in the process epigenitique biosynthese proteins by resonnance effect

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• 2. ［S,S］-EDDS生物合成基因和蛋白和用于生物合成S,S-EDDS的方法 [P] . 中国专利： CN105849083A . 2016-08-10
• 3. in the process epigenetique biosynthese proteins by resonance effect [P] . TNSN93061A1 . 1994-03-17

  机译： 在表观遗传生物合成过程中通过共振作用

• 4. inhibitors of cholesterol biosynthese compounds, their process of preparatio and biosynthese cholesterol. the process of preparation and their therapeutic application. [P] . BE888332A . 1981-10-08

  机译： 胆固醇生物合成化合物的抑制剂，其制备和合成胆固醇的过程。制备过程及其治疗应用。

• 5. process for the production of a protein by biosynthese [P] . RO87225A2 . 1985-12-20

  机译： 生物合成生产蛋白质的方法

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• 1. Changes in physicochemical properties of proteins in Kayserian Pastirma made from the M.semimembranosus muscle of cows during traditional processing [J] . Abdulatef Mrghni Ahhmed ,Gen Kaneko ,Hideki Ushio . 食品科学与人类健康（英文） . 2013,第1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. 一氧化氮合成酶抑制剂对牛肉成熟过程中钙蛋白酶活性和蛋白质降解的影响 [C] . ZHANG Chaoyang ,张朝阳 ,LIU Rui . 第十四届中国肉类科技大会 . 2016
• 4. 表面等离子体共振效应对电荷转移过程影响的SERS探究 [A] . 郭霖 . 2021