynthesis of a series of unprecedented analogs of the TS pycnidione 1 and xenovulene A 2. In a systematic synthetic biology driven approach, we recombined genes from three TS biosynthetic gene clusters (pycnidione 1, xenovulene A 2 and eupenifeldin 3) in the fungal host Aspergillus oryzae NSAR1. Rational design of the reconstituted pathways granted control over the number of hDA reactions taking place, the chemical nature of the fused polyketide moiety (tropolono- vs. monobenzo-pyranyl) and the degree of hydroxylation. Formation of unexpected monobenzopyranyl sesquiterpenoids was investigated using isotope-feeding studies to reveal a new and highly unusual oxidative ring contraction rearrangement. © 2020 Wiley-VCH Gmb

    Drosophila Insulin receptor regulates the persistence of injury-induced nociceptive sensitization

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    Diabetes-associated nociceptive hypersensitivity affects diabetic patients with hard-to-treat chronic pain. Because multiple tissues are affected by systemic alterations in insulin signaling, the functional locus of insulin signaling in diabetes-associated hypersensitivity remains obscure. Here, we used Drosophila nociception/nociceptive sensitization assays to investigate the role of Insulin receptor (Insulin-like receptor, InR) in nociceptive hypersensitivity. InR mutant larvae exhibited mostly normal baseline thermal nociception (absence of injury) and normal acute thermal hypersensitivity following UV-induced injury. However, their acute thermal hypersensitivity persists and fails to return to baseline, unlike in controls. Remarkably, injury-induced persistent hypersensitivity is also observed in larvae that exhibit either type 1 or type 2 diabetes. Cell type-specific genetic analysis indicates that InR function is required in multidendritic sensory neurons including nociceptive class IV neurons. In these same nociceptive sensory neurons, only modest changes in dendritic morphology were observed in the InRRNAi-expressing and diabetic larvae. At the cellular level, InR-deficient nociceptive sensory neurons show elevated calcium responses after injury. Sensory neuron-specific expression of InR rescues the persistent thermal hypersensitivity of InR mutants and constitutive activation of InR in sensory neurons ameliorates the hypersensitivity observed with a type 2-like diabetic state. Our results suggest that a sensory neuron-specific function of InR regulates the persistence of injury-associated hypersensitivity. It is likely that this new system will be an informative genetically tractable model of diabetes-associated hypersensitivity
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