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Sökning: WFRF:(Nilsson Anna) > Malmö universitet

  • Resultat 1-10 av 30
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1.
  • Bexelius, Maria, et al. (författare)
  • 27 forskare : Så kan EU:s murar rivas
  • 2015
  • Ingår i: Dagens samhälle. - : Sveriges kommuner och landsting. - 1652-6511. ; :20150923
  • Tidskriftsartikel (populärvet., debatt m.m.)
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3.
  • Ullmark, Peter, et al. (författare)
  • Design & visuell kommunikation : examensbok 2010
  • 2010
  • Rapport (övrigt vetenskapligt/konstnärligt)abstract
    • Publiceras i samband med den första utexamineringen från kandidatprogrammet Design & Visuell Kommunikation på Malmö högskola. Boken innehåller artiklar om designforskning såväl som personliga presentationer av programmets studenter och deras examensarbeten eller portfolios. Boken definierar vad Design & Visuell Kommunikation står för i studenternas mening.
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4.
  • Acosta, Stefan, et al. (författare)
  • Engaging patients and caregivers in establishing research priorities for aortic dissection
  • 2019
  • Ingår i: SAGE Open Medicine. - : Sage Publications. - 2050-3121. ; 7, s. 1-7
  • Tidskriftsartikel (refereegranskat)abstract
    • Objectives: The aim of this study was to establish the top 10 research uncertainties in aortic dissection together with the patient organization Aortic Dissection Association Scandinavia using the James Lind Alliance concept. Methods: A pilot survey aiming to identify uncertainties sent to 12 patients was found to have high content validity (scale content validity index = 0.91). An online version of the survey was thereafter sent to 30 patients in Aortic Dissection Association Scandinavia and 45 caregivers in the field of aortic dissection. Research uncertainties of aortic dissection were gathered, collated and processed. Results: Together with research priorities retrieved from five different current guidelines, 94 uncertainties were expressed. A shortlist of 24 uncertainties remained after processing for the final workshop. After the priority-setting process, using facilitated group format technique, the ranked final top 10 research uncertainties included diagnostic tests for aortic dissection; patient information and care continuity; quality of life; endovascular and medical treatment; surgical complications; rehabilitation; psychological consequences; self-care; and how to improve prognosis. Conclusion: These ranked top 10 important research priorities may be used to justify specific research in aortic dissection and to inform healthcare research funding decisions.
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5.
  • Alegría, Carlos, et al. (författare)
  • The Complexity of the Lower Envelope of Collections of Various Geometric Shapes
  • 2024
  • Ingår i: 40th European Workshop on Computational Geometry. ; , s. 200-206
  • Konferensbidrag (refereegranskat)abstract
    • We study the problem of determining the complexity of the lower envelope of a collection of n geometric objects. For collections of rays; unit length line segments; and collections of unit squares to which we apply at most two transformations from translation, rotation, and scaling, we prove a complexity of Θ(n). If all three transformations are applied to unit squares, then we show the complexity becomes Θ(nα(n)), where α(n) is the slowly growing inverse of Ackermann’s function.
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6.
  • Anna, Brötzner, et al. (författare)
  • The k-Transmitter Watchman Route Problem is NP-Hard Even in Histograms and Star-Shaped Polygons
  • 2024
  • Ingår i: 40th European Workshop on Computational Geometry. ; , s. 381-387
  • Konferensbidrag (refereegranskat)abstract
    • A k-transmitter g in a polygon P, with n vertices, k-sees a point p ∈ P if the line segment gp intersects P’s boundary at most k times. In the k-Transmitter Watchman Route Problem we aim to minimize the length of a k-transmitter watchman route along which every point in the polygon—or a discrete set of points in the interior of the polygon—is k-seen. We show that the k-Transmitter Watchman Route Problem for a discrete set of points is NP-hard for histograms, uni-monotone polygons, and star-shaped polygons given a fixed starting point. For histograms and uni-monotone polygons it is also NP-hard without a fixed starting point. Moreover, none of these versions can be approximated to within a factor c · log n, for any constant c > 0.
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8.
  • Bagheri, Alireza, et al. (författare)
  • Minsum m watchmen’s routes in Stiegl polygons
  • 2023
  • Ingår i: XX Spanish Meeting on Computational Geometry. ; , s. 41-44
  • Konferensbidrag (refereegranskat)abstract
    • We present an O(n2 · min{m, n}) time and O(n · min{m, n}) storage algorithm to compute the minsum set of m watchmen routes given their starting points in a Stiegl polygon ― a staircase polygon where the floor solely consists of one horizontal and one vertical edge ― with n vertices.
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9.
  • Dieden, Anna, 1984-, et al. (författare)
  • Exploring biomarkers associated with deteriorating vascular health using a targeted proteomics chip : The SABPA study
  • 2021
  • Ingår i: Medicine. - : Lippincott Williams & Wilkins. - 0025-7974 .- 1536-5964. ; 100:20
  • Tidskriftsartikel (refereegranskat)abstract
    • ABSTRACT: In this observational study, by the use of a multiplex proteomic platform, we aimed to explore associations between 92 targeted proteins involved in cardiovascular disease and/or inflammation, and phenotypes of deteriorating vascular health, with regards to ethnicity.Proteomic profiling (92 proteins) was carried out in 362 participants from the Sympathetic activity and Ambulatory Blood Pressure in Africans (SABPA) study of black and white African school teachers (mean age 44.7 ± 9.9 years, 51.9% women, 44.5% Black Africans, 9.9% with known cardiovascular disease). Three proteins with <15% of samples below detectable limits were excluded from analyses. Associations between multiple proteins and prevalence of hypertension as well as vascular health [Carotid intima-media thickness (cIMT) and pulse wave velocity (PWV)] measures were explored using Bonferroni-corrected regression models.Bonferroni-corrected significant associations between 89 proteins and vascular health markers were further adjusted for clinically relevant co-variates. Hypertension was associated with growth differentiation factor 15 (GDF-15) and C-X-C motif chemokine 16 (CXCL16). cIMT was associated with carboxypeptidase A1 (CPA1), C-C motif chemokine 15 (CCL15), chitinase-3-like protein 1 (CHI3L1), scavenger receptor cysteine-rich type 1 protein M130 (CD163) and osteoprotegerin, whereas PWV was associated with GDF15, E-selectin, CPA1, fatty acid-binding protein 4 (FABP4), CXCL16, carboxypeptidase B (CPB1), and tissue-type plasminogen activator. Upon entering ethnicity into the models, the associations between PWV and CPA1, CPB1, GDF-15, FABP4, CXCL16, and between cIMT and CCL-15, remained significant.Using a multiplex proteomic approach, we linked phenotypes of vascular health with several proteins. Novel associations were found between hypertension, PWV or cIMT and proteins linked to inflammatory response, chemotaxis, coagulation or proteolysis. Further, we could reveal whether the associations were ethnicity-dependent or not.
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10.
  • El-Schich, Zahra, et al. (författare)
  • Interfacing antibody-based microarrays and digital holography enables label-free detection for loss of cell volume
  • 2015
  • Ingår i: Future Science OA. - : Future Science Group. - 2056-5623. ; 1:3
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: We introduce the combination of digital holographic microscopy (DHM) and antibody microarrays as a powerful tool to measure morphological changes in specifically antibody-captured cells. The aim of the study was to develop DHM for analysis of cell death of etoposide-treated suspension cells. Result/Methodology: We demonstrate that the cell number, mean area, thickness, and volume were non-invasively measured by using DHM. The cell number was stable over time, but the two cell lines showed changes of cell area and cell irregularity after treatment. The cell volume in etoposide-treated cells was decreased, whereas untreated cells showed stable volume. Conclusions: Our results provide proof of concept for using DHM combined with antibody-based microarray technology for detecting morphological changes in captured cells.
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