142 research outputs found
Beyond The Rhetoric: Asylum In The Obama And Trump Administrations
This paper contrasts the asylum policies in the Trump Administration to those of the Obama Administration. This research performs an intersectional analysis of rhetoric, political affiliation, direct and indirect policy initiatives, and enforcement across these administrations. This paper finds that although rhetoric can alter public opinion, it is often unrelated to the development of policy initiatives and enforcement. The same conclusion is drawn regarding the dissociation between political affiliation and detention practices. The human experience related to asylum is explored, specifically relating to policy implementation in both administrations, including family separation, the Migrant Protection Protocols (MPP), and the “Muslim Ban.” Migrants’ firsthand experiences, as presented in scholarly journals and periodicals, are collated to conclude that harsh detention practices that are often associated with the Trump Administration through public opinion and the media, were developed during the Obama Presidency and continually perpetuated in President Trump’s term. This paper also searches for parallels and variances between executive orders in both administrations, concluding that President Trump signed more extreme executive actions against the asylum system. To support this analysis, both Presidents’ White House press releases and social media posts are examined to conclude that the rhetoric and real policies do not consistently coincide. This research deciphers various scholarly journal articles, news sources, publications from nonprofit organizations, and think tanks from across the political spectrum. As the tides of political control have recently changed, it is vital for constituents to understand the real impacts that these most recent administrations had on the development and implementation of asylum policy in the United States. Via an intensive comparison of both administration’ asylum initiatives, this research will provide a retrospective view that can help the American populous make conclusions about the past and informed decisions about the future.https://orb.binghamton.edu/research_days_posters_2021/1005/thumbnail.jp
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A Toolbox for Spatiotemporal Analysis of Voltage-Sensitive Dye Imaging Data in Brain Slices
Voltage-sensitive dye imaging (VSDI) can simultaneously monitor the spatiotemporal electrical dynamics of thousands of neurons and is often used to identify functional differences in models of neurological disease. While the chief advantage of VSDI is the ability to record spatiotemporal activity, there are no tools available to visualize and statistically compare activity across the full spatiotemporal range of the VSDI dataset. Investigators commonly analyze only a subset of the data, and a majority of the dataset is routinely excluded from analysis. We have developed a software toolbox that simplifies visual inspection of VSDI data, and permits unaided statistical comparison across spatial and temporal dimensions. First, the three-dimensional VSDI dataset (x,y,time) is geometrically transformed into a two-dimensional spatiotemporal map of activity. Second, statistical comparison between groups is performed using a non-parametric permutation test. The result is a 2D map of all significant differences in both space and time. Here, we used the toolbox to identify functional differences in activity in VSDI data from acute hippocampal slices obtained from epileptic Arx conditional knock-out and control mice. Maps of spatiotemporal activity were produced and analyzed to identify differences in the activity evoked by stimulation of each of two axonal inputs to the hippocampus: the perforant pathway and the temporoammonic pathway. In mutant hippocampal slices, the toolbox identified a widespread decrease in spatiotemporal activity evoked by the temporoammonic pathway. No significant differences were observed in the activity evoked by the perforant pathway. The VSDI toolbox permitted us to visualize and statistically compare activity across the spatiotemporal scope of the VSDI dataset. Sampling error was minimized because the representation of the data is standardized by the toolbox. Statistical comparisons were conducted quickly, across the spatiotemporal scope of the data, without a priori knowledge of the character of the responses or the likely differences between them
A New Gd³⁺ Spin Label for Gd³⁺-Gd³⁺ Distance Measurements in Proteins Produces Narrow Distance Distributions
Gd(3+) tags have been shown to be useful for performing distance measurements in biomolecules via the double electron-electron resonance (DEER) technique at Q- and W-band frequencies. We introduce a new cyclen-based Gd(3+) tag that exhibits a relatively narrow electron paramagnetic resonance (EPR) spectrum, affording high sensitivity, and which yields exceptionally narrow Gd(3+)-Gd(3+) distance distributions in doubly tagged proteins owing to a very short tether. Both the maxima and widths of distance distributions measured for tagged mutants of the proteins ERp29 and T4 lysozyme, featuring Gd(3+)-Gd(3+) distances of ca. 6 and 4 nm, respectively, were well reproduced by simulated distance distributions based on available crystal structures and sterically allowed rotamers of the tag. The precision of the position of the Gd(3+) ion is comparable to that of the nitroxide radical in an MTSL-tagged protein and thus the new tag represents an attractive tool for performing accurate distance measurements and potentially probing protein conformational equilibria.This work was supported by the Israel Science Foundation, the
Australian Research Council (ARC), and an AustraliaWeizmann
Making Connections grant. B.G. thanks the ARC
for a Future Fellowship (FT130100838). D.G. holds the Erich
Klieger Professorial Chair in Physical Chemistry
Blood-Brain Barrier Breakdown Following Traumatic Brain Injury: A Possible Role in Posttraumatic Epilepsy
Overcoming artificial broadening in Gd³⁺–Gd³⁺ distance distributions arising from dipolar pseudo-secular terms in DEER experiments
By providing accurate distance measurements between spin labels site-specifically attached to bio-macromolecules, double electron–electron resonance (DEER) spectroscopy provides a unique tool to probe the structural and conformational changes in these molecules. Gd3+-tags present an important family of spin-labels for such purposes, as they feature high chemical stability and high sensitivity in high-field DEER measurements. The high sensitivity of the Gd3+ ion is associated with its high spin (S = 7/2) and small zero field splitting (ZFS), resulting in a narrow spectral width of its central transition at high fields. However, under the conditions of short distances and exceptionally small ZFS, the weak coupling approximation, which is essential for straightforward DEER data analysis, becomes invalid and the pseudo-secular terms of the dipolar Hamiltonian can no longer be ignored. This work further explores the effects of pseudo-secular terms on Gd3+–Gd3+ DEER measurements using a specifically designed ruler molecule; a rigid bis-Gd3+-DOTA model compound with an expected Gd3+–Gd3+ distance of 2.35 nm and a very narrow central transition at the W-band (95 GHz). We show that the DEER dipolar modulations are damped under the standard W-band DEER measurement conditions with a frequency separation, Δν, of 100 MHz between the pump and observe pulses. Consequently, the DEER spectrum deviates considerably from the expected Pake pattern. We show that the Pake pattern and the associated dipolar modulations can be restored with the aid of a dual mode cavity by increasing Δν from 100 MHz to 1.09 GHz, allowing for a straightforward measurement of a Gd3+–Gd3+ distance of 2.35 nm. The increase in Δν increases the contribution of the |−5/2〉 → |−3/2〉 and |−7/2〉 → |−5/2〉 transitions to the signal at the expense of the |−3/2 〉 → |−1/2〉 transition, thus minimizing the effect of dipolar pseudo-secular terms and restoring the validity of the weak coupling approximation. We apply this approach to the A93C/N140C mutant of T4 lysozyme labeled with two different Gd3+ tags that have narrow central transitions and show that even for a distance of 4 nm there is still a significant (about two-fold) broadening that is removed by increasing Δν to 636 MHz and 898 MHz.This research was supported by the Israeli Science Foundation (grant
334/14) and made possible in part by the historic generosity of the
Harold Perlman Family. D. G. holds the Erich Klieger professorial
chair in Chemical Physic
Testing for regularity and stochastic transitivity using the structural parameter of nested logit
We introduce regularity and stochastic transitivity as necessary and well-behaved conditions respectively, for the consistency of discrete choice preferences with the Random Utility Model (RUM). For the specific case of a three-alternative nested logit (NL) model, we synthesise these conditions in the form of a simple two-part test, and reconcile this test with the conventional zero-one bounds on the structural (‘log sum’) parameter within this model, i.e. 0 0. On the other hand, we show that neither regularity nor stochastic transitivity constrain the upper bound at one. Therefore, if the conventional zero-one bounds are imposed in model estimation, preferences which violate regularity and/or stochastic transitivity may either go undetected (if the ‘true’ structural parameter is less than zero) and/or be unknowingly admitted (if the ‘true’ lower bound is greater than zero), and preferences which comply with regularity and stochastic transitivity may be excluded (if the ‘true’ upper bound is greater than one). Against this background, we show that imposition of the zero-one bounds may compromise model fit, inferences of willingness-to-pay, and forecasts of choice behaviour. Finally, we show that where the ‘true’ structural parameter is negative (thereby violating RUM – at least when choosing the ‘best’ alternative), positive starting values for the structural parameter in estimation may prevent the exposure of regularity and stochastic transitivity failures
Revisiting consistency with random utility maximisation: theory and implications for practical work
While the paradigm of utility maximisation has formed the basis of the majority of applications in discrete choice modelling for over 40 years, its core assumptions have been questioned by work in both behavioural economics and mathematical psychology as well as more recently by developments in the RUM-oriented choice modelling community. This paper reviews the basic properties with a view to explaining the historical pre-eminence of utility maximisation and addresses the question of what departures from the paradigm may be necessary or wise in order to accommodate richer behavioural patterns. We find that many, though not all, of the behavioural traits discussed in the literature can be approximated sufficiently closely by a random utility framework, allowing analysts to retain the many advantages that such an approach possesses
A Dynamic View of Domain-Motif Interactions
Many protein-protein interactions are mediated by domain-motif interaction, where a domain in one protein binds a short linear motif in its interacting partner. Such interactions are often involved in key cellular processes, necessitating their tight regulation. A common strategy of the cell to control protein function and interaction is by post-translational modifications of specific residues, especially phosphorylation. Indeed, there are motifs, such as SH2-binding motifs, in which motif phosphorylation is required for the domain-motif interaction. On the contrary, there are other examples where motif phosphorylation prevents the domain-motif interaction. Here we present a large-scale integrative analysis of experimental human data of domain-motif interactions and phosphorylation events, demonstrating an intriguing coupling between the two. We report such coupling for SH3, PDZ, SH2 and WW domains, where residue phosphorylation within or next to the motif is implied to be associated with switching on or off domain binding. For domains that require motif phosphorylation for binding, such as SH2 domains, we found coupled phosphorylation events other than the ones required for domain binding. Furthermore, we show that phosphorylation might function as a double switch, concurrently enabling interaction of the motif with one domain and disabling interaction with another domain. Evolutionary analysis shows that co-evolution of the motif and the proximal residues capable of phosphorylation predominates over other evolutionary scenarios, in which the motif appeared before the potentially phosphorylated residue, or vice versa. Our findings provide strengthening evidence for coupled interaction-regulation units, defined by a domain-binding motif and a phosphorylated residue
Network Formation with Local Complements and Global Substitutes: The Case of R&D Networks
Quantum probability: A new method for modelling travel behaviour
There has been an increasing effort to improve the behavioural realism of mathematical models of choice, resulting in efforts to move away from random utility maximisation (RUM) models. Some new insights have been generated with, for example, models based on random regret minimisation (RRM, μ-RRM). Notwithstanding work using for example Decision Field Theory (DFT), many of the alternatives to RUM tested on real-world data have however only looked at only modest departures from RUM, and differences in results have consequently been small. In the present study, we address this research gap again by investigating the applicability of models based on quantum theory. These models, which are substantially different from the state-of-the-art choice modelling techniques, emphasise the importance of contextual effects, state dependence, interferences and the impact of choice or question order. As a result, quantum probability models have had some success in better explaining several phenomena in cognitive psychology. In this paper, we consider how best to operationalise quantum probability into a choice model. Additionally, we test the quantum model frameworks on a best/worst route choice dataset and demonstrate that they find useful transformations to capture differences between the attributes important in a most favoured alternative compared to that of the least favoured alternative. Similar transformations can also be used to efficiently capture contextual effects in a dataset where the order of the attributes and alternatives are manipulated. Overall, it appears that models incorporating quantum concepts hold significant promise in improving the state-of-the-art travel choice modelling paradigm through their adaptability and efficient modelling of contextual changes
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