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11篇 您的检索式:作者名="Eleazer D"
    题名 作者 年代 出处 被引量
1Flare-up rate in pulpally necrotic molors in one-visit versus two-visit endodontic treatment显示文摘Eleazer P D Eleazer K R 0,,09:1
2Flare up rate in pulpally necrotic molars in one visit versus two visit endodontic treatment显示文摘Eleazer P D Eleazer K R 0,,05:1
3Clearance of biofilms from dental unit waterlines through the use of hydroperoxide ion-phase transfer catalysts显示文摘P A Shepherd M A Shojaei P D Eleazer 2001Quintessence International Dental Digest2001,32,10:1
4A comparison of torque required to fracture rotary files with tips bound in simulated curved canal显示文摘Guilford W I Lemons F E Eleazer P D 2005J Endod2005,31,:1
5Flare-up rate in pulpally necrotic molars in, one-visit versus two-visit endodontic treatment显示文摘Eleazer P D Eleazer K R 1998Journal of Endodontics1998,24,9:1
6Detoxification of endotoxin by endodontic irrigants and calcium hydroxide显示文摘Buck R A Cai J Eleazer P D 2001J Endod2001,27,5:1
7Detoxification of endotoxin by endodonfic imgants and caleinm hydroxide 显示文摘Buckra P Eleazer D 2001J Endod2001,27,5:1
8Flare - up rate in pnlpally necrot- ic molars in one -visit versus two -visit endodontic treatment显示文摘ELEAZER P D ELEAZER K R 1998J Endodon1998,24,9:1
9Geriatric content in medical school curricula: results of a national survey显示文摘Eleazer GP Doshi R Wieland D 2005J Am Geriatr Soc2005,53,1:1
10Hare-up rate in pulpally necrotic molors in one visit verustw-visit endodontic treatment显示文摘Eleazer D Eleazer K 1998J Endod1998,24,9:1
11Inhibition of Rgs10 Expression Prevents Immune Cell Infiltration in Bacteria-induced Inflammatory Lesions and Osteoclast-mediated Bone Destruction显示文摘Regulator of G-protein Signaling 10(Rgs10)plays an important function in osteoclast differentiation.However,the role of Rgs10 in immune cells and inflammatory responses,which activate osteoclasts in inflammatory lesions,such as bacteria-induced periodontal disease lesions,remains largely unknown.In this study,we used an adeno-associated virus(AAV-)mediated RNAi(AAV-shRNA-Rgs10)knockdown approach to study Rgs10’s function in immune cells and osteoclasts in bacteria-induced inflammatory lesions in a mouse model of periodontal disease.We found that AAV-shRNA-Rgs10 mediated Rgs10 knockdown impaired osteoclastogenesis and osteoclast-mediated bone resorption,in vitro and in vivo.Interestingly,local injection of AAV-shRNA-Rgs10 into the periodontal tissues in the bacteria-induced inflammatory lesion greatly decreased the number of dendritic cells,T-cells and osteoclasts,and protected the periodontal tissues from local inflammatory damage and bone destruction.Importantly,AAV-mediated Rgs10 knockdown also reduced local expression of osteoclast markers and pro-inflammatory cytokines.Our results demonstrate that AAVshRNA-Rgs10 knockdown in periodontal disease tissues can prevent bone resorption and inflammation simultaneously.Our data indicate that Rgs10 may regulate dendritic cell proliferation and maturation,as well as the subsequent stimulation of T-cell proliferation and maturation,and osteoclast differentiation and activation.Our study suggests that AAV-shRNA-Rgs10 can be useful as a therapeutic treatment of periodontal disease.Sen Yang Liang Hao Matthew McConnell Xuedong Zhou Min Wang Yan Zhang John D Mountz Michael Reddy Paul D. Eleazer Yi-Ping Li Wei Chen 2013Bone Research2013,1,3:0
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