44 research outputs found
P2 7 What do stars do best? Shine!
In the film ’Stardust’, the magical realm of Stormhold encounters a fallen star in the form a human woman. In the final encounter against the evil witch, she does what stars do and shines as bright as she can to destroy said witch.By modeling the ‘starlight’ as surface power density (surface irradiance) equivalent to the sun at 6.41×10^7Wm−2, we determined a radiation pressure acting on the witch to be 1.48×10^−3Pa at a distance of 3 m. For a radiation pressure strong enough to destroy human skin, we calculated a surface irradiance of 1.17×10^18Wm−2
Monte Carlo Analysis of the SO(3) Lattice Gauge Theory and the Critical Dimensionality of Space-Time
Memory Limitations and Structural Forgetting: The Perception of Complex Ungrammatical Sentences as Grammatical
Changes to the Fossil Record of Insects through Fifteen Years of Discovery
The first and last occurrences of hexapod families in the fossil record are compiled from publications up to end-2009. The major features of these data are compared with those of previous datasets (1993 and 1994). About a third of families (>400) are new to the fossil record since 1994, over half of the earlier, existing families have experienced changes in their known stratigraphic range and only about ten percent have unchanged ranges. Despite these significant additions to knowledge, the broad pattern of described richness through time remains similar, with described richness increasing steadily through geological history and a shift in dominant taxa, from Palaeoptera and Polyneoptera to Paraneoptera and Holometabola, after the Palaeozoic. However, after detrending, described richness is not well correlated with the earlier datasets, indicating significant changes in shorter-term patterns. There is reduced Palaeozoic richness, peaking at a different time, and a less pronounced Permian decline. A pronounced Triassic peak and decline is shown, and the plateau from the mid Early Cretaceous to the end of the period remains, albeit at substantially higher richness compared to earlier datasets. Origination and extinction rates are broadly similar to before, with a broad decline in both through time but episodic peaks, including end-Permian turnover. Origination more consistently exceeds extinction compared to previous datasets and exceptions are mainly in the Palaeozoic. These changes suggest that some inferences about causal mechanisms in insect macroevolution are likely to differ as well
La prescription de méthylphénidate chez l’enfant et l’adolescent en France : caractéristiques et évolution entre 2010 et 2019
Review of Dotocryptus Brèthes (Hymenoptera, Ichneumonidae, Cryptinae), with a New Species from Colombia
BIOLOGY AND LIFE HISTORY OF LIMOTHRIPS CEBEAL1UM HALIDAY AND APTINOTHRIPS RUFUS GMELIN FEEDING ON GRAMINEAE
Paradoxical androgen receptor regulation by small molecule enantiomers
Small molecules that target the androgen receptor (AR) are the mainstay of therapy for lethal castration-resistant prostate cancer (CRPC), yet existing drugs lose their efficacy during continued treatment. This evolution of resistance is due to heterogenous mechanisms which include AR mutations causing the identical drug to activate instead of inhibit the receptor. Understanding in molecular detail the paradoxical phenomenon wherein an AR antagonist is transformed into an agonist by structural mutations in the target receptor is thus of paramount importance. Herein, we describe a reciprocal paradox: opposing antagonist and agonist AR regulation determined uniquely by enantiomeric forms of the same drug structure. The antiandrogen BMS-641988, which has (
R
)-chirality at C-5 encompasses a previously uncharacterized (
S
)-stereoisomer that is, surprisingly, a potent agonist of AR, as demonstrated by transcriptional assays supported by cell imaging studies. This duality was reproduced in a series of novel compounds derived from the BMS-641988 scaffold. Coupled with in silico modeling studies, the results inform an AR model that explains the switch from potent antagonist to high-affinity agonist in terms of C-5 substituent steric interactions with helix 12 of the ligand binding site. They imply strategies to overcome AR drug resistance and demonstrate that insufficient enantiopurity in this class of AR antagonist can confound efforts to correlate structure with function.
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