Institution
Renji Hospital
Healthcare•Shanghai, China•
About: Renji Hospital is a healthcare organization based out in Shanghai, China. It is known for research contribution in the topics: Medicine & Biology. The organization has 1112 authors who have published 714 publications receiving 15442 citations. The organization is also known as: Rénjì Yīyuàn.
Topics: Medicine, Biology, Internal medicine, Chemistry, Cancer
Papers published on a yearly basis
Papers
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TL;DR: Compared with montelukast, low-dose budesonide led to fewer exacerbation events, lower costs, and slightly more quality-adjusted life years over 1 year, which may improve the use of low- dose budesonides, an economically and clinically preferable treatment in pediatric patients.
Abstract: Aim: To compare the cost-effectiveness of low-dose budesonide versus montelukast among patients aged 1-5 years from a Chinese patient and healthcare payer perspective. Materials & methods: A Markov model based on exacerbation states was developed. Exacerbation was defined as the need for rescue therapy (mild exacerbation) or hoscopitalization (moderate-to-severe exacerbation). Inputs including efficacy (i.e., exacerbation rates), mortality, utilities, costs and treatment adherence were obtained from literature. Results: Compared with montelukast, low-dose budesonide led to fewer exacerbation events (1.44 vs 2.15), lower costs (¥3675 vs 4130) and slightly more quality-adjusted life years (0.974 vs 0.967) over 1 year. Conclusion: These findings may improve the use of low-dose budesonide, an economically and clinically preferable treatment to montelukast in pediatric patients.
2 citations
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TL;DR: In this article , a dual-targeting circular aptamer (DTCA) was proposed to enhance the recognition power of monovalent aptamers in oncology, which can recognize two different biomarkers on living cells to augment aptamer-receptor interactions.
Abstract: Currently, the broad use of monovalent aptamers in oncology faces challenges, including insufficient recognition and internalization caused by a finite number of receptors on the cell surface, as well as a confined recognition spectrum. Herein, we describe the development of a dual-targeting circular aptamer (DTCA) that can recognize two different biomarkers on living cells to augment aptamer–receptor interactions, thus enhancing recognition of the target cells. This improvement not only boosts binding and internalization abilities, but also expands the recognition spectrum of these aptamers to different leukemia cells. Moreover, the stability of DTCA in serum can be significantly improved by an enzyme-promoted terminal ligation strategy. The chemical incorporation of 5-fluorodeoxyuridine into DTCA resulted in a pharmaceutically functional aptamer that exhibited excellent selectivity, as demonstrated by its high cytotoxicity against target cancer cells, but not to normal cells. The superiority of our newly developed strategy was further highlighted by its precise tumor-imaging capability.
2 citations
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TL;DR: It is indicated that antigenic epitope of beta 2 GP1 might be located in its fifth domain and detection of anti-r beta 2GP1 antibodies may be of potential value for evaluating the risk of thrombosis and/or other APS associated symptom.
Abstract: OBJECTIVE To investigate cloning and expression of beta 2-glycoprotein 1 (beta 2GP1) recognized by antiphospholipid antibodies and to study the clinical significance of anti-beta 2GP1 antibodies in patients with autoimmune disease. METHODS By using reverse transcription-PCR method, two kinds of expression plasmid which expressed beta 2GP1 and the fifth domain of beta 2-glycoprotein 1 (beta 2GP1-D5) proteins respectively were constructed in this study. Their antigenic activities were identified by immunoblots using rabbit anti-beta 2GP1 antibodies. Anti-r beta 2GP1 and anti-r beta 2GP1-D5 antibodies in the 112 patents were detected by ELISA using r beta 2GP1 and r beta 2GP1-D5 as coating antigens. RESULTS A significant correlation in statistics (r = 0.667, P < 0.01) between the levels of anti-r beta 2GP1 and anticardiolipin antibodies (aCL) was found. The presence of anti-r beta 2GP1 antibodies was associated with an increased frequency of history of thrombosis and/or recurrent abortion. Anti-r beta 2GP1 assay provided better specificity than conventional aCL assay. The binding of anti-r beta 2GP1 from the sera of patients with antiphospholipid syndrome (APS) to r beta 2GP1 was inhibited by r beta 2GP1-D5. Meanwhile, of 28 patients who had positive anti-r beta 2GP1 antibodies in sera, 27 (96.4%) had positive anti-r beta 2GP1-D5 antibodies. CONCLUSION It is indicated that antigenic epitope of beta 2 GP1 might be located in its fifth domain. Detection of anti-r beta 2GP1 antibodies may be of potential value for evaluating the risk of thrombosis and/or other APS associated symptom.
2 citations
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TL;DR: In this paper , self-stable precipitation polymerization was used to prepare an enzyme-immobilized microsphere composite, which was successfully immobilized on Ni2+ charged pyridine-derived particles.
Abstract: Self-stable precipitation polymerization was used to prepare an enzyme-immobilized microsphere composite. Phosphomannose isomerase (PMI) with His-tag was successfully immobilized on Ni2+ charged pyridine-derived particles. The maximum amount of PMI immobilized on such particles was ∼184 mg/g. Compared with free enzyme, the activity of the immobilized enzymes was significantly improved. In addition, the immobilized enzymes showed a much better thermostability than free enzymes. At the same time, the immobilized enzymes can be reused for multiple reaction cycles. We observed that the enzyme activity did not decrease significantly after six cycles. We conclude that the pyridine-derived particles can be used to selectively immobilize His-tagged enzymes, which can couple the enzyme purification and catalysis steps and improve the efficiency of enzyme-catalyzed industrial processes.
2 citations
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TL;DR: The risk factors for conversion of LC to OC were attacks of acute cholecystitis, the length of disease, tenderness of upper abdomen, thickening of gallbladder wall and hydrops of gall Bladder.
Abstract: Objective To investigate the risk factors for conversion from laparoscopic(LC) to open cholecystectomy(OC).Methods The clinical data of 2 850 cases of LC were retrospectively analyzed.Results The occurrence rate of conversion was 4.03%.The risk factors for LC conversion to open procedurecomprised:two or more attacks of acute cholecystitis in recent 6 months;history of cholecysfifis2 years;appearedrigh quadrent abdominal signs,thickness of gallbladder wall≥3 mm;and hydrops of gallbladder.Conclusions The risk factors for conversion of LC to OC were attacks of acute cholecystitis,the length of disease,tenderness of upper abdomen,thickening of gallbladder wall and hydrops of gallbladder.A detailed history,clinical examination with suitable imaging test,proper selection of patients and improving the skill of operators,may decrease the occurrence of the LC conversion rate and the complicationafter operation.OC should be selected for the patients with the above risk factors.
2 citations
Authors
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Name | H-index | Papers | Citations |
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Jaap Stoker | 66 | 404 | 15532 |
Nan Shen | 56 | 238 | 13592 |
Carola G. Vinuesa | 54 | 128 | 17433 |
Jing-Yuan Fang | 54 | 289 | 10826 |
Honglan Li | 53 | 199 | 8285 |
Matthew C. Cook | 43 | 119 | 9708 |
Guido N. J. Tytgat | 40 | 102 | 6175 |
Jianrong Xu | 37 | 226 | 4915 |
Eric J.H. Meuleman | 37 | 126 | 6184 |
Xiong Ma | 35 | 127 | 3587 |
Gang Huang | 34 | 116 | 3122 |
Jinke Cheng | 33 | 97 | 4120 |
Jie Xu | 32 | 83 | 3150 |
Steven R. Lindheim | 30 | 186 | 3594 |
Qiang Wu | 29 | 75 | 4203 |