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Träfflista för sökning "WFRF:(Rubio C. Ignacio) "

Sökning: WFRF:(Rubio C. Ignacio)

  • Resultat 1-7 av 7
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2.
  • Hudson, Lawrence N, et al. (författare)
  • The database of the PREDICTS (Projecting Responses of Ecological Diversity In Changing Terrestrial Systems) project
  • 2017
  • Ingår i: Ecology and Evolution. - : John Wiley & Sons. - 2045-7758. ; 7:1, s. 145-188
  • Tidskriftsartikel (refereegranskat)abstract
    • The PREDICTS project-Projecting Responses of Ecological Diversity In Changing Terrestrial Systems (www.predicts.org.uk)-has collated from published studies a large, reasonably representative database of comparable samples of biodiversity from multiple sites that differ in the nature or intensity of human impacts relating to land use. We have used this evidence base to develop global and regional statistical models of how local biodiversity responds to these measures. We describe and make freely available this 2016 release of the database, containing more than 3.2 million records sampled at over 26,000 locations and representing over 47,000 species. We outline how the database can help in answering a range of questions in ecology and conservation biology. To our knowledge, this is the largest and most geographically and taxonomically representative database of spatial comparisons of biodiversity that has been collated to date; it will be useful to researchers and international efforts wishing to model and understand the global status of biodiversity.
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3.
  • Beal, Jacob, et al. (författare)
  • Robust estimation of bacterial cell count from optical density
  • 2020
  • Ingår i: Communications Biology. - : Springer Science and Business Media LLC. - 2399-3642. ; 3:1
  • Tidskriftsartikel (refereegranskat)abstract
    • Optical density (OD) is widely used to estimate the density of cells in liquid culture, but cannot be compared between instruments without a standardized calibration protocol and is challenging to relate to actual cell count. We address this with an interlaboratory study comparing three simple, low-cost, and highly accessible OD calibration protocols across 244 laboratories, applied to eight strains of constitutive GFP-expressing E. coli. Based on our results, we recommend calibrating OD to estimated cell count using serial dilution of silica microspheres, which produces highly precise calibration (95.5% of residuals <1.2-fold), is easily assessed for quality control, also assesses instrument effective linear range, and can be combined with fluorescence calibration to obtain units of Molecules of Equivalent Fluorescein (MEFL) per cell, allowing direct comparison and data fusion with flow cytometry measurements: in our study, fluorescence per cell measurements showed only a 1.07-fold mean difference between plate reader and flow cytometry data.
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4.
  • Cajander, Sara, 1980-, et al. (författare)
  • Profiling the dysregulated immune response in sepsis : overcoming challenges to achieve the goal of precision medicine
  • 2024
  • Ingår i: The Lancet Respiratory Medicine. - : Elsevier. - 2213-2600 .- 2213-2619. ; 12:4, s. 305-322
  • Forskningsöversikt (refereegranskat)abstract
    • Sepsis is characterised by a dysregulated host immune response to infection. Despite recognition of its significance, immune status monitoring is not implemented in clinical practice due in part to the current absence of direct therapeutic implications. Technological advances in immunological profiling could enhance our understanding of immune dysregulation and facilitate integration into clinical practice. In this Review, we provide an overview of the current state of immune profiling in sepsis, including its use, current challenges, and opportunities for progress. We highlight the important role of immunological biomarkers in facilitating predictive enrichment in current and future treatment scenarios. We propose that multiple immune and non-immune-related parameters, including clinical and microbiological data, be integrated into diagnostic and predictive combitypes, with the aid of machine learning and artificial intelligence techniques. These combitypes could form the basis of workable algorithms to guide clinical decisions that make precision medicine in sepsis a reality and improve patient outcomes.
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5.
  • Osuchowski, Marcin F., et al. (författare)
  • The COVID-19 puzzle : deciphering pathophysiology and phenotypes of a new disease entity
  • 2021
  • Ingår i: The Lancet Respiratory Medicine. - : Elsevier. - 2213-2600 .- 2213-2619. ; 9:6, s. 622-642
  • Forskningsöversikt (refereegranskat)abstract
    • The zoonotic SARS-CoV-2 virus that causes COVID-19 continues to spread worldwide, with devastating consequences. While the medical community has gained insight into the epidemiology of COVID-19, important questions remain about the clinical complexities and underlying mechanisms of disease phenotypes. Severe COVID-19 most commonly involves respiratory manifestations, although other systems are also affected, and acute disease is often followed by protracted complications. Such complex manifestations suggest that SARS-CoV-2 dysregulates the host response, triggering wide-ranging immuno-inflammatory, thrombotic, and parenchymal derangements. We review the intricacies of COVID-19 pathophysiology, its various phenotypes, and the anti-SARS-CoV-2 host response at the humoral and cellular levels. Some similarities exist between COVID-19 and respiratory failure of other origins, but evidence for many distinctive mechanistic features indicates that COVID-19 constitutes a new disease entity, with emerging data suggesting involvement of an endotheliopathy-centred pathophysiology. Further research, combining basic and clinical studies, is needed to advance understanding of pathophysiological mechanisms and to characterise immuno-inflammatory derangements across the range of phenotypes to enable optimum care for patients with COVID-19.
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6.
  • Winkler, Martin S., et al. (författare)
  • Bridging animal and clinical research during SARS-CoV-2 pandemic : A new-old challenge
  • 2021
  • Ingår i: EBioMedicine. - : Elsevier. - 2352-3964. ; 66
  • Forskningsöversikt (refereegranskat)abstract
    • Many milestones in medical history rest on animal modeling of human diseases. The SARS-CoV-2 pandemic has evoked a tremendous investigative effort primarily centered on clinical studies. However, several animal SARS-CoV-2/COVID-19 models have been developed and pre-clinical findings aimed at supporting clinical evidence rapidly emerge. In this review, we characterize the existing animal models exposing their relevance and limitations as well as outline their utility in COVID-19 drug and vaccine development. Concurrently, we summarize the status of clinical trial research and discuss the novel tactics utilized in the largest multi-center trials aiming to accelerate generation of reliable results that may subsequently shape COVID-19 clinical treatment practices. We also highlight areas of improvement for animal studies in order to elevate their translational utility. In pandemics, to optimize the use of strained resources in a short time-frame, optimizing and strengthening the synergy between the preclinical and clinical domains is pivotal.
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7.
  • Giritli Nygren, Katarina, 1971-, et al. (författare)
  • Thoughts about intersectionality and risk. Interviews with key scholar
  • 2024
  • Ingår i: Journal of Risk Research. - : Routledge. - 1366-9877 .- 1466-4461.
  • Tidskriftsartikel (refereegranskat)abstract
    • Since the early twenty first century, feminist and intersectional approaches to risk research have gained momentum, initially emerging from studies on HIV risks within health studies. Over the past decade, these approaches have expanded to other fields. As editors of this special issue, Katarina Giritli Nygren and Anna Olofsson introduce a reflection piece anchoring the issue. The reflection piece includes insights from seven influential scholars in the intersectionality, equality, and risk fields: Lisa Bowleg, Dean Curran, Kelly Hannah Moffat, Claudia Mitchell, Lori Peek, Ignacio Rubio C., and Jens O. Zinn. Each scholar offers personal reflections on the development of intersectional analyses in risk research, highlighting key areas for future research. Three themes emerged: challenging risk as a neutral concept, addressing the complexity of risks in everyday life, and navigating between social structures and identity struggles. Contributors argue for contextualising risk within broader societal structures, embracing complexity, and understanding the intertwined nature of inequalities. Some, but not all, also advocate for intersectionality as a critical concept for studies of systemic change and equality. Overall, the reflections underscore the importance of centring intersectionality in understanding the dimensions of inequality and risk. The piece concludes by calling for further conversations and reflections to deepen our understanding of risk mobilisations and their links to inequality, both locally and globally. Such conversations can challenge assumptions and revitalize risk research, envisioning alternative worlds that prioritize equality.
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