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Träfflista för sökning "WFRF:(Marten Lutz) "

Sökning: WFRF:(Marten Lutz)

  • Resultat 1-8 av 8
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1.
  • Bartholomay, S., et al. (författare)
  • Cross-talk compensation for blade root flap-and edgewise moments on an experimental research wind turbine and comparison to numerical results
  • 2018
  • Ingår i: Proceedings of the ASME Turbo Expo. - : ASME Press. - 9780791851180
  • Konferensbidrag (refereegranskat)abstract
    • In the current paper a method to correct cross-talk effects for strain-gauge measurements is presented. Themethod is demonstrated on an experimental horizontal axiswind turbine. The procedure takes cross-moments (flapwise on edgewise moments and vice versa) as well as axialacceleration into account. The results from the experimental setup are compared to numerical URANS calculationsand the medium-fidelity code Qblade for a baseline caseand two yawed inflow situations.
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2.
  • Downing, Laura J., 1954, et al. (författare)
  • Clausal morphosyntax and information structure
  • 2019
  • Ingår i: The Bantu Languages / edited by Mark Van de Velde, Koen Bostoen, Derek Nurse, and Gérard Philippson. - New York : Routledge. - 9781138799677 ; , s. 270-307
  • Bokkapitel (refereegranskat)abstract
    • This chapter surveys the following main themes in Bantu clausal morphosyntax: word order, agreement in the phrase and the clause, valency-changing morphosyntax, non-verbal predication, complex clause structure and dependent clauses, and the phonology-syntax interface.
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3.
  • Holmes, Michael V., et al. (författare)
  • Secretory Phospholipase A(2)-IIA and Cardiovascular Disease
  • 2013
  • Ingår i: Journal of the American College of Cardiology. - : Elsevier. - 0735-1097 .- 1558-3597. ; 62:21, s. 1966-1976
  • Tidskriftsartikel (refereegranskat)abstract
    • Objectives This study sought to investigate the role of secretory phospholipase A(2) (sPLA(2))-IIA in cardiovascular disease. less thanbrgreater than less thanbrgreater thanBackground Higher circulating levels of sPLA(2)-IIA mass or sPLA(2) enzyme activity have been associated with increased risk of cardiovascular events. However, it is not clear if this association is causal. A recent phase III clinical trial of an sPLA(2) inhibitor (varespladib) was stopped prematurely for lack of efficacy. less thanbrgreater than less thanbrgreater thanMethods We conducted a Mendelian randomization meta-analysis of 19 general population studies (8,021 incident, 7,513 prevalent major vascular events [MVE] in 74,683 individuals) and 10 acute coronary syndrome (ACS) cohorts (2,520 recurrent MVE in 18,355 individuals) using rs11573156, a variant in PLA2G2A encoding the sPLA(2)-IIA isoenzyme, as an instrumental variable. less thanbrgreater than less thanbrgreater thanResults PLA2G2A rs11573156 C allele associated with lower circulating sPLA(2)-IIA mass (38% to 44%) and sPLA(2) enzyme activity (3% to 23%) per C allele. The odds ratio (OR) for MVE per rs11573156 C allele was 1.02 (95% confidence interval [CI]: 0.98 to 1.06) in general populations and 0.96 (95% CI: 0.90 to 1.03) in ACS cohorts. In the general population studies, the OR derived from the genetic instrumental variable analysis for MVE for a 1-log unit lower sPLA(2)-IIA mass was 1.04 (95% CI: 0.96 to 1.13), and differed from the non-genetic observational estimate (OR: 0.69; 95% CI: 0.61 to 0.79). In the ACS cohorts, both the genetic instrumental variable and observational ORs showed a null association with MVE. Instrumental variable analysis failed to show associations between sPLA2 enzyme activity and MVE. less thanbrgreater than less thanbrgreater thanConclusions Reducing sPLA(2)-IIA mass is unlikely to be a useful therapeutic goal for preventing cardiovascular events.
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4.
  • Jung, Christian, et al. (författare)
  • A comparison of very old patients admitted to intensive care unit after acute versus elective surgery or intervention
  • 2019
  • Ingår i: Journal of critical care. - : W B SAUNDERS CO-ELSEVIER INC. - 0883-9441 .- 1557-8615. ; 52, s. 141-148
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: We aimed to evaluate differences in outcome between patients admitted to intensive care unit (ICU) after elective versus acute surgery in a multinational cohort of very old patients (80 years; VIP). Predictors of mortality, with special emphasis on frailty, were assessed.Methods: In total, 5063 VIPs were induded in this analysis, 922 were admitted after elective surgery or intervention, 4141 acutely, with 402 after acute surgery. Differences were calculated using Mann-Whitney-U test and Wilcoxon test. Univariate and multivariable logistic regression were used to assess associations with mortality.Results: Compared patients admitted after acute surgery, patients admitted after elective surgery suffered less often from frailty as defined as CFS (28% vs 46%; p < 0.001), evidenced lower SOFA scores (4 +/- 5 vs 7 +/- 7; p < 0.001). Presence of frailty (CFS >4) was associated with significantly increased mortality both in elective surgery patients (7% vs 12%; p = 0.01), in acute surgery (7% vs 12%; p = 0.02).Conclusions: VIPs admitted to ICU after elective surgery evidenced favorable outcome over patients after acute surgery even after correction for relevant confounders. Frailty might be used to guide clinicians in risk stratification in both patients admitted after elective and acute surgery. 
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7.
  • Marten, Lutz, et al. (författare)
  • Linguistic variation and the dynamics of language documentation: Editing in ‘pure’ Kagulu
  • 2016
  • Ingår i: Language Documentation & Conservation. - 1934-5275. ; 10, s. 105-129
  • Tidskriftsartikel (refereegranskat)abstract
    • The Tanzanian ethnic community language Kagulu is in extended language contact with the national language Swahili and other neighbouring community languages. The effects of contact are seen in vocabulary and structure, leading to a high degree of linguistic variation and to the development of distinct varieties of ‘pure’ and ‘mixed’ Kagulu. A comprehensive documentation of the language needs to take this variation into account and to provide a description of the different varieties and their interaction. The paper illustrates this point by charting the development of a specific text within a language documentation project. A comparison of three versions of the text – a recorded oral story, a transcribed version of it and a further, edited version in which features of pure Kagulu are edited in – shows the dynamics of how the different versions of the text interact and provides a detailed picture of linguistic variation and of speakers’ use and exploitation of it. We show that all versions of the text are valid, ‘authentic’ representations of their own linguistic reality, and how all three of them, and the processes of their genesis, are an integral part of a comprehensive documentation of Kagulu and its linguistic ecology.
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8.
  • Sakornsakolpat, Phuwanat, et al. (författare)
  • Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations
  • 2019
  • Ingår i: Nature Genetics. - : Springer Science and Business Media LLC. - 1061-4036 .- 1546-1718. ; 51:3, s. 494-505
  • Tidskriftsartikel (refereegranskat)abstract
    • Chronic obstructive pulmonary disease (COPD) is the leading cause of respiratory mortality worldwide. Genetic risk loci provide new insights into disease pathogenesis. We performed a genome-wide association study in 35,735 cases and 222,076 controls from the UK Biobank and additional studies from the International COPD Genetics Consortium. We identified 82 loci associated with P < 5 x 10-8; 47 of these were previously described in association with either COPD or population-based measures of lung function. Of the remaining 35 new loci, 13 were associated with lung function in 79,055 individuals from the SpiroMeta consortium. Using gene expression and regulation data, we identified functional enrichment of COPD risk loci in lung tissue, smooth muscle, and several lung cell types. We found 14 COPD loci shared with either asthma or pulmonary fibrosis. COPD genetic risk loci clustered into groups based on associations with quantitative imaging features and comorbidities. Our analyses provide further support for the genetic susceptibility and heterogeneity of COPD.
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