161,288 research outputs found
Transatlantic Trade Policy: US Market Opening Strategies. European Policy Paper #1
[Introduction.] Since the 1950s, the European Community (EC) has been trying to build up a new independent legal and economic order. This exercise has been difficult and gradual. Indeed, each step forward in the build-up of the community's legal and economic order requires a new compromise formula between the member states--for example, between the free traders and the economic interventionists; between the more service-oriented, the more industrial-oriented, and the more agricultural economies; and between the richer and the poorer regions. Obviously, the Community is not developing in a vacuum. Since the Community is a major player in international trade relations, its development has an effect, not only within the EC, but also on third countries. Naturally, since Community measures also affect third countries, those third countries, including the United States (US), have been trying to influence or even control the final shape of the EC's legal and economic order. As Jeffrey Garten, the US Under Secretary of Commerce for International Trade, has recently explained, the US is determined to try and shape its trading partners' economic system in view of the US market opening objective. According to Garten, Washington would use its power to try to pry open markets even if it meant challenging "the very industrial organization of countries"(cited in Friedman, 1995). As a result, tension has developed between, on the one hand, the EC's sovereign right to set up its own legal order and, on the other, the outside world's interest in monitoring and influencing the EC's development. This paper examines this tension as it arises in the relationship between the Community and the United States. More specifically, the paper deals with the institutional strategies (multilateral, bilateral, and unilateral) used by the United States to monitor the EC's development and to keep the Common Market open for US exports. The main question is how far each of the institutional strategies was able to help resolve, or better, help prevent, "market opening" conflicts between the US and the EC. At the end of the paper, the current US market opening options toward the EC will be analyzed, including the recent suggestion to create a Transatlantic Free Trade Area (TAFTA) similar to the North American Free Trade Agreement (NAFTA)
The rediscovery of uromodulin (Tamm-Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease.
A role for CFTR in human autosomal dominant polycystic kidney disease
Pages C389-C399: K. Hanaoka, O. Devuyst, E. M. Schwiebert, P. D. Wilson, and W. B. Guggino. “A role for CFTR in human autosomal dominant polycystic kidney disease.” Page C395, Fig. 5: because of a photographic processing error, panels B and D, which both show unstained cells, were mislabeled and incorrectly reproduced. The corrected figure appears below. (See PDF) </jats:p
Variations on the Author
“Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship
Going Beyond Counting First Authors in Author Co-citation Analysis
The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Aquaporin-1: New developments and perspectives for peritoneal dialysis
Peritoneal dialysis involves diffusive and convective transport and osmosis through the highly vascularized peritoneal membrane. Several lines of evidence have demonstrated that the water channel aquaporin-1 (AQP1) corresponds to the ultrasmall pore predicted by the model of peritoneal transport. Proof-of-principle studies have shown that upregulation of the expression of AQP1 in peritoneal capillaries results in increased water permeability and ultrafiltration, without affecting the osmotic gradient or small solute permeability. Conversely, studies in Aqp1 mice have shown that haplo-insufficiency for AQP1 results in significant attenuation of water transport. Recent studies have demonstrated that AQP1 is involved in the migration of different cell types, including endothelial cells. In parallel, chemical screening has identified lead compounds that could act as antagonists or agonists of AQPs, with description of putative binding sites and potential mechanisms of gating the water channel. By modulating water transport, these pharmacological agents could have clinically relevant effects in targeting specific tissues or disease states.Olivier Devuyst and Andrea J. Yoo
Larry O. Spencer, Conference Author Presentation
Gen. Larry O. Spencer, USAF (Ret.), author of Dark Horse: A Journey from the Horseshoe to the Pentago
Expression of mutant uromodulin leads to progressive tubulointerstitial damage and renal defects in transgenic mice.
Allelic effects on uromodulin aggregates drive autosomal dominant tubulointerstitial kidney disease
Missense mutations in the uromodulin (UMOD) gene cause autosomal dominant tubulointerstitial kidney disease (ADTKD), one of the most common monogenic kidney diseases. The unknown impact of the allelic and gene dosage effects and fate of mutant uromodulin leaves open the gap between postulated gain-of-function mutations, end-organ damage and disease progression in ADTKD. Based on two prevalent missense UMOD mutations with divergent disease progression, we generated Umod(C171Y) and Umod(R186S) knock-in mice that showed strong allelic and gene dosage effects on uromodulin aggregates and activation of ER stress and unfolded protein and immune responses, leading to variable kidney damage. Deletion of the wild-type Umod allele in heterozygous Umod(R186S) mice increased the formation of uromodulin aggregates and ER stress. Studies in kidney tubular cells confirmed differences in uromodulin aggregates, with activation of mutation-specific quality control and clearance mechanisms. Enhancement of autophagy by starvation and mTORC1 inhibition decreased uromodulin aggregates. These studies substantiate the role of toxic aggregates as driving progression of ADTKD-UMOD, relevant for therapeutic strategies to improve clearance of mutant uromodulin
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