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Institution

University of Patras

EducationPátrai, Greece
About: University of Patras is a education organization based out in Pátrai, Greece. It is known for research contribution in the topics: Population & Catalysis. The organization has 13372 authors who have published 31263 publications receiving 677159 citations. The organization is also known as: Panepistímio Patrón.


Papers
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Journal ArticleDOI
TL;DR: The time-expanded approach turns out to be more robust for modeling more complex scenarios, whereas the time-dependent approach shows a clearly better performance.
Abstract: We consider two approaches that model timetable information in public transportation systems as shortest-path problems in weighted graphs. In the time-expanded approach, every event at a station, e.g., the departure of a train, is modeled as a node in the graph, while in the time-dependent approach the graph contains only one node per station. Both approaches have been recently considered for (a simplified version of) the earliest arrival problem, but little is known about their relative performance. Thus far, there are only theoretical arguments in favor of the time-dependent approach. In this paper, we provide the first extensive experimental comparison of the two approaches. Using several real-world data sets, we evaluate the performance of the basic models and of several new extensions towards realistic modeling. Furthermore, new insights on solving bicriteria optimization problems in both models are presented. The time-expanded approach turns out to be more robust for modeling more complex scenarios, whereas the time-dependent approach shows a clearly better performance.

232 citations

Journal ArticleDOI
TL;DR: It may be concluded that P. fruticosa leaves avoid severe photoinhibitory and oxidative damage during the long, warm, dry and sunny Mediterranean summer by reducing light harvesting and electron flow capacity, whilst maintaining an adequate photoprotective ability.
Abstract: Photosynthetic pigments and relative water content of young leaves of P. fruticosa decreased considerably with the onset of the summer dry period and stabilized at low values for the last two summer months, while leaf growth was arrested. Corresponding decreases in photochemical efficiency of photosystem II, as judged by chlorophyll fluorescence measurements of predarkened leaves, were, however, negligible. Following the first autumn heavy rains, growth was restored and photosynthetic pigments and relative water content increased to the pre-drought values. The results indicate that the reduction of chlorophylls does not result from severe photoinhibitory damage but, instead, it may be an adaptive response against the adverse conditions of the Mediterranean summer. Some photosynthetic and photoprotective characteristics of P. fruticosa leaves at two stages of their development, i.e. at the severely dehydrated state with arrested growth during late summer and after their revival following the first heavy autumn rains were compared. Apart from the chlorophyll loss, the photon yield of O 2 evolution and the photosynthetic capacity at saturated CO 2 were considerably suppressed during the summer, indicating that the extremely low net photosynthetic rates observed in the field were the combined result of stomatal and mesophyll limitations. Epoxidation state was low at midday during the summer, indicating an active, photodissipative xanthophyll cycle. Although zeaxanthin content did not increase at midday after the rains, the potential of the cycle was maintained in the revived leaves, as judged by the high concentrations of the cycle components. After the rains, the activities of the anti-oxidant enzymes (superoxide dismutase, ascorbate peroxidase) remained relatively unchanged on a chlorophyll basis, but increased when expressed on a leaf surface area or protein basis. It may be concluded that P. fruticosa leaves avoid severe photoinhibitory and oxidative damage during the long, warm, dry and sunny Mediterranean summer by reducing light harvesting and electron flow capacity, whilst maintaining an adequate photoprotective ability. The preservation of a remarkable photodissipative and anti-oxidative potential after the rains may be related to the low predictability of precipitation even during the rainy winter.

231 citations

Journal ArticleDOI
TL;DR: An interdisciplinary summary of the current body of knowledge on autumn colours is provided, and unresolved issues and future avenues of research are discussed that might help reveal the evolutionary meaning of this spectacle of nature.
Abstract: Leaf colour change is commonly observed in temperate deciduous forests in autumn. This is not simply a side effect of leaf senescence, and, in the past decade, several hypotheses have emerged to explain the evolution of autumn colours. Yet a lack of crosstalk between plant physiologists and evolutionary ecologists has resulted in slow progress, and so the adaptive value of this colour change remains a mystery. Here we provide an interdisciplinary summary of the current body of knowledge on autumn colours, and discuss unresolved issues and future avenues of research that might help reveal the evolutionary meaning of this spectacle of nature.

231 citations

Journal ArticleDOI
TL;DR: A recent published breakthrough introduced a new chemical platform for synthesis and discovery of a wide range of diverse macrolides, leading to a macrolide renaissance, increasing the hope for novel and safe therapeutic agents to combat serious human infectious diseases.
Abstract: Macrolides represent a large family of protein synthesis inhibitors of great clinical interest due to their applicability to human medicine. Macrolides are composed of a macrocyclic lactone of different ring sizes, to which one or more deoxy-sugar or amino sugar residues are attached. Macrolides act as antibiotics by binding to bacterial 50S ribosomal subunit and interfering with protein synthesis. The high affinity of macrolides for bacterial ribosomes, together with the highly conserved structure of ribosomes across virtually all of the bacterial species, is consistent with their broad-spectrum activity. Since the discovery of the progenitor macrolide, erythromycin, in 1950, many derivatives have been synthesised, leading to compounds with better bioavailability and acid stability and improved pharmacokinetics. These efforts led to the second generation of macrolides, including well-known members such as azithromycin and clarithromycin. Subsequently, in order to address increasing antibiotic resistance, a third generation of macrolides displaying improved activity against many macrolide resistant strains was developed. However, these improvements were accompanied with serious side effects, leading to disappointment and causing many researchers to stop working on macrolide derivatives, assuming that this procedure had reached the end. In contrast, a recent published breakthrough introduced a new chemical platform for synthesis and discovery of a wide range of diverse macrolide antibiotics. This chemical synthesis revolution, in combination with reduction in the side effects, namely, 'Ketek effects', has led to a macrolide renaissance, increasing the hope for novel and safe therapeutic agents to combat serious human infectious diseases.

231 citations

Journal ArticleDOI
TL;DR: It is concluded that Ang-2 by itself stimulates the extravasation of cell-poor fluid, but in the presence of ongoing inflammation it reduces cellular infiltration in tissues.
Abstract: Angiopoietins (Angs) are endothelium-selective ligands that exert most of their actions through the Tie-2 receptor. It is widely accepted that Ang-1 promotes the structural integrity of blood vessels and exhibits anti-inflammatory properties. In contrast, the role of Ang-2 remains less clear because it has been shown to behave as a Tie-2 agonist or antagonist under different experimental conditions. To define the role of Ang-2 in acute inflammation, we studied the effects of recombinant Ang-2 administration in vivo. We show herein that Ang-2, but not Ang-1, induces edema formation in the mouse paw in a dose-dependent manner; the edema seems to be fast-peaking (maximum at 30 min) and resolves within 4 h. The effect of Ang-2 is blocked by the coadministration with a soluble form of the Tie-2 receptor or Ang-1. NO and prostaglandin E 2 levels in mouse paw following the injection of Ang-2 remained unaltered, suggesting that the action of Ang-2 does not involve these mediators. In addition, Ang-2 exerted a weak stimulatory effect on leukocyte migration in the mouse paw. Similarly, Ang-2 injected into the mouse air pouch produced only a modest effect on cell extravasation that peaked at 30 min. However, when cell migration was elicited using zymosan, Ang-2 significantly inhibited leukocyte migration. We conclude that Ang-2 by itself stimulates the extravasation of cell-poor fluid, but in the presence of ongoing inflammation it reduces cellular infiltration in tissues.

231 citations


Authors

Showing all 13529 results

NameH-indexPapersCitations
Thomas J. Meyer120107868519
Thoralf M. Sundt11275555708
Chihaya Adachi11290861403
Eleftherios P. Diamandis110106452654
Roland Siegwart105115451473
T. Geralis9980852221
Spyros N. Pandis9737751660
Michael Tsapatsis7737520051
George K. Karagiannidis7665324066
Eleftherios Mylonakis7544821413
Matthias Mörgelin7533218711
Constantinos C. Stoumpos7519427991
Raymond Alexanian7521121923
Mark J. Ablowitz7437427715
John Lygeros7366721508
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202395
2022250
20211,738
20201,672
20191,469
20181,443