A method to detect signs of gust of synchronisation of color changed to avoid copies of a program of glass.

• 1. 一种基于机器视觉的检测溶液颜色变化的自动滴定装置及检测方法 [P] . 中国专利： CN105717111A . 2016-06-29
• 2. 一种依据颜色变化通过肉眼检测硫氰酸根的离子传感器及其制备方法和应用 [P] . 中国专利： CN110146498B . 2021.03.26
• 3. Method and apparatus for detecting modified color burst signals to prevent the copying of a video program [P] . 韩国专利： KR100531968B1 . 2005-11-30

  机译： 用于检测修改的色同步信号以防止复制视频节目的方法和设备

• 4. Method for detecting color burst signals modified to prevent a video program is copied. [P] . ES2192766T3 . 2003-10-16

  机译： 复制用于防止视频节目的彩色猝发信号的检测方法被复制。

• 5. Method and apparatus for detecting modified color burst signals to prevent the copying of a video program [P] . 美国专利： US6600873B1 . 2003-07-29

  机译： 用于检测修改的色同步信号以防止复制视频节目的方法和设备

• 1. Nonconvex Quadratic Programming Method for κ-Coloring Problem: Algorithm and Computation [J] . Cao Jiaming 现代交通学报（英文版） . 1994,第002期
• 2. Nonconvex Quadratic Programming Method for k－Coloring Problem：Algorithm and Computation [J] . 现代交通学报：英文版 . 1994,第002期
• 3. Method for Incorporation of Controllability in Heat Exchanger Network Synthesis by Integrating Mathematical Programming and Knowledge Engineering [J] . 李志红 中国化学工程学报：英文版 . 2002,第006期
• 4. A Method of Traffic Sign Detecting Based on Color Similarity [C] . Lin Chuan, Pan Shenghui, Zhang Fan, Third International Measuring Technology and Mechatronics Automation . 2011
• 5. Remote Sensing Methods and Applications for Detecting Change in Forest Ecosystems [D] . Gudex-Cross, David J. 2018
• 6. A scale-space method for detecting recurrent DNA copy number changes with analytical false discovery rate control [O] . Ewald van Dyk, Marcel J.T. Reinders, Lodewyk F.A. Wessels 2013
• 7. ACC/AHA 2002 guideline update for exercise testing: summary article A report of the American college of cardiology/American heart association task force on practice guidelines (committee to update the 1997 exercise testing guidelines) 11The ACC/AHA Task Force on Practice Guidelines makes every effort to avoid any actual or potential conflicts of interest that might arise as a result of an outside relationship or personal interest of a member of the writing panel. Specifically, all members of the writing panel are asked to provide disclosure statements of all such relationships that might be perceived as real or potential conflicts of interest. These statements are reviewed by the parent task force, reported orally to all members of the writing panel at the first meeting, and updated as changes occur.22This document was approved by the American College of Cardiology Foundation Board of Trustees in July 2002 and by the American Heart Association Science Advisory and Coordinating Committee in June 2002. When citing this document, the American College of Cardiology Foundation and the American Heart Association would appreciate the following citation format: Gibbons RJ, Balady GJ, Bricker JT, Chaitman BR, Fletcher GF, Froelicher VF, Mark DB, McCallister BD, Mooss AN, O’Reilly MG, Winters WL Jr. ACC/AHA 2002 guideline update for exercise testing: summary article: a report of the ACC/AHA Task Force on Practice Guidelines (Committee to Update the 1997 Exercise Testing Guidelines). J Am Coll Cardiol 2002;40:1531–40.33Copies: This document is available on the World Wide Web sites of the ACC (www.acc.org) and the AHA (www.americanheart.org). A single copy of the complete guidelines is available by calling 800-253-4636 (US only) or writing the American College of Cardiology, Resource Center, 9111 Old Georgetown Road, Bethesda, MD 20814-1699. Ask for reprint No. 71-0231. To obtain a copy of the Executive Summary published in the October 1, 2002 issue of Circulation, ask for reprint No. 71-0232. To purchase additional reprints (specify version and reprint number): up to 999 copies, call 800-611-6083 (US only) or fax 413-665-2671; 1000 or more copies, call 410-528-4426, fax 410-528-4264, or e-mail kbradle@lww.com.44(J Am Coll Cardiol 2002;40:1531–40.)55©2002 by the American College of Cardiology Foundation and the American Heart Association, Inc. [O] . Gibbons Raymond J, Balady Gary J, Timothy Bricker J, 2002
• 8. Optimization of the Flat Panel Display Color and Color Coding Methods for Improved Diagnostic Performance of Soft-Copy Digital Mammography. [R] . Kanicki, J. 2001

• 1. Impact of a colorectal cancer screening program implantation on delays and prognosis of non-screening detected colorectal cancer [J] . Joaquin Cubiella ,María Lorenzo ,Franco Baiocchi . 世界胃肠病学杂志:英文版 . 2021,第39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. 测量镀膜中空玻璃颜色值推断单片镀膜玻璃颜色值的方法 [C] . 王秀丽 ,郭明 . 2009年中国玻璃行业年会暨技术研讨会 . 2009
• 4. 一种基于颜色和形状的人脸检测方法 [A] . 周宗恒 . 2001