EAR LABEL FOR FILLING A CATTLE,METHOD OF CREATING THE IDENTIFIING MARKS ON ITS BASIC BODY AND A STAMP TO PERFORM THIS METHOD

• 1. 无线识别标签、其制作方法、制作装置、无线识别标签用的薄片部件、及用于无线识别标签制作的安装在其制作装置上的箱 [P] . 中国专利： CN1784690A . 2006-06-07
• 2. 内容创建系统、内容创建方法、用于执行该内容创建方法的计算机可执行程序、包括该程序的计算机可读记录介质、图形用户接口系统、以及显示控制方法 [P] . 中国专利： CN1781086A . 2006-05-31
• 3. Label Creating Apparatus, Non-Transitory Storage Medium Storing Program Readable by the Label Creating Apparatus, and Method of Label Cutting Processing Performed by the Label Creating Apparatus [P] . 美国专利： US2018251252A1 . 2018-09-06

  机译： 标签创建设备，标签创建设备可读的非暂时性存储介质存储程序以及标签创建设备执行的标签切割处理方法

• 4. EAR MARKS FOR LIVESTOCK REGISTRATION, PRINTING METHOD FOR EAR MARKS, AND IDENTIFICATION METHOD USING THE EAR MARKS [P] . CA2320320C . 2007-07-10

  机译： 用于牲畜登记的耳标，耳标的打印方法以及使用耳标的识别方法

• 5. EAR MARKS FOR LIVESTOCK REGISTRATION, PRINTING METHOD FOR EAR MARKS, AND IDENTIFICATION METHOD USING THE EAR MARKS [P] . IL137780A . 2004-05-12

  机译： 用于牲畜登记的耳标，耳标的打印方法以及使用耳标的识别方法

• 1. Comparison of β-Amyloid Plaque Labeling Methods:Antibody Staining, Gallyas Silver Staining,and Thioflavin-S Staining [J] . Xinze Shi, Xuan Wei, Longze Sha, 中国医学科学杂志（英文版） . 2018,第003期
• 2. Diagnosing Graves’ Disease and Non-Graves Hyperthyroidism Using TSH Receptor Antibody Test versus Non-TSH Receptor Antibody Test Methods of Diagnosis [J] . Mohammed Qader Meena 内分泌与新陈代谢疾病期刊（英文） . 2020,第002期
• 3. Stamping Plant 4.0 - Basics for the Application of Data Mining Methods in Manufacturing Car Body Parts [C] . Stephan Purr, Josef Meinhardt, Arnulf Lipp International Conference on Sheet Metal . 2015
• 4. Investigating methods for using ractopamine hydrochloride in domestic beef cattle and factors affecting body condition of cattle on Il N'gwesi Group Ranch in Kenya, Africa [D] . Culp, Kyle Christian. 2010
• 5. Mirror-Mark Tests Performed on Jackdaws Reveal Potential Methodological Problems in the Use of Stickers in Avian Mark-Test Studies [O] . Manuel Soler, Tomás Pérez-Contreras, Juan Manuel Peralta-Sánchez -1
• 6. A comparison of methods for smoothing and gap filling time series Biogeosciences Discussions A comparison of methods for smoothing and gap filling time series of remote sensing observations: application to MODIS LAI products A comparison of methods for smoothing and gap filling time series [O] . Kandasamy, S, Baret, Frédéric, Verger, A, 2012

• 1. The Effect of Different Filling Methods on the Microleakage of the Tooth Edge after Bulk Resin Filling [J] . Xin Gao ,Jing Di . 抗癌研究 . 2020,第006期
• 2. OPTIMIZATION OF AUTOBODY PANEL STAMPING PROCESS BASED ON DYNAMIC EXPLICIT FINITE ELEMENT METHOD [J] . X. G. Bao ,D. N. He ,D. Lu . 金属学报：英文版 . 2000,第1期
• 3. 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
• 4. PIT标签标记大黄鱼方法的评估 [C] . 蔡明夷 ,陈建林 ,刘贤德 . 2007年全国海水养殖学术研讨会 . 2007
• 5. 基于生物信息学方法从牛和绵羊表达序列标签中筛选SSR标记的初步研究 [A] . 闫秋良 . 2007