106 research outputs found

    Loss of hyperbolicity and tachyons in generalized Proca theories

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    Various groups recently demonstrated that the time evolution of simplest self-interacting vector fields, those with self-interaction potentials, can break down after a finite duration in what is called loss of hyperbolicity. We establish that this is not an isolated issue, and other generalizations of the Proca theory suffer from the same problem. Specifically, we show that vector field theories with derivative self-interactions have a similar pathology. For this, we derive the effective metric that governs the dynamics, and show that it can change signature during time evolution. We also show that, generalized Proca theories may suffer from tachyonic instabilities as well, which lead to another form of unphysical behavior.Comment: 10 pages, 4 figure

    Constraining scalar-tensor theories using neutron star mass and radius measurements

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    We use neutron star mass and radius measurements to constrain the spontaneous scalarization phenomenon in scalar-tensor theories using Bayesian analysis. Neutron star structures in this scenario can be significantly different from the case of general relativity, which can be used to constrain the theory parameters. We utilize this idea to obtain lower bounds on the coupling parameter β\beta for the case of massless scalars. These constraints are currently weaker than the ones coming from binary observations, and they have relatively low precision due to the approximations in our method. Nevertheless, our results clearly demonstrate the power of the mass-radius data in testing gravity, and can be further improved with future observations. The picture is different for massive scalars, for which the same data is not able to effectively constrain the theory parameters in an unexpected manner. We identify the main reason for this to be a large high-likelihood region in the parameter space where deviations from general relativity are relatively small. We hope this initial study to be an invitation to use neutron star structure measurements more effectively to test alternative theories in general.Comment: 19 pages, 13 figure

    Entanglement in Coupled Harmonic Oscillators via Unitary Transformation

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    We develop an approach to study the entanglement in two coupled harmonic oscillators. We start by introducing an unitary transformation to end up with the solutions of the energy spectrum. These are used to construct the corresponding coherent states through the standard way. To evaluate the degree of the entanglement between the obtained states, we calculate the purity function in terms of the coherent and number states, separately. The result is yielded to two parameters dependance of the purity, which can be controlled easily. Interesting results are derived by fixing the mixing angle of such transformation as \pi/2. We compare our results with already published work and point out the relevance of these findings to a systematic formulation of the entanglement effect in two coupled harmonic oscillators.Comment: 19 pages, 6 figures, clarification and reference added, misprints corrected. Version published in JSTA

    Management of bipolar disorder in the intercontinental region: an international, multicenter, non-interventional, cross-sectional study in real-life conditions

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    Most of the existing data on real-life management of bipolar disorder are from studies conducted in western countries (mostly United States and Europe). This multinational, observational cohort study aimed to describe the management and clinical outcomes of bipolar patients in real-life conditions across various intercontinental countries (Bangladesh, Egypt, Iran, Israel, Tunisia, and Ukraine). Data on socio-demographic and disease characteristics, current symptomatology, and pharmacological treatment were collected. Comparisons between groups were performed using standard statistical tests. Overall, 1180 patients were included. The median time from initial diagnosis was 80 months. Major depressive disorder was the most common initial diagnosis. Mood stabilizers and antipsychotics were the most common drugs being prescribed at the time of the study. Antidepressants (mainly selective serotonin uptake inhibitors [SSRIs]) were administered to 36.1% of patients. Patients with bipolar I disorder received higher number of antipsychotics and anxiolytics than those with bipolar II disorder (p < 0.001). Presence of depressive symptoms was associated with an increase in antidepressant use (p < 0.001). Bipolar disorder real-life management practice, irrespective of region, shows a delay in diagnosis and an overuse of antidepressants. Clinical decision-making appears to be based on a multidimensional approach related to current symptomatology and type of bipolar disorder

    FANCA Gene Mutations in North African Fanconi Anemia Patients

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    Populations in North Africa (NA) are characterized by a high rate of consanguinity. Consequently, the proportion of founder mutations might be higher than expected and could be a major cause for the high prevalence of recessive genetic disorders like Fanconi anemia (FA). We report clinical, cytogenetic, and molecular characterization of FANCA in 29 North African FA patients from Tunisia, Libya, and Algeria. Cytogenetic tests revealed high rates of spontaneous chromosome breakages for all patients except two of them. FANCA molecular analysis was performed using three different molecular approaches which allowed us to identify causal mutations as homozygous or compound heterozygous forms. It included a nonsense mutation (c.2749C > T; p.Arg917Ter), one reported missense mutation (c.1304G > A; p.Arg435His), a novel missense variant (c.1258G > A; p.Asp409Glu), and the FANCA most common reported mutation (c.3788_3790delTCT; p.Phe1263del). Furthermore, three founder mutations were identified in 86.7% of the 22 Tunisian patients: (1) a deletion of exon 15, in 36.4% patients (8/22); (2), a deletion of exons 4 and 5 in 23% (5/22) and (3) an intronic mutation c.2222 + 166G > A, in 27.3% (6/22). Despite the relatively small number of patients studied, our results depict the mutational landscape of FA among NA populations and it should be taken into consideration for appropriate genetic counseling

    Relationship between epistasis and aggressiveness in resistance of pepper (Capsicum annuum L.) to Phytophthora nicotianae

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    This study evaluated the types of gene action governing the inheritance of resistance to Phytophthora nicotianae necrosis in populations derived from two crosses involving two susceptible (Beldi and Nabeul II) and one resistant (CM334) cultivars of pepper (Capsicum annuum L.). Populations, composed of Pr, Ps, F1 , F 2 , BC 1 Pr, and BC 1 Ps generations, were inoculated with six P. nicotianae isolates. Generation means analysis indicated that an additive-dominance model was appropriate for P. nicotianae isolates Pn Ko1 , Pn Ko2 and Pn Kr1 , which showed low aggressiveness in the two crosses. For the more aggressive isolates Pn Bz1 , Pn Bz2 and Pn Kr2 , epistasis was an integral component of resistance in the two crosses. The presence of epistasis in the resistance of pepper to P. nicotianae was dependent on the level of aggressiveness of the isolates. Selection in pepper with less aggressive isolates was efficient, but not with more aggressive isolates; on the other hand, selection with more aggressive isolates was more stable. The minimum number of genes controlling resistance was estimated at up to 2.71. In the majority of cases, the additive variance was significant and greater than the environmental and dominance variance

    The effect of tobacco, XPC, ERCC2 and ERCC5 genetic variants in bladder cancer development

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    <p>Abstract</p> <p>Background</p> <p>In this work, we have conducted a case-control study in order to assess the effect of tobacco and three genetic polymorphisms in <it>XPC, ERCC2 and ERCC5 </it>genes (rs2228001, rs13181 and rs17655) in bladder cancer development in Tunisia. We have also tried to evaluate whether these variants affect the bladder tumor stage and grade.</p> <p>Methods</p> <p>The patients group was constituted of 193 newly diagnosed cases of bladder tumors. The controls group was constituted of non-related healthy subjects. The rs2228001, rs13181 and rs17655 polymorphisms were genotyped using a polymerase chain reaction-restriction fragment length polymorphism technique.</p> <p>Results</p> <p>Our data have reported that non smoker and light smoker patients (1-19PY) are protected against bladder cancer development. Moreover, light smokers have less risk for developing advanced tumors stage. When we investigated the effect of genetic polymorphisms in bladder cancer development we have found that ERCC2 and ERCC5 variants were not implicated in the bladder cancer occurrence. However, the mutated homozygous genotype for XPC gene was associated with 2.09-fold increased risk of developing bladder cancer compared to the control carrying the wild genotype (p = 0.03, OR = 2.09, CI 95% 1.09-3.99). Finally, we have found that the XPC, ERCC2 and ERCC5 variants don't affect the tumors stage and grade.</p> <p>Conclusion</p> <p>These results suggest that the mutated homozygous genotype for XPC gene was associated with increased risk of developing bladder. However we have found no association between rs2228001, rs13181 and rs17655 polymorphisms and tumors stage and grade.</p
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