Training content creation controller, training content creation control method and training content creation control program

• 1. 程序创建辅助装置、程序创建辅助装置的控制方法、以及程序创建辅助装置的控制程序 [P] . 中国专利： CN108780306A . 2018-11-09
• 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. Training content creation controller, training content creation control method and training content creation control program [P] . JPWO2021019799A1 . 2021-09-13

  机译： 培训内容创建控制器，培训内容创建控制方法和培训内容创建控制程序

• 4. Training content creation device, training content creation method, and training content creation program [P] . JP6928724B2 . 2021-09-01

  机译： 培训内容创建设备，培训内容创建方法和培训内容创建程序

• 5. Training content creation device, training content creating method and training content creation program [P] . JPWO2021019598A1 . 2021-09-13

  机译： 培训内容创建设备，培训内容创建方法和培训内容创建程序

• 1. Content Creation and Production Choice： Film, Television and Related Production Enterprises [J] . Michael B. Hoggan 新闻与大众传媒：英文版 . 2017,第005期
• 2. A nurse-led long-term pelvic floor muscle training program in the management of female patients with overactive bladder e A study protocol for a randomized controlled trial [J] . Tu-Zhen Xu, Qiu-Hua Sun, Xiao Huang, 国际护理科学（英文） . 2015,第002期
• 3. MATERIAL PROTECTION, CONTROL, AND ACCOUNTING (MPCA) TRAINING NEEDS ASSESSMENT AND PROPOSAL FOR THE CREATION OF A NATIONAL TRAINING CENTER IN THE REPUBLIC OF KAZAKHSTAN [C] . T. Zhantikin, A. Kim, T. Dairbekov, INMM annual meeting . 2008
• 4. Enhancing Training Outcomes in the Context of e-Learning: The Impact of Objective Learner Control, Training Content Complexity, Cognitive Load, Learning Goal Orientation, and Metacognitive Strategies. [D] . Granger, Benjamin P. 2012
• 5. Creation of novel training programmes mapped to the Joint Royal Colleges of Physicians Training Board Internal Medicine stage 1 curriculum [O] . Marie McNulty, Elizabeth Carty, Indranil Chakravorty, 2019
• 6. Modeling the Process of Development and Creation of the Professional Training Content for Applied Bachelors [O] . V.A. Shterenzon 2020

• 1. Creation of a Training Course Program for Cancer-Patient Group Facilitators and Its Effects [J] . Masami Chujo . 护理学期刊（英文） . 2017,第2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. Creation of Digital Content as a Service Learning in Teaching Foreign Language in High School [J] . Héctor Rubén Ríos Santana . 中美英语教学 . 2021,第009期
• 4. 使用气体或其他低闪点燃料船舶船员培训内容与实施建议 [C] . 曹亮 ,张守俊 ,李荣辉 . 中国交通教育研究会航海教育研究分会2020年学术年会 . 2020
• 5. 艺术类体育舞蹈专项考生考前培训内容优化措施研究 [A] . 陈思宇 . 2020