Institution
University of Sydney
Education•Sydney, New South Wales, Australia•
About: University of Sydney is a education organization based out in Sydney, New South Wales, Australia. It is known for research contribution in the topics: Population & Health care. The organization has 61532 authors who have published 187345 publications receiving 6114218 citations. The organization is also known as: Sydney University & USyd.
Papers published on a yearly basis
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King Juan Carlos University1, University of Sydney2, University of New South Wales3, University of Córdoba (Spain)4, Technical University of Madrid5, Pablo de Olavide University6, Nicolaus Copernicus University in Toruń7, Northern Arizona University8, Instituto Potosino de Investigación Científica y Tecnológica9, University of La Serena10, Central University of Venezuela11, University of Chile12, Ferdowsi University of Mashhad13, Ohio State University14, Northeast Normal University15, Agricultural Research Organization, Volcani Center16
TL;DR: It is suggested that changes in aridity, such as those predicted by climate-change models, may reduce microbial abundance and diversity, a response that will likely impact the provision of key ecosystem services by global drylands.
Abstract: Soil bacteria and fungi play key roles in the functioning of terrestrial ecosystems, yet our understanding of their responses to climate change lags significantly behind that of other organisms. This gap in our understanding is particularly true for drylands, which occupy ∼41% of Earth´s surface, because no global, systematic assessments of the joint diversity of soil bacteria and fungi have been conducted in these environments to date. Here we present results from a study conducted across 80 dryland sites from all continents, except Antarctica, to assess how changes in aridity affect the composition, abundance, and diversity of soil bacteria and fungi. The diversity and abundance of soil bacteria and fungi was reduced as aridity increased. These results were largely driven by the negative impacts of aridity on soil organic carbon content, which positively affected the abundance and diversity of both bacteria and fungi. Aridity promoted shifts in the composition of soil bacteria, with increases in the relative abundance of Chloroflexi and α-Proteobacteria and decreases in Acidobacteria and Verrucomicrobia. Contrary to what has been reported by previous continental and global-scale studies, soil pH was not a major driver of bacterial diversity, and fungal communities were dominated by Ascomycota. Our results fill a critical gap in our understanding of soil microbial communities in terrestrial ecosystems. They suggest that changes in aridity, such as those predicted by climate-change models, may reduce microbial abundance and diversity, a response that will likely impact the provision of key ecosystem services by global drylands.
641 citations
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TL;DR: Research synthesizing the current state of knowledge about physiological plasticity in ectotherms shows that freshwater and marine animals seem to have a greater capacity for acclimation than terrestrial ones.
Abstract: Acclimation, a form of physiological plasticity, is the capacity for organisms to physiologically adjust to temperature variation. Such changes can potentially reduce climate change impacts on animal populations. Research synthesizing the current state of knowledge about physiological plasticity in ectotherms shows that freshwater and marine animals seem to have a greater capacity for acclimation than terrestrial ones.
641 citations
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TL;DR: It is shown that the MaSC pool increases 14-fold during maximal progesterone levels at the luteal dioestrus phase of the mouse, demonstrating a key role for progester one in propelling this expansion.
Abstract: Reproductive history is the strongest risk factor for breast cancer after age, genetics and breast density. Increased breast cancer risk is entwined with a greater number of ovarian hormone-dependent reproductive cycles, yet the basis for this predisposition is unknown. Mammary stem cells (MaSCs) are located within a specialized niche in the basal epithelial compartment that is under local and systemic regulation. The emerging role of MaSCs in cancer initiation warrants the study of ovarian hormones in MaSC homeostasis. Here we show that the MaSC pool increases 14-fold during maximal progesterone levels at the luteal dioestrus phase of the mouse. Stem-cell-enriched CD49fhi cells amplify at dioestrus, or with exogenous progesterone, demonstrating a key role for progesterone in propelling this expansion. In aged mice, CD49fhi cells display stasis upon cessation of the reproductive cycle. Progesterone drives a series of events where luminal cells probably provide Wnt4 and RANKL signals to basal cells which in turn respond by upregulating their cognate receptors, transcriptional targets and cell cycle markers. Our findings uncover a dynamic role for progesterone in activating adult MaSCs within the mammary stem cell niche during the reproductive cycle, where MaSCs are putative targets for cell transformation events leading to breast cancer.
640 citations
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TL;DR: Examination of attention and executive function in a cross-section of 408 healthy persons across the adult life span shows that BMI was inversely related to performance on all cognitive tests and suggests that this relationship does not vary with age.
640 citations
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TL;DR: Post-infective fatigue syndrome is a valid illness model for investigating one pathophysiological pathway to chronic fatigue syndrome and persists in a significant minority of patients for six months or more after clinical infection with several different viral and non-viral micro-organisms.
Abstract: Objective To delineate the risk factors, symptom patterns, and longitudinal course of prolonged illnesses after a variety of acute infections.
Design Prospective cohort study following patients from the time of acute infection with Epstein-Barr virus (glandular fever), Coxiella burnetii (Q fever), or Ross River virus (epidemic polyarthritis).
Setting The region surrounding the township of Dubbo in rural Australia, encompassing a 200 km geographical radius and 104 400 residents.
Participants 253 patients enrolled and followed at regular intervals over 12 months by self report, structured interview, and clinical assessment.
Outcome measures Detailed medical, psychiatric, and laboratory evaluations at six months to apply diagnostic criteria for chronic fatigue syndrome. Premorbid and intercurrent illness characteristics recorded to define risk factors for chronic fatigue syndrome. Self reported illness phenotypes compared between infective groups.
Results Prolonged illness characterised by disabling fatigue, musculoskeletal pain, neurocognitive difficulties, and mood disturbance was evident in 29 (12%) of 253 participants at six months, of whom 28 (11%) met the diagnostic criteria for chronic fatigue syndrome. This post-infective fatigue syndrome phenotype was stereotyped and occurred at a similar incidence after each infection. The syndrome was predicted largely by the severity of the acute illness rather than by demographic, psychological, or microbiological factors.
Conclusions A relatively uniform post-infective fatigue syndrome persists in a significant minority of patients for six months or more after clinical infection with several different viral and non-viral micro-organisms. Post-infective fatigue syndrome is a valid illness model for investigating one pathophysiological pathway to chronic fatigue syndrome.
639 citations
Authors
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Name | H-index | Papers | Citations |
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Salim Yusuf | 231 | 1439 | 252912 |
David J. Hunter | 213 | 1836 | 207050 |
Rob Knight | 201 | 1061 | 253207 |
Eric B. Rimm | 196 | 988 | 147119 |
Michael Marmot | 193 | 1147 | 170338 |
Nicholas G. Martin | 192 | 1770 | 161952 |
Jing Wang | 184 | 4046 | 202769 |
David R. Williams | 178 | 2034 | 138789 |
Jasvinder A. Singh | 176 | 2382 | 223370 |
Rory Collins | 162 | 489 | 193407 |
David W. Johnson | 160 | 2714 | 140778 |
Tien Yin Wong | 160 | 1880 | 131830 |
Barbara E.K. Klein | 160 | 856 | 93319 |
Peter B. Reich | 159 | 790 | 110377 |
Nicholas J. Talley | 158 | 1571 | 90197 |