METHOD OF PREPARING COLUMNAR BODY OF FOLDED PRINTED PAPER AND STACKER FOR COLUMNAR BODY FOR SAID METHOD

• 1. 一种树脂表面亲水化方法、等离子体处理装置、叠层体、及叠层体的制备方法 [P] . 中国专利： CN113841217A . 2021-12-24
• 2. 叠层体缺陷部位的表示方法 [P] . 中国专利： CN100388094C . 2008.05.14
• 3. RESIN COMPOSITION FOR COLUMNAR FORMED BODIES, METHOD FOR PRODUCING SUBSTRATE WITH COLUMNAR FORMED BODY, AND SUBSTRATE WITH COLUMNAR FORMED BODY [P] . 世界知识产权组织专利： WO2016076252A1 . 2016-05-19

  机译： 立柱式车身的树脂组成，用立柱式车身制造基质的方法以及用立柱式车身的基质

• 4. METHOD FOR LEADING GROUNDING CONDUCTOR INTO COLUMNAR BODY, SUCH AS HOLLOW POLE, BETWEEN PAIR OF UPPER AND LOWER LEAD-IN HOLES IN THE COLUMNAR BODY AND GRIPPING TOOL FOR ROPE FOR LEADING GROUNDING CONDUCTOR IN THE COLUMNAR BODY [P] . 日本专利： JP2001025117A . 2001-01-26

  机译： 在上，下铅垂对中将接地导体引入圆柱体（例如空心柱）的方法和用于在接地体中导引接地线的夹线工具

• 5. Caulked assembly of metal plate body with columnar body, caulked assembly of resin molded body with columnar body, and method for producing the same [P] . 美国专利： US7918007B2 . 2011-04-05

  机译： 金属板体与柱状体的铆接组件，树脂成型体与柱状体的铆接组件及其制造方法

• 1. 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
• 2. Nanobody-based immunosensing methods for safeguarding public health [J] . Jiarong Zhang, Hui Sun, Wei Pei, 生物医学研究杂志：英文版 . 2021,第004期
• 3. Analysis on the Applicability of the Post-stack Seismic Attribute Recognition Method in the Sand Bodies of the River-way of Fuyang Oil Layer [C] . Xinrong ZHANG, Shi FANG, Jinping LIU, International Symposium on Linear Drives for Industry Applications . 2013
• 4. Development and Testing of Manufacturing Methods for a Piezoelectric Composite Stacked Generator to Improve the Success Rate of Interbody Spinal Fusion [D] . Tobaben, Eric 2014
• 5. A Method for Preparing Photographs of Petri Dish Cultures by Direct Contact Printing on Photographic Paper [O] . John T. Buchholz, I. M. Lewis 1930
• 6. ABSTRACT Various body parts or organs can be analysed to identify the different diseases in the human body. Fingernail analysis is one of the ways to identify disease in the human body. Nails are the body part which are farthest from the heart and therefore receive oxygen at last. As a result the nails are the first who show the symptoms of a disease in the human body. Fingernails can be easily captured for diagnosis and there are no heavy equipment or no specific conditions required to use nail image for disease diagnosis, like in other tests and scanning processes. Human nails deliver beneficial information about complaints or any nutritive imbalances in the human body depending upon their shape, texture and colour. In human beings, numerous systemic and skin diseases can be easily analyzed through careful examination of nails of both the limbs. A lot of nail illnesses have been found to be primary signs of numerous underlying systemic illnesses. The colour, texture or shape changes in nails are signs of many diseases mainly affecting nails. Considering all these properties of nails a system is proposed that uses digital image processing (DIP) methods for identifying such changes in the human nail to get more precise results and predict numerous diseases effortlessly. With the emerging Internet of Things (IOT) concept the generated report is made available remotely, this will help users to reduce transportation efforts. As the system has to deal with large and private data, the security of data must be ensured. To keep the data confidential, the Blockchain concept which is one of the most emerging concepts in the field of data management is used. The paper contains the implementation of the digital image processing for feature extraction of nail images, usage of IOT (ThingSpeak cloud) for data storage and implementation of Blockchain to keep the system secured and theft free. KEY WORDS: Int ernet of thin gs (IOT), Image proc essin g, Thin gSpeak, RG B vavalues, Mean pi xel vavalues, Bloc kchain , Hash key. Disease Diagnostic System: Abnormalities in Human Nail [O] . Pranav S. Wazarkar 2020

• 1. 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
• 2. A Novel Human Antibody,HF,against HER2/erb-B2 Obtained by a Computer-Aided Antibody Design Method [J] . Chunxia Qiao ,Ming Lv ,Xinying Li . 工程(英文) . 2021,第11期
• 3. Recent Developments in SARS-CoV-2 Neutralizing Antibody Detection Methods [J] . Jo-Lewis BANGA NDZOUBOUKOU ,Yan-di ZHANG ,Xiong-lin FAN . 当代医学科学(英文) . 2021,第6期
• 4. 基于”产品工程”的中药浸膏粉体定向设计研究策略与制备方法探讨 [C] . ZHU Hua-xu ,朱华旭 ,唐志书 . 2016中国中药制剂大会暨世界中医药学会中药新型给药系统专业委员会第七届学术年会、世界中医药学会中药药剂专业委员会第十一届学术年会、中华中医药学会制剂分会第十七次学术年会 . 2016
• 5. 原位生长柱状晶复合增韧氧化铝陶瓷制备方法及机理研究 [A] . 荣守范 . 2008