84 research outputs found
Landau-Zener transitions in a linear chain
We present an exact asymptotic solution for electron transition amplitudes in
an infinite linear chain driven by an external homogeneous time-dependent
electric field. This solution extends the Landau-Zener theory for the case of
infinite number of states in discrete spectrum. In addition to transition
amplitudes we calculate an effective diffusion constant.Comment: 3 figure
Active Amplification of the Terrestrial Albedo to Mitigate Climate Change: An Exploratory Study
This study explores the potential to enhance the reflectance of solar
insolation by the human settlement and grassland components of the Earth's
terrestrial surface as a climate change mitigation measure. Preliminary
estimates derived using a static radiative transfer model indicate that such
efforts could amplify the planetary albedo enough to offset the current global
annual average level of radiative forcing caused by anthropogenic greenhouse
gases by as much as 30 percent or 0.76 W/m2. Terrestrial albedo amplification
may thus extend, by about 25 years, the time available to advance the
development and use of low-emission energy conversion technologies which
ultimately remain essential to mitigate long-term climate change. However,
additional study is needed to confirm the estimates reported here and to assess
the economic and environmental impacts of active land-surface albedo
amplification as a climate change mitigation measure.Comment: 21 pages, 3 figures. In press with Mitigation and Adaptation
Strategies for Global Change, Springer, N
Whole-genome sequencing reveals host factors underlying critical COVID-19
Critical COVID-19 is caused by immune-mediated inflammatory lung injury. Host genetic variation influences the development of illness requiring critical care1 or hospitalization2,3,4 after infection with SARS-CoV-2. The GenOMICC (Genetics of Mortality in Critical Care) study enables the comparison of genomes from individuals who are critically ill with those of population controls to find underlying disease mechanisms. Here we use whole-genome sequencing in 7,491 critically ill individuals compared with 48,400 controls to discover and replicate 23 independent variants that significantly predispose to critical COVID-19. We identify 16 new independent associations, including variants within genes that are involved in interferon signalling (IL10RB and PLSCR1), leucocyte differentiation (BCL11A) and blood-type antigen secretor status (FUT2). Using transcriptome-wide association and colocalization to infer the effect of gene expression on disease severity, we find evidence that implicates multiple genesâincluding reduced expression of a membrane flippase (ATP11A), and increased expression of a mucin (MUC1)âin critical disease. Mendelian randomization provides evidence in support of causal roles for myeloid cell adhesion molecules (SELE, ICAM5 and CD209) and the coagulation factor F8, all of which are potentially druggable targets. Our results are broadly consistent with a multi-component model of COVID-19 pathophysiology, in which at least two distinct mechanisms can predispose to life-threatening disease: failure to control viral replication; or an enhanced tendency towards pulmonary inflammation and intravascular coagulation. We show that comparison between cases of critical illness and population controls is highly efficient for the detection of therapeutically relevant mechanisms of disease
Perspective: Advanced particle imaging
Contains fulltext :
174577.pdf (Publisherâs version ) (Open Access
Subsurface penetration of chemisorbed hydrogen isotopes into the Ru(0001) crystal surface
0-73. Pharmacokinetic interaction between letrozole and tamoxifen in postmenopausal patients with advanced breast cancer
Cage Hydrocarbons as Linkers in Dimeric Drug Design: Case Studies with Trimethoprim and Tedizolid
The looming threat of a âpost-antibiotic eraâ has been caused by a rapid rise in antibacterial resistance and subsequent depletion of effective antibiotic agents in the clinic. An efficient strategy to address this shortfall lies in the reengineering of pre-existing and commercially available antibiotic drugs. This is exemplified by dimerization, a design concept in which two pharmacophores are covalently linked to form a new chemical entity. The cage hydrocarbons cubane (1), bicyclo[2.2.2]octane (BCO) (2), adamantane (3), and bicyclo[1.1.1]pentane (BCP) (4) present themselves as an attractive family of linkers in this regard. In this report, all four hydrocarbon cages were employed as linkers in a series of dimers based on the commercially available antibiotics trimethoprim and tedizolid. A detailed synthetic roadmap for the protection and deprotection of each pharmacophore is outlined. Several members of the trimethoprim series showed activity on par with that of their trimethoprim progenitor, although this was not the case for the tedizolid series. The design strategy outlined herein highlights the utility of the group as a platform for the rapid and modular construction of future novel antibiotics.Biljana Vujcic, Jessica Wyllie, Tania, Jed Burns, Keith F. White, Simon Cromwell, David W. Lupton, Jason L. Dutton, Tatiana P. Soares da Costa, Sevan D. Housto
Visual outcomes in the subfoveal radiotherapy study:A randomized controlled trial of teletherapy for age-related macular degeneration
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