232 research outputs found
Does input trade liberalization boost downstream firms’ exports? Theory and firm-level evidence
We analyze the impact of input tariffs on the export status and export performance of heterogeneous processing firms. Using a theoretical model with downstream firms exhibiting different levels of productivity, we show that lower input tariffs may increase the export sales of high-productivity firms at the expense of low-productivity firms and may decrease the probability of firms entering foreign markets. We compare the predictions of the theoretical model with firm-level data from the French agrifood sector by developing a two-stage estimation procedure that uses an equation for selection into export markets in the first stage and an exports equation in the second stage. The liberalization of agricultural trade appears to favor the reallocation of market share from low- to high-productivity agrifood firms. In addition, our results suggest that, whether lower input tariffs increase total exports sales (and jobs), a large fraction of the least productive exporting firms may lose from an additional decrease in agricultural input tariffs
Memory effects in classical and quantum mean-field disordered models
We apply the Kovacs experimental protocol to classical and quantum p-spin
models. We show that these models have memory effects as those observed
experimentally in super-cooled polymer melts. We discuss our results in
connection to other classical models that capture memory effects. We propose
that a similar protocol applied to quantum glassy systems might be useful to
understand their dynamics.Comment: 24 pages, 12 figure
Mycofactocin Is Associated with Ethanol Metabolism in Mycobacteria
Tuberculosis is caused by Mycobacterium tuberculosis, and the increasing emergence of multidrug-resistant strains renders current treatment options ineffective. Although new antimycobacterial drugs are urgently required, their successful development often relies on complete understanding of the metabolic pathways—e.g., cholesterol assimilation—that are critical for persistence and for pathogenesis of M. tuberculosis. In this regard, mycofactocin (MFT) function appears to be important because its biosynthesis genes are predicted to be essential for M. tuberculosisin vitro growth in cholesterol. In determining the metabolic basis of this genetic requirement, our results unexpectedly revealed the essential function of MFT in ethanol metabolism. The metabolic dysfunction thereof was found to affect the mycobacterial growth in cholesterol which is solubilized by ethanol. This knowledge is fundamental in recognizing the bona fide function of MFT, which likely resembles the pyrroloquinoline quinone-dependent ethanol oxidation in acetic acid bacteria exploited for industrial production of vinegar.Mycofactocin (MFT) belongs to the class of ribosomally synthesized and posttranslationally modified peptides conserved in many Actinobacteria. Mycobacterium tuberculosis assimilates cholesterol during chronic infection, and its in vitro growth in the presence of cholesterol requires most of the MFT biosynthesis genes (mftA, mftB, mftC, mftD, mftE, and mftF), although the reasons for this requirement remain unclear. To identify the function of MFT, we characterized MFT biosynthesis mutants constructed in Mycobacterium smegmatis, M. marinum, and M. tuberculosis. We found that the growth deficit of mft deletion mutants in medium containing cholesterol—a phenotypic basis for gene essentiality prediction—depends on ethanol, a solvent used to solubilize cholesterol. Furthermore, functionality of MFT was strictly required for growth of free-living mycobacteria in ethanol and other primary alcohols. Among other genes encoding predicted MFT-associated dehydrogenases, MSMEG_6242 was indispensable for M. smegmatis ethanol assimilation, suggesting that it is a candidate catalytic interactor with MFT. Despite being a poor growth substrate, ethanol treatment resulted in a reductive cellular state with NADH accumulation in M. tuberculosis. During ethanol treatment, mftC mutant expressed the transcriptional signatures that are characteristic of respirational dysfunction and a redox-imbalanced cellular state. Counterintuitively, there were no differences in cellular bioenergetics and redox parameters in mftC mutant cells treated with ethanol. Therefore, further understanding of the function of MFT in ethanol metabolism is required to identify the cause of growth retardation of MFT mutants in cholesterol. Nevertheless, our results establish the physiological role of MFT and also provide new insights into the specific functions of MFT homologs in other actinobacterial systems
Static properties of the dissipative random quantum Ising ferromagnetic chain
We study the zero temperature static properties of dissipative ensembles of
quantum Ising spins arranged on periodic one dimensional finite clusters and on
an infinite chain. The spins interact ferro-magnetically with nearest-neighbour
pure and random couplings. They are subject to a transverse field and coupled
to an Ohmic bath of quantum harmonic oscillators. We analyze the coupled system
using Monte Carlo simulations of the classical two-dimensional counterpart
model. The coupling to the bath enhances the extent of the ordered phase, as
found in mean-field spin-glasses. In the case of finite clusters we show that a
generalization of the Caldeira-Leggett localization transition exists. In the
case of the infinite random chain we study the effect of dissipation on the
transition and the Griffiths phase.Comment: 21 pages, 10 figure
Effects of dissipation on disordered quantum spin models
We study the effects of the coupling to an Ohmic quantum reservoir on the
static and dynamical properties of a family of disordered SU(2) spin models in
a transverse magnetic field using a method of direct spin summation. The
tendency to form a glassy phase increases with the strength of the coupling of
the system to the environment. We study the influence of the environment on the
features of the phase diagram of the various models as well as the stability of
the possible phases.Comment: 24 pages, 8 fig
A-ring modifications on the triazafluorenone core structure and their mGluR1 antagonist properties
Tricyclic thienopyridine\u2013pyrimidones/thienopyrimidine\u2013pyrimidones as orally efficacious mGluR1 antagonists for neuropathic pain
Advanced Differentiated Thyroid Cancer. A Complex Condition Needing a Tailored Approach
Differentiated thyroid cancers (DTCs) are slow-growing malignant tumours, including papillary and follicular carcinomas. Overall, prognosis is good, although it tends to worsen when local invasion occurs with bulky cervical nodes, or in the case of distant metastases. Surgery represents the main treatment for DTCs. However, radical excision is challenging and significant morbidity and functional loss can follow the treatment of the more advanced forms. Literature on advanced thyroid tumours, both differentiated and undifferentiated, does not provide clear and specific guidelines. This emerges the need for a tailored and multidisciplinary approach. In the present study, we report our single-centre experience of 111 advanced (local, regional, and distant) DTCs, investigating the rate of radical excision, peri-procedural and post-procedural complications, quality of life, persistence, recurrence rates, and survival rates. Results are critically appraised and compared to the existing published evidence review
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