19 research outputs found
Optical symmetries and anisotropic transport in high-Tc superconductors
A simple symmetry analysis of in-plane and out-of-plane transport in a family
of high temperature superconductors is presented. It is shown that generalized
scaling relations exist between the low frequency electronic Raman response and
the low frequency in-plane and out-of-plane conductivities in both the normal
and superconducting states of the cuprates. Specifically, for both the normal
and superconducting state, the temperature dependence of the low frequency
Raman slope scales with the axis conductivity, while the
Raman slope scales with the in-plane conductivity. Comparison with experiments
in the normal state of Bi-2212 and Y-123 imply that the nodal transport is
largely doping independent and metallic, while transport near the BZ axes is
governed by a quantum critical point near doping holes per
CuO plaquette. Important differences for La-214 are discussed. It is also
shown that the axis conductivity rise for is a consequence of
partial conservation of in-plane momentum for out-of-plane transport.Comment: 16 pages, 8 Figures (3 pages added, new discussion on pseudogap and
charge ordering in La214
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
EDF-based Real-time Message Scheduling of Periodic Messages on a Master-Slave-Based Synchronized Switched Ethernet
Abstract. Switched Ethernet has many features for real-time communications but cannot guarantee the timely delivery of a real-time message due to possible collisions on the output ports. This paper first suggests a feasible condition for real-time communication of periodic messages on a master-slave-based synchronized switched Ethernet. Then an EDF (Earliest Deadline First)-based scheduling algorithm that satisfies the proposed scheduling condition is proposed. The master node checks the feasible condition for messages and makes a message transmission schedule for feasible messages. The proposed scheduling algorithm can handle dynamic message requests and performs the real-time communication without any modification in the switch. The performance of the proposed scheduling algorithm has been evaluated by simulation to show the timely delivery of real-time messages and the real-time communication capacity of the switched Ethernet
Development and use of real-time PCR to detect and quantify Mycoplasma haemocanis and "Candidatus Mycoplasma haematoparvum" in dogs
Two canine haemoplasma species have been recognised to date; Mycoplasma haemocanis (Mhc), which has been associated with anaemia in splenectomised or immunocompromised dogs, and "Candidatus Mycoplasma haematoparvum" (CMhp), recently described in an anaemic splenectomised dog undergoing chemotherapy. The study aim was to develop quantitative real-time PCR assays (qPCRs) incorporating an endogenous internal control to detect Mhc and CMhp and to apply these assays to DNA samples extracted from canine blood collected in Northern Tanzania (n = 100) and from dogs presented to a Trinidadian veterinary hospital (n = 185). QPCRs specific for Mhc and CMhp were designed using 16S rRNA gene sequence data, and each was duplexed with an assay specific for canine glyceraldehyde-3-phosphate dehydrogenase (GAPDH). The assays detected <= 10 copies of a sequence-specific haemoplasma plasmid per reaction and neither assay showed cross-reactivity with 10(6) copies of the sequence-specific plasmid from the non-target canine haemoplasma species. Nineteen of the 100 Tanzanian samples (19%) were positive for Mhc alone and one (1%) was dually infected. One Trinidadian sample was negative for canine GAPDH DNA and was excluded from the study. Of the 184 remaining Trinidadian samples, nine (4.9%) were positive for Mhc alone, five (2.7%) for CMhp alone, and two (1.1%) dually infected. This is the first report of canine haemoplasma qPCR assays that use an internal control to confirm the presence of amplifiable sample DNA, and their application to prevalence studies. Mhc was the most commonly detected canine haemoplasma species