25 research outputs found
Research on SLM Algorithm for PAPR reduction in MB-OFDM UWB Systems
AbstractMultiband orthogonal frequency division multiplexing (MB-OFDM) is one of the key techniques of ultra wideband (UWB) systems. A major drawback of MB-OFDM technique is the high peak-to-average power ratio (PAPR) of the transmit signal. In this paper, a novel phase sequence of selected mapping algorithm which makes the side information not needed is designed to lower the PAPR of MB-OFDM UWB signals. It is also shown that comparable PAPR reduction performance with the original SLM algorithm can be achieved with a small increase in signal power. Simulation results show that there must be equilibriums between SLM computational complexity and PAPR performance. The objective of the new algorithm is to lower PAPR close to ordinary SLM technique with reduced computational complexity with little performance degradation and achieves better system resource utilization
The Error Performance and Fairness of CUWB Correlated Channels
AbstractThe symbol period becomes smaller compared to the channel delay in multiband orthogonal frequency division multiplexing (MB-OFDM) cognitive ultra wideband (CUWB) wireless communications, the transmitted signals experiences frequency-selective fading and leads to performance degradation. In this paper, a new design method for space-time trellis codes in MB-OFDM systems with correlated Rayleigh fading channels is introduced. This method converts the single output code symbol into several STTC code symbols, which are to be transmitted simultaneously from multiple transmitter-antennas. By using Viterbi optimal soft decision decoding algorithm, we investigate both quasi-static and interleaved channels and demonstrate how the spatial fading correlation affects the performance of space–time codes over these two different MB-OFDM wireless channel models. Simulation results show that the performance of space–time code is to be robust to spatial correlation. When the system bandwidth increases, the long term fairness quality will gradually become better and finally converges to 1
Expression of calcitonin gene-related peptide in efferent vestibular system and vestibular nucleus in rats with motion sickness.
UNLABELLED: Motion sickness presents a challenge due to its high incidence and unknown pathogenesis although it is a known fact that a functioning vestibular system is essential for the perception of motion sickness. Recent studies show that the efferent vestibular neurons contain calcitonin gene-related peptide (CGRP). It is a possibility that the CGRP immunoreactivity (CGRPi) fibers of the efferent vestibular system modulate primary afferent input into the central nervous system; thus, making it likely that CGRP plays a key role in motion sickness. To elucidate the relationship between motion sickness and CGRP, the effects of CGRP on the vestibular efferent nucleus and the vestibular nucleus were investigated in rats with motion sickness. METHODS: An animal model of motion sickness was created by subjecting rats to rotary stimulation for 30 minutes via a trapezoidal stimulation pattern. The number of CGRPi neurons in the vestibular efferent nucleus at the level of the facial nerve genu and the expression level of CGRPi in the vestibular nucleus of rats were measured. Using the ABC method of immunohistochemistry technique, measurements were taken before and after rotary stimulation. The effects of anisodamine on the expression of CGRP in the vestibular efferent nucleus and the vestibular nucleus of rats with motion sickness were also investigated. RESULTS AND DISCUSSION: Both the number of CGRPi neurons in the vestibular efferent nucleus and expression level in the vestibular nucleus increased significantly in rats with motion sickness compared to that of controls. The increase of CGRP expression in rats subjected to rotary stimulation 3 times was greater than those having only one-time stimulation. Administration of anisodamine decreased the expression of CGRP within the vestibular efferent nucleus and the vestibular nucleus in rats subjected to rotary stimulation. In conclusion, CGRP possibly plays a role in motion sickness and its mechanism merits further investigation
Steroid nuclear receptor coactivator 2 controls immune tolerance by promoting induced Treg differentiation via up-regulating Nr4a2
Steroid nuclear receptor coactivator 2 (SRC2) is a member of a family of transcription coactivators. While SRC1 inhibits the differentiation of regulatory T cells (Tregs) critical for establishing immune tolerance, we show here that SRC2 stimulates Treg differentiation. SRC2 is dispensable for the development of thymic Tregs, whereas naive CD4+ T cells from mice deficient of SRC2 specific in Tregs (SRC2fl/fl/Foxp3YFP-Cre) display defective Treg differentiation. Furthermore, the aged SRC2fl/fl/Foxp3YFP-Cre mice spontaneously develop autoimmune phenotypes including enlarged spleen and lung inflammation infiltrated with IFNγ-producing CD4+ T cells. SRC2fl/fl/Foxp3YFP-Cre mice also develop severer experimental autoimmune encephalomyelitis (EAE) due to reduced Tregs. Mechanically, SRC2 recruited by NFAT1 binds to the promoter and activates the expression of Nr4a2, which then stimulates Foxp3 expression to promote Treg differentiation. Members of SRC family coactivators thus play distinct roles in Treg differentiation and are potential drug targets for controlling immune tolerance
Analysis of the Influence of Aviation Logistics on the Regional Ecological Economic Development of Jilin Province
Cloning, Expression, and Characterization of a Thermophilic Endoglucanase, AcCel12B from Acidothermus cellulolyticus 11B
The gene ABK52392 from the thermophilic bacterium Acidothermus cellulolyticus 11B was predicted to be endoglucanase and classified into glycoside hydrolase family 12. ABK52392 encodes a protein containing a catalytic domain and a carbohydrate binding module. ABK52392 was cloned and functionally expressed in Escherichia coli. After purification by Ni-NTA agarose affinity chromatography and Q-Sepharose® Fast Flow chromatography, the properties of the recombinant protein (AcCel12B) were characterized. AcCel12B exhibited optimal activity at pH 4.5 and 75 °C. The half-lives of AcCel12B at 60 and 70 °C were about 90 and 2 h, respectively, under acidic conditions. The specific hydrolytic activities of AcCel12B at 70 °C and pH 4.5 for sodium carboxymethylcellulose (CMC) and regenerated amorphous cellulose (RAC) were 118.3 and 104.0 U·mg−1, respectively. The Km and Vmax of AcCel12B for CMC were 25.47 mg·mL−1 and 131.75 U·mg−1, respectively. The time course of hydrolysis for RAC was investigated by measuring reducing ends in the soluble and insoluble phases. The total hydrolysis rate rapidly decreased after the early stage of incubation and the generation of insoluble reducing ends decreased earlier than that of soluble reducing ends. High thermostability of the cellulase indicates its potential commercial significance and it could be exploited for industrial application in the future
Expression of CGRPi fibers in the vestibular nuclei (magnification:10×10).
<p>I; triple rotary stimulation with undoesd; II: single rotary stimulation with undoesd; III:single rotary stimulation with saline dosed; IV:single rotary stimulation with anisodamine dosed; V: control group. Arrows show the CGRPi fibers in the vestibular nuclei.</p
Comparison of intake volume of saccharin solution before and after rotary stimulation in the four experimental groups.
<p>A: rotary stimulation undosed; B: rotary stimulation saline dosed; C: rotary stimulation anisodamine dosed; D: control group. *<i>P</i><0.05 as compared with the before rotary stimulation respectively. The reduction in group C was significantly less than those of group A and group B in the three 24 h intervals after rotary stimulation.</p
The numbers of CGRP positive cells in the efferent nucleus.
<p>I: triple rotary stimulation with undoesd; II: single rotary stimulation with undoesd; III: single rotary stimulation with saline dosed; IV: single rotary stimulation with anisodamine dosed; V: control group.*<i>P</i><0.05 for group I vs. group V and group II vs. group V; #<i>P</i><0.05 for group IV vs. group II.</p
The mean optical density of CGRP immunoreactivity in the vestibular nuclei of rats.
<p>I: triple rotary stimulation with undoesd; II: single rotary stimulation with undoesd; III: single rotary stimulation with saline dosed; IV: single rotary stimulation with anisodamine dosed; V: control group. *<i>P</i><0.05 for group I vs. group V and group II vs. group V; #<i>P</i><0.05 for group IV vs. group II.</p