1,558 research outputs found

    The Journey Home: Flight Related Factors on Refugee Decisions to Return

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    The international refugee regime promotes voluntary repatriation as the preferred solution to refugee crises. It is commonly held that it is safe for refugees to return once conditions are stable in the country of origin, which typically translates to when the violence between combatants ceases. However, the empirical record suggests that refugee returns are far from uniform in relationship to the presence or absence or level of violence in a conflict setting. In other words, we know remarkably little about the conditions under which refugee returns actually occur. In response to this shortfall in knowledge, we ask: how do refugees form decisions on when and whether they should return despite ongoing violence and instability in their country of origin? We focus upon one crucial part of the picture, in particular: how does prior exposure to violence in the country of origin affect refugees’ subsequent decisions to return? To explore this relationship, we designed an original survey, implemented among 2,000 Syrian refugees hosted in Lebanon to causally identify the effects of prior conflict exposure on refugees’ decisions to return. We find that Syrian refugees are more willing to leave Lebanon and return home when they have prior experience of violence in Syria. We explain this counter-intuitive finding as a reflection of these particular refugees as “experts” who are better able to understand and assess their risk tolerance of violence. In contrast, refugees more removed from violence before fleeing their homes harbor more uncertainty of the threats associated with returning and are unwilling to accept the risk of doing so

    The Journey Home: Flight Related Factors on Refugee Decisions to Return

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    Normative practice for forced displacement is to voluntarily repatriate refugees once conditions are stable in the country of origin, which typically translates to the end of violence. However, Syrian refugees have been returning over the past few years even though there is yet to be a definitive end to the Syrian civil war. Therefore, this paper asks how refugees form decisions on when and whether they should return despite ongoing violence and instability in their country of origin? For now, we focus upon one part of the picture: how prior exposure to violence in the country of origin affects their subsequent decision to return home from their host country. To explore this relationship, we designed an original survey, implemented among Syrian refugees hosted in Lebanon (N=2,000), to causally identify the effects of prior conflict exposure on refugees’ decisions to return. We find that Syrian refugees are more willing to leave Lebanon and return home when they have prior experience of violence in Syria. We explain this initially counterintuitive finding as reflecting that they better understand their tolerance to violence, because they are “experts” and are more capable of assessing risk. In contrast, refugees who were not directly exposed to violence before fleeing their homes are more unsure of the threats associated to returning and are unwilling, therefore, to accept the risk of doing so

    Using survey experiments to explore refugee resettlement preferences

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    BEX3 contributes to cisplatin chemoresistance in nasopharyngeal carcinoma

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    Studies have been performed on the radiation hardness of the type of VCSELs**2 Vertical Cavity Surface Emitting Lasers. that will be used in the ATLAS SemicConductor Tracker. The measurements were made using 30 MeV proton beams, 24 GeV/c proton beams and a gamma source. The lifetime of the devices after irradiation was studied

    Timed inhibition of CDC7 increases CRISPR-Cas9 mediated templated repair.

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    Repair of double strand DNA breaks (DSBs) can result in gene disruption or gene modification via homology directed repair (HDR) from donor DNA. Altering cellular responses to DSBs may rebalance editing outcomes towards HDR and away from other repair outcomes. Here, we utilize a pooled CRISPR screen to define host cell involvement in HDR between a Cas9 DSB and a plasmid double stranded donor DNA (dsDonor). We find that the Fanconi Anemia (FA) pathway is required for dsDonor HDR and that other genes act to repress HDR. Small molecule inhibition of one of these repressors, CDC7, by XL413 and other inhibitors increases the efficiency of HDR by up to 3.5 fold in many contexts, including primary T cells. XL413 stimulates HDR during a reversible slowing of S-phase that is unexplored for Cas9-induced HDR. We anticipate that XL413 and other such rationally developed inhibitors will be useful tools for gene modification
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