739 research outputs found
A robot arm simulation with a shared memory multiprocessor machine
A parallel processing scheme for a single chain robot arm is presented for high speed computation on a shared memory multiprocessor. A recursive formulation that is derived from a virtual work form of the d'Alembert equations of motion is utilized for robot arm dynamics. A joint drive system that consists of a motor rotor and gears is included in the arm dynamics model, in order to take into account gyroscopic effects due to the spinning of the rotor. The fine grain parallelism of mechanical and control subsystem models is exploited, based on independent computation associated with bodies, joint drive systems, and controllers. Efficiency and effectiveness of the parallel scheme are demonstrated through simulations of a telerobotic manipulator arm. Two different mechanical subsystem models, i.e., with and without gyroscopic effects, are compared, to show the trade-off between efficiency and accuracy
Spacecraft Docking System
A method and apparatus for docking a spacecraft. The apparatus comprises elongate members, movement systems, and force management systems. The elongate members are associated with a docking structure for a spacecraft. The movement systems are configured to move the elongate members axially such that the docking structure for the spacecraft moves. Each of the elongate members is configured to move independently. The force management systems connect the movement systems to the elongate members and are configured to limit a force applied by the each of the elongate members to a desired threshold during movement of the elongate members
Cloning and expression profiling of the VLDLR gene associated with egg performance in duck (Anas platyrhynchos)
<p>Abstract</p> <p>Background</p> <p>The very low density lipoprotein receptor gene (<it>VLDLR</it>), a member of the low density lipoprotein receptor (<it>LDLR</it>) gene family, plays a crucial role in the synthesis of yolk protein precursors in oviparous species. Differential splicing of this gene has been reported in human, rabbit and rat. In chicken, studies showed that the VLDLR protein on the oocyte surface mediates the uptake of yolk protein precursors into growing oocytes. However, information on the <it>VLDLR </it>gene in duck is still scarce.</p> <p>Methods</p> <p>Full-length duck <it>VLDLR </it>cDNA was obtained by comparative cloning and rapid amplification of cDNA ends (RACE). Tissue expression patterns were analysed by semi-quantitative reverse-transcription polymerase chain reaction (RT-PCR). Association between the different genotypes and egg performance traits was investigated with the general linear model (GLM) procedure of the SAS<sup>® </sup>software package.</p> <p>Results</p> <p>In duck, two <it>VLDLR </it>transcripts were identified, one transcript (variant-a) containing an O-linked sugar domain and the other (variant-b) not containing this sugar domain. These transcripts share ~70 to 90% identity with their counterparts in other species. A phylogenetic tree based on amino acid sequences showed that duck VLDLR proteins were closely related with those of chicken and zebra finch. The two duck <it>VLDLR </it>transcripts are differentially expressed i.e. <it>VLDLR-a </it>is mainly expressed in muscle tissue and <it>VLDLR-b </it>in reproductive organs. We have localized the duck <it>VLDLR </it>gene on chromosome Z. An association analysis using two completely linked SNP sites (T/C at position 2025 bp of the ORF and G/A in intron 13) and records from two generations demonstrated that the duck <it>VLDLR </it>gene was significantly associated with egg production (P < 0.01), age of first egg (P < 0.01) and body weight of first egg (P < 0.05).</p> <p>Conclusions</p> <p>Duck and chicken <it>VLDLR </it>genes probably perform similar function in the development of growing oocytes and deposition of yolk lipoprotein. Therefore, <it>VLDLR </it>could be a candidate gene for duck egg performance and be used as a genetic marker to improve egg performance in ducks.</p
Towards an analytical framework of corporate performance measurement in chemical industry: balanced scorecard perspective
MyD88-5 links mitochondria, microtubules, and JNK3 in neurons and regulates neuronal survival
The innate immune system relies on evolutionally conserved Toll-like receptors (TLRs) to recognize diverse microbial molecular structures. Most TLRs depend on a family of adaptor proteins termed MyD88s to transduce their signals. Critical roles of MyD88-1–4 in host defense were demonstrated by defective immune responses in knockout mice. In contrast, the sites of expression and functions of vertebrate MyD88-5 have remained elusive. We show that MyD88-5 is distinct from other MyD88s in that MyD88-5 is preferentially expressed in neurons, colocalizes in part with mitochondria and JNK3, and regulates neuronal death. We prepared MyD88-5/GFP transgenic mice via a bacterial artificial chromosome to preserve its endogenous expression pattern. MyD88-5/GFP was detected chiefly in the brain, where it associated with punctate structures within neurons and copurified in part with mitochondria. In vitro, MyD88-5 coimmunoprecipitated with JNK3 and recruited JNK3 from cytosol to mitochondria. Hippocampal neurons from MyD88-5–deficient mice were protected from death after deprivation of oxygen and glucose. In contrast, MyD88-5–null macrophages behaved like wild-type cells in their response to microbial products. Thus, MyD88-5 appears unique among MyD88s in functioning to mediate stress-induced neuronal toxicity
Binary Star Evolution in Different Environments: Filamentary, Fractal, Halo and Tidal-tail Clusters
Using membership of 85 open clusters from previous studies (Pang et al.
2021a,b, 2022b; Li et al. 2021) based on Gaia DR3 data, we identify binary
candidates in the color-magnitude diagram, for systems with mass ratio q > 0.4.
The binary fraction is corrected for incompleteness at different distances due
to the Gaia angular resolution limit. We find a decreasing binary fraction with
increasing cluster age, with substantial scatter. For clusters with a total
mass > 200, the binary fraction is independent of cluster mass. The
binary fraction depends strongly on stellar density. Among four types of
cluster environments, the lowest-density filamentary and fractal stellar groups
have the highest mean binary fraction: 23.6% and 23.2%, respectively. The mean
binary fraction in tidal-tail clusters is 20.8%, and is lowest in the densest
halo-type clusters: 14.8%. We find clear evidence of early disruptions of
binary stars in the cluster sample. The radial binary fraction depends strongly
on the cluster-centric distance across all four types of environments, with the
smallest binary fraction within the half-mass radius , and increasing
towards a few . Only hints of mass segregation is found in the target
clusters. The observed amount of mass segregation is not significant to
generate a global effect inside the target clusters. We evaluate the bias of
unresolved binary systems (assuming a primary mass of 1) in 1D
tangential velocity, which is 0.1-1. Further studies are
required to characterize the internal star cluster kinematics using Gaia proper
motions
Subtype classification for prediction of prognosis of breast cancer from a biomarker panel: correlations and indications
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