23 research outputs found

    3 Existential Threats to Our Elections

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    This report underscores three existential threats facing U.S. elections:  an exodus of election officials due to threats and harassment, the potential of election manipulation by partisan actors, and inadequate funding of our critical election infrastructure. It calls for federal action to address these troubling trends, including combatting election disinformation, preventing efforts to subvert future elections, increasing federal and state funding for elections, and protecting election workers from threats of violence

    Fair Pay: Why Congress Needs to Invest in Junior Staff

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    Legislative staff are crucial to the daily operations of Congress, both on Capitol Hill and in district offices. Congressional staffers help craft policy, advance legislation, and handle inquiries from constituents and the press. But despite their responsibilities, staffers in lawmakers' personal offices, congressional policy committees, and district offices are widely and consistently undercompensated for their work, especially in entry-level positions.While significant progress has been made recently to address inadequate staff pay in the House of Representatives under the leadership of Speaker Nancy Pelosi (D-CA), further steps are needed to ensure that entry-level staffers from all socioeconomic backgrounds are able to thrive in both chambers of Congress.Fairly compensating congressional staff, especially junior-level staffers, will help Congress attract and retain a diverse and capable workforce. Giving staff both the financial incentive and ability to stay in their roles and advance upward means that members of Congress won't need to keep retraining employees and that valuable institutional knowledge will be retained. In these ways, better financial compensation for staff will both help curb the brain drain from Capitol Hill to K Street and guard against the undue influence of special-interest lobbyists

    Extreme Gerrymanderers

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    Gerrymandering is the intentional practice of manipulating the boundaries of congressional districts to provide an unfair advantage for a specific party or group. The practice has increasingly created barriers to representative democracy and allows politicians to select their voters, rather than allowing voters to pick their politicians.New maps that create the boundaries between congressional districts are drawn every 10 years, following each decennial census. In the wake of the 2020 Census, state legislators crafted a number of hyperpartisan and discriminatory gerrymanders. This report highlights a dozen of the worst

    Open-label add-on treatment trial of minocycline in fragile X syndrome

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    <p>Abstract</p> <p>Background</p> <p>Fragile X syndrome (FXS) is a disorder characterized by a variety of disabilities, including cognitive deficits, attention-deficit/hyperactivity disorder, autism, and other socio-emotional problems. It is hypothesized that the absence of the fragile X mental retardation protein (FMRP) leads to higher levels of matrix metallo-proteinase-9 activity (MMP-9) in the brain. Minocycline inhibits MMP-9 activity, and alleviates behavioural and synapse abnormalities in <it>fmr1 </it>knockout mice, an established model for FXS. This open-label add-on pilot trial was conducted to evaluate safety and efficacy of minocycline in treating behavioural abnormalities that occur in humans with FXS.</p> <p>Methods</p> <p>Twenty individuals with FXS, ages 13-32, were randomly assigned to receive 100 mg or 200 mg of minocycline daily. Behavioural evaluations were made prior to treatment (baseline) and again 8 weeks after daily minocycline treatment. The primary outcome measure was the Aberrant Behaviour Checklist-Community Edition (ABC-C) Irritability Subscale, and the secondary outcome measures were the other ABC-C subscales, clinical global improvement scale (CGI), and the visual analog scale for behaviour (VAS). Side effects were assessed using an adverse events checklist, a complete blood count (CBC), hepatic and renal function tests, and antinuclear antibody screen (ANA), done at baseline and at 8 weeks.</p> <p>Results</p> <p>The ABC-C Irritability Subscale scores showed significant improvement (p < 0.001), as did the VAS (p = 0.003) and the CGI (p < 0.001). The only significant treatment-related side effects were minor diarrhea (n = 3) and seroconversion to a positive ANA (n = 2).</p> <p>Conclusions</p> <p>Results from this study demonstrate that minocycline provides significant functional benefits to FXS patients and that it is well-tolerated. These findings are consistent with the <it>fmr1 </it>knockout mouse model results, suggesting that minocycline modifies underlying neural defects that account for behavioural abnormalities. A placebo-controlled trial of minocycline in FXS is warranted.</p> <p>Trial registration</p> <p>ClinicalTrials.gov Open-Label Trial NCT00858689.</p

    Blocking microglial pannexin-1 channels alleviates morphine withdrawal in rodents

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    Opiates are essential for treating pain, but termination of opiate therapy can cause a debilitating withdrawal syndrome in chronic users. To alleviate or avoid the aversive symptoms of withdrawal, many of these individuals continue to use opiates. Withdrawal is therefore a key determinant of opiate use in dependent individuals, yet its underlying mechanisms are poorly understood and effective therapies are lacking. Here, we identify the pannexin-1 (Panx1) channel as a therapeutic target in opiate withdrawal. We show that withdrawal from morphine induces long-term synaptic facilitation in lamina I and II neurons within the rodent spinal dorsal horn, a principal site of action for opiate analgesia. Genetic ablation of Panx1 in microglia abolished the spinal synaptic facilitation and ameliorated the sequelae of morphine withdrawal. Panx1 is unique in its permeability to molecules up to 1 kDa in size and its release of ATP. We show that Panx1 activation drives ATP release from microglia during morphine withdrawal and that degrading endogenous spinal ATP by administering apyrase produces a reduction in withdrawal behaviors. Conversely, we found that pharmacological inhibition of ATP breakdown exacerbates withdrawal. Treatment with a Panx1-blocking peptide (10panx) or the clinically used broad-spectrum Panx1 blockers, mefloquine or probenecid, suppressed ATP release and reduced withdrawal severity. Our results demonstrate that Panx1-mediated ATP release from microglia is required for morphine withdrawal in rodents and that blocking Panx1 alleviates the severity of withdrawal without affecting opiate analgesia

    A micro-solid oxide fuel cell system as battery replacement

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    The concept and the design of a micro-solid oxide fuel cell system is described and discussed. The system in this study is called the ONEBAT system and consists of the fuel cell PEN (positive electrode - electrolyte - negative electrode) element, a gas processing unit, and a thermal system. PEN elements of free-standing multi-layer membranes are fabricated on Foturan® and on Si substrates using thin film deposition and microfabrication techniques. Open circuit voltages of up to 1.06 V and power of 150 mW cm−2 are achieved at 550°C. The membranes are stable up to 600°C. The gas processing unit allows butane conversion of 95% and hydrogen selectivity of 83% at 550°C in the reformer and efficient after-burning of hydrogen, carbon monoxide, and lower hydrocarbons in the post-combustor. Thermal system simulations prove that a large thermal gradient of more than 500 °C between the hot module and its exterior are feasible. The correlation between electrical power output – system size and thermal conductivity – heat-transfer coefficient of the thermal insulation material are shown. The system design studies show that the single sub-systems can be integrated into a complete system and that the requirements for portable electronic devices can be achieved with a base unit of 2.5 W and a modular approach
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