216 research outputs found
STOCHASTIC SCHEDULING WITH ASYMMETRIC EARLINESS AND TARDINESS PENALTIES UNDER RANDOM MACHINE BREAKDOWNS
Damping multi-model adaptive switching controller design for electronic air suspension system
This paper presents the design and verification of a damping multi-model adaptive switching controller for electronic air suspension (EAS) system. In order to improve the convergence rate of identification algorithm of conventional adaptive controller, multiple local linear full-car vehicle models of EAS system with fixed parameters are established according to the actual damping control process of EAS for different vehicle driving conditions and an adaptive model whose initial value of parameters can be re-assigned is introduced to enhance the system control precision. The model switching control strategy based on minimum error is used to select the best matching model online and the optimum damping force is regulated by adaptive control algorithm, thus constituting the damping multi-model adaptive control for EAS. Simulation results show that the control method proposed in this paper can improve the damping regulating performance of EAS effectively in wide range driving conditions, especially for the case of sudden change in driving conditions
Mesodermal Nkx2.5 is necessary and sufficient for early second heart field development
AbstractThe vertebrate heart develops from mesoderm and requires inductive signals secreted from early endoderm. During embryogenesis, Nkx2.5 acts as a key transcription factor and plays essential roles for heart formation from Drosophila to human. In mice, Nkx2.5 is expressed in the early first heart field, second heart field pharyngeal mesoderm, as well as pharyngeal endodermal cells underlying the second heart field. Currently, the specific requirements for Nkx2.5 in the endoderm versus mesoderm with regard to early heart formation are incompletely understood. Here, we performed tissue-specific deletion in mice to dissect the roles of Nkx2.5 in the pharyngeal endoderm and mesoderm. We found that heart development appeared normal after endodermal deletion of Nkx2.5 whereas mesodermal deletion engendered cardiac defects almost identical to those observed on Nkx2.5 null embryos (Nkx2.5−/−). Furthermore, re-expression of Nkx2.5 in the mesoderm rescued Nkx2.5−/− heart defects. Our findings reveal that Nkx2.5 in the mesoderm is essential while endodermal expression is dispensable for early heart formation in mammals
Limited Regeneration Potential with Minimal Epicardial Progenitor Conversions in the Neonatal Mouse Heart after Injury
The regeneration capacity of neonatal mouse heart is controversial. In addition, whether epicardial cells provide a progenitor pool for de novo heart regeneration is incompletely defined. Following apical resection of the neonatal mouse heart, we observed limited regeneration potential. Fate-mapping of Tbx18MerCreMer mice revealed that newly formed coronary vessels and a limited number of cardiomyocytes were derived from the T-box transcription factor 18 (Tbx18) lineage. However, further lineage tracing with SM-MHCCreERT2 and Nfactc1Cre mice revealed that the new smooth muscle and endothelial cells are in fact derivatives of pre-existing coronary vessels. Our data show that neonatal mouse heart can regenerate but that its potential is limited. Moreover, although epicardial cells are multipotent during embryogenesis, their contribution to heart repair through "stem" or "progenitor" cell conversion is minimal after birth. These observations suggest that early embryonic heart development and postnatal heart regeneration are distinct biological processes. Multipotency of epicardial cells is significantly decreased after birth
Vehicle Detection Based on Deep Dual-Vehicle Deformable Part Models
Vehicle detection plays an important role in safe driving assistance technology. Due to the high accuracy and good efficiency, the deformable part model is widely used in the field of vehicle detection. At present, the problem related to reduction of false positivity rate of partially obscured vehicles is very challenging in vehicle detection technology based on machine vision. In order to address the abovementioned issues, this paper proposes a deep vehicle detection algorithm based on the dual-vehicle deformable part model. The deep learning framework can be used for vehicle detection to solve the problem related to incomplete design and other issues. In this paper, the deep model is used for vehicle detection that consists of feature extraction, deformation processing, occlusion processing, and classifier training using the back propagation (BP) algorithm to enhance the potential synergistic interaction between various parts and to get more comprehensive vehicle characteristics. The experimental results have shown that proposed algorithm is superior to the existing detection algorithms in detection of partially shielded vehicles, and it ensures high detection efficiency while satisfying the real-time requirements of safe driving assistance technology
Hybrid model predictive control of damping multi-mode switching damper for vehicle suspensions
This paper investigates the design and verification of a hybrid model predictive controller of a damping multi-mode switching damper for application in vehicle suspensions. Since the damping mode switches induce different modes of operation, the vehicle suspension system including this damper poses challenging hybrid control problem. To solve this problem, a novel approach to the modelling and controller design problem is proposed based on hybrid modelling and model predictive control techniques. The vehicle suspension system with the damping multi-mode switching damper is formulated as a mixed logical dynamical model comprising continuous and discrete system inputs. Based on this model, a constrained optimal control problem is solved to manage the switching sequences of the damping mode with respect to the suspension performance requirements. Numerical simulation results demonstrate the effectiveness of the proposed control methodology finally
Sox2 in the Dermal Papilla Niche Controls Hair Growth by Fine-Tuning BMP Signaling in Differentiating Hair Shaft Progenitors
How dermal papilla (DP) niche cells regulate hair follicle progenitors to control hair growth remains unclear. Using Tbx18Cre to target embryonic DP precursors, we ablate the transcription factor Sox2 early and efficiently, resulting in diminished hair shaft outgrowth. We find that DP niche expression of Sox2 controls the migration rate of differentiating hair shaft progenitors. Transcriptional profiling of Sox2 null DPs reveals increased Bmp6 and decreased Bmp inhibitor Sostdc1, a direct Sox2 transcriptional target. Subsequently, we identify upregulated Bmp signaling in knockout hair shaft progenitors and demonstrate that Bmps inhibit cell migration, an effect that can be attenuated by Sostdc1. A shorter and Sox2-negative hair type lacks Sostdc1 in the DP and shows reduced migration and increased Bmp activity of hair shaft progenitors. Collectively, our data identify Sox2 as a key regulator of hair growth that controls progenitor migration by fine-tuning Bmp-mediated mesenchymal-epithelial crosstalk
Genetic identification of a common collagen disease in Puerto Ricans via identity-by-descent mapping in a health system
Achieving confidence in the causality of a disease locus is a complex task that often requires supporting data from both statistical genetics and clinical genomics. Here we describe a combined approach to identify and characterize a genetic disorder that leverages distantly related patients in a health system and population-scale mapping. We utilize genomic data to uncover components of distant pedigrees, in the absence of recorded pedigree information, in the multi-ethnic BioMe biobank in New York City. By linking to medical records, we discover a locus associated with both elevated genetic relatedness and extreme short stature. We link the gene, COL27A1, with a little-known genetic disease, previously thought to be rare and recessive. We demonstrate that disease manifests in both heterozygotes and homozygotes, indicating a common collagen disorder impacting up to 2% of individuals of Puerto Rican ancestry, leading to a better understanding of the continuum of complex and Mendelian disease
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