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Lost in translation: ethnocentric tendency in website communication

This paper reports on an exploratory case study investigating the proposition that a locally-embedded organization may exhibit a natural tendency towards ethnocentric perspectives in website communication. Particularly, in multicultural audience environments, such as exist in international tourism, ethnocentric website communication may impede the consistent formation of desired organizational ima

NPM and change management in asset management organisations

Purpose: Effective engineering asset management is essential in delivering public services safely whilst avoiding breakdowns and accidents. To ensure asset safety and sustainability, public sector firms have to adopt new processes and practices. It is the role of supervisors to implement the changes, and as part of the New Public Management (NPM) public sector reforms, public sector asset managers

Impact assessment of policies promoting fiber-to-fiber recycling of textiles

As part of the Mistra Future Fashion Research Program, IVL Swedish Environmental Research Institute (IVL), the International Institute for Industrial Environmental Economics (IIIEE) and PlanMiljø have investigated policy options promoting (fiber-to-fiber) recycling of textile waste. The ambition was to contribute to and broaden the discussion regarding potential policy measures in the textile fiel

Diversity in Education : Crossing cultural, disciplinary and professional divides

International and interdisciplinary programmes for students from diverse cultural and professional backgrounds entail many benefits—perhaps the most essential is learning how to work with people holding different perspectives. However, they also bring many challenges.How can we support students from abroad, both inside and beyond the classroom? How can we equip students from diverse backgrounds wi

Recurrent otitis media : genetic immunoglobulin markers in children and their parents

The likelihood that hereditary factors play a significant role in the development of recurrent acute otitis media (rAOM) in children has been suggested. The genetically determined immunoglobulin variants, Gm and Km, are useful tools for mapping out the genetic loci involved in antibody responses. Certain Gm and Km types, G2m(23) and Km(1), appear to be linked to genes which regulate the concentrat

Homozygous APC-resistance combined with inherited type I protein S deficiency in a young boy with severe thrombotic disease

Inherited resistance to activated protein C (APC) is a frequent cause of familial thrombosis. It is associated with a factor V gene point mutation replacing arginine506 in the APC-cleavage site with a glutamine. Thrombotic events are rare during childhood even in patients with homozygous APC-resistance. We now wish to report on a case of severe venous thrombosis, in a 10-year-old boy. He was found

Inherited resistance to activated protein C caused by presence of the FV:Q506 allele as a basis of venous thrombosis

Inherited resistance to activated protein C (APC) was recently discovered as a cause of familial thrombophilia and is now known to be the most common genetic risk factor for venous thrombosis. In a majority of cases, APC resistance is associated with a single point mutation in the factor V gene, which results in substitution of arginine (R) at position 506 by glutamine (Q) (FV:Q506). The mutation

Activated protein C resistance due to a common factor V gene mutation is a major risk factor for venous thrombosis

Inherited resistance to activated protein C (APC) was recently discovered to be a cause of familial thrombophilia and is now known to be the most common genetic risk factor for venous thrombosis. It is caused by a single point mutation in the gene for factor V, which predicts substitution or arginine (R) at position 506 with a glutamine (Q). Accordingly, the activated form of mutated factor V (FVa

Factor V:Q506 mutation and anticardiolipin antibodies in systemic lupus erythematosus

Inherited resistance to activated protein C (APC resistance) is an important risk factor of venous thrombosis. It is caused by a point mutation in the gene coding for coagulation factor V, called FV:Q506. Arterio-venous thrombosis is a common and serious medical problem in patients with systemic lupus erythematosus (SLE). We studied the prevalence of the factor V mutation associated with APC resis

Structural determinants in ApoA-I amyloidogenic variants explain improved cholesterol metabolism despite low HDL levels

Twenty Apolipoprotein A-I (ApoA-I) variants are responsible for a systemic hereditary amyloidosis in which protein fibrils can accumulate in different organs, leading to their failure. Several ApoA-I amyloidogenic mutations are also associated with hypoalphalipoproteinemia, low ApoA-I and high-density lipoprotein (HDL)-cholesterol plasma levels; however, subjects affected by ApoA-I-related amyloid

Plasma stem cell factor levels are associated with risk of cardiovascular disease and death

OBJECTIVE: Stem cell factor (SCF) is a key growth factor for several types of stem and progenitor cells. There is experimental evidence that such cells are of importance for maintaining the integrity of the cardiovascular system. We investigated the association between circulating levels of SCF and risk for development of cardiovascular events and death.METHODS: SCF was analysed by the proximity e

Molecular mechanisms controlling phosphate-induced downregulation of the yeast Pho84 phosphate transporter

In Saccharomyces cerevisiae, phosphate uptake is mainly dependent on the proton-coupled Pho84 permease under phosphate-limited growth conditions. Phosphate addition causes Pho84-mediated activation of the protein kinase A (PKA) pathway as well as rapid internalization and vacuolar breakdown of Pho84. We show that Pho84 undergoes phosphate-induced phosphorylation and subsequent ubiquitination on am

Bridging across length scales : multi-scale ordering of supported lipid bilayers via lipoprotein self-assembly and surface patterning

We show that a two-step process, involving spontaneous self-assembly of lipids and apolipoproteins and surface patterning, produces single, supported lipid bilayers over two discrete and independently adjustable length scales. Specifically, an aqueous phase incubation of DMPC vesicles with purified apolipoprotein A-I results in the reconstitution of high density lipoprotein (rHDL), wherein nanosca