method формировани  signals дл  распознавани  plants and other heterogeneity characterization

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• 2. 图像特征的识别信号产生装置及图像特征的识别信号产生方法 [P] . 中国专利： CN1531709A . 2004-09-22
• 3. method формировани  signals дл  распознавани  plants and other heterogeneity characterization [P] . SU482137A1 . 1975-08-30

  机译： 识别植物和其他异质性特征的信号产生方法

• 4. the device дл  распознавани  plants and heterogeneity characterization based on [P] . SU472625A1 . 1975-06-05

  机译： 设备длраспознавани植物和基于

• 5. METHODS AND AN APPARATUS FOR HETEROGENEITY CHARACTERIZATION AND DETERMINATION OF THERMAL CONDUCTIVITY OF MATERIALS [P] . 美国专利： US2014294039A1 . 2014-10-02

  机译： 材料非均质性表征和热导率测定的方法和装置

• 1. Characterization of plant genomic SSR loci and exploration of an experiential method of developing SSR markers [J] . Xiaodong ZHU, Linhai WANG, Jingyin YU, 中国油料作物学报（英文） . 2016,第001期
• 2. Characterization of plant genomic SSR loci and exploration of an experiential method of developing SSR markers [J] . Xiaodong, ZHU, Linhai, 中国油料作物学报（英文版） . 2016,第001期
• 3. Mass Spectrometry Characterization of the Heterogeneity of a Plant-Derived Therapeutic Monoclonal Antibody [C] . Yanyan Lu, Catherine E. Costello ASMS Conference on Mass Spectrometry and Allied Topics . 2014
• 4. Characterization of multiple regulatory networks and responses to environmental signals in Pseudomonas syringae during its association with plants. [D] . Yu, Xilan. 2013
• 5. Simple and efficient methods to generate split roots and grafted plants useful for long-distance signaling studies in Medicago truncatula and other small plants [O] . Tessema K Kassaw, Julia A Frugoli 2012
• 6. Beyond the Canon: Within-Plant and Population-Level Heterogeneity in Jasmonate Signaling Engaged by Plant-Insect Interactions [O] . Dapeng Li, Ian T. Baldwin, Emmanuel Gaquerel 2016
• 7. Evaluation of Selected Signal Processing Methods for the Characterization of Steam Generator Eddy Current Signals [R] . Brown, S. D., Hayford, D. T. 1980

• 1. Characterization of the Modified Lifting Scheme Compression Method of EMG Signals [J] . Ele Pierre ,Ntsama Eloundou Pascal ,Tonye Emmanuel . 通讯和计算机 . 2011,第011期
• 2. BACKGROUND： Vibrio vulnifi cus inside the body could activate the NF-!B signaling pathwayand initiate the inflammatory cascade. The lung is one of the earliest organs affected by sepsisassociated with acute lung injury. High mobility group protein B1 （HMGB1） is an important late-actingpro-infl ammatory cytokine involving in the pathophysiology of sepsis. It is also involved in the injuryprocess in the lung, liver and intestine. There has been no report on the involvement of HMGB1 inVibrio vulnifi cus sepsis-induced lung injury.METHODS： Sixty rats were randomly divided into a normal control group （group A, n=10） anda Vibrio vulnificus sepsis group （group B, n=50）. Sepsis was induced in the rats by subcutaneousinjection of Vibrio vulnificus （concentration 6×108 cfu/mL, volume 0.1 mL/100g）） into the left lowerlimbs. The rats in group B were sacrifi ced separately 1, 6, 12, 24, and 48 hours after the infection.Their lungs were stored as specimens, lung water content was measured, and lung pathology wasobserved under a light microscope. The expressions of the HMGB1 gene and protein in the lungswere detected by RT-PCR and Western blot. Data were analyzed with one-way analysis of variance（ANOVA） and the LSD method for pair-wise comparison between the two groups. P〈0.05 wasconsidered statistically signifi cant.RESULTS： Compared to group A （0.652±0.177）, HMGB1 mRNA expression in the lungs ofgroup B was signifi cantly higher at 0 hour （1.161±0.358, P=0.013）, 24 hours （1.679±0.235, P=0.000）,and 48 hours （1.258±0.274, P=0.004） （P〈0.05）, and peaked at 24 hours. Compared to group A（0.594±0.190）, HMGB1 protein expression at 6 hours （1.408±0.567, P=0.026） after infection wassignificantly increased （P〈0. 05）, and peaked at 24 hours （2.415±1.064, P=0.000） after infection.Compared to group A （0.699±0.054）, lung water content was significantly increased at 6 hours（0.759±0.030, P=0.001）,12 hours （0.767±0.023, P=0.000）, 24 hours （0.771±0.043, P=0.000） and 48hours （0.789±0.137, P=0.000） after infection （P〈0.05）. Compared to group A, pathological changesat 12 hours in group B indicate marked pulmonary vascular congestion, interstitial edema andinfl ammatory infi ltration. Alveolar cavity collapse and boundaries of the alveolar septum could not beclearly identifi ed.CONCLUSION： Vibrio vulnifi cus sepsis can lead to injury in rat lungs, and increased HMGB1expression in lung tissue may be one of the mechanisms for injury from Vibrio vulnifi cus sepsis. [J] . Qiao-meng Qiu ,Zhong-wang Li ,Lu-ming Tang . 世界急诊医学杂志(英文) . 2011,第4期
• 3. Synthesis of Chromium(III) Oxide Nanoparticles by Electrochemical Method and Mukia Maderaspatana Plant Extract, Characterization, KMnOsub4 /subDecomposition and Antibacterial Study [J] . Rakesh nbsp ,S. Ananda ,Netkal M. Made Gowda . 催化剂现代研究（英文） . 2013,第4期
• 4. 基于识别的线性特征增强方法的实现及改进 [C] . 段晓旭 ,姚长利 ,郑元满 . 中国地球物理学会第二十九届年会 . 2013
• 5. 基于可区分性特征学习的说话人识别方法研究 [A] . 黄多林 . 2020