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Institution

Queensland University of Technology

EducationBrisbane, Queensland, Australia
About: Queensland University of Technology is a education organization based out in Brisbane, Queensland, Australia. It is known for research contribution in the topics: Population & Poison control. The organization has 14188 authors who have published 55022 publications receiving 1496237 citations. The organization is also known as: QUT.


Papers
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Journal ArticleDOI
TL;DR: In this paper, the authors identify the main factors driving or hindering construction innovation and explore the relationships between innovation influences and other aspects of business strategy and environment, in the context of broader societal considerations.
Abstract: The goal of this paper is to identify the main factors driving or hindering construction innovation. An analysis of the relevant literature indicates there are six primary influences: (i) clients and manufacturers; (ii) the structure of production; (iii) relationships between individuals and firms within the industry and between the industry and external parties; (iv) procurement systems; (v) regulations/standards; and (vi) the nature and quality of organisational resources. Attention to these factors by businesses and public-policy makers would be a key component of effective innovation strategy and policy. Further research is needed, however, to explore the relationships between innovation influences; and between innovation influences and other aspects of business strategy and environment, in the context of broader societal considerations. Further research should also identify quantitative estimates of the impact of innovation on the construction industry.

549 citations

Journal ArticleDOI
TL;DR: This paper showed that tumor cells without mitochondrial DNA (mtDNA) showed delayed tumor growth, and that tumor formation is associated with acquisition of mtDNA from host cells, leading to partial recovery of mitochondrial function in cells derived from primary tumors grown from cells without mtDNA and a shorter lag in tumor growth.

548 citations

01 Jan 2013
TL;DR: It is demonstrated that it is possible to develop multifunctional scaffolds by combining enhanced angiogenesis potential, osteostimulation, and antibacterial properties for the treatment of large bone defects.
Abstract: It is of great importance to develop multifunctional bioactive scaffolds, which combine angiogenesis capacity, osteostimulation, and antibacterial properties for regenerating lost bone tissues. In order to achieve this aim, we prepared copper (Cu)-containing mesoporous bioactive glass (Cu-MBG) scaffolds with interconnective large pores (several hundred micrometer) and well-ordered mesopore channels (around 5 nm). Both Cu-MBG scaffolds and their ionic extracts could stimulate hypoxia-inducible factor (HIF)-1a and vascular endothelial growth factor(VEGF) expression in human bone marrow stromal cells(hBMSCs). In addition, both Cu-MBG scaffolds and their ionic extracts significantly promoted the osteogenic differentiation of hBMSCs by improving their bone-related gene expression (alkaline phosphatase (ALP), osteopontin(OPN) and osteocalcin (OCN)). Furthermore, Cu-MBG scaffolds could maintain a sustained release of ibuprofen and significantly inhibited the viability of bacteria. This study indicates that the incorporation of Cu2þ ions into MBG scaffolds significantly enhances hypoxia-like tissue reaction leading to the coupling of angiogenesis and osteogenesis. Cu2þ ions play an important role to offer the multifunctional properties of MBG scaffold system. This study has demonstrated that it is possible to develop multifunctional scaffolds by combining enhanced angiogenesis potential, osteostimulation, and antibacterial properties for the treatment of large bone defects.

545 citations

Journal ArticleDOI
TL;DR: A novel approach to estimate the viral Load emitted by a contagious subject on the basis of the viral load in the mouth, the type of respiratory activity, respiratory physiological parameters, and activity level is proposed and shows that high quanta emission rates can be reached by an asymptomatic infectious SARS-CoV-2 subject performing vocalization during light activities.

541 citations

Journal ArticleDOI
TL;DR: The Bactrocera dorsalis complex of tropical fruit flies contains 75 described species, largely endemic to Southeast Asia, and development of a phylogeny of the group is considered a high priority to provide a framework for future evolutionary and ecological studies.
Abstract: The Bactrocera dorsalis complex of tropical fruit flies (Diptera: Tephritidae: Dacinae) contains 75 described species, largely endemic to Southeast Asia. Within the complex are a small number of polyphagous pests of international significance, including B. dorsalis sensu stricto, B. papayae, B. carambolae, and B. philippinensis. Most species within the complex were described in 1994 and since then substantial research has been undertaken in developing morphological and molecular diagnostic techniques for their recognition. Such techniques can now resolve most taxa adequately. Genetic evidence suggests that the complex has evolved in only the last few million years, and development of a phylogeny of the group is considered a high priority to provide a framework for future evolutionary and ecological studies. As model systems, mating studies on B. dorsalis s.s. and B. cacuminata have substantially advanced our understanding of insect use of plant-derived chemicals for mating, but such studies have not been applied to help resolve the limits of biological species within the complex. Although they are commonly regarded as major pests, there is little published evidence documenting economic losses caused by flies of the B. dorsalis complex. Quantification of economic losses caused by B. dorsalis complex species is urgently needed to prioritize research for quarantine and management. Although they have been documented as invaders, relatively little work has been done on the invasion biology of the complex and this is an area warranting further work.

541 citations


Authors

Showing all 14597 results

NameH-indexPapersCitations
Nicholas G. Martin1921770161952
Paul M. Thompson1832271146736
Christopher J. O'Donnell159869126278
Robert G. Parton13645959737
Tim J Cole13682792998
Daniel I. Chasman13448472180
David Smith1292184100917
Dmitri Golberg129102461788
Chao Zhang127311984711
Shi Xue Dou122202874031
Thomas H. Marwick121106358763
Peter J. Anderson12096663635
Bruno S. Frey11990065368
David M. Evans11663274420
Michael Pollak11466357793
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023205
2022641
20214,218
20204,026
20193,623
20183,374