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In the ordinary course of business, the Company's subsidiaries CIFG Europe and CIFG NA have issued financial guaranty contracts in favor of special purpose entities SPEs ; . Specifically, CIFG Europe has issued financial guaranty contracts in favor of Mogador Ltd., a corporation established in Jersey, which is owned by Mogador Trust, a Jersey-based charitable trust. CIFG NA has issued contracts in favor of several distinct New York state business trusts, collectively known as the New Generation Funding Trusts. The contracts generally provide credit protection to protection buyers who have entered into credit default swap CDS ; transactions with the SPEs. The CIFG Group receives premiums at market rates but does not hold any equity positions or subordinated debt in these SPEs and accordingly, the financial statements of the SPEs are not consolidated with the financial statements of the group or any of its subsidiaries. As of 31 December 2002, 1.5 billion of par exposure was transacted with these SPEs and included in the table in Note VI a. As December 2002 the aggregate fair value of the credit default swaps represents a loss of K 1.7. Other than the transactions described above, the SPEs own no assets and have no outstanding debt. The aggregate summary financial statements of those SPEs are reflected in the following table as of and for the year ending 31 December 2002: in 000's Euros.
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Up 10 wk ; another ofthe seven patients developed irreversible CHF when LVEF finally dropped significantly. These prelim mary results suggest that a ; a fall in diastolic parameters may represent the first sign of anthracycline toxicity, and b ; dia stolic as well as systolic parameters should be monitored in pts undergoing anthracycline therapy. Advantages of Modified Oblique Cardiac MRI Projections. W. 1. Ganz, A. Serafini, A. Gentili, University of Medicine. Miami, FL. To optimize magnetic resonance imaging MRI ; imaging of cardiovascular anatomy, a modified oblique projection MOP ; is proposed.Twenty subjectswerestudied in this MOP using a Picker 0.35 Tesla MRI system with gated multislice spin echo sequences. In the MOP. the patient's right side is elevated 30 at the diaphragm, and the shoulders are depressed so that they are symmetrical on the imaging table. This position provides advantages in imaging the cardiovascular system in all orthogonal projections. In the transaxial projec tion, 1 ; the ventricular mass, 2 ; the four chamber view demonstrating the atrio-ventricular septum and valves: 3 ; aortopulmonary relation and 4 ; the aortic origin of both left and right coronary arteries can usually be visualized. In the coronal projection, the connection of I ; pulmonary vessels.
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DMD #372R References: Belinsky MG, Chen ZS, Shchaveleva I, Zeng H and Kruh GD 2002 ; Characterization of the drug resistance and transport properties of multidrug resistance protein 6 MRP6, ABCC6 ; . Cancer Res 62: 6172-6177. Bodo A, Bakos E, Szeri F, Varadi A and Sarkadi B 2003 ; Differential Modulation of the Human Liver Conjugate Transporters MRP2 and MRP3 by Bile Acids and Organic Anions. J Biol Chem 278: 23529-23537. Boyer JL and Meier PJ 1990 ; Characterizing mechanisms of hepatic bile acid transport utilizing isolated membrane vesicles. Methods Enzymol 192: 517-533. Chen ZS, Hopper-Borge E, Belinsky MG, Shchaveleva I, Kotova E and Kruh GD 2003 ; Characterization of the transport properties of human multidrug resistance protein 7 MRP7, ABCC10 ; . Mol Pharmacol 63: 351-358. Chu X, Huskey SE, Braun MP, Sarkadi B, Evans DC and Evers R 2004 ; Transport of ethinylestradiol glucuronide and ethinylestradiol sulfate by the multidrug resistance proteins MRP1, MRP2, and MRP3. J Pharmacol Exp Ther 309: 156-164. Crocenzi FA, Mottino AD, Cao J, Veggi LM, Pozzi EJ, Vore M, Coleman R and Roma MG 2003 ; Estradiol-17beta-D-glucuronide induces endocytic internalization of Bsep in rats. J Physiol Gastrointest Liver Physiol 285: G449-459. Cui Y, Konig J, Buchholz JK, Spring H, Leier I and Keppler D 1999 ; Drug resistance and ATPdependent conjugate transport mediated by the apical multidrug resistance protein, MRP2, permanently expressed in human and canine cells. Mol Pharmacol 55: 929-937. Evers R, de Haas M, Sparidans R, Beijnen J, Wielinga PR, Lankelma J and Borst P 2000 ; Vinblastine and sulfinpyrazone export by the multidrug resistance protein MRP2 is associated with glutathione export. Br J Cancer 83: 375-383. Gerk and Vore M 2002 ; Regulation of expression of the multidrug resistance-associated protein 2 MRP2 ; and its role in drug disposition. J Pharmacol Exp Ther 302: 407-415. Gerk PM, Yang Y, Ho RH, Li W, Kim RB and Vore M 2003 ; Effects of human MRP2 mutations on its transport and ATPase activities and activation by ursodiol. Hepatology 38: 382A. Hagenbuch B and Meier PJ 2003 ; The superfamily of organic anion transporting polypeptides. Biochim Biophys Acta 1609: 1-18. Hagmann W, Schubert J, Konig J and Keppler D 2002 ; Reconstitution of transport-active multidrug resistance protein 2 MRP2; ABCC2 ; in proteoliposomes. Biol Chem 383: 1001-1009. Haussinger D, Schmitt M, Weiergraber O and Kubitz R 2000 ; Short-term regulation of canalicular transport. Semin Liver Dis 20: 307-321. Hirohashi T, Suzuki H and Sugiyama Y 1999 ; Characterization of the transport properties of cloned rat multidrug resistance-associated protein 3 MRP3 ; . J Biol Chem 274: 1518115185. Huang L, Hoffman T and Vore M 1998 ; Adenosine triphosphate-dependent transport of estradiol-17beta beta-D- glucuronide ; in membrane vesicles by MDR1 expressed in insect cells. Hepatology 28: 1371-1377. Ito K, Oleschuk CJ, Westlake C, Vasa MZ, Deeley RG and Cole SP 2001a ; Mutation of Trp1254 in the multispecific organic anion transporter, multidrug resistance protein 2 MRP2 ; ABCC2 ; , alters substrate specificity and results in loss of methotrexate transport activity. J Biol Chem 276: 38108-38114.
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| Sulfinpyrazone treatmentPrior to chemotherapy in cancer patients. J Med 1980; 69: 491-97 Hansen HH, Dombernowsky P. hirsch FR. Staging procedures and prognostic features in small cell anaplastic bronchogenic carcinoma. Semin Oncol 1978; 5: 280-85 Hirsch FR, Hansen HH, Hainau B. Bilateral hone marrow examinations in small cell anaplastic carcinoma of the lung. Acta Pathol Microbiol Scand 1979; 87: 59-62 Stahel HA, Mabry M, Skarin AT, Speak J, Bernal SD. Detection of bone marrow metastasis in small cell lung cancer by mono clonal antihod J Clin Oncol 1985; 3: 455-61 Levenson RM, Sauerbninn BJL, Ihde DC. Small cell lung cancer: radionucleide hone scans for assessment of tumor extent and response. AJR 1981; 137: 31-5 and surmontil.
Fear of malpractice lawsuits [16, 29, 30]. To try to resolve the latter dilemma, for example, the US president recently signed into law the Patient Safety and Quality Improvement Act of 2005 S.544 ; , which has clarified legislative aspects of liability by providing legal protection to health care professionals who report their errors. However, as we explain below, without a profound managerial change that creates open and communicative organizations, we doubt the extent to which legislation can discourage `silence' [31]. According to the management literature, employees decide whether to raise issues with management by `reading the context' for clues concerning context favorability. A favorable context is when physicians perceive management either top management or ward managers ; to be willing to listen and be supportive, and that error reporting has relatively little negative consequences [32]. In general, underreporting of adverse events indicates that physicians perceive their organizations' context as unfavorable. An unfavorable context is characterized by the shared beliefs that speaking up about problems in the organization is not worth the effort and that voicing one's opinions and concerns is dangerous to their jobs. Why do physicians perceive the health care context as unfavorable? We suggest an answer based on the concept of psychological contracts [33]. Psychological contracts within organizations refer to the employees' shared beliefs, based upon promises expressed or implied, about the terms of an exchange agreement between them and the organization [33]. In general, the shared implicit psychological contract in health care organizations is a contract of blame in which an error is believed to be the responsibility of the employee who commits the error s ; . Indeed, a recent trend in the health care industry is to use `cards' that publicly report physicians' success and error rates [34]. By publicly reporting error rates, physicians may compromise their employability and may also expose themselves to malpractice lawsuits. Consequently, silence prevails. A different possible psychological contract between physicians and their organization is a `no-blame' contract in which both sides agree that errors are because of systemic flaws, which must be detected and corrected. This removes the fear of personal liability and eliminates incentives to hide errors. Hence, one would voice an error to avoid potential hazards and to improve the system [2]. It is our observation that a `no-blame' psychological contract exists within groups, for example within a team, a ward, or a profession. Ambiguous professional work is executed within the ingroup [35]; hence, the professionals and the profession perceive an error as an opportunity to learn and develop. However, although the profession supports internal learning and change, it blocks externally oriented sources of change and learning [36]. This occurs because a psychological contract of `blame' tends to exist between groups, for example between management or regulators and those who are managed or supervised. As a result, reports will not cross the profession's borders. For example, physicians tend to be suspicious about external monitoring because `they don't understand our work' whereas are ready to conduct fierce internal reviews of.
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Treatment attenuated NFAT nuclear translocation compared to controls 131%; p 0.05 ; . The impact of glucosamine, alloxan and PUGNAc on NFAT translocation, was remarkably similar to their effects on viability seen in Fig. 4A and symlin
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Effects of BK on [Cu2 + i-The study of [Ca2 + ]i the use of by Fura-2 in suspensions of intact cells is complicated by a slow leakage of the indicator to the incubation medium, which results in a progressive increase of base-line fluorescence 24, 25 ; . Recently, DiVirgilio e t ul. 25 ; have demonstrated that inhibitors of organic anion transportcan efficiently block the dye leakage in the macrophage cell line, 5774. Using one such drug, sulfinpyrazone, which by itself has no effect on either A$ or [Caz + ]i PC12 cells, no leakage of Fura-2 for up to 20 min of incubation at 37 "C, and no modification of either the size or kinetics of the [Ca2 + Ii transientsinduced by various agents, including BK, could be detected. Because of this, all the [Ca2 + ]i experiments presented here have been performed in cells pretreated with sulfinpyrazone 250 p M ; . first series of experiments Figs. 1 and 2 ; , the concentration dependence of the BK effect on [Ca2 + Ii was investigated. Concentrations of the peptide between 10-8-10-6 M and symmetrel.
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1. Contestants may only enter 1 recipe. 2. Give your recipes to your dietitian no later than August 1, 2002. Patients in the satellite units must ask their nurse to pass along recipes to the dietitian ; . 3. Recipes will be divided into either the Hemo dialysis or Peritoneal Dialysis group. If you have any questions about the nutrient content of your recipe, ask your dietitian. 4. A third, second and first place winner will be chosen for both people on Hemodialysis and Peritoneal Dialysis. 5. The 6 winning recipes will be featured in the summer 2002 edition of the Renal Nutrition Update. A variety of prizes will be awarded to the winners and synagis.
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Bacterial strains used in this study are described in the Table. P. aeruginosa strains PAO1, ML5087 and PAO2375, S. maltophilia strains ATCC 13637 and ULA-511, and B. cepacia strains K127 and K131 were used as wild-type and reference strains.3, 8, 9 Most multidrug-resistant or efflux pump-deficient mutants derived from these strains were selected or constructed as reported previously, 3, 8, 9 and their susceptibilities to -lactams, ciprofloxacin, aminoglycosides, macrolides, tetracycline and or chloramphenicol have been reported.3, 8, 9 The PAO1 nfxB mutant, strain K1536, was and synvisc
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