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Ayanthi A. Richards

Researcher at University of Queensland

Publications -  16
Citations -  1999

Ayanthi A. Richards is an academic researcher from University of Queensland. The author has contributed to research in topics: Adiponectin & Adipokine. The author has an hindex of 14, co-authored 16 publications receiving 1913 citations. Previous affiliations of Ayanthi A. Richards include Princess Alexandra Hospital.

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Lipid rafts and caveolae as portals for endocytosis: new insights and common mechanisms.

TL;DR: This review examines the current evidence for the involvement of rafts and caveolae in endocytosis and the molecular players involved in their regulation.
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Adiponectin--a key adipokine in the metabolic syndrome.

TL;DR: Given the low levels of adiponectin in subjects with the metabolic syndrome, and the beneficial effect of the adipokine in animal studies, there is exciting potential for adiponECTin replacement therapy in insulin resistance and related disorders.
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Adiponectin Multimerization Is Dependent on Conserved Lysines in the Collagenous Domain: Evidence for Regulation of Multimerization by Alterations in Posttranslational Modifications

TL;DR: Gl glucose-induced increases in HMW multimer production from human adipose explants correlated with changes in the two-dimensional electrophoresis profile of adiponectin isoforms, suggesting that adiponECTin multimer composition is affected by changes in PTM in response to physiological factors.
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Acute lipopolysaccharide priming boosts inflammasome activation independently of inflammasome sensor induction.

TL;DR: It is demonstrated that rapid LPS priming ofNLRP3 inflammasome activation can occur independently of NLRP3 induction, since the priming effect of LPS is still apparent at short pre-treatment times in which NLRP2 protein expression remains unchanged.
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Inhibitors of COP-mediated Transport and Cholera Toxin Action Inhibit Simian Virus 40 Infection

TL;DR: It is shown that SV40 requires COPI- and COPII-dependent transport steps for successful infection and a potent inhibition of SV40 infection by the dipeptide N-benzoyl-oxycarbonyl-Gly-Phe-amide, which also inhibits late events in cholera toxin action is demonstrated.