Institute of Pharmacology and Toxicology Academy of Military Medical Sciences Pla China

Boe Technology Group Co., Ltd.

Hefei Boe Display Technology Co., Ltd.

Beijing Boe Technology Development Co., Ltd.

China University of Petroleum

Beijing Boe Health Technology Co., Ltd.

Chinese Academy of Sciences

China National Petroleum Corporation

Ieit Systems Co., Ltd.

Chinese Academy of Medical Sciences

Hongliang Wang

Song Li

Wu Zhong

Junhai Xiao

Zhibing Zheng

Xinbo Zhou

Xingzhou Li

Yunde Xie

Xiaokui Wang

Ke Dai

Lili Wang

Lin Zhang

Guoming Zhao

Xian Wei Zhang

Fang Zhai

Yanyang Hu

Gang Wang

Lei Guo

Yanping Liao

Lin Li

Yang Sun

Feng Guo

Chunming Xu

Jinsen Gao

Wei Liu

Lan Jiang

Hualin Liao

Chengyu Jiang

Jilei Niu

Ruiyuan Cao

Baojian Shen

Yuling Liu

Guoqiang Zhang

Xuejun Xia

Jiao Huang

Wujun Dong

Fuchen Tian

Shuai Yang

Lin Dong

Renyun Wang

Yandong Yang

Zhihui Song

Haolin Liu

Shengcai Lu

Yubin Zhou

Changyin Dong

Dujia Jin

Cuiping Zhou

Fangyuan Cao

Libao Xu

Xiaoye Zhang

Yue Xu

Wenhao Ma

Chenggang Li

Shuan Rao

Xian Zhang

Disclosed are an asynchronous FIFO read/write control method and system, and an electronic device, belonging to the technical field of data read/write technology. The asynchronous FIFO read/write control method comprises: parsing data received by a front-end interface to obtain a data packet length and valid video data; determining an almost empty threshold of a first FIFO queue and a second FIFO queue according to the data packet length, and writing the valid video data into the first FIFO queue and the second FIFO queue in a ping-pong manner; determining a minimum time interval of FIFO readings according to a sending time sequence of a back-end interface, and reading data from the first FIFO queue and the second FIFO queue in the ping-pong manner according to the almost empty threshold and the minimum time interval, so as to output the read data through the back-end interface.

Asynchronous FIFO read/write control method and system, and electronic device

A public event administrating system is disclosed. The public event involves a plurality of individuals and the administrating system includes: a data collecting module, a data processing module, a medical resource scheduling module, and a grid administrating module. The data collecting module is configured to acquire initial data about the public event from a plurality of data sources. The data processing module is configured to process the initial data to acquire processed data. The medical resource scheduling module is configured to receive an individual service request and allocate currently available medical resources to an individual requesting service at least according to the individual service request. And, the grid administrating module is configured to divide a geographic region managed by the administrating system into a plurality of grids, and assign a plurality of grid administrators to the plurality of grids to respectively administrate individuals in the plurality of grids.

Public event administrating system

A data processing method, a detection device administration server, a user terminal, a network server, and a data processing system are provided. The data processing method is applicable to a detection device administration server and includes: communicating with a first detection device; sending, in response to a user terminal of a user binding the first detection device through first identification information of the first detection device, a first detection request to the first detection device; and receiving, after the user completes the first detection, first detection data sent by the first detection device.

Data processing method, user terminal and servers

The present disclosure relates to a display panel. The display panel may include a first substrate, a second substrate opposite the first substrate, and a frame supporting structure between the first substrate and the second substrate in a frame area of the display panel. The frame area of the display panel may surround a display area of the display panel. The frame supporting structure may include a first frame supporting portion on at least one part of a circumference of the display area, the first frame supporting portion comprises an elastic material, and an elastic recovery rate of the elastic material is above about 80%.

Display panel and preparation method thereof

According to a liquid crystal display panel and a display device in the present disclosure, since at least one of a first polarizer and a second polarizer has a light scattering structure, polarized light of corresponding colors transmitted by sub-pixel units with different colors in a liquid crystal display structure can be uniformly diffused by the light scattering structure. That is to say, the light scattering structure plays a role for uniformly mixing the polarized light of different colors. Therefore, the rainbow pattern phenomenon is effectively improved or even eliminated, and the display quality is improved.

Liquid crystal display panel and display device

A display panel having a display area and a peripheral area is provided. The display panel includes a first display substrate; a second display substrate facing the first display substrate; a sealant layer in the peripheral area and between the first display substrate and the second display substrate, configured to seal the first display substrate and the second display substrate together to form a cell; and an elastic support layer in the peripheral area and between the first display substrate and the second display substrate. The elastic support layer encircled by the sealant layer and spaced apart from the sealant layer. The elastic support layer substantially surrounds the display area. The elastic support layer is configured to be in direct contact with the first display substrate and in direct contact with the second display substrate.

Display panel, display apparatus, method of fabricating display panel, and operating method of operating display panel

A simulation device for integrated evaluation experiment for sand control wellbore plugging and plugging removal, including a wellbore system, a whole sand control well plugging system, a local sand control well plugging system and a plugging removal system. The wellbore system simulates downhole working conditions of the sand control wellbore. Perforations of the whole sand control well plugging system and sand-filled pipe of the local sand control well plugging system are applied on the casing pipe of the wellbore system. The plugging process of the sand control well system is simulated by pumping a sand-laden slurry into the wellbore system. The plugging removal process is simulated by setting the plugging removal tool of plugging removal system through an oil tube in the wellbore system. The plugging removal effect of the plugging removal tool is analyzed and evaluated according to the reliable data measured by the pressure gauge, flowmeter, etc.

Simulation device and method for integrated evaluation experiment for sand control wellbore plugging and plugging removal

The present invention relates to a 2,3-epoxy succinyl derivative, a preparation method and a use thereof, in particular, the present invention relates to a compound represented by Formula (1), a racemate or an optical isomer thereof, a solvate thereof, or a pharmaceutically acceptable salt thereof. The compound according to the present invention has good inhibitory activity and/or selectivity against cathepsin, especially Cathepsin B, can be used in the treatment of multiple diseases associated with cathepsin, for example, osteoporosis, rheumatoid arthritis and osteoarthritis that are associated with Cathepsin K, Ebola virus infection, a degenerative disease and an autoimmune disease that are associated with Cathepsin L, S, especially Cathepsin B-related tumor diseases, such as gastric cancer, cervical cancer, lung cancer, breast cancer, prostate cancer, bladder cancer, colon cancer, neuroglioma, and melanoma. 

2,3-epoxy succinyl derivative, preparation method and use thereof

The present invention relates to a compound represented by Formula I, a racemate or optical isomer thereof, or a pharmaceutically acceptable salt, a solvate or a hydrate thereof, a pharmaceutical composition comprising the compound, and a use thereof in the manufacture of a medicament for preventing and/or treating a disease or disorder associated with a viral infection. 

4-oxo-4,5-dihydrothiazole derivative, preparation method and use thereof

Provided are an insulin-lipid complex, a preparation method thereof, and a formulation thereof. The insulin-lipid complex is prepared by compounding insulin and a lipid material in an organic solvent system containing a low boiling point acid, and drying. The mass ratio of insulin to the lipid material is 1:3&#x2dc;1:20. An oil solution of the insulin-lipid complex and vesicles containing insulin are further provided.

Insulin-lipid complex, preparation method therefor, and preparation thereof

The present invention provides a method for processing low-grade heavy oil, comprising: providing a riser-bed reactor; preheating the low-grade heavy oil and injecting it into the riser reactor to react with solid catalyst particles at the temperature of 550-610&#xb0; C.; oil-gas, after reacting with the solid catalyst particles in the riser reactor, being introduced into the fluidized bed reactor to continue to react at temperature of 440-520&#xb0; C. and weight hourly space velocity of 0.5-5 h; and the oil-gas, after reacting in the fluidized bed reactor, being separated from coked solid catalyst particles carried therein, and the separated oil-gas being introduced into a fractionation system. The method can effectively remove carbon residues, heavy metals, asphaltenes and other impurities from the low-grade heavy oil, and obtain high liquid product yield in a simple process.

Method of processing low-grade heavy oil

Disclosed are pyridazine derivatives represented by Formula I or pharmaceutically acceptable salts or hydrates thereof, pharmaceutical compositions comprising the compounds, methods of treating and/or preventing diseases or disorders associated with viral infections in patients using the compounds, and the use of the compounds in preparing the medicaments for treating and/or preventing diseases or disorders associated with viral infections. The compounds represented by Formula I have antiviral activity, especially anti-microRNA viral activity. Symbols in the compounds represented are described in the specification. 

Pyridazine derivatives and use thereof as medicaments for treating microRNA viral infection

Disclosed is as a substituted thiazolamine derivative represented by Formula I or a pharmaceutically acceptable salt thereof or a hydrate thereof (the definitions of each group in the formula are as presented in the description), and the application thereof in the prevention and/or treatment of viral diseases induced by picornavirus. Also disclosed is a pharmaceutical composition containing the compound. 

Thiazolamine derivative and use thereof as anti-picornaviral infection medicament

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Beijing, China

Hongliang Wang