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Institution

Jagiellonian University

EducationKrakow, Poland
About: Jagiellonian University is a education organization based out in Krakow, Poland. It is known for research contribution in the topics: Population & Catalysis. The organization has 17438 authors who have published 44092 publications receiving 862633 citations. The organization is also known as: Academia Cracoviensis & Akademia Krakowska.


Papers
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Journal ArticleDOI
TL;DR: Gingipains seem to be key players in subverting host defense systems with, significantly, the complement and neutrophils being the main target and a strong effect on mechanisms controlling host matrix metalloproteinase activity at the level of gene expression and zymogen activation.
Abstract: Recently accumulated large bodies of evidence have strongly implicated proteolytic enzymes released by subgingival plaque bacteria in the pathogenicity of periodontal disease. With regard to proteolytic power, however, the contribution from different microbial species considered as periodontal pathogens is not equal. Two of these bacteria, P. gingivalis and T. denticola, have developed an elaborate proteolytic systems composed of several surface-located or secreted enzymes, which apparently serve a role to provide bacteria with nutrients in the form of small peptides and amino acids. Of these two species, proteinases of P. gingivalis are the most intensively studied, and during the last decade an impressive array of information has been accumulated with respect to the biochemical characterization of purified proteinases and structure of the genes encoding them, the regulation of expression and the effects of these enzymes on host systems. In addition, studies on proteinase-deficient isogenic mutants has shed light on both their housekeeping functions and potential role(s) in the pathogenicity of periodontitis. Among several proteinases produced by P. gingivalis, the cysteine proteinases, referred to as gingipains, are clearly in the spotlight. They are the subject of several recent reviews and generally considered as the major virulence factors of this periodontal pathogen (59, 105, 139, 182, 183, 186, 281, 284, 286, 289). Gingipains seem to be key players in subverting host defense systems with, significantly, the complement and neutrophils being the main target. In addition, through uncontrolled activation of kallikrein/kinin pathway and coagulation cascade they contribute to local generation of bradykinin and thrombin, two synergistically working pro-inflammatory reagents with a strongly, although indirectly, stimulatory effect on bone resorption. Furthermore, the ability to interact with the cytokine networking systems has the potential to dysregulate the local inflammatory reaction. Finally, gingipains have a strong effect on mechanisms controlling host matrix metalloproteinase activity at the level of gene expression and zymogen activation (Fig. 10). Collectively, at the periodontal lesion site, the non-restrained action of gingipains, supported by other proteinases locally produced by subgingival plaque bacteria, would dysregulate most mechanisms controlling inflammatory reaction. Although successful in limiting infection to the periodontium, the ultimate effect of uncontrolled inflammatory processes would be the destruction of periodontal connective tissue, certainly the hallmark of periodontitis.

359 citations

Journal ArticleDOI
Markus Ackermann1, Marco Ajello1, W. B. Atwood2, Luca Baldini  +205 moreInstitutions (31)
TL;DR: In this paper, the results of analysis of cosmic-ray electrons using about 8 x 10(6) electron candidates detected in the first 12 months on-orbit by the Fermi Large Area Telescope were presented.
Abstract: We present the results of our analysis of cosmic-ray electrons using about 8 x 10(6) electron candidates detected in the first 12 months on-orbit by the Fermi Large Area Telescope. This work extend ...

359 citations

Journal ArticleDOI
TL;DR: Inhibition of HO-1 can be suggested as a potential therapeutic approach sensitizing tumors to radiation, chemotherapy, or photodynamic therapy, as well as an enzyme facilitating tumor progression.
Abstract: Heme oxygenase-1 (HO-1) catalyzes the oxidation of heme to biologically active products: carbon monoxide (CO), biliverdin, and ferrous iron. It participates in maintaining cellular homeostasis and plays an important protective role in the tissues by reducing oxidative injury, attenuating the inflammatory response, inhibiting cell apoptosis, and regulating cell proliferation. HO-1 is also an important proangiogenic mediator. Most studies have focused on the role of HO-1 in cardiovascular diseases, in which its significant, beneficial activity is well recognized. A growing body of evidence indicates, however, that HO-1 activation may play a role in carcinogenesis and can potently influence the growth and metastasis of tumors. HO-1 is very often upregulated in tumor tissues, and its expression is further increased in response to therapies. Although the exact effect can be tissue specific, HO-1 can be regarded as an enzyme facilitating tumor progression. Accordingly, inhibition of HO-1 can be suggested as a p...

359 citations

Journal ArticleDOI
Céline Bellenguez1, Steve Bevan2, Andreas Gschwendtner3, Spencer Cca.1, Annette I. Burgess1, Matti Pirinen1, Caroline A. Jackson4, Matthew Traylor2, Amy Strange1, Zhan Su1, P D Syme5, Rainer Malik3, Joanna Pera6, N. Bo7, Robin Lemmens8, Robin Lemmens9, Colin Freeman1, R. Schanz10, T James2, D Poole1, Lee Murphy4, Helen Segal1, L Cortellini11, Cheng Y-C.12, Daniel Woo13, Mike A. Nalls14, Bertram Müller-Myhsok15, Christa Meisinger, Udo Seedorf16, Helen Ross-Adams6, Steven Boonen8, D. Wloch-Kopec6, V Valant11, Julia Slark10, Karen L. Furie17, Hossein Delavaran7, Cordelia Langford18, Panos Deloukas18, Sarah Edkins18, Sarah E. Hunt18, Emma Gray18, Serge Dronov18, Leena Peltonen18, Solveig Gretarsdottir19, Gudmar Thorleifsson19, Unnur Thorsteinsdottir19, Unnur Thorsteinsdottir20, Kari Stefansson20, Kari Stefansson19, Giorgio B. Boncoraglio, Eugenio Parati, John Attia21, Elizabeth G. Holliday21, Christopher R Levi21, Franzosi M-G., Anuj Goel1, Anna Helgadottir1, Anna Helgadottir19, Jenefer M. Blackwell22, Jenefer M. Blackwell23, Elvira Bramon24, Matthew A. Brown25, Juan P. Casas26, Juan P. Casas27, Aiden Corvin28, Audrey Duncanson29, Janusz Jankowski1, Janusz Jankowski30, Christopher G. Mathew24, Palmer Cna.31, Robert Plomin24, Anna Rautanen1, Stephen Sawcer23, Richard C. Trembath24, Ananth C. Viswanathan32, Nicholas W. Wood27, B. B. Worrall33, Steven J. Kittner12, Steven J. Kittner34, Braxton D. Mitchell12, Brett M. Kissela13, James F. Meschia35, Vincent Thijs9, Vincent Thijs8, Arne Lindgren7, Mary Joan MacLeod5, Agnieszka Slowik6, Matthew Walters36, Jonathan Rosand11, Jonathan Rosand17, Pankaj Sharma10, Martin Farrall1, Sudlow Clm.4, Peter M. Rothwell1, Martin Dichgans3, Peter Donnelly1, Hugh S. Markus2 
TL;DR: A new association for large vessel stroke within HDAC9 (encoding histone deacetylase 9) on chromosome 7p21.1 is identified, which suggests distinct genetic architectures for different stroke subtypes.
Abstract: Genetic factors have been implicated in stroke risk, but few replicated associations have been reported. We conducted a genome-wide association study (GWAS) for ischemic stroke and its subtypes in 3,548 affected individuals and 5,972 controls, all of European ancestry. Replication of potential signals was performed in 5,859 affected individuals and 6,281 controls. We replicated previous associations for cardioembolic stroke near PITX2 and ZFHX3 and for large vessel stroke at a 9p21 locus. We identified a new association for large vessel stroke within HDAC9 (encoding histone deacetylase 9) on chromosome 7p21.1 (including further replication in an additional 735 affected individuals and 28,583 controls) (rs11984041; combined P = 1.87 × 10(-11); odds ratio (OR) = 1.42, 95% confidence interval (CI) = 1.28-1.57). All four loci exhibited evidence for heterogeneity of effect across the stroke subtypes, with some and possibly all affecting risk for only one subtype. This suggests distinct genetic architectures for different stroke subtypes.

358 citations

Journal ArticleDOI
Morad Aaboud1, Georges Aad2, Brad Abbott3, Ovsat Abdinov4  +2954 moreInstitutions (225)
TL;DR: In this paper, a search for new phenomena in final states with an energetic jet and large missing transverse momentum is reported, and the results are translated into exclusion limits in models with pair-produced weakly interacting dark-matter candidates, large extra spatial dimensions, and supersymmetric particles in several compressed scenarios.
Abstract: Results of a search for new phenomena in final states with an energetic jet and large missing transverse momentum are reported. The search uses proton-proton collision data corresponding to an integrated luminosity of 36.1 fb−1 at a centre-of-mass energy of 13 TeV collected in 2015 and 2016 with the ATLAS detector at the Large Hadron Collider. Events are required to have at least one jet with a transverse momentum above 250 GeV and no leptons (e or μ). Several signal regions are considered with increasing requirements on the missing transverse momentum above 250 GeV. Good agreement is observed between the number of events in data and Standard Model predictions. The results are translated into exclusion limits in models with pair-produced weakly interacting dark-matter candidates, large extra spatial dimensions, and supersymmetric particles in several compressed scenarios.

358 citations


Authors

Showing all 17729 results

NameH-indexPapersCitations
Roxana Mehran141137899398
Brad Abbott137156698604
M. Morii1341664102074
M. Franklin134158195304
John Huth131108785341
Wladyslaw Dabrowski12999079728
Rostislav Konoplich12881173790
Michel Vetterli12890176064
Francois Corriveau128102275729
Christoph Falk Anders12673468828
Tomasz Bulik12169886211
Elzbieta Richter-Was11879369127
S. H. Robertson116131158582
S. J. Chen116155962804
David M. Stern10727147461
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023162
2022510
20212,769
20202,777
20192,736
20182,735