http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Hydraulic regenerative braking system studies based on a nonlinear dynamic model of a full vehicle
Ning Li,Xiaobin Ning,Qiucheng Wang,Jiliang Li 대한기계학회 2017 JOURNAL OF MECHANICAL SCIENCE AND TECHNOLOGY Vol.31 No.6
To obtain a reasonable match of the main parameters of a hydraulic regenerative braking system and to improve the energy recovery efficiency, this paper establishes the corresponding mathematical models and testbed for a hydraulic regenerative braking system. The proposed system is analysed and verified through simulation and experiments. Then, the linear and nonlinear mathematical models of a full vehicle are built, with joint simulation of the hydraulic regenerative braking system, and the influence of the hydraulic regenerative braking system on braking performance under different running conditions is discussed. The results indicate that the deviations in the simulation results between the linear and nonlinear dynamic models are very small. When the brake deceleration and road adhesion coefficient are 0.2, deviations are within 1.38 %. With an increase in the braking deceleration and road adhesion coefficient, the deviations in braking time and distance between the systems become larger and larger. When the braking deceleration and road adhesion coefficient are 0.7, the deviation reaches 30 %. Finally, with braking energy recovery efficiency and braking distance as the optimization objectives, the nonlinear braking energy recovery system parameters are optimized. After optimization, the energy recovery efficiency of the nonlinear system reaches 76.3 %, and the braking distance is 22.8 m.
Sequence Analysis of cytb Gene in Echinococcus granulosus from Western China
Xiuqin Zhong,Ning Wang,Dandan Hu,Jiahai Wang,Tianyu Liu,Xiaobin Gu,Shuxian Wang,Xuerong Peng,Guangyou Yang 대한기생충학열대의학회 2014 The Korean Journal of Parasitology Vol.52 No.2
Echinococcus granulosus is the causative agent of cystic echinococcosis with medical and veterinary importance in China. Our main objective was to discuss the genotypes and genetic diversity of E. granulosus present in domestic animals and humans in western China. A total of 45 hydatid cyst samples were collected from sheep, humans, and a yak and subjected to an analysis of the sequences of mitochondrial cytochrome b (cytb) gene. The amplified PCR product for all samples was a 1,068 bp band. The phylogenetic analysis showed that all 45 samples were identified as E. granulosus (genotype G1). Ten haplotypes were detected among the samples, with the main haplotype being H1. The haplotype diversity was 0.626, while the nucleotide diversity was 0.001. These results suggested that genetic diversity was low among our samples collected from the west of China based on cytb gene analysis. These findings may provide more information on molecular characteristics of E. granulosus from this Chinese region.
A brain somatic RHEB doublet mutation causes focal cortical dysplasia type II
Shanshan Zhao,Zhenghui Li,Muxian Zhang,Lingliang Zhang,Honghua Zheng,Jinhuan Ning,Yanyan Wang,Feng-Peng Wang,Xiaobin Zhang,Hexia Gan,Yuanqing Wang,Xian Zhang,Hong Luo,Guojun Bu,Huaxi Xu,Yi Yao,Yun-wu 생화학분자생물학회 2019 Experimental and molecular medicine Vol.51 No.-
Focal cortical dysplasia type II (FCDII) is a cerebral cortex malformation characterized by local cortical structure disorganization, neuronal dysmorphology, and refractory epilepsy. Brain somatic mutations in several genes involved in the PI3K/AKT/mTOR pathway are associated with FCDII, but they are only found in a proportion of patients with FCDII. The genetic causes underlying the development FCDII in other patients remain unclear. Here, we carried out whole exome sequencing and targeted sequencing in paired brain–blood DNA from patients with FCDII and identified a brain somatic doublet mutation c.(A104T, C105A) in the Ras homolog, mTORC1 binding (RHEB) gene, which led to the RHEB p.Y35L mutation in one patient with FCDII. This RHEB mutation carrier had a dramatic increase of ribosomal protein S6 phosphorylation, indicating mTOR activation in the region of the brain lesion. The RHEB p.Y35L mutant protein had increased GTPλS-binding activity compared with wild-type RHEB. Overexpression of the RHEB p. Y35L variant in cultured cells also resulted in elevated S6 phosphorylation compared to wild-type RHEB. Importantly, in utero electroporation of the RHEB p.Y35L variant in mice induced S6 phosphorylation, cytomegalic neurons, dysregulated neuron migration, abnormal electroencephalogram, and seizures, all of which are found in patients with FCDII. Rapamycin treatment rescued abnormal electroencephalograms and alleviated seizures in these mice. These results demonstrate that brain somatic mutations in RHEB are also responsible for the pathogenesis of FCDII, indicating that aberrant activation of mTOR signaling is a primary driver and potential drug target for FCDII.