Method and apparatus for the conversion of an arbitrary ETI signal in an ETI signal with DAB-mode 3

• 1. 将用户比特流转换为编码比特流的方法、检测信号中同步模式的方法、记录载体、信号、记录设备和重放设备 [P] . 中国专利： CN101023588A . 2007-08-22
• 2. 用信号通知用于跳过和合并模式的多假设的方法和装置、以及用信号通知具有运动矢量差的合并中的距离偏移表的方法和装置 [P] . 中国专利： CN112806002A . 2021-05-14
• 3. METHOD AND DEVICE FOR CONVERSION OF A ETI-SIGNAL TO ETI-SIGNAL WITH DAB-MODE 3 [P] . 韩国专利： KR20080063185A . 2008-07-03

  机译： 用DAB模式3将ETI信号转换为ETI信号的方法和装置

• 4. The device and method for the temporal synchronization of a signal eti [P] . 法国专利： FR3003419B1 . 2018-11-30

  机译： 用于信号eti的时间同步的设备和方法

• 5. DEVICE AND METHOD FOR TIME SYNCHRONIZATION OF AN ETI SIGNAL [P] . 法国专利： FR3003419A1 . 2014-09-19

  机译： ETI信号时间同步的装置和方法

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• 2. GEOMETRIC METHOD FOR BLIND SIGNAL SEPARATION OF MULTICHANNEL MPSK SIGNALS [J] . Fang Yong, Ji Shuai, Wang Min 电子科学学刊：英文版 . 2012,第003期
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• 1. Enrichment of Low Grade Eti Mine-Espey Colemanite Stocks Using Microwave Methods [J] . Ramazan Butuner1 ,Ahmet Aydm2 . 环境科学与工程：A . 2016,第007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. Arbitrary-Dimensional Frequency Estimation of Complex Sinusoid Signals [J] . Zhang Zhan College of Electronic Information Wuhan University Wuhan 430072 China . 武汉大学自然科学学报：英文版 . 1997,第4期
• 4. 产生任意波形信号的系统及其在标准微位移发生装置中的应用研究 [C] . 叶孝佑 ,薛梓 . 2008年全国几何量精密测量技术学术交流会 . 2008
• 5. 基于M etis图划分算法的图平衡划分方法 [A] . 赵一明 . 2014